Patent Application
20230340621
The present invention relates to a method of detecting diseases in turf grass caused by fungal pathogens with a loop-mediated isothermal amplification (LAMP) assay of a sample of such turf grass to detect nucleic acids from one or more fungi.
LAMP or Loop-mediated Isothermal Amplification as described in e.g. U.S. Pat. No. 6,410,278 (Eiken) is a DNA amplification method characterized by the use of at least 4 or more different primers (See, e.g., http://loopamp.elken.co.ip/e/lamp/primer.html) that are specifically designed to recognize 6 distinct regions on the target gene and the reaction process proceeds at a constant temperature using strand displacement reaction. Amplification and detection of target nucleic acid of interest can be completed in a single step, by incubating the mixture of the biological sample or a nucleic acid extract thereof, primers, DNA polymerase with strand displacement activity and substrates at a constant temperature (about 65′C). It provides high amplification efficiency, with DNA being amplified numerous times in 15-60 minutes. Because of its high specificity, the presence of amplified product can indicate the presence of target gene (http://loopamp.eiken.co.jp/e/lamp/principle.html).
There are numerous problems that turf grass managers face in maintaining turf grass at a standard of quality expected by users. While the problems are many, those relating to disease (including diseases caused by fungal pathogens) are particularly challenging to manage and control. For example, disease can affect turf grass plants on golf courses causing a loss of revenue from reduced quality including playability. One example of a common problem for golf course managers is knowing which disease is present so that appropriate and timely management techniques can be taken. Relevant turf diseases caused by turf pathogenic microorganisms include, for example, anthracnose, take-all patch, summer patch, snow mold, pythium blight, brown patch and dollar spot.
Agricultural active chemicals for controlling pathogens, such as fungicides, are typically applied on golf courses as needed depending on the extent of disease pressure, pathogen population, weather, and the like. However, fungicide applications are highly controlled by course budget, availability of appropriate equipment, and availability of qualified personnel for applying the agricultural active chemicals.
In view of these problems, a rapid and reliable assay for detection of turf pathogenic fungi would be extremely useful. Known PCR assays are not practical to use in golf course or other intensively managed turf grass or professional landscape settings, as PCR requires specialised laboratory skills and instruments. Certain other molecular biology methods for decting fungal disease in turf grass are known and described, for example, in WO2009147017 which relates to a TRFLP methodology.
The present invention accordingly relates to a LAMP assay for detecting the presence of DNA in a turf sample which is associated with selected fungal pathogens that cause relevant turf diseases including, for example, anthracnose, take-all patch, summer patch, snow mold, pythium blight, brown patch and dollar spot.
To facilitate timely and efficient detection of turf grass disease pathogens and to improve the cost and effectiveness of turf grass disease treatments, a LAMP assay according to the invention can be utilized to earlier detect DNA associated with fungal pathogens which cause relevant turf diseases. In accordance with the invention, the LAMP method suitably uses a primer set of at least four and preferably six or more nucleic acid sequences derived from the target disease pathogens. More particularly, the inventive method provides that each primer used in the selected primer set for the LAMP assay has from 15 to 50 nucleic acids and where the primers in the set are selected from a specific DNA loci within the target fungi.
In accordance with the present invention, a method for detecting fungal DNA in a turf grass sample with a loop-mediated isothermal amplification (LAMP) assay is provided which contains primers for fungal DNA (nucleic acids) of a turf pathogenic fungi selected from the group consisting of Sclerotinia homoeocarpa, Rhizoctonia solani spp., Pythium aphanidermatum, Gaeumannomyces graminis spp., Microdochium nivale spp., Magnaporthe poae, Colletotrichum graminicola, Colletotrichum cereale and Pythium ultimum var. ultimum(target fungi). The LAMP assay of the present invention uses a primer set of at least four and preferably six or more nucleic acid sequences with each primer in the set having from 15 to 50 nucleic acids, and where the fungal DNA to be detected is obtained from a target fungal pathogen. The primers useful in the present LAMP assay method are selected from specific internal transcribed spacer regions or genes of the target fungi to provide improved assay results.
In a particular embodiment, the Microdochium nivale spp. target fungi are selected from Microdochium nivale var. nivale and Microdochium nivale var. majus. In another embodiment, the Gaeumannomyces graminis spp. target fungi are selected from Gaeumannomyces graminis var. avenae, Gaeumannomyces graminis var. graminis and Gaeumannomyces graminis var. tritici. In a further embodiment, the Rhizoctonia solani spp. target fungi are selected from Rhizoctonia solani AG2-21V and Rhizoctonia solani AG2-2111B.
