Patent Application
20220267829
The present invention relates to the field of multiplex based viral pathogen detection and analysis. More particularly, the present invention relates to detecting the presence of clade variants of SARS-COVID-2 virus in patient and environmental samples.
The COVID-19 pandemic has increased awareness that viral infection can be an existential threat to health, public safety and the US economy. More fundamentally, there is a recognition that the viral risks are exceedingly dangerous and complex and require new approaches to diagnostics and screening.
The next pandemic wave is expected to have more pronounced flu-like symptoms (seasonal influenza A and/or B) coupled with the COVID-19, or COVID-19 variants that will coexist with the Coronavirus already responsible for the common cold. These complexities are expected to pose significant challenges to public health and the healthcare system in diagnosing multi-symptom conditions accurately and efficiently.
The COVID-19 pandemic has also led to the realization of an additional level of complexity that the realization that human health and environmental contamination are linked in a fundamental way that affects collection efficiency and increases risk to the healthcare workers (1, 2). Alternatives to nasopharyngeal collection methods such as for example, saliva collection are needed to enable scalability among millions of individuals.
Q-RT-PCR technology has dominated COVID-19 diagnostics and public health screening. Independent of the test developer, Q-RT-PCR has been shown to have an unusually high false negative rate (15% up to 30%). As of May 2020, the CDC has recorded 613, 041 COVID-19 tests. With a 15% false negative rate, approximately 91, 956 people would thus be falsely classified as free of infection. Meta-analysis has shown that the false negative rate for Q-RT-PCR is high below day 7 of infection when viral load is still low. This renders Q-RT-PCR ineffective as a tool for early detection of weak symptomatic carriers while also lessening its value in epidemiology.
As for other organisms, genetic variations in SARS-COVID-2 are grouped into clades. There are over 52, 600 complete and high-coverage genomes available on the Global Initiative on Sharing Avian Influenza Data (GISAID). Presently, WHO has identified 10, 022 SARS-COVID-2 genomes from 68 different countries and detected 65, 776 variants and 5, 775 distinct variants that comprised missense mutations, synonymous mutations, mutations in non-coding regions, non-coding deletions, in-frame deletions, non-coding insertions, stop-gained variants, frameshift deletions and in-frame insertions among others. Identifying these clade variants in population and environmental samples while a daunting task, is critical for global public health management directed to controlling the pandemic.
When first identified, it was widely assumed that COVID-19 would mutate slowly, based on a relatively stable genome that would experience minimal genetic drift as the pandemic spread. Unfortunately, perhaps as a function of environmental selection pressure (crowding) physical selection pressure (PPE) and therapeutic selection pressure (vaccination) the original Wuhan clade has evolved into a very large number of clade variants. Consequently, in the past 3 months there has been an international effort to discover and track the full range of clade variant evolution.
Next Generation Sequencing (NGS), primarily Targeted Resequencing of the CoV-2 Spike gene, has been instrumental in elucidating the patterns of genetic variation which define the growing set of clade variants of present international concern (UK, South Africa, Brazil, India, US California, US NY, US Southern) with others emerging at an expanding rate. Whereas NGS is without equal as a discovery tool in genetic epidemiology, it is not ideally suited for field-deployed, public health screening at population scale due to complexities associated with purchasing and managing the kits supply chain, setting up and training personnel, especially when compared to Q-RT-PCR, which is the present standard for nucleic acid based COVID-19 screening. Conversely, while Q-RT-PCR (especially TaqMan) is now the clear standard in COVID-19 testing laboratories for simple positive/negative screening, its suitability for screening clade variants is limited. Deploying TaqMan for COVID-19 clade Identification requires running about 10-15 TaqMan kits on each sample to generate sequence content equivalent to Spike targeted NGS, thereby negating the benefits of costs and logistics with Q-RT-PCR.
Thus, there is a need in the art for superior tools to not only administer and stabilize sample collection for respiratory viruses from millions of samples in parallel obtained from diverse locations including, clinic, home, work, school and in transportation hubs, but also to detect and identify clade variants in the population at the highest levels of sensitivity and specificity. The present invention fulfills this longstanding need and desire in the art.
The present invention is directed to a method for detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a subject. In the method a sample is obtained from the subject and total RNA is isolated therefrom. In a single assay a combined reverse transcription and asymmetric PCR amplification reaction is performed on the total RNA using a plurality of fluorescently labeled primer pairs comprising an unlabeled primer and a fluorescently labeled primer that are selective for target sequences within a Spike gene in the SARS-CoV-2 virus to generate a plurality of fluorescent labeled SARS-CoV-2 amplicons. The plurality of fluorescently labeled SARS-CoV-2 amplicons are hybridized to a plurality of nucleic acid probes comprising universal probes, wild type probes and mutant probes, each having a sequence that specifically base-pairs with one of the target sequences in the fluorescently labeled SARS-CoV-2 amplicons and at least one control probe to which the fluorescently labeled SARS-CoV-2 amplicons do not hybridize and where each of the nucleic acid probes is attached to specific positions on a solid microarray support. The microarray is washed at least once. The microarray is imaged to detect fluorescent signals above a threshold for all the nucleic acid probes upon hybridization to the fluorescently labeled SARS-CoV-2 amplicons.
The present invention is directed to a related method for detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a subject where the Spike gene is genotyped at each target sequence. In the related method further comprises measuring the fluorescent signal from hybridization of the fluorescently labeled SARS-CoV-2 amplicons to the wild type probes and from the hybridation of the fluorescently labeled SARS-CoV-2 amplicons to the mutant probes is measured at each of the target sequences. A relative size of the fluorescent signal from hybridization to the mutant probes vs. the fluorescent signal from hybridization to the wild type probes is analyzed directly to produce a hybridization pattern of wild type vs. mutant genotyping among all the target sites in SARS-CoV-2. The hybridization pattern is compared to a known pattern of wild type vs. mutant genotype variation among known SARS-CoV-2 variants to identify the SARS-CoV-2 in the sample as a known variant of concern or a known variant of interest or a combination thereof or as an unknown variant.
The present invention also is directed to a method for detecting, genotyping and identifying a variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) a subject. In the method a sample is obtained from the subject and total RNA is isolated therefrom. In a single assay a combined reverse transcription and asymmetric PCR amplification reaction is performed on the total RNA using a set of fluorescently labeled primer pairs, each comprising an unlabeled primer and a fluorescently labeled primer, that are selective for sequences within a Spike gene in the SARS-CoV-2 virus to generate a plurality of fluorescent labeled SARS-CoV-2 amplicons. The plurality of fluorescently labeled SARS-CoV-2 amplicons are hybridized to a plurality of nucleic acid probes comprising a set of universal probes, wild type probes and mutant probes, each having a sequence that specifically base-pairs with one of the target sequences in the fluorescently labeled SARS-CoV-2 amplicons and at least one control probe to which the fluorescently labeled SARS-CoV-2 amplicons do not hybridize and where each of the nucleic acid probes attached to a specific position on a solid microarray support. The microarray is washed at least once. The microarray is imaged to detect fluorescent signals above threshold for all the nucleic acid probes produced upon hybridization to the fluorescently labeled SARS-CoV-2 amplicons. At least N fluorescent signals above the threshold from hybridization of the fluorescently labeled SARS-CoV-2 amplicons to the universal probes are measured thereby detecting the SARS-CoV-2 in the sample. The Spike gene is genotyped at each target sequence. During genotyping the fluorescent signals from hybridization of the fluorescently labeled SARS-CoV-2 amplicons to the wild type probes and from the hybridation of the fluorescently labeled SARS-CoV-2 amplicons are compared to the mutant probes at each position on the microarray. A relative size of the fluorescent signal from hybridization to the mutant probes vs. the fluorescent signal from hybridization to the wild type probes is directly analyzed to produce a hybridization pattern of wild type vs. mutant genotyping at each target sequence in SARS-CoV-2. A variant of SARS-CoV-2 is identified as a known variant of concern or a known variant of interest or a combination thereof or as an unknown variant by comparing the hybridization pattern to a known pattern of wild type vs. mutant genotype variation among known SARS-CoV-2 variants.
Other and further aspects, features, and advantages of the present invention will be apparent from the following description of the presently preferred embodiments of the invention. These embodiments are given for the purpose of disclosure.
So that the matter in which the above-recited features, advantages and objects of the invention, as well as others which will become clear, are attained and can be understood in detail, more particular descriptions and certain embodiments of the invention briefly summarized above are illustrated in the appended drawings. These drawings form a part of the specification. It is to be noted, however, that the appended drawings illustrate preferred embodiments of the invention and therefore are not to be considered limiting in their scope.
As used herein, the term “a” or “an” when used in conjunction with the term “comprising” in the claims and/or the specification may mean “one,” but it is also consistent with the meaning of “one or more,” “at least one,” and “one or more than one.” Some embodiments of the invention may consist of or consist essentially of one or more elements, method steps, and/or methods of the invention. It is contemplated that any method described herein can be implemented with respect to any other method described herein.
As used herein, the term “or” in the claims is used to mean “and/or” unless explicitly indicated to refer to alternatives only or the alternatives are mutually exclusive, although the disclosure supports a definition that refers to only alternatives and “and/or”.
As used herein, “comprise” and its variations, such as “comprises” and “comprising” will be understood to imply the inclusion of a stated item, element or step or group of items, elements or steps but not the exclusion of any other item, element or step or group of items, elements or steps unless the context requires otherwise. Similarly, “another” or “other” may mean at least a second or more of the same or different claim element or components thereof.
