z-logo
open-access-imgOpen Access
Sensitive Detection of Xanthomonas oryzae Pathovars oryzae and oryzicola by Loop-Mediated Isothermal Amplification
Author(s) -
Jillian M. Lang,
Paul Langlois,
Marian Hanna R. Nguyen,
Lindsay R. Triplett,
Laura Purdie,
Timothy A. Holton,
Appolinaire Djikeng,
Casiana M. Vera Cruz,
Valérie Verdier,
Jan E. Leach
Publication year - 2014
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.00274-14
Subject(s) - loop mediated isothermal amplification , xanthomonas oryzae , xanthomonas oryzae pv. oryzae , biology , pathovar , xanthomonas , pathogen , genomic dna , microbiology and biotechnology , bacterial disease , bacteria , genetics , dna , pseudomonadaceae , pseudomonas
Molecular diagnostics for crop diseases can enhance food security by enabling the rapid identification of threatening pathogens and providing critical information for the deployment of disease management strategies. Loop-mediated isothermal amplification (LAMP) is a PCR-based tool that allows the rapid, highly specific amplification of target DNA sequences at a single temperature and is thus ideal for field-level diagnosis of plant diseases. We developed primers highly specific for two globally important rice pathogens,Xanthomonas oryzae pv. oryzae, the causal agent of bacterial blight (BB) disease, andX. oryzae pv. oryzicola, the causal agent of bacterial leaf streak disease (BLS), for use in reliable, sensitive LAMP assays. In addition to pathovar distinction, two assays that differentiateX. oryzae pv. oryzae by African or Asian lineage were developed. Using these LAMP primer sets, the presence of each pathogen was detected from DNA and bacterial cells, as well as leaf and seed samples. Thresholds of detection for all assays were consistently 104 to 105 CFU ml−1 , while genomic DNA thresholds were between 1 pg and 10 fg. Use of the unique sequences combined with the LAMP assay provides a sensitive, accurate, rapid, simple, and inexpensive protocol to detect both BB and BLS pathogens.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom