Patent Application
20150190487
The present invention relates to a mutant strain of Neospora spp, the use thereof in a pharmaceutical composition and the use thereof in a vaccine composition.
Neospora caninum is an intracellular parasite, responsible for neosporosis. It belongs to the phylum of the Apicomplexans (a branch of the Apicomplexa) which includes a large number of predominantly intracellular parasites. These parasites are responsible for diseases such as neosporosis, toxoplasmosis, malaria, coccidiosis and cryptosporidiosis. They have in common a specific process for the invasion of host cells in several steps, leading to the formation of a parasitophorous vacuole in which the parasite develops.
The life cycle of Neospora caninum has two distinct phases: an asexual phase in an intermediate host such as the mouse, ovines and bovines which leads to the production of tachyzoites and then cysts containing bradyzoites, and a sexual phase in the definitive host (mainly the dog) which leads to the production of oocysts, containing sporozoites, which are eliminated in the faeces.
Animal neosporosis is an significant economic problem in the area of livestock farming and in particular in cattle rearing, where it causes a decrease in the weight gain of calves, a decrease in fertility, a decrease in milk production but in particular is recognized as being one of the major causes of abortions. Thus, every year throughout the world, 30 to 40 million abortions are caused by Neospora caninum in the bovine population. In contrast to Toxoplasma gondii, the maternal-foetal transmission of the parasite and the congenital infection of the foetus occur not only in the case of primary infection during gestation but also in cows chronically infected prior to gestation.
The contamination of cattle may occur by two quite distinct routes:
These consequences obviously have important economic repercussions for livestock farms. Thus, neosporosis is responsible for a loss of £35 million per 1.2 million dairy cows in California (Dubey, J. Am. Vet. Med. Assoc., 1999, April 15; 214(8): 1160-3), of £19 million per 1.6 million cows in the Netherlands (Bartels et al., Vet. Parasitol., 2006, April 15; 137(1-2): 17-27) and of £10 million per 0.7 million cows in Switzerland (Häsler et al., Prev. Vet. Med., 2006, December 18; 77(3-4): 230-53).
The development of a vaccine is a major objective for combating neosporosis. Several strategies for constructing a vaccine against neosporosis are currently under investigation:
Despite the serious economic consequences in cattle rearing, no vaccine that is effective, safe and simple to use vaccine is currently marketed or in the development phase. There is consequently a real need to make a vaccine available that is both effective against neosporosis, easy to use and displays excellent safety.
Surprisingly, the inventors found that the suppression of the function of the NcMIC3 protein alone, or the suppression of the function of the two NcMIC3 and NcMIC1 proteins, in a strain of Neospora caninum, leads to a mutant strain that has infectious and immunogenic properties, conferring on mammals a vaccine protection against the harmful effects of neosporosis.
The present invention therefore relates to a mutant strain of Neospora spp in which the function of the NcMIC3 protein and/or the function of the NcMIC1 protein is suppressed.
The present invention therefore also relates to a mutant strain of Neospora spp in which the function of the NcMIC3 protein is suppressed, in particular by the inhibition of the expression of the ncmic3 gene, and/or the function of the NcMIC1 protein is suppressed, in particular by the inhibition of the expression of the ncmic1 gene.
The present invention therefore relates to a mutant strain of Neospora spp in which the function of the NcMIC3 protein is suppressed.
The present invention therefore relates to a mutant strain of Neospora spp in which the function of the NcMIC1 protein is suppressed.
The present invention therefore relates to a mutant strain of Neospora spp in which the function of the protein NcMIC3 and optionally the function of the NcMIC1 protein are suppressed.
The present invention therefore relates to a mutant strain of Neospora spp in which the function of the NcMIC3 protein is suppressed, in particular by the inhibition of the expression of the ncmic3 gene, and optionally the function of the NcMIC1 protein is suppressed, in particular by the inhibition of the expression of the ncmic1 gene.
Proteins are the effectors of cellular activity. The suppression of the function of a protein may result from its absence from biosynthesis or from its non-functionality. The origin of this dysfunction may be linked to disturbances occurring during transcription of the gene encoding the protein, during its translation or may occur during the process of maturation of the protein (post-translational modifications). The deletion of the gene also explains why no protein can be synthesized.
The NcMIC1 and NcMIC3 proteins are proteins of the micronemes, secretory organelles of the apicomplexans which play a central role in the recognition and the adhesion to the host cells. In Neospora caninum, the NcMIC1 protein is a protein of 460 amino acids encoded by the ncmic1 gene, which comprises 4 exons. The polypeptide sequence of NcMIC1 contains a signal peptide of 20 amino acids followed by two repeat regions (48 amino acids and 44 amino acids) in tandem (Keller et al., Infect Immune. 2002 June; 70(6): 3187-98).
The NcMIC3 protein of Neospora caninum is encoded by the ncmic3 gene, which comprises a single exon. This protein has 362 amino acids.
The inventors have constructed a mutant strain of Neospora caninum called Neo ncmic1-3 KO, in which the function of the NcMIC1 protein and the function of the NcMIC3 protein have been suppressed, a mutant strain Neo ncmic3 KO, in which only the function of the NcMIC3 protein has been suppressed, and a mutant strain Neo ncmic1 KO, in which only the function of the NcMIC1 protein has been suppressed. These three mutant strains of Neospora caninum are the first example of attenuated live strains of Neospora caninum obtained by the controlled and targeted deletion of virulence genes or by the controlled and targeted suppression of the functions of virulence proteins.
In the present invention, by “the function of the NcMIC1 protein is suppressed” is meant either the absence of expression of the NcMIC1 protein, or is meant the expression of a non-functional NcMIC1 protein, for example the expression of a protein not having the function of the NcMIC1 protein and having a certain amino acid sequence identity with that of the NcMIC1 protein.
By “the function of the NcMIC3 protein is suppressed” is meant either the absence of the expression of NcMIC3, or the expression of a non-functional NcMIC3 protein, for example a protein not having the function of the NcMIC3 protein and having a certain amino acid sequence identity with that of the NcMIC3 protein.
The absence of the expression of the NcMIC1 protein or of the NcMIC3 protein may result from the deletion of the whole of the ncmic1 or ncmic3 gene, or of its coding region, or from a mutation, a deletion or an insertion of one or more nucleotides in the coding region of the ncmic1 or ncmic3 gene leading to the absence of the expression of the proteins or to proteins with little amino acid sequence identity with the NcMIC1 or NcMIC3 proteins, or a dysfunction of the promoter region or regulatory region cis or trans of the ncmic1 or ncmic3 gene, or a dysfunction of one or more transcription factors able to bind to said promoter region, or a dysfunction of the translation of messenger RNA, or some epigenetic modifications that are well known to a person skilled in the art. Thus, by “inhibition of the expression of the ncmic1 or ncmic3 gene” is meant all the mechanisms that disturb the transcription of the ncmic1 or ncmic3 gene to messenger RNAs or all the mechanisms that disturb the translation of the messenger RNA to NcMIC1 or NcMIC3 proteins, these two steps being necessary for the synthesis of a functional NcMIC1 or NcMIC3 protein.
A non-functional NcMIC1 protein or a non-functional NcMIC3 protein is a protein that does not have the capacity to recognize the host cells or that does not allow the adhesion of the parasite to said host cells. A non-functional protein may result from a mutation, a deletion or an insertion of one or more nucleotides in the coding region of the ncmic1 or ncmic3 gene. In this case, the modification of the nucleic acid of the coding region does not block the mechanism of the expression of the protein, which may optionally retain a certain amino acid sequence identity with that of the NcMIC1 protein or that of the NcMIC3 protein, but changes the reading frame of the corresponding mRNA during translation of the protein. The non-functionality of the NcMIC3 protein, or of the NcMIC1 protein, may also be the consequence of post-translational modifications that are ineffective or insufficient (i.e. glycosylation, isoprenylation, phosphorylation, sulphation, amidation, acetylation, alkylation, etc.) and which allow it to perform its function.
The function of the NcMIC3 protein, or of the NcMIC1 protein, may also be suppressed indirectly, in particular by altering or suppressing the expression of one or more other proteins (in particular other adhesins) which bind to the NcMIC3 protein, or to the NcMIC1 protein, to form a functional complex. The destructuring of such a complex leads to a loss of function of the NcMIC3 protein, or of the NcMIC1 protein.
In a particular embodiment, the invention relates to a mutant strain of Neospora in which only the function of the NcMIC3 protein is suppressed.
The inventors found that the suppression of the function of the NcMIC3 protein alone in Neospora caninum makes it possible to significantly reduce the virulence of the parasite in vivo. Nevertheless, the double suppression of the function of the NcMIC3 protein and of the function of the NcMIC1 protein in Neospora caninum further accentuates the attenuation of the virulence of the parasite.
In a particular embodiment, the invention relates to a mutant strain of Neospora spp in which the function of the NcMIC3 protein and the function of the NcMIC1 protein are suppressed.
In a particular embodiment, the invention relates to a mutant strain of Neospora spp in which both the function of the NcMIC3 protein and the function of the NcMIC1 protein are suppressed by the inhibition of expression of the two ncmic3 and ncmic1 genes.