In one embodiment of the present invention there is provided a method for detecting clade variants in a Coronavirus disease 2019 virus (COVID-19) in a sample, comprising obtaining the sample; harvesting viruses from the sample; isolating a total RNA from the harvested viruses; performing a combined reverse transcription and first amplification reaction on the total RNA using at least one first primer pair selective for all COVID-19 viruses to generate COVID-19 virus cDNA amplicons; performing a second amplification using the COVID-19 virus cDNA amplicons as template and at least one fluorescent labeled second primer pair selective for a target nucleotide sequence in the COVID-19 virus cDNA to generate at least one fluorescent labeled COVID-19 virus amplicon; hybridizing the fluorescent labeled COVID-19 virus amplicons to a plurality of nucleic acid probes, each having a sequence corresponding to a sequence determinant that discriminates among the clade variants of the COVID-19 virus, where the nucleic acid probes are attached to a solid microarray support; washing the microarray at least once; and imaging the microarray to detect at least one fluorescent signal from the hybridized fluorescent labeled COVID-19 virus amplicons, thereby detecting the clade variants of the COVID-19 virus in the sample. In a related embodiment after the imaging step, a step is performed of generating an intensity distribution profile from the at least one fluorescent signal that is unique to one of the clade variants thereby detecting the clade variant of the COVID-19 virus in the sample.
A total RNA potentially comprising RNA from COVID-19 virus and other contaminating pathogens and human cells is isolated from the sample. Commercially available RNA isolation kits such as for example, a Quick-DNA/RNA Viral MagBead Kit from Zymo Research are used for this purpose. The total RNA thus isolated is used without further purification. Alternatively, intact virus may be captured with magnetic beads, using kits such as that from Ceres Nanosciences (e.g., CERES NANOTRAP technology), or by first precipitating the virus with polyethylene glycol (PEG), followed by lysis of the enriched virus by heating with a “PCR-Friendly” lysis solution such as 1% NP40 in Tris-EDTA buffer and then used without additional purification.
The COVID-19 virus RNA in the total RNA isolate is used as a template for amplifying a COVID-19 virus specific sequence. This comprises first performing a combined reverse transcriptase enzyme catalyzed reverse transcription reaction and a first amplification reaction using a first primer pair selective for the virus to generate COVID-19 virus cDNA amplicons. In this embodiment, the first primer pairs have forward (odd numbers) and reverse (even number) sequences shown in SEQ ID NO: 1 to SEQ ID NO: 8 (Table 1).). Commercially available reverse transcriptase enzyme and buffers are used in this step. Controls including, but not limited to a RNAse P control having first primer pair (forward primer SEQ ID NO: 130, reverse primer SEQ ID NO: 131) are also used herein (Table 1). The COVID-19 virus cDNA amplicons generated in the first amplification reaction are used as a template for a second amplification that employs at least one fluorescent labeled second primer pair selective for a target nucleotide sequence in the COVID-19 virus cDNA to generate at least one fluorescent labeled COVID-19 virus amplicon.
The fluorescent labeled COVID-19 virus amplicons hybridize to the nucleic acid probes, which are attached at specific positions on a microarray support, for example, a 3-dimensional lattice microarray support. After hybridization, the microarray is washed at least once to remove unhybridized amplicons. Washed microarrays are imaged to detect a fluorescent signal from the hybridized fluorescent labeled COVID-19 virus amplicons to detect the Clade variants of the COVID-19 virus in the sample.
Further to this embodiment, prior to the harvesting step, the method comprises mixing the sample with an RNA stabilizer. A representative RNA stabilizer is a chemical stabilizer that protects the RNA from degradation during storage and transportation.
In both embodiments at least one of the fluorescent labeled second primer pair is selective for a panel of target nucleotide sequences within a target region of a gene in the COVID-19 virus; and the nucleic acid probes are specific to the target region of the gene, whereby the at least one fluorescent labeled COVID-19 virus amplicon generated is hybridized to the nucleic acid probe thereby discriminating the clade variants of the COVID-19 virus in the sample. Further to this embodiment the imaging and generating steps comprise detecting the at least one fluorescent signal from the hybridized at least one fluorescent labeled COVID-19 virus amplicons associated with the panel of target nucleotide sequences within the target region of the gene; and generating an intensity distribution profile unique to each of the clade variants, whereby each of the clade variants is distinguishable from others. Particularly, the gene may be a Spike gene.
In a non-limiting example, the target region may be in the Spike gene and/or Nucleoprotein gene in the COVID-19 virus and the fluorescent labeled second primer pairs may have forward (odd numbers) and reverse (even number) sequences shown in SEQ ID NO: 9 to SEQ ID NO: 29 (Tables 2 and 11) and the paired fluorescent labeled second primer sequences shown in Table 27. Controls including, but not limited to a RNAse P control having primer pair (forward primer SEQ ID NO: 132, reverse primer SEQ ID NO: 133) are also used herein (Table 2).
Any fluorescent label may be used in the fluorescent labeled second primer pairs including, but not limited to, a CY3, a CY5, SYBR Green, a DYLIGHT™ DY647, a ALEXA FLUOR 647, a DYLIGHT™ DY547 and a ALEXA FLUOR 550.
In all embodiments the clade variant of the COVID-19 virus is identified as a variant of concern, a variant of interest, or a Wuhan variant, or a combination thereof. Particularly, the clade variants of the COVID-19 virus may be Denmark, UK (B.1.1.7), South African (B.1.351), Brazil/Japan (P1), Brazil(B1.1.28), California USA, L452R (1.429), India (N440K), or Wuhan, or a combination thereof. The COVID-19 virus is a Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV 2) or a mutated form thereof. A combination of these variants also may be detected simultaneously.
Also in all embodiments the first primer pair may comprise the nucleotide sequences of SEQ ID NO: 1 and SEQ ID NO: 2, or SEQ ID NO: 3 and SEQ ID NO: 4, or SEQ ID NO: 5 and SEQ ID NO: 6, or SEQ ID NO: 7 and SEQ ID NO: 8, or SEQ ID. NO: 264 or SEQ ID NO: 265, or a combination thereof. Sequences of the first primer pairs for the Spike gene and Nucleocapsid gene are shown in Table 1.
In addition in all embodiments the fluorescent labeled second primer pair may comprise the nucleotide sequences of SEQ ID NO: 9 and SEQ ID NO: 10, or SEQ ID NO: 11 and SEQ ID NO: 12, or SEQ ID NO: 13 and SEQ ID NO: 14, or SEQ ID NO: 15 and SEQ ID NO: 16, or SEQ ID NO: 17 and SEQ ID NO: 18, SEQ ID NO: 19 and SEQ ID NO: 20, SEQ ID NO: 21 and SEQ ID NO: 22, SEQ ID NO: 23 and SEQ ID NO: 24, SEQ ID NO: 25 and SEQ ID NO: 26, SEQ ID NO: 27 and SEQ ID NO: 28, SEQ ID NO: 29 and SEQ ID NO: 24, SEQ ID NO: 137 and SEQ ID NO: 20, or SEQ ID NO: 9 and SEQ ID NO: 138, or SEQ ID NO: 11 and SEQ ID NO: 139, or SEQ ID NO: 140 and SEQ ID NO: 16, or SEQ ID NO: 141 and SEQ ID NO: 18, or SEQ ID NO: 142 and SEQ ID NO: 143 or a combination thereof. Sequences of the fluorescent labeled second primer pairs are shown in Tables 2, 11 and 27.
Furthermore, in all embodiments the nucleic acid probes may comprise at least one nucleotide sequence selected from the group consisting of SEQ ID NOS: 30-129 and/or 144-263. The nucleic acid probes may have a sequence corresponding to a sequence determinant that discriminates among the Clade variants of the COVID-19 virus. The nucleic acid probes are specific to the target region of the gene in the COVID-19 virus as discussed supra. This enables hybridization of the one fluorescent labeled COVID-19 virus amplicon generated to the Spike gene-specific nucleic acid probe thereby discriminating the Clade variants of the COVID-19 virus in the sample. In a non-limiting example, the target region is in a Spike gene or nucleoprotein gene in the COVID-19 virus and the nucleic acid probes have a sequence shown in SEQ ID NO: 30 to SEQ ID: 129 (Tables 3, 10 and 14) or SEQ ID NO: 144 to SEQ ID NO: 263 (Tables 28A and 28B). Controls including, but not limited to, a RNAse P control nucleic acid probe (SEQ ID NO: 68 and SEQ ID NO: 69) and a negative control nucleic acid probe (SEQ ID NO: 70) are also used herein (Table 3).
Further still in all embodiments the sample may comprise at least one of a nasopharyngeal swab, a nasal swab, a mouth swab, a mouthwash, an aerosol, or a swab from a hard surface. In one aspect the sample may be any sample obtained from a subject including, but not limited to, a nasopharyngeal swab, a nasal swab, a mouth swab, and a mouthwash (sample obtained by rinsing the subject's buccal cavity). A pooled sample obtained by combining two or more of these samples or by combining samples from multiple subjects also may be used. In another aspect, the sample is an environmental sample obtained from inanimate sources include, but are not limited to, an aerosol and a hard surface. The aerosol samples may be obtained using commercial air samplers such as for example a Coriolis Micro Air Sampler. A sample from a hard surface may be obtained using a swab. In both aspects, the viruses from samples obtained on swabs are dispersed in a liquid such as phosphate buffered saline. Aerosol samples are transferred into a volume of a liquid such as phosphate buffered saline.
In another embodiment of the present invention, there is provided a method for detecting Clade variants in the Coronavirus disease 2019 virus (COVID-19) in a sample, comprising obtaining the sample; harvesting viruses from the sample; isolating total RNA from the harvested viruses; performing a combined reverse transcription and asymmetric PCR amplification reaction on the total RNA using at least one fluorescent labeled primer pair comprising an unlabeled primer, and a fluorescently labeled primer, selective fora target sequence in all COVID-19 viruses to generate at least one fluorescent labeled COVID-19 virus amplicon; hybridizing the fluorescent labeled COVID-19 virus amplicons to a plurality of nucleic acid probes, each having a sequence corresponding to a sequence determinant that discriminates among the clade variants of the COVID-19 virus, where the nucleic acid probes are attached to a solid microarray support; washing the microarray at least once; and imaging the microarray to detect at least one fluorescent signal from the hybridized fluorescent labeled COVID-19 virus amplicons, thereby detecting the clade variants of the COVID-19 virus in the sample. In a related embodiment after the imaging step, a step is performed of generating an intensity distribution profile from the at least one fluorescent signal that is unique to one of the clade variants thereby detecting the clade variant of the COVID-19 virus in the sample.
