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 in | The Journal of infectious diseases Vol. 166; no. 5; pp. 1173 - 1177 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Chicago, IL
The University of Chicago Press
01.11.1992
University of Chicago Press |
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Abstract | 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. |
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AbstractList | 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. 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. 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.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. |
Author | Bailey, Robin L. Clarke, Ian N. Ward, Michael E. Hayes, Lyn J. Mabey, David C. W. Pickett, Mark A. Watt, Peter J. |
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Keywords | Chain reaction Prognosis Etiopathogenesis Trachoma Exploration Genotype Medical screening Endemy Epidemiology Result Infection Spectrometry Enzymatic activity Immunological investigation Risk factor Bacteriosis Chlamydiosis Diagnosis |
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SubjectTerms | Amino acids Antigens Bacterial Outer Membrane Proteins - genetics Base Sequence Biological and medical sciences Chlamydia trachomatis Chlamydia trachomatis - genetics Chlamydia trachomatis - isolation & purification Concise Communications DNA DNA, Bacterial - genetics DNA, Bacterial - isolation & purification Enzyme-Linked Immunosorbent Assay Eyes Gambia Genes, Bacterial Genetic Variation Genotype Genotypes Humans Infectious diseases Medical sciences Membrane proteins Molecular Sequence Data Oligodeoxyribonucleotides Polymerase chain reaction Polymerase Chain Reaction - methods Restriction Mapping Sequencing Trachoma Trachoma - epidemiology Trachoma - microbiology |
Title | Genotyping of Chlamydia trachomatis from a Trachoma-Endemic Village in The Gambia by a Nested Polymerase Chain Reaction: Identification of Strain Variants |
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