Rapid detection of Phytophthora cinnamomi based on a new target gene Pcinn13739
Phytophthora cinnamomi causes crown and root wilting in more than 5,000 plant species and represents a significant threat to the health of natural ecosystems and horticultural crops. The early and accurate detection of P. cinnamomi is a fundamental step in disease prevention and appropriate manageme...
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Published in | Frontiers in cellular and infection microbiology Vol. 12; p. 923700 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
25.08.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Phytophthora cinnamomi
causes crown and root wilting in more than 5,000 plant species and represents a significant threat to the health of natural ecosystems and horticultural crops. The early and accurate detection of
P. cinnamomi
is a fundamental step in disease prevention and appropriate management. In this study, based on public genomic sequence data and bioinformatic analysis of several
Phytophthora
,
Phytopythium
, and
Pythium
species, we have identified a new target gene, Pcinn13739; this allowed us to establish a recombinase polymerase amplification–lateral flow dipstick (RPA-LFD) assay for the detection of
P. cinnamomi
.
Pcinn13739
-RPA-LFD assay was highly specific to
P. cinnamomi
. Test results for 12 isolates of
P. cinnamomi
were positive, but negative for 50 isolates of 25 kinds of
Phytophthora
species, 13 isolates of 10 kinds of
Phytopythium
and
Pythium
species, 32 isolates of 26 kinds of fungi species, and 11 isolates of two kinds of
Bursaphelenchus
species. By detecting as little as 10 pg.µl
−1
of genomic DNA from
P. cinnamomi
in a 50-µl reaction, the RPA-LFD assay was 100 times more sensitive than conventional PCR assays. By using RPA-LFD assay,
P. cinnamomi
was also detected on artificially inoculated fruit from
Malus pumila
, the leaves of
Rhododendron pulchrum
, the roots of sterile
Lupinus polyphyllus
, and the artificially inoculated soil. Results in this study indicated that this sensitive, specific, and rapid RPA-LFD assay has potentially significant applications to diagnosing
P. cinnamomi
, especially under time- and resource-limited conditions. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Thuy Le, Duke University, United States Reviewed by: Davide Palmieri, University of Molise, Italy; Sameh S.M. Soliman, University of Sharjah, United Arab Emirates This article was submitted to Fungal Pathogenesis, a section of the journal Frontiers in Cellular and Infection Microbiology |
ISSN: | 2235-2988 2235-2988 |
DOI: | 10.3389/fcimb.2022.923700 |