The total RNA is isolated as described supra and any COVID-19 virus RNA in the total RNA isolate is used as a template in a combined reverse transcription/amplification reaction (RT-PCR). In this step, the nucleic acid sequences in the COVID-19 virus RNA are transcribed using a reverse transcriptase enzyme to generate COVID-19 complementary DNA (cDNA) that is amplified in the same reaction using COVID-19 virus selective fluorescent labeled primer pairs to generate fluorescent labeled COVID-19 virus amplicons. Each fluorescent labeled primer pair comprises an unlabeled primer and a fluorescently labeled primer in about 4-fold to about 8-fold excess of the unlabeled primer whereby, upon completion of the reaction, the fluorescently labelled amplicon is primarily single stranded (that is, the reaction is a type of “asymmetric PCR”).
Hybridization of the fluorescent labeled COVID-19 virus amplicons to the plurality of nucleic acid probes attached at specific positions on a microarray support is performed as described supra. The nucleic acid probes may have a sequence corresponding to a sequence determinant that discriminates among the Clade variants of the COVID-19 virus and are specific to the target region of the gene in the COVID-19 virus, as discussed supra. This enables hybridization of the one fluorescent labeled COVID-19 virus amplicon generated to the Spike gene-specific nucleic acid probe or nucleoprotein specific nucleic acid probe thereby discriminating the Clade variants of the COVID-19 virus in the sample. In a non-limiting example, the target region is in a Spike gene and/or a nucleoprotein gene in the COVID-19 virus and the nucleic acid probes have a sequence shown in SEQ ID NO: 31 to SEQ ID: 63 (Table 3). Controls are as described supra and shown in (Table 3).
Further to this embodiment, prior to the harvesting step, the method comprises mixing the sample with an RNA stabilizer. A representative RNA stabilizer is a chemical stabilizer, as described supra.
In both embodiments at least one of the fluorescent labeled second primer pair is selective for a panel of target nucleotide sequences within a target region of a gene in the COVID-19 virus; and the nucleic acid probes are specific to the target region of the gene, whereby the at least one fluorescent labeled COVID-19 virus amplicon generated is hybridized to the nucleic acid probe thereby discriminating the clade variants of the COVID-19 virus in the sample. Further to this embodiment the method comprises detecting the at least one fluorescent signal from the hybridized at least one fluorescent labeled COVID-19 virus amplicons associated with the panel of target nucleotide sequences within the target region of the gene; and generating an intensity distribution profile unique to each of the clade variants, whereby each of the clade variants is distinguishable from others. Particularly, the gene may be the Spike gene and/or a nucleoprotein gene.
In a non-limiting example, the target region may be in the Spike gene and/or a nucleoprotein gene in the COVID-19 virus and the fluorescent labeled second primer pairs may have forward (odd numbers) and reverse (even number) sequences shown in SEQ ID NO: 9 to SEQ ID NO: 29 (Tables 2 and 11) and the paired fluorescent labeled second primer sequences shown in Table 27. Controls including, but not limited to a RNAse P control having a primer pair with forward primer SEQ ID NO: 66 and reverse primer SEQ ID NO: 67 are also used herein (Table 2).
In all embodiments the COVID-19 gene, the clade variants of the COVID-19 virus, the at least one fluorescent labeled primer pair, the fluorescent label, the nucleic acid probes, and the samples are as described supra. Also in all embodiments the fluorescently labeled primer may be in an excess of about 4-fold to about 8-fold over the unlabeled primer in the fluorescent labeled primer pair. Exemplary nucleotide sequences for the fluorescent labeled primer pairs including, for example, RNAse P controls, are shown in Tables 2, 11 and 27. Exemplary nucleotide sequences for the nucleic acid probes, including, for example, RNAse P controls and negative controls, are shown in Tables 3, 28A and 28B.
In yet another embodiment of the present invention there is provided a method for detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a subject, comprising obtaining a sample from the subject; isolating total RNA from the sample; performing in a single assay a combined reverse transcription and asymmetric PCR amplification reaction on the total RNA using a plurality of fluorescently labeled primer pairs comprising an unlabeled primer and a fluorescently labeled primer, selective for target sequences within a Spike gene in the SARS-CoV-2 virus to generate a plurality of fluorescent labeled SARS-CoV-2 amplicons; hybridizing the plurality of fluorescently labeled SARS-CoV-2 amplicons to a plurality of nucleic acid probes comprising a plurality of universal probes, wild type probes and mutant probes, each having a sequence that specifically base-pairs with one of the target sequences in the fluorescently labeled SARS-CoV-2 amplicons and at least one control probe to which the fluorescently labeled SARS-CoV-2 amplicons do not hybridize, each of the nucleic acid probes attached to specific positions on a solid microarray support; washing the microarray at least once; imaging the microarray to detect fluorescent signals above a threshold for all the nucleic acid probes upon hybridization to the fluorescently labeled SARS-CoV-2 amplicons.
Further to this embodiment the Spike gene is genotyped at each target sequence where the method further comprises measuring the fluorescent signal from hybridization of the fluorescently labeled SARS-CoV-2 amplicons to the wild type probes and from the hybridation of the fluorescently labeled SARS-CoV-2 amplicons to the mutant probes at each of the target sequences; analyzing directly a relative size of the fluorescent signal from hybridization to the mutant probes vs. the fluorescent signal from hybridization to the wild type probes to produce a hybridization pattern of wild type vs. mutant genotyping among all the target sites in SARS-CoV-2; and comparing the hybridization pattern to a known pattern of wild type vs. mutant genotype variation among known SARS-CoV-2 variants to identify the SARS-CoV-2 in the sample as a known variant of concern or a known variant of interest or a combination thereof or as an unknown variant.
In one aspect of both embodiments the plurality of fluorescently labeled primer pairs may be a set of nucleotide sequences comprising SEQ ID NO: 266 and SEQ ID NO: 138, SEQ ID NO: 11 and SEQ ID NO: 139, SEQ ID NO: 267 and SEQ ID NO: 141, SEQ ID NO: 268 and SEQ ID NO: 16, and SEQ ID NO: 141 and SEQ ID NO: 269. Further to this aspect the plurality of fluorescently labeled primer pairs comprises an internal control primer pair to amplify RNase P and the control probe comprises a sequence that specifically base-pairs with a fluorescently labeled RNase P amplicon. In this further aspect the internal control primer pair may comprise the nucleotide sequences of SEQ ID NO: 132 and SEQ ID NO: 270. Also the control probe may comprise the nucleotide sequence of SEQ ID NO: 134.
In another aspect of both embodiments the universal probes may comprise the nucleotide sequences of SEQ ID NOS: 33, 36, 42, 61, 153, 174, 235, 236, 251-252, 256, 259, 283, 287, 291, 293-294, 299, 301, 302 304, and 305. In yet another aspect the wild type probes may comprise the nucleotide sequences of SEQ ID NOS: 37, 40, 43, 47, 52, 59, 62, 126, 154, 164, 179, 182, 235, 282, 288, and 298. In yet another aspect the mutant probes may comprise the nucleotide sequences of SEQ ID NOS: 35, 38, 41, 44, 45, 53, 54, 129, 155, 161, 176, 180, 183, 189, 190, 236, 289, 290, 292, 295, 296, 297, 300, 303, 306, and 307.
In both embodiments and all aspects thereof during the imaging step, SARS-CoV-2 may be detected by measuring at least N fluorescent signals above the threshold from hybridizing of the fluorescently labeled SARS-CoV-2 amplicons to the universal probes. Also in both embodiments and all aspects thereof the fluorescently labeled primer may be in an excess of about 4-fold to about 8-fold over the unlabeled primer in the fluorescent labeled primer pair. In addition the sample may be, but is not limited to, a nasopharyngeal swab, a nasal swab, a mouth swab, or saliva.
In yet another embodiment of the present invention there is provided a method for detecting, genotyping and identifying a variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a subject, comprising obtaining a sample from the subject; isolating total RNA from the sample; performing in a single assay a combined reverse transcription and asymmetric PCR amplification reaction on the total RNA using a set of fluorescently labeled primer pairs, each comprising an unlabeled primer and a fluorescently labeled primer, selective for sequences within a Spike gene in the SARS-CoV-2 virus to generate a plurality of fluorescent labeled SARS-CoV-2 amplicons; hybridizing the plurality of fluorescently labeled SARS-CoV-2 amplicons to a plurality of nucleic acid probes comprising a set of universal probes, wild type probes and mutant probes, each having a sequence that specifically base-pairs with one of the target sequences in the fluorescently labeled SARS-CoV-2 amplicons and at least one control probe to which the fluorescently labeled SARS-CoV-2 amplicons do not hybridize, each of the nucleic acid probes attached to specific positions on a solid microarray support; washing the microarray at least once; imaging the microarray to detect fluorescent signals above threshold for all the nucleic acid probes produced upon hybridization to the fluorescently labeled SARS-CoV-2 amplicons; measuring at least N fluorescent signals above the threshold from hybridization of the fluorescently labeled SARS-CoV-2 amplicons to the universal probes thereby detecting the SARS-CoV-2 in the sample; genotyping the Spike gene at each target sequence, the step comprising comparing the fluorescent signals from hybridization of the fluorescently labeled SARS-CoV-2 amplicons to the wild type probes and from the hybridation of the fluorescently labeled SARS-CoV-2 amplicons to the mutant probes at each position on the microarray; and analyzing directly a relative size of the fluorescent signal from hybridization to the mutant probes vs. the fluorescent signal from hybridization to the wild type probes to produce a hybridization pattern of wild type vs. mutant genotyping at each target sequence in SARS-CoV-2; and identifying a variant of SARS-CoV-2 as a known variant of concern or a known variant of interest or a combination thereof or as an unknown variant by comparing the hybridization pattern to a known pattern of wild type vs. mutant genotype variation among known SARS-CoV-2 variants.
In one aspect of this embodiment the set of fluorescently labeled primer pairs may comprise the nucleotide sequences of SEQ ID NO: 266 and SEQ ID NO: 138, SEQ ID NO: 11 and SEQ ID NO: 139, SEQ ID NO: 267 and SEQ ID NO: 141, SEQ ID NO: 268 and SEQ ID NO: 16, SEQ ID NO: 141 and SEQ ID NO: 269, and SEQ ID NO: 132 and SEQ ID NO: 270. The fluorescently labeled primer pairs are described in Table 29.