In the context of the present invention, detection of fungal DNA with the inventive LAMP assay in a turf sample may be indicative of the presence of fungal pathogens and can also assist in assesing the onset or presence of a turf disease condition as follows:
Sclerotinia homoeocarpa
Rhizoctonia solani spp.
Microdochium nivale spp.
Pythium aphanidermatum
Gaeumannomyces graminis spp.
Magnaporthe poae
Colletotrichum graminicola
Colletotrichum cereale
Pythium ultimum
In one embodiment,
Preferably the LAMP primer sets sutiable for use in detecting fungi DNA in turf samples according to the present invention comprise four primers including: a pair of forward (FIP) and reverse (BIP) inner primers, and a pair of forward (F3) and reverse (B3) outer primers. More preferably, the LAMP primer sets sutiable for use in the present invention include the addition of loop forward (LF) and/or loop back (LB) primers to accelerate amplification of nucleic acid present in the turf sample and to reduce the detection time of any target fungi that may be present in such turf sample. The LAMP primer set embodiments listed below relate to the detection of the target fungi DNA in turf samples in accordance with the method of the invention.
In the description of the embodiments which follow that are associated with the primers of SEQ ID Nos. 14-91 according to the invention, it will be understood that the primers useful in the present invention each independently and respectively have a sequence which is at least 90%, preferably at least 95%, more preferably at least 96%, and even more preferably at least 97% identical to the primers of SEQ IDs of 14-91.
In a particularly prefered embodiment, the primers useful in the present invention each independently and respectively have a sequence which is at least at least 98%, more preferably at least 99% identical to the primers of SEQ IDs of 14-91. Most preferably, the primers useful in the present invention each independently and respectively have a sequence which is identical to SEQ IDs of 14-91.
Accordingly, the present invention provides a method for detecting fungal DNA in a turf grass sample with a loop-mediated isothermal amplification (LAMP) assay which contains primers for fungal DNA of at least one turf pathogenic fungi selected from Sclerotinia homoeocarpa, Rhizoctonia solani spp., Pythium aphanidermatum, Gaeumannomyces graminis spp., Microdochium nivale spp., Magnaporthe poae, Colletotrichum graminicola, Colletotrichum cereale and Pythium ultimum var. ultimum, comprising: subjecting the turf sample to a LAMP reaction wherein the LAMP reaction uses a primer set of four or more nucleic acid sequences with each primer in the set having from 15 to 50 nucleic acids, and wherein the set of primers comprises at least one primer set as described below.
In one embodiment, the primer set for detecting Sclerotinia homoeocarpa DNA comprises or is selected from SEQ ID NOs: 15 and 27.
In another embodiment, the primer set for detecting Sclerotinia homoeocarpa DNA comprises or is selected from SEQ ID NOs:14, 15, 16 and 17.
In a further embodiment, the primer set for detecting Sclerotinia homoeocarpa DNA comprises or is selected from SEQ ID NOs: 14, 15, 16, 17, 18 and 19.
In a further embodiment, the primer set for detecting Rhizoctonia solani DNA comprises or is selected from SEQ ID NO: 23.
In another embodiment, the primer set for detecting Rhizoctonia solani DNA comprises or is selected from SEQ ID Nos: 63, 64 and 65.
In another embodiment, the primer set for detecting Rhizoctonia solani DNA comprises or is selected from SEQ ID NO: 20, 21, 22 and 23.
In another embodiment, the primer set for detecting Rhizoctonia solani DNA comprises or is selected from SEQ ID NO: 62, 63. 66 and 67.
In yet another embodiment, the primer set for detecting Rhizoctonia solani DNA comprises or is selected from SEQ ID Nos: 62, 63, 64, 65, 66 and 67.
In another embodiment, the primer set for detecting Rhizoctonia solani DNA comprises or is selected from SEQ ID Nos: 20, 21, 22, 23, 24 and 25.
In another embodiment, the primer set for detecting Microdochium nivale spp. (preferably Microdochium nivale var. nivale) DNA comprises or is selected from SEQ ID Nos: 27, 28 and 29.