The function of the NcMIC3 protein of the mutant strain of Neospora spp may be suppressed by:
The function of the NcMIC1 protein of the mutant strain of Neospora spp may be suppressed by:
By “mutation of one or more nucleotides” is meant the substitution, the permutation or the replacement of one or more nucleotides of a nucleotide sequence with one or more nucleotides not present in the wild-type sequence. By “wild-type sequence” is meant the nucleotide sequence found in the natural state in the wild-type strain of the parasite. The wild-type sequence is by definition devoid of all human intervention by genetic engineering. In the present invention, the reference wild-type strain of N. caninum is the strain NC1.
By “deletion of one or more nucleotides” is meant the suppression of one or more nucleotides of a nucleotide sequence.
By “insertion of one or more nucleotides” is meant the addition or the integration of one or more nucleotides into a nucleotide sequence.
The mutation, the deletion or the insertion of one or more nucleotides may take place within one or more exons of the corresponding gene and may consequently modify the coding region of said gene, or else may take place within one or more introns and may modify the splice site of a relevant intron. This modification of the splicing site consequently changes the reading frame of the mRNA and leads to the translation of a new protein the amino acid sequence of which differs from the sequence of the so-called wild-type protein.
By “destabilization of the messenger RNA” is meant a decrease in its half-life, i.e. the period of time during which a messenger RNA is available to allow its translation into a protein. The stabilization of messenger RNAs is provided by cis elements (the 5′ and 3′ UTR sequences flanking the coding sequences of a gene) and trans elements, in proteins capable of binding to the cis elements. The half-life of a messenger RNA may vary in response to various stimuli such as environmental factors, growth factors or hormones. A modification, carried out in vitro by genetic engineering, of the nucleotide sequences of the cis elements is capable of modifying the half-life of the messenger RNA.
By “inhibition of the translation of the messenger RNA of a gene” is meant blocking the translation of the messenger RNA into the protein corresponding to it. In this case, the messenger RNA of a gene is present in the cell, whereas the protein corresponding to it is absent. The inhibition of translation of the messenger RNA of a gene may result from dysfunction of an element of the translation machinery, in particular of the ribosomes, of the ribosomal RNAs (rRNA) or of the transfer RNAs (tRNA), or of the aminoacyl-tRNA synthetases.
In a particular embodiment, the invention relates to a mutant strain of Neospora spp, in which:
In a more particular embodiment, the invention relates to a mutant strain of Neospora spp, in which:
Such a mutation, deletion or insertion of one or more nucleotides in the nucleotide sequence of the ncmic3 gene or of the ncmic1 gene may lead to the absence of the expression of the NcMIC3 or NcMIC1 protein, or to the production of a non-functional protein, which may or may not have a certain amino acid sequence identity with that of the NcMIC3 or NcMIC1 protein.
More particularly, the invention relates to a mutant strain of Neospora spp, in which both the function of the NcMIC3 protein and the function of the NcMIC1 protein are suppressed by a mutation, a deletion or an insertion of one or more nucleotides in the nucleotide sequences of the ncmic3 and ncmic1 genes.
In another particular embodiment, the invention relates to a mutant strain of Neospora spp, in which:
In another more particular embodiment, the invention relates to a mutant strain of Neospora spp, in which:
By “deletion of the gene” is meant the suppression of the whole gene, i.e. the introns and the exons, or the entire coding region of the gene, i.e. only the exons. By “promoter region” is meant the nucleotide sequence situated upstream of the transcribed but untranslated 5′ UTR region, which serves as a box for the regulation of the expression of a gene.
More particularly, the invention relates to a mutant strain of Neospora spp, in which the function of the NcMIC3 protein is suppressed by the deletion of a part or the whole of the ncmic3 gene or of its promoter region and the function of the NcMIC1 protein is suppressed by the deletion of a part or the whole of the ncmic1 gene or of its promoter region.
In another particular embodiment, the invention relates to a mutant strain of Neospora spp, in which:
In another more particular embodiment, the invention relates to a mutant strain of Neospora spp, in which:
More particularly, the invention relates to a mutant strain of Neospora spp, in which
In a particular embodiment, the mutant strain of Neospora spp according to the present invention is a mutant strain of Neospora caninum.
The present invention also has the objective of providing a pharmaceutical composition comprising a mutant strain of Neospora in which the function of the NcMIC3 protein, and/or the function of the NcMIC1 protein, are suppressed.
The present invention also has the objective of providing a pharmaceutical composition comprising a mutant strain of Neospora in which the function of the NcMIC3 protein, and optionally the function of the NcMIC1 protein, are suppressed.
Said pharmaceutical composition comprising a mutant strain as described above and a pharmaceutically acceptable vehicle.
More particularly, a pharmaceutical composition of this kind is administered in a unit dose varying from 102 to 109 tachyzoites of a mutant strain of Neospora spp.
More particularly, a pharmaceutical composition of this kind is administered in a unit dose varying from 102 to 109 tachyzoites of the strain Neo ncmic1-3 KO.
Even more particularly, such a pharmaceutical composition is administered in a unit dose varying from 103 to 108, in particular from 104 to 107, in particular from 105 to 106 tachyzoites of the strain Neo ncmic1-3 KO.
Even more particularly, such a pharmaceutical composition is administered in a unit dose varying from 102 to 108, in particular from 102 to 107, in particular from 102 to 106, in particular from 102 to 105, in particular from 102 to 104, in particular from 102 to 103 tachyzoites of the strain Neo ncmic1-3 KO.
Even more particularly, such a pharmaceutical composition is administered in a unit dose of 102, 103, 104, 105, 106, 107, 108, or 109 tachyzoites of the strain Neo ncmic1-3 KO.
In a more particular embodiment, the first administration may be followed by possible subsequent boosters, according to the unit doses stated above.
Moreover, the present invention has the objective of supplying a vaccine composition comprising a Neospora spp mutant strain according to the present invention and a pharmaceutically acceptable vehicle.
Such a pharmaceutical composition or vaccine composition may be administered by parenteral route (intravenous, subcutaneous, intradermal, intramuscular, and intraperitoneal) or by enteral route.
The choice of an acceptable pharmaceutical vehicle contained in such a pharmaceutical composition or vaccine composition may be made in relation to the method of administration envisaged, based on the knowledge of a person skilled in the art.
Such a pharmaceutical or vaccine composition may be used for the treatment of neosporosis of primary infection, of reactivation or of reinfection in pet animals, such as dogs and horses, and farm animals, such as ovines, caprins, bovines, porcines, camelids and cervids.
More particularly, such a pharmaceutical or vaccine composition may be used for the treatment of neosporosis of primary infection, of reactivation or of reinfection in companion animals, such as dogs and horses, and farm animals, such as ovines, caprins, bovines, porcines, camelids and cervids and in particular for preventing the maternal-foetal transmission of the parasite in order to reduce the number of abortions but also the risk of vertical contamination from mothers to their offspring.
Even more particularly, such a pharmaceutical or vaccine composition may be used for the treatment of neosporosis of primary infection, of reactivation or of reinfection in pet animals, such as dogs and horses, and farm animals, such as ovines, caprins, bovines, porcines, camelids and cervids and in particular for preventing the maternal-foetal transmission of the parasite in order to reduce the number of abortions but also the risk of vertical contamination from mothers to their offspring in the case of infection during gestation (i.e. acute infection) but also prior to gestation (i.e. chronic infection).
The invention also relates to a method of in vitro diagnostics for differentiating the animals vaccinated with the mutant strains Neo ncmic1 KO, Neo ncmic3 KO, Neo ncmic1-3 KO and animals naturally infected by the wild-type strains of N. caninum. These diagnostic tests, called DIVA (Differentiating Infected from Vaccinated Animal), are being required more and more by the regulatory authorities in particular for purposes of pharmacovigilance and epidemiological studies but also in order to identify the possible causes of abortions occurring in the vaccinated animals.
The present invention also relates to a method of in vitro differential diagnostics for discriminating a mammal vaccinated with the compositions of the invention from an unvaccinated mammal, said method comprising a step of:
The present invention also relates to a method of in vitro differential diagnostics for discriminating a mammal vaccinated with the compositions of the invention from an unvaccinated mammal, said method comprising the following steps:
According to a particular embodiment, the method of the invention may be implemented on a biological sample selected from the group constituted by blood and serum but also certain tissues and organs such as the placenta, the brain, the muscles, etc.
The wild-type strains of Neospora caninum have the ncmic1 and ncmic3 genes in their genome and express the NcMIC1 and NcMIC3 proteins.
The mutant strains of Neospora caninum as defined according to the present invention have, respectively:
Diagnostics between animals vaccinated with the mutant strains of the invention and animals infected by wild-type strains of N. caninum may be indirect, based on the detection and the identification of antibodies, or direct, based on the detection of the infectious agent with immunology or molecular technologies.
The present invention also relates to a method for the detection, in a biological sample in particular selected from the group constituted by blood and serum obtained from a mammal, of an anti-NcMIC1 antibody and/or an anti-NcMIC3 antibody and/or an anti-DHFR antibody and/or an anti-CAT-GFP antibody, said method comprising the following step:
By “immune complex” is meant the physical interaction between an antigen and an antibody specifically directed against this antigen. In the present invention, this interaction takes place in vitro between the NcMIC1, NcMIC3, DHFR, CAT-GFP proteins and the antibodies specifically directed against each of these proteins.