In another aspect of this embodiment the probes are described in Tables 30 and 31. Particularly, the probe hybridizing to the fluorescently labeled RNase P amplicon may comprise the nucleotide sequence of SEQ ID NO: 134. Also the universal probes may comprise the nucleotide sequences of SEQ ID NOS: 33, 36, 42, 61, 153, 174, 235, 236, 251-252, 256, 259, 283, 287, 291, 293-294, 299, 301, 302 304, and 305. In addition the wild type probes may comprise the nucleotide sequences of SEQ ID NOS: 37, 40, 43, 47, 52, 59, 62, 126, 154, 164, 179, 182, 235, 282, 288, and 298. Furthermore the mutant probes may comprise the nucleotide sequences of SEQ ID NOS: 35, 38, 41, 44, 45, 53, 54, 129, 155, 161, 176, 180, 183, 189, 190, 236, 289, 290, 292, 295, 296, 297, 300, 303, 306, and 307.
In this embodiment and aspects thereof N may be equal to or greater than 6 fluorescent signals. Also in this embodiment and aspects thereof the excess of the fluorescently labeled primer in the primer pair and the sample are as described supra.
In yet another embodiment of the present invention, there is a provided a method for detecting a pathogen in a subject comprising obtaining a sample from the subject; isolating total nucleic acids from the sample; performing in a single assay a combined reverse transcription and/or an asymmetric PCR amplification reaction on the total nucleic acids using a plurality of fluorescently labeled primer pairs comprising an unlabeled primer and a fluorescently labeled primer, selective for target sequences within a gene of interest in the pathogen to generate a plurality of fluorescently labeled pathogen amplicons; hybridizing the plurality of fluorescently labeled pathogen amplicons to a plurality of nucleic acid probes comprising a plurality of universal probes, wild type probes and mutant probes, each having a sequence that specifically base-pairs with one of the target sequences in the fluorescently labeled pathogen amplicons and at least one control probe to which the fluorescently labeled pathogen amplicons do not hybridize, each of the nucleic acid probes attached to specific positions on a solid microarray support; washing the microarray at least once; imaging the microarray to detect fluorescent signals above a threshold for all the nucleic acid probes upon hybridization to the fluorescently labeled pathogen amplicons.
Further to this embodiment the gene of interest is genotyped at each target sequence where the method comprises measuring the fluorescent signal from hybridization of the fluorescently labeled pathogen amplicons to the wild type probes and from the hybridation of the fluorescently labeled pathogen amplicons to the mutant probes at each of the target sequences; analyzing directly a relative size of the fluorescent signal from hybridization to the mutant probes vs. the fluorescent signal from hybridization to the wild type probes to produce a hybridization pattern of wild type vs. mutant genotyping among all the target sites in the pathogen; and comparing the hybridization pattern to a known pattern of wild type vs. mutant genotype variation among known pathogens to identify the variant.
In one aspect of both embodiments the pathogen may be an RNA virus or a DNA virus. For example, the RNA virus may be, but is not limited to, an influenza virus, such as influenza A or influenza B. A DNA virus may be, but is not limited to, an adenovirus, a herpesviruses, a papillomavirus, or a smallpox virus. In another aspect the pathogen may be a pathogenic bacteria, such as, but not limited to, a respiratory disease-causing bacterium, for example, a Mycobacterium species, a Streptococcus species, a Mycoplasma species, an Enterococcus species, a Haemophilus species, a Klebsiella species, a Moraxella species, a Corynebacterium species, or a combination thereof. In yet another aspect the pathogen may be a pathogenic fungus, such as, but not limited to, a disease-causing molds and yeasts, for example, a Histoplasma species, a Coccidioides species, a Blastomyces species, a Rhizopus species, an Aspergillus species, a Pneumocystis species, a Candida species or a Cryptococcus species, or a combination thereof.
In this embodiment and aspects thereof during the imaging step, the pathogen is detected by measuring at least N fluorescent signals above the threshold from hybridizing of the fluorescently labeled pathogen amplicons to the universal probes. Particularly, N is equal to or greater than 6 fluorescent signals. In this embodiment and aspects thereof the fluorescently labeled primer may be in an excess of about 4-fold to about 8-fold over the unlabeled primer in the fluorescent labeled primer pair. In addition in this embodiment and aspects thereof the sample may be an individual sample or a pooled sample from a nasopharyngeal swab, a nasal swab, a mouth swab, a mouthwash, an aerosol, or a swab from a hard surface or a combination thereof.
Provided herein are methods of nucleic acid analysis to detect stable genetic variation such as a clade variation in a viral pathogen which is based on simultaneous analysis of multiple sequence domains in a gene, such as for example the Spike (S) gene in the RNA genome of CoV-2, or the Nucleoprotein (N) gene in SARS-CoV-2 or a combination of the Spike gene and the Nucleoprotein gene in SARS-CoV-2 to measure clade variation in SARS-CoV-2.
In one method for detecting the stable genetic variation, total RNA from the harvested viruses is isolated and used in a combined reverse transcription and first amplification reaction (RT-PCR) to generate COVID-19 virus cDNA amplicons. These amplicons are used as template in a second amplification reaction that uses fluorescent labeled second primer pair selective for a panel of target nucleotide sequences within a target region of a gene in the COVID-19 virus such as for example, the gene for the Spike protein, to generate fluorescent labeled COVID-19 virus amplicons. In a second method, a combined reverse transcription and asymmetric PCR amplification reaction is performed using at least one fluorescent labeled primer pair selective for the panel of target nucleotide sequences within a target region of a gene in the COVID-19 virus to generate fluorescent labeled COVID-19 virus amplicons. In either method, the fluorescent labeled COVID-19 virus amplicons are hybridized to nucleic acid probes attached at specific positions on a microarray.
This method allows positive hybridization signals to be validated on each sample tested based on internal “mismatched” and “sequence specific” controls. Additionally, at least one fluorescent signal from the hybridized amplicons associated with the panel of target nucleotide sequences within the target region of the gene is detected and an intensity distribution profile unique to each of the Clade variants generated, whereby each of the Clade variants is distinguishable from others.
In the embodiments described supra, the solid microarray support is made of any suitable material known in the art including but not limited to borosilicate glass, a thermoplastic acrylic resin (e.g., poly(methyl methacrylate-VSUVT) a cycloolefin polymer (e.g. ZEONOR 1060R), a metal including, but not limited to gold and platinum, a plastic including, but not limited to polyethylene terephthalate, polycarbonate, nylon, a ceramic including, but not limited to TiO2, and Indium tin oxide (ITO) and engineered carbon surfaces including, but not limited to graphene. A combination of these materials may also be used. The solid support has a front surface and a back surface and is activated on the front surface by chemically activatable groups for attachment of the nucleic acid probes. In this embodiment, the chemically activatable groups include but are not limited to epoxysilane, isocyanate, succinimide, carbodiimide, aldehyde and maleimide. These materials are well known in the art and one of ordinary skill in this art would be able to readily functionalize any of these supports as desired. In a preferred embodiment, the solid support is epoxysilane functionalized borosilicate glass support.
The nucleic acid probes are attached either directly to the solid microarray support, or indirectly attached to the support using bifunctional polymer linkers. In this embodiment, the bifunctional polymer linker has a top domain and a bottom end. On the bottom end is attached a first reactive moiety that allows covalent attachment to the chemically activatable groups in the solid support. Examples of first reactive moieties include but are not limited to an amine group, a thiol group and an aldehyde group. In one aspect the first reactive moiety is an amine group. On the top domain of the bifunctional polymer linker is provided a second reactive moiety that allows covalent attachment to the oligonucleotide probe. Examples of second reactive moieties include but are not limited to nucleotide bases like thymidine, adenine, guanine, cytidine, uracil and bromodeoxyuridine and amino acid like cysteine, phenylalanine, tyrosine glycine, serine, tryptophan, cystine, methionine, histidine, arginine and lysine. The bifunctional polymer linker may be an oligonucleotide such as OLIGOdT, an amino polysaccharide such as chitosan, a polyamine such as spermine, spermidine, cadaverine and putrescine, a polyamino acid, with a lysine or histidine, or any other polymeric compounds with dual functional groups which can be attached to the chemically activatable solid support on the bottom end, and the nucleic acid probes on the top domain. Preferably, the bifunctional polymer linker is OLIGOdT having an amine group at the 5′ end.
The bifunctional polymer linker may be unmodified with a fluorescent label. Alternatively, the bifunctional polymer linker has a fluorescent label attached covalently to the top domain, the bottom end, or internally. The second fluorescent label is different from the fluorescent label in the fluorescent labeled primers. Having a fluorescent label (fluorescent tag) attached to the bifunctional polymer linker is beneficial since it allows the user to image and detect the position of the individual nucleic acid probes (“spot”) printed on the microarray. By using two different fluorescent labels, one for the bifunctional polymer linker and the second for the amplicons generated from the viral RNA being queried, the user can obtain a superimposed image that allows parallel detection of those nucleic acid probes which have been hybridized with amplicons. This is advantageous since it helps in identifying the virus comprised in the sample using suitable computer and software, assisted by a database correlating nucleic acid probe sequence and microarray location of this sequence with a known RNA signature in viruses. Examples of fluorescent labels include, but are not limited to CY5, DYLIGHT™ DY647, ALEXA FLUOR 647, CY3, DYLIGHT™ DY547, or ALEXA FLUOR 550. The fluorescent labels may be attached to any reactive group including but not limited to, amine, thiol, aldehyde, sugar amido and carboxy on the bifunctional polymer linker. In one aspect, the bifunctional polymer linker is CY5-labeled OLIGOdT having an amino group attached at its 3′terminus for covalent attachment to an activated surface on the solid support.
Moreover, when the bifunctional polymer linker also is fluorescently labeled a second fluorescent signal image is detected in the imaging step. Superimposing the first fluorescent signal image and second fluorescent signal image allows identification of the virus by comparing the sequence of the nucleic acid probe at one or more superimposed signal positions on the microarray with a database of signature sequence determinants for a plurality of viral RNA. This embodiment is particularly beneficial since it allows identification of more than one type of virus in a single assay.
The following examples are given for the purpose of illustrating various embodiments of the invention and are not meant to limit the present invention in any fashion.
Provided herein is a method of nucleic acid analysis to detect stable genetic variation in a pathogen which is based on simultaneous analysis of multiple sequence domains in a gene, such as the Spike gene in the RNA genome of CoV-2, to measure clade variation in SARS-CoV-2. For CoV-2, the sequence domains are processed for nucleic acid analysis by converting them into a set of amplicons via a multiplex RT-PCR reaction. In a present preferred implementation, the sequence of those multiplex RT-PCR products is identified relative to that of the underlying CoV-2 Spike gene, by the Horizontal Black Bars in the bottom of Tables 4-8.
The product of that multiplex RT-PCR reaction is analyzed by hybridization to a matrix of synthetic oligonucleotide probes positioned as a microarray test (see the boxes in Tables 4-8). As seen in Tables 4-8, in a preferred implementation of the present invention for CoV-2, there are (15) such Spike Gene Target Regions containing meaningful local sequence variation. (See top Row of Tables 4-8 for their identification).
In terms of detailed test design, the oligonucleotide probes resident at each Target Region of the Spike surface protein are each produced as 3 closely related probe variants, which may be referred to as “Wild Type”, “Mutant” and “Universal”.
In the present invention, a “Wild Type” probe refers to an oligonucleotide probe sequence, generally 14-25 bases long that is specific to the Wuhan progenitor Clade sequence. The pattern of Multiplex RT-PCR amplicon binding to such Wild Type Probes in the present invention are displayed as superscript “2” in Table 4 and as superscript “1” in Table 6.
“Mutant” probes correspond to an oligonucleotide probe sequence, also 15-25 bases long specific to the Sequence Change relative to the Wuhan progenitor manifest at the Spike gene location of interest are displayed as superscript “1” in Table 4 and as superscript “1” in Table 5.
A “Universal” probe refers to an oligonucleotide probe sequence (15-30 bases long) which has been designed to bind to both “Wild Type” and “Mutant” sequences at each site with similar affinity. The patterns of Multiplex RT-PCR amplicon binding to such “Universal” Probes in the present invention are displayed are displayed as superscript “1” in Table 7.
1AA mutation - hybridizes to mutation specific probe
2AA identical to hCoV-19/Wuhan/WIV04/2019 (WIV04) - official reference sequence employed by GISAID (EPI_ISL_402124) Hybridizes to reference specific probe
3Potential probe target
1AA mutation - hybridizes to mutation specific probe
indicates data missing or illegible when filed
1AA identical to hCoV-19/Wuhan/WIV04/2019 (WIV04) - official reference sequence employed by GISAID (EPI_ISL_402124) Hybridizes to reference specific probe
1Both Mutant and Wuhan reference sequence virus hybridize to Locus specific probe
1AA of hCoV-19/Wuhan/WIV04/2019 (WIV04) - official reference sequence employed by GISAID (EPI_ISL_402124)
2AA Identical to (WIV04) - hybridizes to Wuhan reference probe
3AA mutation - hybridizes to mutation specific probe
4Potential probe target identical to (WIV04)
5Potential AA mutation probe target
The oligonucleotide probes of the microarray and the PCR primers to generate RT-PCR amplicons were developed to accommodate a specific CoV-2 Clade Variant set of international interest in 2021, as specified in the Left-most Column in Tables 4-8. But, as can already be seen among the Clade Variant strain these tables, the pattern of local sequence change manifest in each Clade Variant comprises a unique combination derived from a larger set of specific local sequence variation chosen at discrete sites in the Spike gene.
For the Spike protein of the CoV-2 virus and for pathogens more universally, spontaneous local mutation in a surface protein such as Spike is likely to inactivate the protein, thus disabling the pathogen. As such, most spontaneous mutations in surface proteins do not propagate and hence go undetected.
On occasion, however, such random mutation produces a surface protein change that confers a selective advantage to a pathogen, such as enhanced infectivity, better resistance to vaccination or drug therapy and thus the mutation propagates in an infection and ultimately be detected at population scale. Such positively selected local mutational changes are generally rare and thus localized to a relatively small number of discrete segments within a pathogen surface protein such as Spike, often localized to specific sites where the protein contacts host cells, or sites which present peptides for interaction with a protective host antibody or sites where a drug might bind. In many cases such altered surface protein features may function in an additive way (enhanced cell binding+diminished neutralizing antibody binding may be selected for, concurrently) to produce a Clade Variant presenting a combination derived from the set of available local sequence changes that confer functional superiority to the pathogen.
The present invention takes advantage of the fundamental matrix-like character of such selectable (discrete, local) surface protein changes and the ability of a matrix of hybridization probes (as in a microarray) to query many sites of local surface protein sequence change simultaneously (Tables 4-7). As such, this oligonucleotide probe set can interrogate (at the nucleic acid level) many possible combinations of such surface protein change as a single combinatorial test.
Based on the core design test design embodied in Tables 4-7, new, as-yet unknown, functionally relevant local sequence change can be added, once known, as new probes to the microarray (cells with superscript “3” in Table 4). It is expected that many other CoV-2 Clades could be detected and discriminated, in a similar combinatorial fashion, via such relatively minor expansion of the core invention depicted in Table 4.
The present implementation of such an oligonucleotide probe panel for analysis of the CoV-2 Spike gene is based upon detection of 15 positively selected local mutational changes in the Spike gene, i.e. Tables 4-7, each with 3 probe sequence variants at each site, “Mutant”, “Wild Type”, “Universal”, thus generating a set of 15×3=45 oligonucleotide probes to be used for the purpose of combinatorial Clade Variant Analysis.
In the present implementation, if that set of 45 probes is manufactured in triplicate, a 3×45=135 probe microarray is thus generated, which when printed along with positive and negative controls appropriate for CoV-2 testing (such as RNAse P) the present Clade Chip Assay consumes the full microarray content capacity presented by the standard 150 probe, 96-Well format described in applications U.S. Ser. No. 16/950,171 and U.S. Ser. No. 16/950,210, both hereby incorporated by reference in their entireties.
It is useful to note that the information content of such a 150-probe microarray becomes resident in a single well of the 96-well microarray format and thus generates information content similar to that of re-sequencing of the entire gene and content that is equivalent to that obtained from 150 q-RT-PCR assays performed in parallel. As seen below, a first preferred implementation of such a Clade Chip prototype has been fabricated via standard mass production methods described in the above-referenced patent applications.
In a first preferred implementation, the sample preparation methods of the Clade Chip are optimized for both NP-Swab and Saliva collection and designed to detect CoV-2 at 5 virus/RT-PCR reaction sensitivity (500 cp/ml) and resolve multiple CoV-2 Clade variants of present international concern (Denmark, UK, S Africa, Brazil/Japan, India, CA L452R, Wuhan), as depicted in Tables 4-7.
So long as any new CoV-2 Clade may be detected and discriminated via its pattern of Spike gene gRNA sequence change, that additional Clade sequence content (cells with superscript “3” in Table 4) can be designed and added to the manufacture of the present invention in less than 2-weeks, as the need for new or broader-range CoV-2 Clade Variant detection emerges.
The Clade-Chip Assay in the present preferred implementation is based on a standard 96-well plate microarray processing workflow already described in applications having U.S. Ser. No. 16/950,171 and U.S. Ser. No. 16/950,210 both hereby incorporated by reference in their entireties and is deployed in that standard 96-well format as a manual or automated test. However, the matrix of oligonucleotide probes of the present invention to detect CoV-2 Clade Variants via Combinatorial Analysis could, in principle, be implemented by other methods of microarray manufacture or via alternative methods of bead-based solution phase nucleic acid hybridization. Additionally, the same principles of Combinatorial Analysis could be used to develop analogous tests for clade variation in other viruses, bacterial and fungi in the microarray or other hybridization formats.
The Clade Chip Test Design summary is shown in Table 9 and is suited for combinatorial analysis among multiple Spike Targets. The following are its features;
A Clade Chip Probe layout was set up in duplicate. The probe content included three (3) probes for each Spike target site (Universal, Mutant, Wild Type). Validation testing was used to pick the best” of the two closely related “redundant” lead designs for each of the three probes. In addition to the core set of 11 spike targets, new probe designs were included to expand the content of the assay. The full set of redundant probe content was printed in duplicate as a 12×16 probe array in a 96-well format (Table 10). The forward (odd numbers) and reverse (even numbers) primer sequences for each amplimer employed in this assay are shown in Table 11.
Samples Used for Testing. Analysis was performed with a highly characterized, purified Wuhan gRNA standard (Quantitative Standard obtained from ATCC-BEI) or with synthetic “mutant” targets designed by PDx, obtained by SGI fabrication (IDT).
RT-PCR Conditions. RT-PCR was performed using the [UNG+One-Step RT-PCR] protocol. As is customary in optimization of multiplex RT-PCR, the data presented comprise the use of Single PCR primer pairs as a single reaction. Based on these data multiplex RT-PCR conditions are optimized.
Clade Array Hybridization & Imaging. Conditions of Hybridization, Washing and Imaging were exactly as described. Following the completion of the multiplex RT-PCR, the DNA microarray was prepared for hybridization with brief water washes, and an incubation in prehybridization buffer (0.6M NaCl, 0.06M sodium citrate solution, 0.1% Ficoll, 0.1% Polyvinylpyrrolidone 0.1% Bovine Serum Albumin). Following aspiration of the prehybridization buffer, a mixture of amplicon and hybridization buffer (0.6M NaCl, 0.06M sodium citrate solution, 0.1% Ficoll, 0.1% Polyvinylpyrrolidone 0.1% Bovine Serum Albumin) was added to the DNA microarray and allowed to incubate for 2 hours. The microarray was prepared for imaging with one quick wash of wash buffer (22.5 mM NaCl, 2.25 mM sodium citrate solution) and a 10-minute incubation (22.5 mM NaCl, 2.25 mM sodium citrate solution). The microarray plate was then spun dry for 5 minutes at 2200 rpm. The underside of the plate was wiped clean with 70% ethanol and lens tissue until all dust particles were removed. The plate was scanned on the Sensospot utilizing Sensovation software. Cy5 exposure time was set at 312 ms, and the Cy3 exposure times at 115 ms and 578 ms. Upon image scanning completion, the folder containing all of the scanned data was saved to a thumb drive and uploaded to Dropbox for Augury Analysis.
