Genotyping of Chlamydia trachomatis from a Trachoma-Endemic Village in The Gambia by a Nested Polymerase Chain Reaction: Identification of Strain Variants

Direct amplification of the major outer membrane protein (MOMP) gene by polymerase chain reaction (PCR) was used to identify Chlamydia trachomatis in eye swabs from clinically active cases of endemic trachoma in a Gambian village. Chlamydial DNA was detected in 51% of 96 subjects with clinically act...

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Published inThe Journal of infectious diseases Vol. 166; no. 5; pp. 1173 - 1177
Main Authors Hayes, Lyn J., Bailey, Robin L., Mabey, David C. W., Clarke, Ian N., Pickett, Mark A., Watt, Peter J., Ward, Michael E.
Format Journal Article
LanguageEnglish
Published Chicago, IL The University of Chicago Press 01.11.1992
University of Chicago Press
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Summary:Direct amplification of the major outer membrane protein (MOMP) gene by polymerase chain reaction (PCR) was used to identify Chlamydia trachomatis in eye swabs from clinically active cases of endemic trachoma in a Gambian village. Chlamydial DNA was detected in 51% of 96 subjects with clinically active disease and in 5% of 37 clinically negative individuals. The PCR detection was combined with typing, using nested primers to variable sequences (VS) 1, 2, and 4 of the MOMP genes to distinguish between trachoma genotypes A, B, and C, respectively. Genotypes A and B were detected in the village, with some individuals harboring both genotypes within the same eye. DNA sequencing revealed strain variants of both genotypes. Typing of genotype and strain variants is now in progress to study trachoma transmission within the village.
Bibliography:ark:/67375/HXZ-ST18X8XP-5
istex:7F359F2A4026E2F77B8462070A5F1CE8509BEE4B
Reprints or correspondence: Dr. Lyn Hayes, Molecular Microbiology Group, Southampton General Hospital, Southampton SO9 4XY, UK.
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ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/166.5.1173