In another embodiment, the primer set for detecting Microdochium nivale spp. (preferably Microdochium nivale var. nivale) DNA comprises or is selected from SEQ ID NO: 26, 27, 28, and 29.
In a further embodiment, the primer set for detecting Microdochium nivale spp. (preferably Microdochium nivale var. nivale) DNA comprises or is selected from SEQ ID Nos: 26, 27, 28, 29, 30 and 31.
In one embodiment, the primer set for detecting Pythium aphanidermatum DNA comprises or is selected from SEQ ID NOs:33, 36 and 37.
In another embodiment, the primer set for detecting Pythium aphanidermatum DNA comprises or is selected from SEQ ID NO: 32, 33, 36, and 37.
In another embodiment, the primer set for detecting Pythium aphanidermatum DNA comprises or is selected from SEQ ID NOs: 32, 33, 34, 35, 36 and 37.
In another embodiment, the primer set for detecting Pythium aphanidermatum DNA comprises or is selected from SEQ ID NOs:69, 70 and 71.
In another embodiment, the primer set for detecting Pythium aphanidermatum DNA comprises or is selected from SEQ ID NO: 68, 69, 72 and 73.
In another embodiment, the primer set for detecting Pythium aphanidermatum DNA comprises or is selected from SEQ ID NOs: 68, 69, 70, 71, 72 and 73.
In one embodiment, the primer set for detecting Gaeumannomyces graminis spp. (preferably Gaeumannomyces graminis var. avenae, Gaeumannomyces graminis var. graminis or Gaeumannomyces graminis var. tritici) DNA comprises or is selected from SEQ ID NO: 60.
In another embodiment, the primer set for detecting Gaeumannomyces graminis spp. (preferably Gaeumannomyces graminis var. avenae, Gaeumannomyces graminis var. graminis or Gaeumannomyces graminis var. tritici) DNA comprises or is selected from SEQ ID NOs: 42 and 43.
In a further embodiment, the primer set for detecting Gaeumannomyces graminis spp. (preferably Gaeumannomyces graminis var. avenae, Gaeumannomyces graminis var. graminis or Gaeumannomyces graminis var. tritici) DNA comprises or is selected from SEQ ID NO: 38, 39, 42 and 43.
In a further embodiment, the primer set for detecting Gaeumannomyces graminis spp. (preferably Gaeumannomyces graminis var. avenae, Gaeumannomyces graminis var. graminis or Gaeumannomyces graminis var. tritici) DNA comprises or is selected from SEQ ID NO: 56, 57, 60 and 61.
In another embodiment, the primer set for detecting Gaeumannomyces graminis spp. (preferably Gaeumannomyces graminis var. avenae, Gaeumannomyces graminis var. graminis or Gaeumannomyces graminis var. tritici) DNA comprises or is selected from SEQ ID NOs: 38, 39, 40, 41, 42 and 43.
In another embodiment, the primer set for detecting Gaeumannomyces graminis spp. (preferably Gaeumannomyces graminis var. avenae, Gaeumannomyces graminis var. graminis or Gaeumannomyces graminis var. tritici) DNA comprises or is selected from SEQ ID NO: 56, 57, 58, 59, 60 and 61.
In one embodiment, the primer set for detecting Microdochium nivale spp. (preferably Microdochium nivale var. majus) DNA comprises or is selected from SEQ ID Nos: 48 and 49.
In a further embodiment, the primer set for detecting Microdochium nivale spp. (preferably Microdochium nivale var. majus) DNA comprises or is selected from SEQ ID NO: 44, 45, 48 and 49.
In yet another embodiment, the primer set for detecting Microdochium nivale spp. (preferably Microdochium nivale var. majus) DNA comprises or is selected from SEQ ID Nos: 44, 45, 46, 47, 48 and 49.
In another embodiment, the primer set for detecting Magnaporthe poae DNA comprises or is selected from SEQ ID NOs: 54 and 55.
In a further embodiment, the primer set for detecting Magnaporthe poae DNA comprises or is selected from SEQ ID NO: 50, 51, 54 and 55.
In another embodiment, the primer set for detecting Magnaporthe poae DNA comprises or is selected from SEQ ID NOs: 50, 51, 52, 53, 54, and 55.
In one embodiment, the primer set for detecting Colletotrichum graminicola DNA comprises or is selected from SEQ ID NOs:74, 76 and 77.
In a further embodiment, the primer set for detecting Colletotrichum graminicola DNA comprises or is selected from SEQ ID NO: 74 75, 78 and 79.