Data Analysis. Data for all (11) Core Spike Target Sites are presented in
The Clade Array Probe Content was found to be fully functional. An optimized shorter probe was seen to improve Cov-2 mutant analysis at target sites D80A and E484K.
A second 15 Plate Manufacturing Run (#2) of DETECTX-Cv, similar to the one described in Experiment 1 above was implemented to complete validation of the Multiplex assay. In this assessment, print quality passed the test for all 96 (160 probe) arrays among all 15 plates.
The second set of validation tests sought to evaluate the preferred method of multiplexing of the RT-PCR reaction, using the UNG combined with One Step RT-PCR condition. The primary goal was to deliver a first RT-PCR Multiplex capable of distinguishing the five prevalent Clade Variants—UK (B.1.1.7), S Africa (B.1.351) Brazil (P.1) Brazil (P.2) US California (B.1.429) shown in Table 12. The validation materials comprised a purified Wuhan gRNA reference (ATCC-BEI). The data obtained subsequent to RT-PCR, hybridization and washing revealed that an initial deployment of a specific 4-plex RT-PCR reaction, comprising amplimers [2, 3, 6, 8] was sufficient to distinguish, as a single multiplex assay, these five prevalent Clade variants (
A third round of validation was performed to evaluate the preferred method of multiplexing of the RT-PCR reaction, using the UNG combined with One Step RT-PCR condition. The primary goal was to deliver a second (N=5) RT-PCR Multiplex capable of distinguishing the six (6) prevalent US Clade Variants—UK (B.1.1.7), S Africa (B.1.351) Brazil (P.1) Brazil (P.2) a second redundant target in US California (B.1.429) and India N440K. shown in Table 12. The validation materials comprised a purified Wuhan gRNA reference (ATCC-BEI). The data obtained subsequent to RT-PCR, hybridization and washing revealed that a second deployment of a specific 5-plex RT-PCR reaction, comprising a N=5 multiplex of amplimers [2, 3, 5, 6, 8] was sufficient to distinguish, as a single multiplex assay, these six prevalent Clade Variants (
Table 13 shows the information content for the fully multiplexed (2, 3, 5, 6, 8) data obtained via the multiplex RT-PCR reaction in this DETECTX-Cv assay, which is sufficient to discriminate the five clade variants (superscript “1”). It was determined that including Amplimer 5 to the multiplex adds redundancy (superscript “2”) thereby allowing unambiguous discrimination of the India Mutant (B.1.36.29). Similarly, addition of amplimer 4 (for NY B.1.526) and Q677P/H probes (for Southern US B.1.596/13.1.2) to the multiplex enabled discrimination of Southern US and NY Clade variants (superscript “3”). Importantly, the emerging Southern US Clade variants (B.1.596/1.1.2) does not require modification of the present multiplex reaction since inclusion of probes at Q677P/H would be sufficient. Analytical specificity was established as described earlier via analysis of both wild type (Wuhan) gRNA and synthetic, Clade specific fragments.
Current deployment of Augury software was modified to include automated capacity for determining “Wild-Type” vs “Mutant” at each of the (11) Spike target sites of the present DETECTX-Cv assay described above (the columns in Table 12. As modified, Augury is capable of calling the identity of the clade variant, based on the pattern of mutant presentation among the sites (that is, a “look-up” table comprising the pattern of each row of Table 12). Coding to enable such autonomous calling is based on allelotyping methods previously developed for HLA allelotyping. In the present case, the clade variant test is also an exercise in spike gene allelotyping. Such spike gene allelotypes (the rows in Table 12) have already been determined as being the preferred marker for CoV-2 Clade Variation.
Augury Modification with Clade ID Module
The current deployment of the Augury software for wild type COV-2 was modified to include automated capacity for determining “Wild-Type” vs “Mutant” at each of the Spike target sites of the DETECTX-Cv assay (the columns in Table 15) and to identify the Clade variant based on the pattern of mutant presentation among the sites (the rows in Tables 15 and 16). Coding for the software is based on allelotyping formalism previously developed for HLA allelotyping.
All DETECTX-Cv probe sequences and their information content were added to a database (“Dot Score” file) within Augury. This database defined the DETECTX-Cv probe content (Mutant, Wild Type, Universal) at each of the eleven (11) Spike target regions (the columns in Table 15).
The Augury Software is configured to read the bar code associated with each 96-well plate of microarrays for DETECTX-Cv and use the information in the bar code to create a “Dot Score” file for the probe content introduced into DETECTX-Cv. Further, Augury is configured to incorporate a new “Dot Score” file as appropriate for any new Clade Variant content with additional probes in the array (Table 15). Additionally, Augury is intrinsically cloud enabled and configured to deploy software modification downloaded from the cloud. When useful for analysis of DETECTX-Cv, data such as those from the RADx Rosalind initiative can also be introduced directly into Augury autonomously, to update the list of prevalent clade variants.
The core functionality of Augury has been used as a manual product for deployment at TriCore. This version of Augury automatically is enabled to read DETECTX-Cv plate bar codes, perform microarray image analysis, create “Dot Score” files and present the resulting averaged, background subtracted DETECTX-Cv data as a spread sheet matrix, which can be compared to the Clade Variant Hybridization patterns such as described in Table 15. This manual deployment version has been tested on DETECTX-Cv synthetic Clade variant standards.
All prevalent Cov-2 Clades have been programmed into Augury to generate a “Look-up Table” (equivalent in content to the pattern of boxes having superscript 1 and 2 in Table 15). The Augury internal “Lookup Table” is formatted to function as part of a Boolean pattern search as developed previously for allelotype analysis of all genes.
1Information obtained by adding Amplimers 2, 3, 6 and 8
2Information obtained by adding Amplimer 5
3Information obtained by adding Potential probe content
4Information obtained by adding Amplimer 4 + New Clade variant probes
Multiplex RT-PCR [2, 3, 5, 6, 8] were performed in the absence of template (0 copies/reaction) to obtain the mean and STD from the mean for LoB signals. This “blank” data collection data is used by Augury to obtain the analytical threshold for each probe (3.2×STD+Mean) to yield Mutant threshold (Tm), Wild Type threshold (Tw) and Universal threshold (Tu) values for all thirty-three (33) probes comprising the content of DETECTX-Cv.
Threshold values were introduced as constants into Augury for autonomous Mutant vs Wild Type determination at all eleven (11) sites. This was performed using the following relationship analytical approach;
Delta=([RFUm−Tm]/Tm)−([RFUw−Tw]/Tw) (Equation 1)
where,
If Delta >0, within experimental accuracy, then “Mutant” (i.e. boxes having superscript 1 in Table 15). If Delta <0, within experimental accuracy, then “Wild Type” (i.e. boxes having superscript 2 in Table 15).
1. Analytical LoD Determination. A first determination of analytical LoD was performed for DETECTX-Cv, among all eleven (11) Spike target sites deployed using the [UNG+ One Step RT-PCR] conditions. For this analysis, validation materials comprised a purified Wuhan gRNA reference (ATCC-BEI) and a cocktail of five (5) synthetic fragments designed by PathogenDx and fabricated by Integrated DNA Technologies, Inc. (IDT, Coralville, Iowa), comprising each region targeted for amplification via the [2, 3, 5, 6, 8] multiplex RT-PCR reaction (deployed as N=5 multiplex).
To support the multiplex reaction, all 5 synthetic CoV-2 fragments were mixed [1:1:1:1:1] in strand equivalents. Copy number values listed in Table 15 refer to the copy number of each fragment (in the equimolar mix) applied to the RT-PCR reaction. The primary goal here is to deploy the (N=5) RT-PCR multiplex to obtain a preliminary analytical LoD in units of copies/reaction for each of the probes comprising the set associated with each of the (n) target sites—LoDn (Universal), LoDn (Wild Type), LoDn (Mutant). The analytical LoD associated with the Universal probes (LoDn) were lower than that of either LoDn or LoDn, due to the intentionally longer probe sequence for the universal probe, which is associated with a higher affinity for its complementary amplicon sequence.
Subsequent to RT-PCR the DNA microarray was prepared for hybridization with brief water washes, and an incubation in prehybridization buffer (0.6M NaCl, 0.06M sodium citrate solution, 0.1% Ficoll, 0.1% Polyvinylpyrrolidone 0.1% Bovine Serum Albumin). Following aspiration of the prehybridization buffer, a mixture of amplicon and hybridization buffer (0.6M NaCl, 0.06M sodium citrate, 0.1% Ficoll, 0.1% Polyvinylpyrrolidone 0.1% Bovine Serum Albumin) was added to the DNA microarray and allowed to incubate for 2 hours. The microarray is then washed with wash buffer (22.5 mM NaCl, 2.25 mM sodium citrate) and dried via centrifugation. The glass portion of the microarray was cleaned with lens tissue and 70% ethanol and images were acquired on the Sensospot. Images were then uploaded for Augury analysis. Following image acquisition and upload to Augury, it was found that the 5-plex RT-PCR reaction, comprising a N=5 multiplex of amplimers [2, 3, 5, 6, 8] was sufficient to obtain a first determination of analytical LODs [LoDn (Universal), LoDn (Wild Type), and LoDn (Mutant)].
§LoDn (Wild Type). Analytical LoD Values for Analysis of Wild Type (Wuhan)as defined from the input target density (measured in copies per RT-PCR reaction) at which the signal obtained from the Wild Type probe becomes indistinguishable from background.
¶LoDn (Mutant). Analytical LoD Values for Analysis of Mutant (Synthetic Fragment)as defined from the input target density (measured in copies per RT-PCR reaction) at which the signal obtained from the Mutant probe becomes indistinguishable from background.
