Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-14T04:23:01.056Z Has data issue: false hasContentIssue false
  • English
  • Français

Specific identification, grouping and differentiation of Campylobacter jejuni among thermophilic campylobacters using multiplex PCR

Published online by Cambridge University Press:  28 August 2001

V. KOROLIK ,
D. T. FRIENDSHIP ,
T. PEDURU-HEWA ,
D. A. ALFREDSON ,
B. N. FRY  and
P. J. COLOE
V. KOROLIK
Affiliation:
School of Health Science, Griffith University Gold Coast, QLD, Australia
D. T. FRIENDSHIP
Affiliation:
Applied Biology and Environmental Biology, RMIT University, Melbourne, VIC, Australia
T. PEDURU-HEWA
Affiliation:
Applied Biology and Environmental Biology, RMIT University, Melbourne, VIC, Australia
D. A. ALFREDSON
Affiliation:
School of Health Science, Griffith University Gold Coast, QLD, Australia
B. N. FRY
Affiliation:
Applied Biology and Environmental Biology, RMIT University, Melbourne, VIC, Australia
P. J. COLOE
Affiliation:
Applied Biology and Environmental Biology, RMIT University, Melbourne, VIC, Australia
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Campylobacter species such as C. jejuni and C. coli are recognized as major causes of acute gastroenteritis world-wide. Although C. jejuni and C. coli are usually non-pathogenic in birds and animals, they cause enteric disease in humans and the source of infection is often the consumption of contaminated foodstuffs. In this paper we report on the development and use of a multiplex PCR of C. jejuni genomic DNA which yielded a PCR product with a unique polymorphic site that can be used to quickly and accurately identify and group C. jejuni isolates from any source including DNA, cell culture, skin washings and faecal samples. The test is simple and sensitive and can detect purified DNA from a single bacterium 102 cells from crude lysates, 103 cells in seeded faeces and 120 cells/ml of washing of 1 cm2 skin fragments of chicken skin.

Type
Research Article
Information
Epidemiology & Infection , Volume 127 , Issue 1 , August 2001 , pp. 1 - 5
Copyright
2001 Cambridge University Press