By “detection and identification of antibodies” is meant the detection of specific antibodies of the sought antigens present in the serum of the individuals. The detection of the antibodies is carried out by conventional indirect ELISA or competitive ELISA techniques.
The indirect ELISA techniques are based on the use of antigens fixed on solid supports. The serum from the individuals to be diagnosed is deposited on the support in order to generate interactions between the fixed antigen and any antibodies present in the serum of the individuals to be diagnosed. After washing, the antigen-antibody interaction is detected using labelled secondary antibodies specifically recognizing the conjugated anti-species antibodies. The detection of antibodies directed against the DHFR and/or CAT-GFP proteins will demonstrate previous inoculation of the individual with the mutant strains. Conversely, the detection of antibodies directed against the NcMIC1 and NcMIC3 proteins will demonstrate previous contamination of the individual with a wild-type strain of N. caninum.
Competitive ELISA is based on the competition between the antibodies optionally present in the serum of the individual to be diagnosed and the antibodies present in a detection serum. The antigens are fixed on solid supports. The serum of the individuals to be diagnosed and the competitive serum are deposited on the support. The specific binding of the detection antibody is detected using an appropriate and labelled anti-species conjugate. The possible presence of antibodies in the serum of the individual to be diagnosed generates competition with the antibodies present in the detection serum and leads to a decrease in detection. Indirect ELISA with the DHFR and/or CAT-GFP proteins will make it possible to detect the inoculation of the animal with the mutant strains of the invention. Indirect ELISA with the NcMIC1 and NcMIC3 proteins will make it possible to detect the contamination of the animal with a wild-type strain of N. caninum.
The present invention also relates to a method for the detection, in a biological sample in particular selected from the group constituted by blood and serum but also certain tissues and organs such as the placenta, the brain, the muscles, etc. obtained from a mammal, of the NcMIC1 antigen and/or the NcMIC3 antigen and/or the DHFR antigen and/or the CAT-GFP antigen, said method comprising the following step:
In a more particular embodiment, the present invention relates to a method for the detection of the NcMIC1 and/or NcMIC3 and/or DHFR and/or CAT-GFP antigens and the anti-NcMIC1 and/or anti-NcMIC3 and/or anti-DHFR and/or anti-CAT-GFP antibodies.
By “detection of the infectious agent with immunology technologies” is meant all of the techniques allowing the detection of specific antigenic proteins of the wild-type strains of N. caninum (i.e. NcMIC1 and NcMIC3 proteins) and specific proteins of the mutant strains of the invention (i.e. DHFR and/or CAT-GFP proteins).
The detection of the antigenic proteins may result from experiments of immunohistochemistry, immune transfer, an immuno-enzymatic method with antigen capture (ELISA, enzyme-linked immunosorbent assay), immunochromatography or proteomics that are well known to a person skilled in the art. These assays may be carried out with various biological samples.
By “immunohistochemistry” is meant the detection of antigens in fixed tissues using labelled antibodies directed specifically against the antigen. Immunohistochemistry with specific antibodies of the DHFR and/or CAT-GFP proteins will make it possible to detect the inoculation of the animal with the mutant strains of the invention. Immunohistochemistry with specific antibodies of the NcMIC1 and NcMIC3 proteins will make it possible to detect the contamination of the animal with a wild-type strain of N. caninum.
By “immune transfer” is meant the detection of antigens in biological samples after separation of the proteins of the sample by gel electrophoresis and detection with labelled antibodies directed specifically against the antigen. Immune transfer with specific antibodies of the DHFR and/or CAT-GFP proteins will make it possible to detect the inoculation of the animal with the mutant strains. Immune transfer with specific antibodies of the NcMIC1 and NcMIC3 proteins will make it possible to detect the contamination of the animal with a wild-type strain.
By “enzyme-linked immunosorbent assay (ELISA)” is meant the detection of antigens using capture antibodies directed specifically against the antigen and fixed on a solid plate (indirect ELISA of the sandwich type). The antigen present in the sample is captured by the specific antibody and then its presence is revealed by a second labelled antibody. ELISA with specific antibodies of the DHFR and/or CAT-GFP proteins will make it possible to detect the inoculation of the animal with the mutant strains of the invention. ELISA with specific antibodies of the NcMIC1 and NcMIC3 proteins will make it possible to detect the contamination of the animal with a wild-type strain of N. caninum.
By “immunochromatography” is meant a method for the detection of antigens based on the purification of the sample by affinity chromatography using a specific antibody of the antigen labelled and fixed on a chromatography column Immunochromatography with specific antibodies of the DHFR and/or CAT-GFP proteins will make it possible to detect the inoculation of the animal with the mutant strains of the invention. Immunochromatography with specific antibodies of the NcMIC1 and NcMIC3 proteins will make it possible to detect the contamination of the animal with a wild-type strain of N. caninum.
By “detection of the infectious agent with molecular technologies” is meant the techniques of molecular biology that are well known to a person skilled in the art for the identification of the presence of specific nucleotide sequences of the wild-type strains and the mutant strains and in particular by the amplification by the polymerase chain reaction (PCR), real-time PCR, by diagnostics by restriction fragment length polymorphism (RFLP), which may be linked to PCR methods or by diagnostics using nucleic acid probes.
In a particular embodiment, the invention relates to an oligonucleotide consisting of a nucleic acid sequence selected from the group comprising SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, SEQ ID NO: 26, SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47, SEQ ID NO: 48, SEQ ID NO: 49 or their complementary sequences.
By “oligonucleotide” is meant a nucleic acid sequence that can be used as a primer in an amplification method or as a probe in a detection method. In the present invention, the oligonucleotides consist of a sequence of at least 15, preferably 20 nucleotides, and preferably less than 30 nucleotides, capable of hybridizing to a molecule of genomic DNA or to a complementary DNA. By “hybridization” is meant the physical interaction occurring between two nucleic acid molecules. This hybridization may involve DNA/DNA or RNA/RNA homoduplexes or DNA/RNA heteroduplexes.
By “nucleic acid” is meant a succession of nucleotides joined together by phosphodiester bonds. A nucleic acid molecule may be linear, circular, single-stranded, double-stranded, or partially double-stranded. The nucleic acid sequences are described in the present invention according to the usage that is well known to a person skilled in the art, i.e. they are defined by a sequence numbered in the 5′ to 3′ direction.
By “complementary sequences” is meant two nucleic acid sequences that have complementary nucleotides that may interact with one another via hydrogen bonds. Opposite to an adenine, there is always a thymine or a uracil (in the case of a DNA/RNA heteroduplex); opposite to a cytosine, there is always a guanine. By way of example, without limiting the scope of the invention, the sequence 5′ ATCG 3′ and the sequence 5′ CGAT 3′ are complementary.
The invention also relates to the pairs of oligonucleotides consisting of the pairs of sequences selected from:
or their complementary sequences.
By “pair of oligonucleotides” is meant two nucleotides as defined by their sequences.
Another purpose of the invention is to offer sets of oligonucleotides consisting of the triads of sequences selected from:
or their complementary sequences.
For each triad, the first two SEQ IDs correspond to the primers and the third corresponds to the sequence of the probe.
By “sets of oligonucleotides” is meant groups of three oligonucleotides as defined by their respective sequences.
The wild-type strains of Neospora caninum have the ncmic1 and ncmic3 genes in their genome.
Analysis of a biological sample for the presence and/or the expression level of the four ncmic1, ncmic3, dhfr, cat-gfp genes makes it possible to determine whether the animal is a carrier of a strain of Neospora caninum resulting from an infection by a wild-type strain or resulting from a vaccination with one of the three mutant strains as described in the present invention. The purpose is to be able to establish a differential diagnosis that makes it possible to discriminate the vaccinated animals from the unvaccinated and/or infected animals, within a herd.
The invention also relates to the use of at least one oligonucleotide consisting of a nucleic acid sequence selected from the group comprising SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, SEQ ID NO: 26, SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47, SEQ ID NO: 48, SEQ ID NO: 49 or their complementary sequences, for the detection of ncmic1, and/or ncmic3, and/or dhfr, and/or cat-gfp genes derived from the genome of wild-type strains and/or of the mutant strains Neo ncmic1 KO and/or Neo ncmic3 KO and/or Neo ncmic1-3 KO of Neospora caninum.
In a particular embodiment, the invention relates to the use of at least one oligonucleotide consisting of the sequence selected from SEQ ID NO: 21, SEQ ID NO: 24, SEQ ID NO: 25, SEQ ID NO: 26, SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 35, SEQ ID NO: 39, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47 or their complementary sequence, as a primer for carrying out a hybridization and optionally an amplification of the ncmic1 gene originating from the genome of wild-type strains and/or of the mutant strain Neo ncmic3 KO of Neospora caninum.
