Multiplex assay for the detection of citrus pathogens

US10100373B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10100373-B2
Application numberUS-201615162045-A
CountryUS
Kind codeB2
Filing dateMay 23, 2016
Priority dateJul 18, 2012
Publication dateOct 16, 2018
Grant dateOct 16, 2018

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  1. Title

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  5. First independent claim

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  7. Citations and related patents

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Abstract

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The present invention provides methods and compositions for detecting multiple citrus pathogens using a multiplex branched DNA signal amplification reaction.

First claim

Opening claim text (preview).

What is claimed is: 1. A reaction mixture comprising probes (a) for detecting the presence of two or more citrus pathogens selected from the group consisting of Citrus tristeza virus (CTV) universal, CTV genotype T30, CTV genotype VT, Citrus psorosis virus, Citrus tatter leaf virus, Citrus leaf blotch virus, Citrus exocortis viroid, Hop stunt viroid, and Citrus leprosis virus, wherein the reaction mixture comprises at least one capture extender probe and at least one label extender probe for targeting each of the two or more pathogens selected from a set of detection probes as follows: a capture extender probe that targets CTV universal and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:1, 2, 3, 4, 5, or 6; and a label extender probe that targets CTV universal and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO: 7, 8, 9, 10, 11, or 12; a capture extender probe that targets CTV genotype T30 and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:13, 14, 15, 16, 17, 18, 19, or 20; and a label extender probe that targets CTV genotype T30 and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, or 38; a capture extender probe that targets CTV VT genotype and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:41, 42, 43, 44, 45, or 46; and a label extender probe that targets CTV VT genotype and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, or 66; a capture extender probe that targets Citrus psorosis virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:71, 72, 73, 74, 75, 76, 77, or 78; and a label extender probe that targets Citrus psorosis virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:79, 80, 81, 82, 83, 84, 85, or 86; a capture extender probe that targets Citrus tatter leaf virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:87, 88, 89, 90, 91, or 92; and a label extender probe that targets Citrus tatter leaf virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:93, 94, 95, 96, 97, 98, or 99; a capture extender probe that targets Citrus leaf blotch virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:100, 101, 102, 103, or 104; and a label extender probe that targets Citrus leaf blotch virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:105, 106, 107, 108, 109, 110, 111, 112, 113, or 114: a capture extender probe that targets Citrus exocortis virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:118, 119, 120, 121, 122, or 123; and a label extender probe that targets Citrus exocortis virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:124, 125, 126, 127, 128, 129, 130, or 131; a capture extender probe that targets Hop stunt viroid and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:133, 134, 135, 136, or 137; and a label extender probe that targets Hop stunt viroid and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:138, 139, 140, 141, 142, or 143; and a capture extender probe that targets Citrus leprosis virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:144, 145, 146, 147, 148, or 149; and a label extender probe that targets Citrus leprosis virus comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, or 161, further, wherein the capture extender probe comprises a sequence that hybridizes to a capture probe immobilized on a solid support; and (b) a capture probe that hybridizes to one or more of capture extender probes. 2. The reaction mixture of claim 1 , wherein the reaction comprises multiple capture extender probes and multiple label extender probes that target the pathogen. 3. The reaction mixture of claim 1 , further comprising at least one capture extender probe and at least one label extender probe that target a third, fourth, fifth, sixth, seventh, or eighth pathogen selected from Citrus tristeza virus (CTV) universal, CTV genotype T30, CTV genotype VT, Citrus psorosis virus, Citrus tatter leaf virus, Citrus leaf blotch virus, Citrus exocortis viroid, Hop stunt viroid, or Citrus leprosis virus. 4. The reaction mixture of claim 3 , wherein the reaction comprises multiple capture extender probes and multiple label extender probes that target the third, fourth, fifth, sixth, seventh, or eighth pathogen. 5. The reaction mixture of claim 1 , comprising a capture extender probe and a label extender probe for each of the nine pathogens Citrus tristeza virus (CTV) universal, CTV genotype T30, CTV genotype VT, Citrus psorosis virus, Citrus tatter leaf virus, Citrus leaf blotch virus, Citrus exocortis viroid, Hop stunt viroid, and Citrus leprosis virus. 6. The reaction mixture of claim 5 , comprising multiple capture extender probes and multiple label extender probes that target each of the nine pathogens. 7. A kit for detecting the presence of two or more citrus pathogens selected from Citrus tristeza virus (CTV) universal, CTV genotype T30, CTV genotype VT, Citrus psorosis virus, Citrus tatter leaf virus, Citrus leaf blotch virus, Citrus exocortis viroid, Hop stunt viroid, or Citrus leprosis virus in a plant sample, wherein the kit comprises (a) at least one capture extender probe and at least one label extender probe that target each of the two or more pathogens, wherein the at least one capture extender probe and at least one label extender probe for targeting each of the two or more pathogens is selected from a set of detection probes as follows: a capture extender probe that targets CTV universal and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:1, 2, 3, 4, 5, or 6; and a label extender probe that targets CTV universal and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO: 7, 8, 9, 10, 11, or 12; a capture extender probe that targets CTV genotype T30 and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:13, 14, 15, 16, 17, 18, 19, or 20; and a label extender probe that targets CTV genotype T30 and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, or 38; a capture extender probe that targets CTV VT genotype and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:41, 42, 43, 44, 45, or 46; and a label extender probe that targets CTV VT genotype and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, or 66; a capture extender probe that targets Citrus psorosis virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:71, 72, 73, 74, 75, 76, 77, or 78; and a label extender probe that targets Citrus psorosis virus and comprises at least 8, 9, or 10 contiguous nucleotides of a probe sequence of SEQ ID NO:79, 80, 81, 82, 83, 84, 85, or 86; a capture extender probe that targets Citrus tatter leaf virus and comprises at least 8, 9, or 10 contiguous nucleotides of a pr

Assignees

Inventors

Classifications

  • C12Q1/701Primary

    Specific hybridization probes · CPC title

  • Primer sets for multiplex assays · CPC title

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What does patent US10100373B2 cover?
The present invention provides methods and compositions for detecting multiple citrus pathogens using a multiplex branched DNA signal amplification reaction.
Who is the assignee on this patent?
Univ California
What technology area does this patent fall under?
Primary CPC classification C12Q1/701. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 16 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).