A nested multiplex polymerase chain reaction assay for the differential identification of three zooanthroponotic chlamydial strains in porcine swab samples
Author(s) -
Yingguo Li,
Yu Wang,
Fuping Nie,
Jinwen Xiao,
Guoming Wang,
Ling Yuan,
Zhengguo Li
Publication year - 2011
Publication title -
journal of veterinary diagnostic investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.529
H-Index - 78
eISSN - 1943-4936
pISSN - 1040-6387
DOI - 10.1177/1040638711406972
Subject(s) - amplicon , biology , chlamydiaceae , polymerase chain reaction , chlamydophila , nested polymerase chain reaction , virology , chlamydophila pneumoniae , chlamydiales , multiplex polymerase chain reaction , multiplex , chlamydia , microbiology and biotechnology , pathogen , gene , chlamydia trachomatis , genetics
Porcine chlamydial infection is an enzootic infectious disease caused by multiple members of the family Chlamydiaceae (e.g. Chlamydophila abortus, Chlamydia suis, and Chlamydophila pneumoniae). Rapid and accurate differentiation of these pathogens is critical in the control and prevention of disease. The aim of the current study was to develop a nested multiplex polymerase chain reaction (nmPCR) assay to simultaneously detect the 3 chlamydial pathogens in clinical samples. In the first round of the nmPCR, 1 pair of family-specific primers were used to amplify the 1,100 base pair (bp) fragment of chlamydial ompA gene. In the second round of the nmPCR, 4 inner primers were designed for Ch. abortus, C. suis, and Ch. pneumoniae. Each pathogen produced a specic amplicon with a size of 340 bp, 526 bp, and 267 bp respectively. The assay was sensitive and specic for detecting target pathogens in both cell cultures and clinical specimens. The results, incorporated with the improved rapid DNA extraction protocol, suggest that the nmPCR could be a promising assay for differential identification of different chlamydial strains in pigs.
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