In a more particular embodiment, the invention relates to the use of oligonucleotides consisting of at least one pair of sequences selected from: SEQ ID NO: 21 and SEQ ID NO: 25, SEQ ID NO: 21 and SEQ ID NO: 28, SEQ ID NO: 21 and SEQ ID NO: 35, SEQ ID NO: 21 and SEQ ID NO: 46, SEQ ID NO: 39 and SEQ ID NO: 25, SEQ ID NO: 39 and SEQ ID NO: 28, SEQ ID NO: 39 and SEQ ID NO: 35, SEQ ID NO: 39 and SEQ ID NO: 46, SEQ ID NO: 39 and SEQ ID NO: 24, SEQ ID NO: 27 and SEQ ID NO: 28, SEQ ID NO: 27 and SEQ ID NO: 35, SEQ ID NO: 27 and SEQ ID NO: 46, SEQ ID NO: 27 and SEQ ID NO: 24, SEQ ID NO: 45 and SEQ ID NO: 46, SEQ ID NO: 45 and SEQ ID NO: 24, SEQ ID NO: 47 and SEQ ID NO: 46, SEQ ID NO: 47 and SEQ ID NO: 24, SEQ ID NO: 26 and SEQ ID NO: 24, or their complementary sequences, as primers for carrying out a hybridization and optionally an amplification of the ncmic1 gene originating from the genome of wild-type strains and/or of the mutant strain Neo ncmic3 KO of Neospora caninum.
In another particular embodiment, the invention relates to the use of at least one oligonucleotide consisting of the sequence selected from SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 36, SEQ ID NO: 40, or their complementary sequence, as a primer for carrying out a hybridization and optionally an amplification of the ncmic3 gene originating from the genome of wild-type strains and/or of the mutant strain Neo ncmic1 KO of Neospora caninum.
In another more particular embodiment, the invention relates to the use of oligonucleotides consisting of at least one pair of sequences selected from SEQ ID NO: 11 and SEQ ID NO: 12, SEQ ID NO: 11 and SEQ ID NO: 8, SEQ ID NO: 11 and SEQ ID NO: 40, SEQ ID NO: 11 and SEQ ID NO: 6, SEQ ID NO: 5 and SEQ ID NO: 12, SEQ ID NO: 5 and SEQ ID NO: 8, SEQ ID NO: 5 and SEQ ID NO: 40, SEQ ID NO: 5 and SEQ ID NO: 6, SEQ ID NO: 5 and SEQ ID NO: 14, SEQ ID NO: 7 and SEQ ID NO: 12, SEQ ID NO: 7 and SEQ ID NO: 8, SEQ ID NO: 7 and SEQ ID NO: 40, SEQ ID NO: 7 and SEQ ID NO: 6, SEQ ID NO: 7 and SEQ ID NO: 14, SEQ ID NO: 36 and SEQ ID NO: 8, SEQ ID NO: 36 and SEQ ID NO: 40, SEQ ID NO: 36 and SEQ ID NO: 6, SEQ ID NO: 36 and SEQ ID NO: 14, SEQ ID NO: 36 and SEQ ID NO: 12, SEQ ID NO: 15 and SEQ ID NO: 6, SEQ ID NO: 15 and SEQ ID NO: 14, or their complementary sequences, as primers for carrying out a hybridization and optionally an amplification of the ncmic3 gene originating from the genome of wild-type strains and/or of the mutant strain Neo ncmic1 KO of Neospora caninum.
In yet another particular embodiment, the invention relates to the use of at least one oligonucleotide consisting of the sequence selected from SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 37, SEQ ID NO: 41, SEQ ID NO: 43, SEQ ID NO: 44, or their complementary sequence, as a primer for carrying out a hybridization and optionally an amplification of the dhfr selection gene originating from the genome of the mutant strains Neo ncmic3 KO and/or Neo ncmic1-3 KO of Neospora caninum.
In yet another more particular embodiment, the invention relates to the use of oligonucleotides consisting of at least one pair of sequences selected from: SEQ ID NO: 11 and SEQ ID NO: 13, SEQ ID NO: 11 and SEQ ID NO: 10, SEQ ID NO: 11 and SEQ ID NO: 41, SEQ ID NO: 11 and SEQ ID NO: 44, SEQ ID NO: 11 and SEQ ID NO: 6, SEQ ID NO: 5 and SEQ ID NO: 13, SEQ ID NO: 5 and SEQ ID NO: 10, SEQ ID NO: 5 and SEQ ID NO: 41, SEQ ID NO: 5 and SEQ ID NO: 44, SEQ ID NO: 5 and SEQ ID NO: 6, SEQ ID NO: 5 and SEQ ID NO: 14, SEQ ID NO: 37 and SEQ ID NO: 10, SEQ ID NO: 37 and SEQ ID NO: 41, SEQ ID NO: 37 and SEQ ID NO: 44, SEQ ID NO: 37 and SEQ ID NO: 6, SEQ ID NO: 37 and SEQ ID NO: 14, SEQ ID NO: 9 and SEQ ID NO: 10, SEQ ID NO: 9 and SEQ ID NO: 41, SEQ ID NO: 9 and SEQ ID NO: 44, SEQ ID NO: 9 and SEQ ID NO: 6, SEQ ID NO: 9 and SEQ ID NO: 14, SEQ ID NO: 43 and SEQ ID NO: 44, SEQ ID NO: 43 and SEQ ID NO: 6, SEQ ID NO: 43 and SEQ ID NO: 14, SEQ ID NO: 16 and SEQ ID NO: 44, SEQ ID NO: 16 and SEQ ID NO: 6, SEQ ID NO: 16 and SEQ ID NO: 14, or their complementary sequences, as primers for carrying out a hybridization and optionally an amplification of the dhfr selection gene originating from the genome of mutant strains Neo ncmic3 KO and/or Neo ncmic1-3 KO of Neospora caninum.
In yet another particular embodiment, the invention relates to the use of at least one oligonucleotide consisting of the sequence selected from SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 38, SEQ ID NO: 42, SEQ ID NO: 48, SEQ ID NO: 49 or their complementary sequence, as a primer for carrying out a hybridization and optionally an amplification of the cat-gfp selection gene originating from the genome of the mutant strains Neo ncmic1 KO and/or Neo ncmic1-3 KO of Neospora caninum.
In yet another more particular embodiment, the invention relates to the use of oligonucleotides consisting of at least one pair of sequences selected from: SEQ ID NO: 21 and SEQ ID NO: 22, SEQ ID NO: 21 and SEQ ID NO: 30, SEQ ID NO: 21 and SEQ ID NO: 42, SEQ ID NO: 38 and SEQ ID NO: 30, SEQ ID NO: 38 and SEQ ID NO: 42, SEQ ID NO: 38 and SEQ ID NO: 24, SEQ ID NO: 49 and SEQ ID NO: 30, SEQ ID NO: 49 and SEQ ID NO: 42, SEQ ID NO: 49 and SEQ ID NO: 24, SEQ ID NO: 29 and SEQ ID NO: 30, SEQ ID NO: 29 and SEQ ID NO: 42, SEQ ID NO: 29 and SEQ ID NO: 24, SEQ ID NO: 23 and SEQ ID NO: 30, SEQ ID NO: 23 and SEQ ID NO: 42, SEQ ID NO: 23 and SEQ ID NO: 24, SEQ ID NO: 48 and SEQ ID NO: 30, SEQ ID NO: 48 and SEQ ID NO: 42, SEQ ID NO: 48 and SEQ ID NO: 24, or their complementary sequences, as primers for carrying out a hybridization and optionally an amplification of the cat-gfp selection gene originating from the genome of mutant strains Neo ncmic1 KO and/or Neo ncmic1-3 KO of Neospora caninum.
By “amplification” is meant the increase in the concentration of a specific DNA sequence among a mixture of DNA sequences. The techniques of DNA amplification are techniques that are well known to a person skilled in the art.
The invention also relates to the use of at least one oligonucleotide consisting of a nucleic acid sequence selected from the group comprising SEQ ID NO: 35 to 42, SEQ ID NO: 16, SEQ ID NO: 47, SEQ ID NO: 48, or of its complementary sequence, as a probe for carrying out a hybridization with a nucleic acid originating from the genome of wild-type strains and/or of the mutant strains Neo ncmic1 KO and/or Neo ncmic3 KO and/or Neo ncmic1-3 KO of Neospora caninum.
The invention also relates to the use of the oligonucleotide consisting of a nucleic acid sequence selected from the group comprising SEQ ID NO: 35 to 42, SEQ ID NO: 16, SEQ ID NO: 47, SEQ ID NO: 48, or of its complementary sequence, the aforesaid oligonucleotide being labelled with a fluorophore at one end and optionally with a quencher at the other end.
By “fluorophore” is meant the molecules capable of emitting light when they are excited by a light source. The fluorophores are molecules that are well known to a person skilled in the art, those most used being Fam, Tet, Hex, Tamra, Texas Red, Cy3, Cy5. The purpose of this non limitative list is to illustrate the fluorophore concept but should in no case restrict the present invention to the use of only these fluorophores.
By “quencher” is meant a chemical species capable of deactivating an excited state created in a molecular entity by energy transfer, by electron transfer or by a chemical mechanism. Quenchers are molecules that are well known to a person skilled in the art, those most used being Dabcyl, Eclipse Dark Quencher, Black Hole Quencher. A fluorophore may also serve as a quencher. For this, the emission spectrum of the fluorophore grafted at 5′ must not overlap the excitation spectrum of the fluorophore-quencher grafted at 3′. The purpose of this non limitative list is to illustrate the quencher concept but should in no case restrict the present invention to the use of only these quenchers.
In the present invention, the probes used may come under the definition of Taqman, FRET (Fluorescent Resonance Energy Transfer), Molecular Beacon or Scorpion technology or any other real-time PCR (or RT-PCR) technology that are well known to a person skilled in the art.
The invention also relates to a method for the detection of Neospora caninum by in vitro amplification starting from a biological sample, said method comprising the steps of:
According to a particular embodiment, the detection method according to the invention may be implemented on a biological sample selected from the group consisting of blood, serum or plasma, but also certain tissues and organs such as the placenta, the brain, the muscles, etc.
According to another embodiment, in the method for the detection of Neospora caninum, the nucleic acid of Neospora caninum is amplified by PCR. The PCR may be qualitative, quantitative or semiquantitative. According to whether or not a detection probe is used, it is called real-time PCR or conventional PCR.
According to another more particular embodiment, in the method for the detection of Neospora caninum, the amplification product is detected using at least one of the oligonucleotides of sequence SEQ ID NO: 35 to 42, SEQ ID NO: 16, SEQ ID NO: 47, SEQ ID NO: 48, or its complementary sequence, or any other oligonucleotide with a sequence included in that of the amplicon obtained from the primers allowing the amplification of the gene fragment of interest, labelled with a fluorophore at one end and with a quencher, as probe, at the other end.
The invention also relates to a kit for the amplification of Neospora caninum starting from a biological sample, said kit comprising one of the aforesaid sets of oligonucleotides, or their complementary sequences, and means allowing the amplification of a nucleic acid of Neospora caninum.
According to a particular embodiment, said amplification kit comprises:
By “means for amplifying a nucleic acid” is meant the dNTPs, a Taq Polymerase, the salts and buffers for carrying out a PCR.
By “internal control” is meant a nucleic acid sequence (exogenous DNA) unrelated to the genome of Neospora caninum, primers and a probe allowing the amplification and the detection of this exogenous DNA. This internal control is placed in the mix used for PCR for the detection of Neospora caninum and provides evidence of the correct operation of amplification.
The following figures and examples provide further illustration of the present invention.
Batch i: the female Balb/C mice in this batch were vaccinated by intraperitoneal route with 5×106 tachyzoites of the mutant strain Neo ncmic1-3 KO and then challenged by intraperitoneal route with 2×107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch ii: the female Balb/C mice in this batch were vaccinated by intraperitoneal route with 107 tachyzoites of the mutant strain Neo ncmic1-3 KO and then challenged by intraperitoneal route with 2×107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch iii: the female Balb/C mice in this batch were vaccinated by intraperitoneal route with a first dose of 107 tachyzoites of the mutant strain Neo ncmic1-3 KO, and then a month later with a second dose of 107 tachyzoites of the mutant strain Neo ncmic1-3 KO, and then challenged by intraperitoneal route with 2×107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch iv: the female Balb/C mice in this batch were vaccinated by intraperitoneal route with 5×107 tachyzoites of the mutant strain Neo ncmic1-3 KO and then challenged by intraperitoneal route with 2×107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch v: the female Balb/C mice in this batch were vaccinated by intraperitoneal route with 108 tachyzoites of the mutant strain Neo ncmic1-3 KO and then challenged by intraperitoneal route with 2×107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch vi: the female Balb/C mice in this batch were not vaccinated with the tachyzoites of the mutant strain Neo ncmic1-3 KO but were challenged by intraperitoneal route with 2×107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch i: the female mice in this batch were vaccinated with the tachyzoites of the mutant strain Neo ncmic1-3 KO.
Batch ii: the female mice in this batch were not vaccinated and are therefore naive with respect to neosporosis.
T+: a mouse infected by N. caninum and displaying anti-N. caninum IgG antibodies in its serum. This mouse serves as a positive control.
T−: a naive mouse that does not have anti-N. caninum IgG antibodies in its serum. This mouse serves as a negative control.
Batch i: the female mice in this batch were vaccinated with the tachyzoites of the mutant strain Neo ncmic1-3 KO.
Batch ii: the female mice in this batch were not vaccinated and are therefore naive with respect to neosporosis.
Batch i: (broken grey curve—grey circles): the female sheep in this batch were not vaccinated with the tachyzoites of the mutant strain Neo ncmic1-3 KO but were fertilized, and then challenged at mid-gestation, by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch ii (continuous black curve—black squares): the female sheep in this batch were vaccinated by subcutaneous route with a first dose of 107 tachyzoites of the mutant strain Neo ncmic1-3 KO, and then a month later with a second dose of 107 tachyzoites of the mutant strain Neo ncmic1-3 KO. The ewes were fertilized 2 months after the first vaccination, and then challenged, at mid-gestation, by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch iii (continuous grey curve—grey triangles): the female sheep in this batch were vaccinated by subcutaneous route with a dose of 108 tachyzoites of the mutant strain Neo ncmic1-3 KO. The ewes were fertilized 2 months after vaccination, and then challenged, at mid-gestation, by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch iv (broken black curve—black crosses): the female sheep in this batch were not vaccinated with the tachyzoites of the mutant strain Neo ncmic1-3 KO and were not challenged with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum. They were fertilized at the same time as the ewes in batches (i), (ii) and (iii).
Batch i: (broken grey curve—grey circles): the female sheep in this batch were not vaccinated with the tachyzoites of the mutant strain Neo ncmic1-3 KO but were fertilized, and then challenged, at mid-gestation, by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch ii (continuous black curve—black squares): the female sheep in this batch were vaccinated by subcutaneous route with a first dose of 107 tachyzoites of the mutant strain Neo ncmic1-3 KO, and then a month later with a second dose of 107 tachyzoites of the mutant strain Neo ncmic1-3 KO. The ewes were fertilized 2 months after the first vaccination, and then challenged, at mid-gestation, by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch iii (continuous grey curve—grey triangles): the female sheep in this batch were vaccinated by subcutaneous route with a dose of 108 tachyzoites of the mutant strain Neo ncmic1-3 KO. The ewes were fertilized 2 months after vaccination, and then challenged, at mid-gestation, by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch iv (broken black curve—black crosses): the female sheep in this batch were not vaccinated with the tachyzoites of the mutant strain Neo ncmic1-3 KO and were not challenged with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum. They were fertilized at the same time as the ewes in batches (i), (ii) and (iii).
Batch i: the female sheep in this batch were not vaccinated with the tachyzoites of the mutant strain Neo ncmic1-3 KO but were fertilized, and then challenged at mid-gestation, by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch ii: the female sheep in this batch were vaccinated by subcutaneous route with a first dose of 107 tachyzoites of the mutant strain Neo ncmic1-3 KO, and then a month later with a second dose of 107 tachyzoites of the mutant strain Neo ncmic1-3 KO. The ewes were fertilized 2 months after the first vaccination, and then challenged, at mid-gestation, by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch iii: the female sheep in this batch were vaccinated by subcutaneous route with a dose of 108 tachyzoites of the mutant strain Neo ncmic1-3 KO. The ewes were fertilized 2 months after vaccination, and then challenged, at mid-gestation, by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum.
Batch iv: the female sheep in this batch were not vaccinated with the tachyzoites of the mutant strain Neo ncmic1-3 KO and were not challenged with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum. They were fertilized at the same time as the ewes in batches (i), (ii) and (iii).
In order to prepare the strain of N. caninum with the ncmic1 and ncmic3 genes knocked out, two steps of homologous recombination were carried out. The first step of homologous recombination makes it possible to obtain a simple mutant KO (strain Neo ncmic3 KO). The second step of homologous recombination is carried out in the strain Neo ncmic3 KO in order to obtain a doubly deleted strain (Neo ncmic1-3 KO) (
The haploidy of the genome of Neospora caninum during the proliferative phase allows inactivation of a gene in a single homologous recombination.
All the tachyzoites of the strain NC1 of Neospora caninum used were produced in human fibroblasts (HFF) cultured in Dulbecco's minimum medium (DMEM) supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg of streptomycin. They were harvested after mechanical lysis of the host cells and 3 passes through a 25G syringe.
a) Construction of the Plasmid pNcMic3KO-DHFR
The plasmid pNcMic3KO-DHFR (
The 5′UTR region of the ncmic3 gene was amplified by PCR from the genomic DNA of the strain NC1 of Neospora caninum. For the amplification, the primers 5 HR NCmic3 F KpnI and 5 HR NCmic3 R ClaI (SEQ ID NO: 1 and SEQ ID NO: 2) allow amplification of the 5′UTR region of the ncmic3 gene and creation of two restriction sites, which were used for cloning the 5HR fragment upstream of the DHFR selection cassette in the plasmid pT230 DHFR (KpnI at 5′ and ClaI at 3′ of the PCR fragment).