The (N=5) RT-PCR Multiplex (2, 3, 5, 6, 8) described in Example 7 was deployed to obtain a full eleven (11) site Clade variant profile using standard hybridization and wash procedures described above.
A set of five (5) different “Synthetic Clade Variant Standards” corresponding to UK (B.1.1.7), SA (B.1.351), CA452 (B.1.429), Brazil (P.1) and India N440K (B.1.36.29) were prepared each containing a synthetic gene fragment (IDT, Coralville, Iowa) identical to each of the Spike domains amplified by the present RT-PCR multiplex.
Data were obtained at 100 copies/reaction for each of the five (5) synthetic cocktails. Hybridization analysis was performed, and the hybridization data thus obtained was plotted as described above.
Raw data from this analysis presented in
Clinical LoD Range Finding and Clinical LoD analysis were performed on contrived samples, comprising clinical negatives from healthy volunteers, collected in PURE-SAL™ collection device (OASIS DIAGNOSTICS® Corporation, WA). The samples were contrived with heat attenuated CoV-2 (Wuhan, BEI).
Contrived samples were subjected to viral gRNA capture and purification on Zymo silica magnetic beads or Ceres magnetic beads. Five microliters of purified RNA was added to the RT-PCR mix in a PCR plate. The plate was sealed and placed in a thermocycler to undergo 20 minutes of reverse transcription and 45 cycles of asymmetric PCR. Upon PCR completion, the DNA microarray was prepared for hybridization with brief water washes, and an incubation in prehybridization buffer (0.6M NaCl, 0.06M sodium citrate solution, 0.1% Ficoll, 0.1% Polyvinylpyrrolidone 0.1% Bovine Serum Albumin). Following aspiration of the prehybridization buffer, a mixture of amplicon and hybridization buffer (0.6M NaCl, 0.06M sodium citrate, 0.1% Ficoll, 0.1% Polyvinylpyrrolidone 0.1% Bovine Serum Albumin) was added to the DNA microarray and allowed to incubate for 2 hours. The microarray is then washed with wash buffer (22.5 mM NaCl, 2.25 mM sodium citrate) and dried via centrifugation. The glass portion of the microarray was cleaned with lens tissue and 70% ethanol and images were acquired on the Sensospot. Images were then uploaded for Augury analysis.
Clinical LoD Results: Clinical LoD range finding was performed as described above (N=6 repeats) using clinically negative saliva samples (PURE-SAL™) to which were added heat inactivated CoV-2 that were processed using Zymo bead capture.
Pure-SAL Saliva. Pooling Range Finding.
The ability to pool CoV-2 contrived clinical negative PURE-SAL™ saliva samples was tested. Contrived clinical negative samples were pooled at (1) Positive Clinical Sample (100 IL)+(4) Clinical samples (100 IL each), to yield a final pooled sample where the viral complement of the original contrived clinical positive is diluted 5×. The entire pooled specimen was then subjected to Zymo magnetic bead purification, RT-PCR and Hybridization to DETECTX-Cv as described above. The results shown in
DETECTX-Cv analysis was performed by hands-free, autonomous analysis of raw DETECTX-microarray data obtained from Sensovation Scans to generate “Mutant” vs “Wild Type” calls among the ten (10) Spike target sites Table 19. These calls were subsequently used for Clade identification. The autonomous analysis is presented here along with manual Augury analysis.
The following multiple functional modules were added to Augury to enable autonomous analysis of DETECTX-Cv data as follows;
Five (5) synthetic Clade variant standards described earlier (UK, SA, CA452, Brazil P.1, India, Examples 8 and 9) were used for on-site validation. Each standard contained a synthetic gene fragment (IDT) identical to each of the Spike domains amplified by the RT-PCR multiplex. DETECTX-Cv data were obtained at TriCore at 100 copies/reaction for each of the five (5) synthetic cocktails. Analysis of the hybridization data were plotted as described previously. Table 20 shows a plate map, PCR recipe and cycling conditions for this analysis. DNA fragment cocktails were utilized as reference.
1AA mutation - hybridizes to mutation specific probe
2AA identical to hCoV-19/Wuhan/WIV04/2019 (WIV04) - official reference sequence employed by GISAID (EPI_ISL_402124)
3Potential probe target
The Biomerieux EASYMAG® Magnetic Bead platform (bioMérieux, St. Louis, Mo.) was used to extract Covid-19 RNA from 28 clinical positive (NP-VTM) samples (positivity previously determined by Cobas 6800 analysis). The extracted RNA (5 IL) was processed using the DETECTX-Cv method. Table 22 shows a plate map for 28 SARS-CoV-2 positive clinical samples. The PCR recipe and cycling conditions were as described in Table 20.
Results
Sixty (60) clinical positive NP-VTM samples collected by TriCore were sent to PathogenDx for DETECTX-Cv analysis. RNA was extracted from these samples using the Zymo Magnetic Bead platform. The extracted RNA (5 IL) was processed using the DETECTX-Cv method. The PCR recipe and cycling conditions were as described in Table 20.
The method of nucleic acid analysis to detect stable genetic variations in a pathogen is based on simultaneous analysis of multiple sequence domains in a gene or group of genes, such as the Spike gene or the LINK domain of the Nucleoprotein (N) gene in SARS-CoV-2 or a combination of the Spike gene and the N gene in the RNA genome to measure clade variations in SARS-CoV-2. For SARS-CoV-2 (CoV-2), the sequence domains are processed for nucleic acid analysis by converting them into a set of amplicons via a multiplex RT-PCR reaction. In one preferred implementation, the sequence of the multiplex RT-PCR products is identified relative to that of the underlying CoV-2 Spike gene, by the Horizontal Black Bars in the bottom of Table 25 or is identified relative to that of the underlying CoV-2 N gene LINK region, by the Horizontal Black Bar at the bottom of Table 26.
The product of the multiplex RT-PCR reaction is analyzed by hybridization to a matrix of synthetic oligonucleotide probes positioned as a microarray. In one preferred implementation of the present invention for CoV-2, there are (32) such Spike Gene Target Regions (Table 25 & 28) and (11) N gene Target Regions (Table 26, 28) containing meaningful local sequence variation which may be used to measure a pattern of mutation for SARS-CoV2, which in combination, can be used for SARS-CoV-2 Variant Identification. See the top Row of Table 25 for localization of those Target sites in the Spike gene and the top row of Table 26 for their location in the LINK domain of the N protein.
In terms of detailed test design, the forward and reverse Primers deployed for multiplex amplification of the Spike gene (Amplicons S:1-S:8) and those for PCR amplification of the N gene LINK region (Amplicon N:9) are listed in Table 27.
In terms of detailed test design, the Hybridization Probes resident at each target region of the Spike surface protein and each target region of the N gene LINK domain are each produced as 3 closely related types of probe variants, which may be referred to as “Wild Type”, “Mutant” and “Universal”. Those Spike gene and N gene Hybridization probe sequences are listed in Table 28.
The number associated with each element of the matrix in Tables 25 and 26 is the prevalence of that mutation at each location in the N Gene being analyzed (columns) across each of the lineages comprising the Combined WHO and CDC VOC/VOI/VUM lists (rows). Those percentages are calculated by use of the informatics tools provided by Latif et al. based on the aggregated GISAID database (Oct. 20, 2021 update). Where there is no number presented, that location remains as Wild Type in that lineage, Wild Type being defined as the original Wuhan reference sequence.
Table 27 lists S-gene primers to generate amplimers S:1-S:8 and N-gene amplimer N:9 in the DetectX-Cv assay.
Table 28A lists S-gene robes used with the N-gene specific probes to detect hybridization to the S gene regions in amplimers S:1-S:8, that are generated via RT-PCR from the representative primer pairs described in Table 27. Table 28B lists N-gene probes used with the S-gene specific probes to detect hybridization to the N gene region (aa183-aa252), amplimer N:9 that are generated via RT-PCR from the representative primer pairs described in Table 27.
“DETECTX-Cv” technology is designed to combine the practicality of field deployable Q-RT-PCR testing with the high-level information content of targeted NGS. Population scale deployment of DETECTX-Cv is enabled in a way that is simple enough that it can be “drop-shipped” with minimal set up cost and training into any laboratory performing conventional Q-RT-PCR based COVID-19 screening. Initial field deployment demonstrated the ability of DETECTX-Cv to identify clinical positives per shift per Q-RT-PCR screening and analysis without additional sample prep for a large panel of CoV-2 clade variants (UK, Denmark, South Africa, Brazil, US (California, New York, Southern US) and Wuhan and the remainder of the present list of Variants of Concern, Variants of Interest and other Variants as known and classified by the World Health Organization; who.int/en/activities/tracking-SARS-CoV-2-variants/) incorporated into the content of the assay.
The technology encompassed in this invention enables DETECTX-Cv to perform very low-cost microarray analyses in a field-deployable format. DETECTX-Cv is based on proprietary technology of PathogenDx for designing DNA microarray probes and so, the resulting microarrays can be mass produced to deliver >24,000 tests/day. DETECTX-Cv also enables sequence-based testing on these microarrays via open-format room temperature hybridization and washing, much like the processing of ELISA assays. Like an ELISA plate, DETECTX-Cv is mass produced in a 96-well format, ready for manual or automated fluid handling and has the capability to handle up to 576 probe spots per well, at full production scale.