In another embodiment, the primer set for detecting Colletotrichum graminicola DNA comprises or is selected from SEQ ID NOs:74, 75, 76, 77, 78 and 79.
In another embodiment, the primer set for detecting Colletotrichum cereale DNA comprises or is selected from SEQ ID Nos 80, 82 and 83.
In a further embodiment, the primer set for detecting Colletotrichum cereale DNA comprises or is selected from SEQ ID NO: 80, 81, 84 and 85.
In another embodiment, the primer set for detecting Colletotrichum cereale DNA comprises or is selected from SEQ ID Nos 80, 81, 82, 83, 84 and 85.
In one embodiment, the primer set for detecting Pythium ultimum var. Ultimum Idin-rc DNA comprises or is selected from SEQ ID Nos: 86, 88 and 89.
In a further embodiment, the primer set for detecting Pythium ultimum var. Ultimum Idin-rc DNA comprises or is selected from SEQ ID NO: 86, 87, 90 and 91.
In another embodiment, the primer set for detecting Pythium ultimum var. Ultimum Idin-rc DNA comprises or is selected from SEQ ID Nos: 86, 87, 88, 89, 90 and 91.
The LAMP assays of the invention can be used for detection, including early detection, of DNA from turf fungi selected from the group consisting of Sclerotinia homoeocarpa, Rhizoctonia solani, Pythium aphanidermatum, Gaeumannomyces graminis spp., Microdochium nivale spp., Magnaporthe poae, Colletotrichum graminicola, Colletotrichum cereale and Pythium ultimum var. Ultimum in turf samples which is easy to obtain and allows management and/or maintenance of the turf grass to be tailored accordingly.
According to the invention, by “turf grass” there is understood an annual or perennial Gramineae. Said gramineae preferably belongs to one or more of the genera Agropyron, Agrostis, Axonopus, Bromus, Buchloe, Cynodon, Eremochloa, Festuca, Lolium, Paspulum, Pennisetum, Phleum, Poa, Stenotaphrum or Zoysia. More preferably, said gramineae belongs to one or more of the genera Agrostis, Buchloe, Cynodon, Eremochloa, Festuca, Lolium, Paspulum, Pennisetum, Poa, Stenotaphrum or Zoysia.
In one embodiment, according to the invention by “turf” is understood as a group of turf grass, which covers a surface area of ground and is subject to regular maintenance.
The present invention can be practiced with all turf grasses, including cool season turf grass and warm season turf grass.
Examples of cool season turf grasses are: Bluegrasses (Poa L.), such as Kentucky Bluegrass (Poa pratensis L.), Rough Bluegrass (Poa trivialis L.), Canada Bluegrass (Poa compressa L.) and Annual Bluegrass (Poa annua L.); Bentgrasses (Agrostis L.), such as Creeping Bentgrass (Agrostis palustris Huds.), Colonial Bentgrass (Agrostis tenius Sibth.), Velvet Bentgrass (Agrostis canina L.) and Redtop (Agrostis alba L.); Fescues (Festuca L.), such as Creeping Red Fescue (Festuca rubra L.), Chewings Fescue (Festuca rubra var. commutate Gaud.), Sheep Fescue (Festuca ovine L.), Hard Fescue (Festuca longifolia), Tall Fescue (Festuca arundinacea Schreb.), Meadow Fescue (Festuca elatior L.); Ryegrasses (Lolium L.), such as Perennial Ryegrass (Lolium perenne L.), Annual (Italian) Ryegrass (Lolium multiflorum Lam.); Wheatgrasses (Agropyron Gaertn.), such as Fairway Wheatgrass (Agropyron cristatum (L.) Gaertn.), Western Wheatgrass (Agropyron smithii Rydb.). Other cool season turf grasses include Smooth Brome (Bromus inermis Leyss.) and Timothy Phleum L.).
Examples of warm season turf grasses are Bermudagrasses (Cynodon L. C. Rich), Zoysiagrasses Zoysia Willd.), St. Augustinegrass (Stenotaphrum secundatum (Walt.) Kuntze), Centipedegrass Eremochloa ophiuroides (Munro.) Hack.), Carpetgrass (Axonopus Beauv.), Bahiagrass (Paspalum notatum Flugge.), Kikuyugrass (Pennisetum clandestinum Hochst. ex Chiov.), Buffalograss (Buchloe dactyloides (Nutt.) Engelm.) and Seashore paspalum (Paspalum vaginatum swartz).