The 3′UTR region of the ncmic3 gene was amplified by PCR from the genomic DNA of the strain NC1 of Neospora caninum. For the amplification, the primers 3 HR NCmic3 F XbaI and 3 HR NCmic3 R NotI (SEQ ID NO: 3 and SEQ ID NO: 4) allow amplification of the 3′UTR region of the ncmic3 gene and creation of two restriction sites, which were used for cloning the 3HR fragment downstream of the DHFR selection cassette in the plasmid pT230 5HR-NcMic3-DHFR (XbaI at 5′ and NotI at 3′ of the PCR fragment). The sequences of the primers are given in Table I below.
b) Conditions for Electroporation and Selection
50 μg of the plasmid pNcMic3KO-DHFR purified and then linearized by NotI was added to 5×107 NC1 tachyzoites of Neospora caninum suspended in the CYTOMIX electroporation medium containing ATP (3 mM) and glutathione (3 mM) (Van den Hoff et al., Nucleic Acid Research, June 11; 20(11): 2902), and electroporation was carried out in a cuvette with a 4-mm gap, in a volume of 800 μL on a BioRad apparatus (parameters: 2000 V, 50 ohms, 25 μF, with two electric shocks).
After electroporation, the tachyzoites were deposited on a monolayer of HFF cells in culture. For selection of the mutants, the culture medium is replaced and supplemented with the selection agent (2 μM pyrimethamine), 24 h after electroporation. Three culture passages are carried out in this medium.
After 16 days of selection, the resistant parasites are cloned by limit dilution in the wells of 96-well plates of HFF cells. After amplification, the lysis plaques caused by the parasite are investigated. The parasites are subcultured and their genomic DNA is extracted for PCR analyses. These PCR analyses should confirm integration of the transgene but should also allow differentiation of the parasites that have randomly integrated the transgene from the parasites of interest the ncmic3 gene of which has been effectively suppressed by homologous recombination.
c) PCR Analysis
Starting from the genomic DNA, PCRs were carried out for:
The sequences of the primers and the size of the amplicons resulting from the different PCRs are shown in Table II and Table III below, respectively.
Neospora
caninum (NC1)
The electrophoretic profiles of the PCR products are presented in
New PCR analyses were carried out on these clones of interest with new sets of primers. These PCRs, called integration PCRs, allow validation of the genetic KO using a primer present on the genome upstream or downstream of the sequences flanking the ncmic3 gene and a second primer present in the selection cassette (dhfr gene) or in the gene of interest (ncmic3) (
In
All of the PCR results demonstrate that homologous recombination has indeed taken place and that the ncmic3 gene has indeed been deleted from the mutant strain Neo ncmic3 KO.
d) Analysis by Immunofluorescence
Analysis was carried out by immunofluorescence. 24 h before immunofluorescence analysis, 5×105 parasites are deposited in a p24 well containing a coverslip covered with a HFF cell lawn.
The cells infected by the parasites are washed twice with 1×PBS and then fixed with paraformaldehyde (3.7% in 1×PBS) for 30 min. After 3 washings with 1×PBS, the cells are permeabilized with Triton solution (0.1% in 1×PBS) for 5 minutes. After 3 washings with 1×PBS, a saturation step is carried out with a solution of 1×PBS/10% FCS for 30 min. The cells are then incubated with the primary antibody diluted in a solution of PBS/2% FCS for 1 hour, washed 3 times and then incubated with the secondary antibody diluted in a solution of PBS/2% FCS for 1 hour. After 2 washings with 1×PBS, the coverslips are mounted on a slide with Immu-Mount and observed with a fluorescence microscope.
The primary antibody used is an antibody that allows detection of expression of the NcMIC3 protein in the parasite (primary antibody: rabbit anti-mic3 antibody and commercial secondary antibody: Alexa Fluor® 594 goat anti-rabbit, Life technologies ref. A-11012).
For the wild-type strain NC1 of Neospora caninum, red fluorescence is observed at the apical pole of the parasite, revealing the presence of the NcMIC3 protein (
a) Construction of the Plasmid pNc mic1KO-CAT-GFP
The plasmid pNcMic1KO-CAT-GFP (
The 3′UTR region of the ncmic1 gene was amplified by PCR from the genomic DNA of the strain NC1 of Neospora caninum. For the amplification, the primers 3 HR NCmic1 F KpnI and 3 HR NCmic1 R HindIII (SEQ ID NO: 17 and SEQ ID NO: 18) allow amplification of the 3′UTR region of the ncmic1 gene and creation of two restriction sites, which were used for cloning the 3HR fragment upstream of the CAT-GFP selection cassette into the plasmid pT230 CAT-GFP (KpnI at 5′ and HindIII at 3′ of the PCR fragment).
The 5′UTR region of the ncmic1 gene was amplified by PCR from the genomic DNA of the strain NC1 of Neospora caninum. For the amplification, the primers 5 HR NCmic1 F BamHI and 5 HR NCmic1 R NotI (SEQ ID NO: 19 and SEQ ID NO: 20) allow amplification of the 5′UTR region of the ncmic1 gene and creation of two restriction sites, which were used for cloning the 5HR fragment downstream of the CAT-GFP selection cassette into the plasmid pT230 3HRNcMic1CAT-GFP (BamHI at 5′ and NotI at 3′ of the PCR fragment). The sequences of the primers are given in Table IV below.
b) Conditions for Electroporation and Selection
50 μg of the plasmid pNcMic1KO-CAT-GFP, purified and then linearized by KpnI, must be added to 5×107 NC1 tachyzoites suspended in CYTOMIX electroporation medium containing ATP (3 mM) and glutathione (3 mM) (Van den Hoff et al., Nucleic Acid Research, June 11; 20(11): 2902), and electroporation must be carried out in a cuvette with a 4-mm gap, in a volume of 800 μL on a BioRad apparatus (parameters: 2000 V, 50 ohms, 25 μF, with two electric shocks).
After electroporation, the tachyzoites will be deposited on a monolayer of HFF cells in culture. For selection of the mutant, the culture medium will be replaced and supplemented with the selection agent (50 μM chloramphenicol), 24 h after electroporation. Three culture passages must be carried out in this medium.
After 15 days of selection, the resistant parasites will be cloned by limit dilution in the wells of 96-well plates of HFF cells. After amplification, the lysis plaques caused by the parasite will be investigated. The parasites will be subcultured and their genomic DNA will be extracted for PCR analyses.
c) PCR Analysis
The sequences of the primers and the expected size of the amplicons resulting from the different PCRs are shown in Table V and Table VI below, respectively.
Neospora
caninum (NC1)
a) Construction of the Plasmid pNc mic1KO CAT-GFP
The construction of the plasmid pNcMic1KO-CAT-GFP is described in Example 2 (2a).
b) Conditions for Electroporation and Selection
50 μg of the plasmid pNcMic1KO-CAT-GFP, purified and then linearized by KpnI, was added to 5×107 Neo ncmic3 KO tachyzoites suspended in the CYTOMIX electroporation medium containing ATP (3 mM) and glutathione (3 mM) (Van den Hoff et al., Nucleic Acid Research, June 11; 20(11): 2902), and electroporation was carried out in a cuvette with a 4-mm gap, in a volume of 800 μL on a BioRad apparatus (parameters: 2000 V, 50 ohms, 25 μF, with two electric shocks).
After electroporation, the tachyzoites were deposited on a monolayer of HFF cells in culture. For selection of the mutants, the culture medium is replaced and supplemented with the selection agent (chloramphenicol 50 μM), 24 h after electroporation. Three culture passages are carried out in this medium.
After 15 days of selection, the resistant parasites are cloned by limit dilution in the wells of 96-well plates of HFF cells. After amplification, the lysis plaques caused by the parasite are investigated. The parasites are subcultured and their genomic DNA is extracted for PCR analyses.
c) PCR Analysis
The sequences of the primers and the size of the amplicons resulting from the different PCRs are shown in Table VII and Table VIII below, respectively.
Neospora
caninum
In
The electrophoretic analyses of the PCR products show that the strain Neo ncmic1-3 KO no longer has the ncmic1 and ncmic3 genes (wells 3, 4, 5, 6, 9 and 11,
d) Immunofluorescence Analysis
Immunofluorescence analysis was carried out solely by direct observation of the fluorescence of the parasite (
The parasites of the two mutant strains are visualized in direct light (images A and C). One and the same microscopic field is visualized in fluorescence. Green fluorescence, due to expression of the recombinant chimeric protein CAT-GFP, is only detected in the mutant strain Neo ncmic1-3 KO (image D) following insertion of the CAT-GFP cassette. Conversely, the strain Neo ncmic3 KO, which does not have a CAT-GFP cassette, does not express the CAT-GFP protein and consequently does not display fluorescence (image B).
The mutant strains Neo ncmic3 KO and Neo ncmic1-3 KO described in Examples 1 and 3 were maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000, November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
Between 60 and 80% of the female Balb/C mice generally die between 8 and 11 days after being infected by intraperitoneal route with 107 tachyzoites of the strain NC1 of Neospora caninum.
The virulence of the mutants Neo ncmic3 KO and Neo ncmic1-3 KO was investigated on a minimum batch of 10 female Balb/C mice by intraperitoneal injection of 107 tachyzoites/mouse. The controls were carried out under the same conditions on batches of 10 female Balb/C mice using the strain NC1 of Neospora caninum.