DETECTX-Cv is a combinatorial assay with several targets in the CoV-2 Spike gene and the N gene comprising an exceptionally large set of gain-of-function Spike and/or N gene mutants, which are believed to be selected for enhanced infectivity or resistance to natural or vaccine induced host immunity. Based on analysis of the rapidly growing CoV-2 resequencing effort (600,000 genomes in GISAID, April 2021 and over 5,000,000 genomes in GISAID, November 2021; gisaid.org) “terminal differentiation” of the Spike gene marker “basis set” into a set of informative Spike gene and N gene target sites is expected, which can be built into and mass produced into the same 96-well format described above. DETECTX-Cv is therefore expected to be beneficial as a true discovery tool that is capable of unbiased identification of new CoV-2 clade variants based on detection of novel combinations of the underlying Spike Variant “basis set”. Thus, DETECTX-Cv is expected to become the basis for field deployed seasonal COVID testing with military and civilian applications
The DETECTX-Cv test content comprises Spike Gene Target sequence analysis among 32 discrete information-rich domains, and N gene Target sequence analysis among 11 discrete information-rich domains produced as triplicate tests per array, with positive and negative controls, to produce core content that is deployed as about 160 independent hybridization tests (per well) on each sample. The DETECTX-Cv technology described here is based on multiplex asymmetric, endpoint RT-PCR amplification of viral RNA purified as for Q-RT-PCR screening. The RT-PCR product resulting from amplification is fluorescently tagged and used as-is without cleanup for the subsequent steps of hybridization and washing, which are performed at room temperature (RT). Subsequent to hybridization and washing, the DETECTX-Cv plate is subjected to fluorescent plate reading, data processing and analysis that occurs automatically with no intervention by a human user to result in an output of detected CoV-2 clades which can be used locally for diagnosis and/or simultaneously uploaded to a secure, cloud-based portal for use by medical officials for military or public health tracking and epidemiology analysis.
Microarray Assay for Qualitative Detection and Genotyping of SARS-CoV-2 DetectX-Cv+ Method and Materials
DetectX-Cv+ microarray assay uses the same technology as DetectX-Rv described herein and is designed to simultaneously detect SARS-CoV-2 and identify single nucleotide polymorphisms and small deletions associated with SARS-CoV-2 variants. The assay utilizes the Zymo Research Quick-DNA/RNA™ Viral MagBead (R2140) magnetic silica bead extraction kit, the Applied Biosystems MiniAmp™ Thermal Cycler and the Sensospot® (Miltenyi Imaging) fluorescence microarray imager. The fluorescence of each signal is measured by the Sensospot imager and analyzed by proprietary Augury™ software using a local computer, and the results are stored in a dedicated folder on a user's computer. The system may be used with upper respiratory specimens such as nasopharyngeal (NP) swabs, oropharyngeal (OP) swabs, mid-turbinate swabs, anterior nasal swabs, nasal aspirates, nasopharyngeal wash/aspirates and bronchoalveolar lavage (BAL) specimens obtained from patients suspected of COVID-19 disease.
SARS-CoV-2 detection is accomplished by hybridization analysis of 18 Spike gene nucleotide sequences, based upon the use of a set of 18 synthetic oligonucleotide probes (universal probes) that are insensitive to mutations that may occur at those 18 sites. Analysis of deletion or single nucleotide polymorphisms (SNPs) in the SARS-CoV-2 Spike gene is performed by hybridization analysis at 18 unique Spike gene sites by using a different set of synthetic oligonucleotide probes, mutant and wild type. During hybridization, the mutant and wild type probes are designed to base pair to labeled amplicons presenting with the wild type or mutant genetic sequence. Post-hybridization, the now immobilized fluorescently labeled amplicon withstands repeated washing away of non-hybridized amplicon. Remaining probe-bound labeled amplicon achieves single base pair specificity. Fluorescence quantification via Augury™ software at each probe site enables determination of presence or absence of mutations or deletions at 16 Spike gene sites.
The universal probe signals are used to detect the simple presence of SARS-CoV-2 independent of variant type. If N, such as, but not limited to, where N=6, universal probes are above their respective thresholds, then the sample is identified as SARS-CoV-2. By using universal probes the detection of SARS-CoV-2 is not materially affected by variant changes. Moreover, by having access to a large number of the universal probes in the same test, for example, 18, it is possible to require that several of the universal probes must be above threshold concurrently, i.e., ≥6, thus greatly diminishing the likelihood of a false positive determination as compared to a test where only the signal from 1 probe would be sufficient to detect the presence of the virus.
Probe Thresholds are assumed to be constant for the DetectX-Cv+ assay and are determined as for the DetectX-Cv. When the measured hybridization signal for each probe is above the probe threshold, the probe is said to be “ON”, i.e. hybridization detected above threshold. When the signal is less than the probe threshold, the probe is said to be “OFF” i.e. hybridization not detected above threshold.
The 18 unique Spike gene sites are located within the 5 segments of the Spike gene that are amplified as a single multiplex assay in the RT-PCR reaction which precedes microarray hybridization analysis. Table 29 identifies the primer target, the primer name, the primer sequence and the amino acid translation of the codons in the primer sequence. The sequence identifier includes the 5′-tag identified separately from the sequence.
The presence of SARS-CoV-2 is determined by concurrent hybridization of the 5 Spike gene amplicons to the 18 universal probes. Table 30 lists and names 61 probes and the sequences thereof for which the 5′-tag sequences and the 3′-tag sequences are identified separately. Thus 18 independent hybridization tests are performed in parallel, within the microarray, on every sample. Table 31 identifies 18 of the probes from Table 30 where the 18 sites of interest in the Spike gene and the universal probes designed to bind to them can be identified by their location in the amino acid sequence in the Spike protein which they will ultimately encode.
---.TCT.GGG.A
--.♦♦♦.---.---
Probes include universal probes, wild type probes and mutant probes. Probe design for DetectX-Cv+ is identical to those for DetectX-Rv. Briefly, all probes are designed to include several thymidine (T) bases at each end, i.e. 5′Tag and 3′Tag, which are used to facilitate probe assembly, by UV crosslinking, subsequent to oligonucleotide printing onto the microarray surface. 61 probes (Table 30) are printed in triplicate to form a single microarray, comprising 183 discrete 100 μm wide spots in a 183-element microarray, with each oligonucleotide probe immobilized on the bottom of each well of a SBS standard 96-well format, i.e., 96 identical microarrays per 96-well plate. Each well is thus capable of providing a complete set (61×3) of microarray hybridization tests for each sample.
As confirmed in Tables 32A-32D experimental specificity analysis of synthetic Spike gene templates with known mutational changes, all mutant probes (Table 30) are designed to bind 5- to 10-fold more tightly to their cognate, perfectly matched mutant spike gene target sequence, as compared to the same spike sequence from the wild type (Wuhan) progenitor. Thus, the wild type and mutant probes themselves have a sequence that differs by only one or a few bases (Table 30) and may be used to discriminate a mutational sequence change at the 16 sites in the SARS-CoV-2 sequence for which they were designed. The probes are designed to interrogate wild type vs mutant sequence change by hybridizing to a template sequence that is 15-20 bases long and, thus, additional mutations that might arise in the surrounding amplicon can only affect probe function if the mutation had occurred in that 15-20 base long probe binding domain.
It was determined that the incidence of such new mutation in those adjacent probe binding domains is seen to be low, among the entirety of the approximately 7 million current entries in the GISAID database. However, if such a mutation were to occur, it would manifest as a significant loss of binding affinity for both the wild type and mutant probes at each site, given that both of these probes are designed to bind much more weakly upon induction of a single base change anywhere in the 15-20 base binding domain. Thus, in the presence of such unforeseen additional mutations, the hybridization signal associated with both wild type and mutant probe binding would be diminished, in parallel, since both would be subject to the same additional base pairing mismatch.
Two outcomes would result. In most cases, the hybridization signal for both the wild type and mutant probes would be reduced to below their respective threshold value. Augury software would report that mutational analysis as un-measurable or not detected at that site. If the addition of a flanking sequence mutation produced a more modest effect (i.e. wild type and mutant probe signals remained above threshold) as would occur if the viral gRNA target the patient sample was highly concentrated, then the Augury software would report the outcome. In that instance, the result would remain correct, as the addition of the extra mutant would affect the two probes equivalently and the resulting Mutation vs Wild Type distinction based on binding affinity difference due to the target mutation would remain accurate. Ultimately, a mutation would be detected and reported at that site. The universal probe at each site would be affected by flanking sequence mutation much as is the case for wild type and mutant probes. Should the universal probe hybridization signal be reduced to below its threshold, it would be reported as “Not Present”
The limit of detection for SARS-CoV-2 is 300 copies/mL as summarized in Table 33.
The ability of DetectX-Cv+ to detect Variants of Interest (VOI) and Variants of Concern (Variants of Concern) was verified using gBlocks and four next-generation sequencing (NGS) sequenced clinical samples. The four sequenced clinical samples were purchased from Fulgent and tested in DetectX-Cv+ according to the Assay Protocol above. The results are summarized in Table 34A.
Reactivity with the variants shown in Tables 32A-32D was verified using synthetic gBlocks. Briefly, stock concentrations at 108 copies/mL were thawed, and centrifuged for 1 minute at 14,000×g. Each stock was serially diluted in nuclease-free water to the working concentrations shown in Table 33 and the assay was performed according to the Assay Protocol above. Zymo MagBead extraction was not included when preparing gBlock samples. RNAse P (1,000 copies/μL) was added to the test wells. A no template control and a positive control composed of B.1.1.7 synthetic DNA (10,000 cp/μL) and RNase P synthetic DNA (100 cp/μL) were included. The samples were tested in replicates of 20 and detection of each individual mutation point was considered valid where at least 19/20 replicates at the mutation sites known for each variant were positive at the concentrations listed. Delta, Lambda and Omicron variant RNA was also tested at 3× and 10× of their cutoffs, along with gamma irradiated SARS-CoV-2 (BEI NR52287), in triplicate (Table 34B).
This continuation-in-part application claims the benefit of priority under 35 U.S.C. § 120 of pending continuation-in-part application U.S. Ser. No. 14/529,666, filed Nov. 18, 2021, which claims the benefit of priority under 35 U.S.C. § 120 of pending non-provisional application U.S. Ser. No. 17/332,837, filed May 27, 2021, which claims the benefit of priority under 35 U.S.C. § 119(e) of provisional application U.S. Ser. No. 63/147,613, filed Feb. 9, 2021, now abandoned, all of which are hereby incorporated by reference in their entireties.
| Number | Date | Country | |
|---|---|---|---|
| 63147613 | Feb 2021 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 17529666 | Nov 2021 | US |
| Child | 17677600 | US | |
| Parent | 17332837 | May 2021 | US |
| Child | 17529666 | US |