The LAMP method invention also contemplates a kit for the detection of fungi in a turf grass sample using a LAMP assay. A test strip containing one or more than one of the primer sets as described herein can be utilized. In one embodiment, multiple primer sets are multiplexed on a test strip for the detection of multiple diseases from turf grass samples collected from a particular locus.
For example, a bijou tube with a ball bearing and a suitable amount of lysis buffer is provided with a 1 cubic cm homogenized turf sample and shaken vigorously for 1 minute. A test strip with sample well containing all the resuspension buffer and drops of this test solution are placed into a sample wells on a test strip wherein the wells have all the ingredients necessary to perform a LAMP reaction (e.g., the primer sets and a reagent such as an isothermal master mix cat no. iso-001 available from Optigene). In one embodiment, the test strips are multiplexed. In another embodiment, the test strip includes 8 wells, two control and 6 for turf diseases of interest. In one embodiment, the test strip is associated with a diagnostic instrument such as a Genie®II or III available from OptiGene.
Primer Design
Highly conserved genes were used for the design of the LAMP primers for the detection of DNA from selected turf grass pathogens (column 1 of TABLE 3). Pure genomic DNA from all fungi of interest was obtained using the NucleoSpin Plant II (MACHEREY-NAGEL). With PCR technology the sequence of interest were amplified using published primer pairs followed by a Sanger sequencing. The following DNA Loci (genes and regions) were sequenced: Internal transcribed spacer (ITS), elongation factor 1-alpha (EF), beta-tubulin (Tub), cytochrome c oxidase subunit 1 (Cox), superoxide dismutase (SOD1) and large subunit nuclear ribosomal RNA (LSU). The raw sequences were aligned using ClustalW alignment method (CLC Main Workbench Software). The BLAST comparisons with sequences from GenBank (NCBI) were used to identify gene homologs. Ideally, a good sequence is defined by successful PCR amplification for all target taxa and no homology with other taxa.
The best sequences (SEQ ID Nos, 1-13) from the sequenced DNA Loci were then used for the design of the LAMP primers for each of the selected turf grass pathogens using LAMP Designer 1.14 (PREMIER Biosoft). Therefore different parameters were tested to get different primer sets per organisms and loci (See TABLE 3 for a correlation of turf pathogen, selected loci and SEQ ID of best sequences used for primer design). The designed primers sets shown in TABLE 1 were then tested for their specificity (TABLE 3) and sensitivity (TABLE 4).
Specificity
To examine the specificity of the reaction (Literature see below), assays using the designed primer sets are tested using pure genomic DNA extracts from the fungal isolates described in TABLE 2. A comprehensive collection of different turf grass pathogens from distinct geographical origins were collected and grow on different media (potato dextrose/malt/cornmeal/cherry/V8). A ten-day old fungal culture was used to extract the DNA from mycelium (NucleoSpin Plant II—MACHEREY-NAGEL). The genomic DNA was diluted with nuclease free water to 5 ng/μl and a portion of 2.5 μl was used for the specificity tests.
The LAMP specificity tests were performed on a LightCycler 480 (Roche) in 96 well plates at 64° C. for 55 min. The amplicon-specific annealing temperature was determined during cooling from 98° C. to 65° C. with a ramp rate of −0.1° C. per second. Real-time LAMP assays were carried out in 10 μl reaction mixtures containing 5 μl of isothermal master mix at a 1× concentration (Optigene), 0.4 μM each external primer, 1.6 μM each internal primer, and 0.8 μM each loop primer (synthesized by Microsynth) and 2.5 μl of genomic DNA.
All reactions were carried out in duplicate and at two different days.