The mice were also infected with increasing quantities of the strain NC1 of Neospora caninum and the mutant strains Neo ncmic3 KO and Neo ncmic1-3 KO. The dose required for 50% mortality (LD50) is 6×106 tachyzoites for the wild-type strain NC1 of Neospora caninum and 22×106 tachyzoites for the strain Neo ncmic3 KO. For the strain Neo ncmic1-3 KO, the LD50 is very much higher than 108 tachyzoites, i.e. 17 times the LD50 of the wild-type strain NC1 of Neospora caninum. In fact, no mortality is observed at this dose with the mutant strain Neo ncmic1-3 KO.
The mutant strain Neo ncmic1-3 KO described in Example 3 was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000, November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
Female Balb/C mice were divided into 6 separate batches: (i) a batch vaccinated by intraperitoneal route with 5×106 tachyzoites of the mutant strain Neo ncmic1-3 KO, (ii) a batch vaccinated by intraperitoneal route with 107 tachyzoites of the mutant strain Neo ncmic1-3 KO, (iii) a batch vaccinated by intraperitoneal route with 107 tachyzoites of the mutant strain Neo ncmic1-3 KO and boosted 1 month after the first injection with 107 tachyzoites of the mutant strain Neo ncmic1-3 KO, (iv) a batch vaccinated by intraperitoneal route with 5×107 tachyzoites of the mutant strain Neo ncmic1-3 KO, (v) a batch vaccinated by intraperitoneal route with 108 tachyzoites of the mutant strain Neo ncmic1-3 KO and (vi) an unvaccinated control batch.
Four months after vaccination, all the mice were challenged by intraperitoneal route with 2×107 tachyzoites of the wild-type strain NC1 of Neospora caninum. The wild-type strain NC1 of Neospora caninum was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000, November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20. The dose used for challenge is sufficient to lead to 100% mortality of the challenged mice. The survival of the mice is then monitored for one month.
The mutant strain Neo ncmic1-3 KO described in Example 3 was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000, November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
Female OF1 mice were divided into 2 separate batches: (i) a batch vaccinated by intraperitoneal route with 107 tachyzoites of the mutant strain Neo ncmic1-3 KO, (ii) an unvaccinated control batch.
Two months after vaccination, the mice were mated (D0) at a rate of three female mice to one male. The pregnant mice are diagnosed by weighing and on the tenth day of gestation are subjected to infectious challenge by intraperitoneal route with 2×106 tachyzoites of the wild-type strain NC1 of Neospora caninum. The wild-type strain NC1 of Neospora caninum was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000, November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
One day before parturition, the female mice were sacrificed. The placentas and the foetuses were isolated and the DNA was extracted. A nested PCR is carried out from the region of the NC5 gene of N. caninum (Yamage et al., J. Parasitol. 1996 April 82(2): 272-9, Baszler et al., J Clin Microbiol, 1999 December, 37(12): 4059-64). The primer pair NC5 FA (SEQ ID NO: 31) and NC5 RA (SEQ ID NO: 32) is used for the primary PCR, and the primer pair NC5 FB (SEQ ID NO: 33) and NC5 RB (SEQ ID NO: 34) is used for the secondary PCR. The sequences of the primers are given in Table IX below.
For each placenta and foetus, three independent PCRs are carried out. The placentas and foetuses are considered positive when Neospora caninum is detected in the case of at least one PCR. The results are presented in Table X below.
These results demonstrate that vaccination with the attenuated mutant strain Neo ncmic1-3 KO considerably reduces the maternal-foetal transmission of the parasite, thus validating the efficacy of the strain Neo ncmic1-3 KO for preventing harmful effects of neosporosis in a murine model of endogenous congenital neosporosis.
a) Experimental Procedure
The mutant strain Neo ncmic1-3 KO described in Example 3 was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000, November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
Romanov ewes seronegative for Neospora caninum and Toxoplasma gondii were divided into 4 separate batches: a batch comprising 14 control ewes not vaccinated with the mutant strain Neo ncmic1-3 KO, challenged by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum (batch i), a batch comprising 15 ewes vaccinated by subcutaneous route with 107 tachyzoites of the mutant strain Neo ncmic1-3 KO and then boosted by subcutaneous route, 1 month after the first injection, with 107 tachyzoites of the mutant strain Neo ncmic1-3 KO and challenged by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum (batch ii), a batch comprising 14 ewes vaccinated by subcutaneous route with 108 tachyzoites of the mutant strain Neo ncmic1-3 KO and challenged by subcutaneous route with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum (batch iii) and a batch comprising 5 control ewes not vaccinated with the mutant strain Neo ncmic1-3 KO and not challenged with the wild-type strain NC1 of Neospora caninum (batch iv).
Two months after the first vaccination, the ewes were artificially inseminated. They were returned to the ram 3 weeks after artificial insemination. Ultrasonography was then carried out and led to the diagnosis that 14 ewes out of 14 were pregnant in batch (i), 13 ewes out of 15 in batch (ii), 13 ewes out of 14 in batch (iii) and 4 ewes out of 5 in batch (iv).
The pregnant ewes in batches (i), (ii) and (iii) were subjected at mid-gestation to infectious challenge with 107 tachyzoites of the wild-type strain NC1 of Neospora caninum. The wild-type strain NC1 of Neospora caninum was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000, November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
b) Temperature Recorded Post-Immunization and Post-Challenge
From 5 days before vaccination to 14 days post-vaccination, the rectal temperatures of the ewes were recorded daily. The mean values of the temperatures post-immunization of batches (i), (ii), (iii) and (iv) are presented in
On the day before infection and during the subsequent days, the rectal temperature was recorded daily. The mean values of the temperatures post-infection of batches (i), (ii), (iii) and (iv) are presented in
c) Analysis of the Humoral Immune Response
The immune response was investigated post-immunization and post-challenge, using ELISA for evaluating the kinetics of appearance of the specific anti-N. caninum IgGs in the serum of the ewes in batches (i), (ii), (iii) and (iv). The sera are taken before immunization (D0) and then on D22, D57 and D107 post-vaccination and finally after challenge (D0 Chal, D29 Chal, D62 Chal). The blood is taken from the jugular vein and the sample is left overnight at 4° C. for clot formation. The serum is recovered by centrifuging the samples at 5000 g for 10 min. The supernatant is recovered and stored at −20° C.
In order to analyse the humoral immune response induced after the vaccination, an extract of N. caninum is prepared. For the preparation of this total parasite extract, the tachyzoites of the strain NC-1 are washed, sonicated twice at 60 W/s for 10 min in ice and centrifuged at 2000 g for 30 minutes at +4° C. The supernatant is recovered and the concentration is determined by BCA assay, which uses bovine serum albumin (BSA) as standard. The aliquots are stored at −80° C. until used.
The total parasite extract of the strain NC1 is diluted in a carbonate buffer, pH 9.6, in order to obtain a final concentration of 10 μg/mL. The plates are then washed three times with the washing buffer (1×PBS−0.05% Tween 20) and then saturated for 1.5 h at 37° C. with a solution of 1×PBS−0.05% Tween 20 supplemented with 4% of bovine serum albumin (BSA) (Sigma). The medium is then removed. The sera to be tested are diluted to 1/50th in a solution of 1×PBS−0.05% Tween 20 and are deposited in duplicate in the wells. After incubation for 1 hour at 37° C. and a new series of washings, anti-sheep IgG secondary antibody coupled to alkaline phosphatase (Jackson ImmunoResearch 713-055—147, donkey anti-Sheep IgG) and diluted to 1/5000th is deposited at a rate of 100 μL per well. The samples are then incubated for one hour at 37° C. After a new series of three washings, the detection is carried out by the addition of 100 μL of a solution of disodium paranitrophenylphosphate (PnPP) (Sigma) at 1 mg/mL, in DEA-HCl buffer, to each well. After incubation for 20 min at ambient temperature, away from the light, the absorbance at 405 nm is measured using a plate reader (Multiskan MCC340 Wallace). The mean values of the results of the ELISA tests on D0, D22, D57 and D107 post-immunization and on D0, D29, D62 post-challenge for the sera from the different batches of ewes diluted to 1/50th are shown in
After immunization, the unvaccinated ewes in control batches (i) and (iv) did not develop a humoral response. However, the ewes in batches (ii) and (iii) developed an anti-neosporosis IgG response starting from D22. This IgG response is boosted at the second vaccination of batch (ii). It then decreases for the two batches (ii) and (iii).
After challenge, the unchallenged ewes in control batch (iv) did not develop a humoral response. However, the ewes in batches (i), (ii) and (iii) developed an anti-neosporosis IgG response. The humoral response of the vaccinated batches (ii) and (iii) is more rapid than for the unvaccinated batch (i).
d) Investigation of Abortions
After challenge, the ewes were monitored daily until parturition and the abortions and stillbirths were recorded.
The results of this study are presented in Table XV below.
These results demonstrate that vaccination with the attenuated mutant strain Neo ncmic1-3 KO considerably reduces the harmful effects of an infection of a ruminant, in particular an ovine, with Neospora caninum.
The mutant strain Neo ncmic1-3 KO described in Example 3 was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000, November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
Female OF1 mice were divided into 2 separate batches: (i) a batch vaccinated by intraperitoneal route with 5.107 tachyzoites of the mutant strain Neo ncmic1-3 KO, (ii) a control batch, unvaccinated but challenged.
