PCR-based restriction fragment length polymorphism analysis of DNA sequence diversity of flagellin genes of Campylobacter jejuni and allied species
Genotypes were analysed within 29 geographically diverse strains of Campylobacter jejuni mainly from human enteritis cases and four strains representing C. coli, C. lari and C. helveticus. A 1723 bp DNA fragment, amplified by the polymerase chain reaction (PCR) from the flagellin ( fla) genes, was u...
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Published in | Molecular and cellular probes Vol. 7; no. 6; pp. 471 - 480 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier Ltd
01.12.1993
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Genotypes were analysed within 29 geographically diverse strains of
Campylobacter jejuni mainly from human enteritis cases and four strains representing
C. coli, C. lari and
C. helveticus. A 1723 bp DNA fragment, amplified by the polymerase chain reaction (PCR) from the flagellin (
fla) genes, was used to probe genomic Southern blots for restriction site variation at homologous loci. Internal
Hin fl restriction fragment length polymorphisms (RFLP) of the
fla gene PCR amplification product were also used to characterize isolates. Copy number and polymorphisms in and around the
fla genes were detected, and strains were grouped into 10 genotypes on the basis of
fla restriction site similarities.
Campylobacter jejuni had a
fla gene copy number of two and the majority (64%) of strains in the species had common internal
fla gene sequences as indicated by
Hin fl restriction analysis. A greater degree of diversity was detected around the
fla loci in
Hae III and
Bgl II genomic Southern blots. The results showed that analysis of
fla genes provided a novel and fundamental approach to grouping strains and offered a basis for defining a predominant clonal evolutionary line within
C. jejuni. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0890-8508 1096-1194 |
DOI: | 10.1006/mcpr.1993.1070 |