Colletotrichum cereale
Colletotrichum cereale
Colletotrichum cereale
Colletotrichum cereale
Colletotrichum cereale
Colletotrichum cereale
Colletotrichum graminicola
Colletotrichum graminicola
Gaeumannomyces graminis
Gaeumannomyces graminis var. avenae
Gaeumannomyces graminis var. avenae
Gaeumannomyces graminis var. avenae
Gaeumannomyces graminis var. graminis
Gaeumannomyces graminis var. graminis
Gaeumannomyces graminis var. graminis
Gaeumannomyces graminis var. tritici
Gaeumannomyces graminis var. tritici
Gaeumannomyces graminis var. tritici
Magnaporthe poae
Magnaporthe poae
Microdochium nivale majus
Microdochium nivale nivale
Microdochium nivale var. nivale
Microdochium nivale var. nivale
Microdochium nivale var. nivale
Pythium aphanidermatum
Pythium aphanidermatum
Pythium aphanidermatum
Pythium aphanidermatum
Pythium aphanidermatum
Pythium aphanidermatum
Pythium ultimum
Pythium ultimum var. sporangiiferum
Pythium ultimum var. ultimum
Pythium ultimum var. ultimum
Pythium ultimum var. ultimum
Pythium ultimum var. ultimum
Pythium ultimum var. ultimum
Pythium ultimum var. ultimum
Pythium ultimum var. ultimum
Pythium ultimum var. ultimum
Rhizoctonia solani AG1.1C
Rhizoctonia solani AG2-2IV
Rhizoctonia solani AG4
Rhizoctonia solani AG
Rhizoctonia solani AG2-2IIIB
Rhizoctonia solani AG1-1A
Rhizoctonia solani AG1-1
Rhizoctonia solani AG1-1A
Rhizoctonia solani AG1-1B
Rhizoctonia solani AG1-1C
Rhizoctonia solani AG1-1A
Rhizoctonia solani AG1-1B
Rhizoctonia solani AG2-2IIIB
Rhizoctonia solani AG4
Sclerotinia homoeocarpa
Sclerotinia homoeocarpa
Sclerotinia homoeocarpa
Sclerotinia homoeocarpa
Sclerotinia homoeocarpa
Sclerotinia homoeocarpa
Sclerotinia homoeocarpa
Sclerotinia homoeocarpa
Sclerotinia homoeocarpa
Sclerotinia homoeocarpa
Thanatephorus cucumeris/Rhizoctonia solani
Thanatephorus cucumeris/Rhizoctonia solani
Thanatephorus cucumeris/Rhizoctonia solani
Thanatephorus cucumeris/Rhizoctonia solani
As summarized in TABLE 3, the specificity of the LAMP assay was checked against the designed specific target for the fungi strains listed in TABLE 2. As an additional confirmation of specificity, a matching melting temperature of 82.6-89.9° C.±0.5° C. was observed for the different amplified products as also shown in TABLE 3.
Sclerotinia homoeocarpa
Rhizoctonia solani AG2-2IIIB
Rhizoctonia solani AG2-2IV
Microdochium nivale var.
nivale
Pythium aphanidermatum
Pythium aphanidermatum
Gaeumannomyces graminis
Gaeumannomyces graminis
Microdochium nivale var.
majus
Magnaporthe poae
Colletotrichum graminicola
Colletotrichum cereale
Pythium ultimum var. ultimum
The sensitivity of the of the described primer sets corresponding to the DNA of Seq ID Nos. 1-13 (Table 1) were determined using serial dilutions of genomic DNA (1 ng to 100 fg) of all fungi of interests, with each reaction made in duplicate at two different days. Pure genomic DNA from all fungi was obtained using the NucleoSpin Plant II (MACHEREY-NAGEL). The LAMP sensitivity tests were performed on a LightCycler 480 (Roche) in 96 well plates at 64° C. for 55 min. The amplicon-specific annealing temperature was determined during cooling from 98° C. to 65° C. with a ramp rate of −0.1° C. per second. Real-time LAMP assays were carried out in 10 μl reaction mixtures containing 5 μl of isothermal master mix at a 1× concentration (Optigene), 0.4 μM each external primer, 1.6 μM each internal primer, and 0.8 μM each loop primer (synthesized by Microsynth) and 2.5 μl of genomic DNA.
Method of Detecting Fungal Pathogen in a Turf Grass Sample
Sample Collection
A tuft of turf sample including grass roots is collected at a location where a fungal pathogen is expected. The turfgrass may also show symptoms. The turf sample is placed in a clean 50 ml tube (Corning) and stored at −20° C. until use. DNA is extracted using Plant Material Lysis Kit (Optigene). A 1 cm3 cube of the turf sample is placed into a Bijou tube containing 1 ml of lysis buffer (Optigene). The homogenization of the turf sample is conducted by shaking the Bijou tube for 1 min. A volume of 10 μl of the lysate is transferred into a dilution tube provided (Optigene) and mixed vigorously by shaking. The diluted lysate is subsequently defined as the template.