One month after vaccination, a submaxillary blood sample is taken. The whole blood is stored for 2 hours at 37° C. before being centrifuged at 5000 g for 10 minutes in order to store the serum. The serum is stored at −20° C. until used.
In order to analyse the humoral immune response induced after vaccination, an extract of N. caninum is prepared. For the preparation of this total parasite extract, the tachyzoites of the strain NC-1 are washed, sonicated twice at 60 W/s for 10 mM in ice and centrifuged at 2000 g for 30 minutes at +4° C. The supernatant is recovered and the concentration is determined by BCA assay, which uses bovine serum albumin (BSA) as standard. The aliquots are stored at −80° C. until used.
Using sera from mice vaccinated with the mutant strain Neo ncmic1-3 KO and from unvaccinated mice, ELISA tests are carried out in order to characterize the humoral immune response induced by the mutant strain Neo ncmic1-3 KO.
a) Investigation for the Total IgGs Specific to N. caninum
The total parasite extract of the strain NC1 is diluted in a carbonate buffer, pH 9.6, in order to obtain a final concentration of 10 μg/mL. 96-well plates with flat-bottomed wells are then sensitized overnight at +4° C. by depositing 100 μL of total extract of N. caninum in each well. The plates are then washed three times with the washing buffer (1×PBS−0.05% Tween 20) and then saturated for 1.5 h at 37° C. with a solution of 1×PBS−0.05% Tween 20 supplemented with 4% of bovine serum albumin (BSA) (Sigma). The medium is then removed. The sera to be tested are diluted to 1/50th in a solution of 1×PBS−0.05% Tween 20 and are deposited in duplicate in the wells. After incubation for 1 hour at 37° C. and a new series of washings, anti-mouse IgG secondary antibody coupled to alkaline phosphatase (Sigma A3562, goat anti-Mouse IgG) and diluted to 1/5000th is deposited at a rate of 100 μL per well. The samples are then incubated for one hour at 37° C. After a new series of three washings, the detection is carried out by the addition of 100 μL of a solution of disodium paranitrophenylphosphate (PnPP) (Sigma) at 1 mg/mL, in DEA-HCl buffer, to each well. After incubation for 20 min at ambient temperature, away from the light, the absorbance at 405 nm is measured using a plate reader (Multiskan MCC340 Wallace). The mice are regarded as seroconverted when the absorbance obtained is 2.5 times higher than the absorbance obtained with the negative control originating from serum from healthy naive mice (
The vaccinated mice in batch (i) all display seroconversion, in contrast to the unvaccinated mice in batch (ii).
b) Isotypic Profile of the Anti-N. caninum IgGs
The total parasite extract of the strain NC-1 is diluted in a carbonate buffer pH9.6 in order to obtain a final concentration of 10 μg/mL. Flat-bottomed 96-well plates are then sensitized overnight at +4° C. by depositing 100 μL of total extract of N. caninum in each well. The plates are then washed three times with the washing buffer (1×PBS−0.05% Tween 20) and then saturated for 1.5 h at 37° C. with a solution of 1×PBS−0.05% Tween 20 supplemented with 4% of bovine serum albumin (BSA) (Sigma). The medium is then removed. The sera to be tested are diluted to 1/100th in a solution of 1×PBS−0.05% Tween 20 and are deposited in duplicate in the wells. After incubation for 1 hour at 37° C. and a new series of washings, the secondary antibodies are deposited. The anti-IgG1 secondary antibodies (BD 557272, rat anti-Mouse IgG1) and anti-IgG2a secondary antibodies (BD 553389, rat anti-Mouse IgG2a) coupled to alkaline phosphatase and diluted to 1/1000th are deposited at a rate of 100 μL per well. The samples are then incubated for one hour at 37° C. After a new series of three washings, the detection is carried out by the addition of 100 μL of a solution of disodium paranitrophenylphosphate (PnPP) (Sigma) at 1 mg/mL, in DEA-HCl buffer, to each well. After incubation for 20 min at ambient temperature, away from the light, the absorbance at 405 nm is measured using a plate reader (Multiskan MCC340 Wallace) (
The anti-N. caninum IgGs of the vaccinated mice in batch (i) are preferably of type IgG2A, an isotypic profile favourable to protection against Neospora caninum (Long et al., J. Parasitol., 1998, April; 84(2): 316-20).
The mutant strain Neo ncmic1-3 KO described in Example 3 was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000, November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
Female OF1 mice were divided into 2 separate batches: (i) a batch of 11 mice vaccinated by intraperitoneal route with 5.107 tachyzoites of the mutant strain Neo ncmic1-3 KO and (ii) a batch of 6 unvaccinated control mice.
Two months after vaccination, the mice were mated (D0) at a rate of three female mice to one male. The pregnant mice in batches (i) and (ii) are diagnosed by weighing and on the tenth day of gestation are subjected to infectious challenge by intraperitoneal route with 2×106 tachyzoites of the wild-type strain NC1 of Neospora caninum. The wild-type strain NC1 of Neospora caninum was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000, November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
One day before parturition, the female mice were sacrificed. The placentas and the foetuses were isolated and the DNA was extracted. A nested PCR is carried out from the region of the NC5 gene of N. caninum (Yamage et al., J. Parasitol 1996 April 82(2): 272-9, Baszler et al., J Clin Microbiol, 1999 December, 37(12): 4059-64). The primer pair NC5 FA (SEQ ID NO: 31) and NC5 RA (SEQ ID NO: 32) is used for the primary PCR, and the primer pair NC5 FB (SEQ ID NO: 33) and NC5 RB (SEQ ID NO: 34) is used for the secondary PCR. The sequences of the primers are given in Table XI below.
For each placenta and foetus, three independent PCRs are carried out. The placentas and foetuses are considered positive when Neospora caninum is detected in the case of at least one PCR. The results are presented in Table XII below.
These results demonstrate that vaccination with the attenuated mutant strain Neo ncmic1-3 KO reduces the maternal-foetal transmission of the parasite considerably, thus validating the efficacy of the strain Neo mic-1-3 KO for preventing harmful effects of neosporosis in a murine model of endogenous congenital neosporosis.
The mutant strain Neo ncmic1-3 KO described in Example 3 was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS); 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000 November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
Female OF1 mice were divided into 3 separate batches:
One hundred and seven days after the start of the experiments, the mice were mated at a rate of 3 female mice to one male. The pregnant mice are diagnosed by weighing.
At 18 days of gestation, i.e. one day before theoretical parturition, the female mice are sacrificed. The foetuses are isolated and the DNA is extracted.
A nested PCR is carried out from the region of the NC5 gene of N. caninum (Yamage et al., J. Parasitol, 1996 April, 82(2): 272-9, Baszler et al., J. Clin. Microbiol, 1999 December, 37(12): 4059-64). The primer pair NC5 FA (SEQ ID NO: 31) and NC5 RA (SEQ ID NO: 32) is used for the primary PCR, and the primer pair NC5 FB (SEQ ID NO: 33) and NC5 RB (SEQ ID NO: 34) is used for the secondary PCR. The sequences of the primers are given in Table XIII below.
For each foetus, 3 independent PCRs are carried out. The foetus is regarded as positive when Neospora caninum is detected in the case of at least one PCR. The results are presented in Table XIV below.
These results demonstrate that vaccination with the attenuated mutant strain Neo ncmic1-3 KO significantly reduces (Chi2 test, p<0.05) the maternal-foetal transmission of the parasite when the mothers are infected before gestation, thus validating the prophylactic and therapeutic efficacy of the strain Neo ncmic1-3 KO for preventing harmful effects of neosporosis in a murine model of congenital neosporosis with infection of the mother before gestation.
The mutant strain Neo ncmic1-3 KO described in Example 3 was maintained by regular passages on HFF cells cultured in DMEM medium supplemented with 10% of foetal calf serum (FCS); 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. As the passages on HFF cells reduce the virulence of the parasites (Baszler et al., Clin. Diagn. Lab. Immunol., 2000 November; 7(6)893-898 and Bartley et al., Parasitology, 2006, October; 133(4): 421-32), the number of passages on HFF cells is deliberately limited to 20.
Female Balb/C mice were divided into 2 separate batches:
The mice were sacrificed. The brains of the mice are then removed and ground in RPMI medium using a Potter. A proportion of the ground material is then deposited on HFF cells in DMEM medium supplemented with 10% of foetal calf serum (FCS), 2 mM of glutamine, 50 U/mL of penicillin and 50 μg/mL of streptomycin. The parasites are then harvested and their genomic DNA is extracted.
Starting from the genomic DNA, PCRs were carried out for:
The sequences of the primers and the size of the amplicons originating from the different PCRs are shown in Tables XVI and XVII below, respectively.
Neospora
caninum
The amplicons obtained by PCR from samples originating from vaccinated mice and those obtained from samples originating from mice challenged with the strain NC-1 (
These results confirm that it is possible to differentiate the vaccinated animals from the infected animals.
| Number | Date | Country | Kind |
|---|---|---|---|
| 12/57544 | Aug 2012 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/FR2013/051877 | 8/2/2013 | WO | 00 |
