Premium
Rapid, specific, simple, in‐field detection of Xanthomonas campestris pathovar musacearum by loop‐mediated isothermal amplification
Author(s) -
Hodgetts J.,
Hall J.,
Karamura G.,
Grant M.,
Studholme D.J.,
Boonham N.,
Karamura E.,
Smith J.J.
Publication year - 2015
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1111/jam.12959
Subject(s) - pathovar , library science , political science , sociology , biology , computer science , pseudomonas , genetics , pseudomonadaceae , bacteria
Aims To develop and evaluate a loop‐mediated isothermal amplification ( LAMP ) assay for Xanthomonas campestris pathovar musacearum ( Xcm ), the causal agent of banana Xanthomonas wilt, a major disease of banana in Africa. Methods and Results LAMP primers were designed to the general secretion pathway protein D gene and tested against 17 isolates of Xcm encompassing the known genetic and geographic diversity of the bacterium and all isolates were detected. Seventeen other Xanthomonas isolates, including closely related Xanthomonas vasicola , other bacterial pathogens/endophytes of Musa and two healthy Musa varieties gave negative results with the LAMP assay. The assay showed good sensitivity, detecting as little as 51 fg of Xcm DNA , a greater level of sensitivity than that of an Xcm PCR assay. Amplification with the LAMP assay was very rapid, typically within 9 min from bacterial cultures. Symptomatic field samples of Musa from Uganda were tested and all produced amplification in less than 13 min. Conclusions The LAMP assay provides rapid, sensitive detection of the pathogen that is ideally suited for deployment in laboratories with basic facilities and in‐field situations. Significance and Impact of the Study This is the first LAMP assay for Xcm which provides a significant improvement compared to existing diagnostics.