LAMP Reaction
In some embodiments, the LAMP reaction is performed at about 60° C. to about 70° C., such as about 64° C. to about 67° C., or about 64° C. to about 66° C. In specific examples, the LAMP reaction is performed at 64° C.
In some embodiments, the LAMP reaction is allowed to proceed for about 15 to about 45 minutes, such as about 20 minutes to about 40 minutes, or about 25 minutes to about 35 minutes.
In some embodiments, the concentration of primers in the LAMP reaction according to the present invention is 1.4-1.8 μM, more specifically 1.6 μM for the forward (FIP) and reverse (BIP) inner primers, 0.2-0.4 μM, more specifically 0.4 μM for forward (F3) and reverse (B3) outer primers, and 0.4-0.8 μM, more specifically 0.8 μM, loop forward (LF) and/or loop back (LB) primers that are useful to accelerate amplification of nucleic acid present in the turf sample and to reduce the detection time of any target fungi DNA that may be present in such turf sample.
Suitable buffer systems useful in the reaction of LAMP assay include:
Suitable enzyme systems (DNA polymerase, etc.) useful in the reaction of LAMP assay include:
In one embodiment, the LAMP reactions are performed on a Genie instrument (Optigene) in a test strip with dried reagents (Optigene). In one embodiment, the strips have eight 150 μl wells (2 control and 6 for assays). Real-time LAMP assays are carried out in 25 μl reaction mixtures containing 15 μl of isothermal master mix at a 1× concentration (Optigene), 0.4 μM each external primer, 1.6 μM each internal primer, and 0.8 μM each loop primer (synthesized by Microsynth) selected from at least one of the primer sets of Table 1. Prior to adding the template, the lyophilized reaction strip is resuspended in 22 μl resuspension buffer (Optigene). All test strips include a negative control and a positive plant control primer set provided by Optigene. For all assays, 3 μl of template is added per reaction and well. The reaction is held at 64° C. for 30-55 min followed by an anneal program. The temperature profile of the anneal program is determined during cooling from 98° C. to 65° C. with a ramp rate of −0.1° C. per second.
The isothermal master mix contains a fluorescent double-stranded DNA binding dye to permit the real-time detection of the amplicons. The assays are optimized in terms of reaction time, temperature, and the volume of DNA added per reaction.
The fluorescence data that is acquired during amplification phase at 64° C. is reported as amplification time. The fluorescence derivative data that is acquired during the anneal phase is reported as an annealing temperature.
Alternatively, the LAMP assay reaction does not include an anneal program in which case a pH-sensitive indicator dye can be used to assess the presence of target fungal DNA. In some examples, the pH-sensitive indicator dye is a colored dye detectable in visible light. In particular examples, the colored dye comprises cresol red, phenol red, m-cresol purple, bromocresol purple, neutral red, naphtholphthalein, thymol blue or naphtolphthalein. In other examples, the pH-sensitive indicator dye is a fluorescent indicator dye. In particular examples, the fluorescent dye comprises 2′,7′-bis-(2-carboxyethyl)-5(6)-carboxyfluorescein, 5(6)-carboxy-2′,7′-dichlorofluorescein, 5(6)-carboxyfluorescein, 3,6-diacetoxyphthalonitrile, 6,8-dihydroxy-1,3-pyrenedisulfonic acid, or 5-(and-6)-carboxyl seminaphthorhodafluor.
Following the foregoing procedures, the detection of the presence of fungal pathogen DNA (Table 3) in a turf sample may indicate the presence of a turf fungal pathogen that may cause relevant turf diseases (including, for example, anthracnose, take-all patch, summer patch, snow mold, pythium blight, brown patch and dollar spot). Early and efficient detection provides suitable turf grass disease management decisions to be undertaken.
| Number | Date | Country | Kind |
|---|---|---|---|
| 18155093.0 | Feb 2018 | EP | regional |
| 18159821.0 | Mar 2018 | EP | regional |
This application is a divisional of U.S. application Ser. No. 16/967,319, filed Aug. 4, 2020, which is a 371 National Stage application of International Application No. PCT/EP2019/052803, filed Feb. 5, 2019, which claims priority to EP 18159821.0, filed Mar. 2, 2018, and EP 18155093.0, filed Feb. 5, 2018, the entire contents of which are incorporated by reference herein.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16967319 | Aug 2020 | US |
| Child | 18185738 | US |
