Risk factors for infection with Campylobacter jejuni flaA genotypes
Unicomb, LE
O'Reilly, LC
Kirk, MD
Stafford, RJ
Smith, HV
Becker, NG
Patel, MS
Gilbert, GL
Adamson, P
Ashbolt, R
Cheung, K
Combs, B
Dalton, C
Djordjevic, S
Doyle, R
Ferguson, J
Gilbert, L
Givney, R
Gordon, D
Gregory, J
Hogg, G
Inglis, T
Jelfs, P
Lalor, K
Lanser, J
Mickan, L
Rios, R
Sarna, M
Sharma, H
Smith, H
Unicomb, L
Valcanis, M
- Publication Type:
- Journal Article
- Citation:
- Epidemiology and Infection, 2008, 136 (11), pp. 1480 - 1491
- Issue Date:
- 2008-01-01
Open Access
Copyright Clearance Process
- Recently Added
- In Progress
- Open Access
This item is open access.
Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Unicomb, LE | en_US |
dc.contributor.author | O'Reilly, LC | en_US |
dc.contributor.author | Kirk, MD | en_US |
dc.contributor.author | Stafford, RJ | en_US |
dc.contributor.author | Smith, HV | en_US |
dc.contributor.author | Becker, NG | en_US |
dc.contributor.author | Patel, MS | en_US |
dc.contributor.author | Gilbert, GL | en_US |
dc.contributor.author | Adamson, P | en_US |
dc.contributor.author | Ashbolt, R | en_US |
dc.contributor.author | Cheung, K | en_US |
dc.contributor.author | Combs, B | en_US |
dc.contributor.author | Dalton, C | en_US |
dc.contributor.author |
Djordjevic, S https://orcid.org/0000-0001-9301-5372 |
en_US |
dc.contributor.author | Doyle, R | en_US |
dc.contributor.author | Ferguson, J | en_US |
dc.contributor.author | Gilbert, L | en_US |
dc.contributor.author | Givney, R | en_US |
dc.contributor.author | Gordon, D | en_US |
dc.contributor.author | Gregory, J | en_US |
dc.contributor.author | Hogg, G | en_US |
dc.contributor.author | Inglis, T | en_US |
dc.contributor.author | Jelfs, P | en_US |
dc.contributor.author | Lalor, K | en_US |
dc.contributor.author | Lanser, J | en_US |
dc.contributor.author | Mickan, L | en_US |
dc.contributor.author | Rios, R | en_US |
dc.contributor.author | Sarna, M | en_US |
dc.contributor.author | Sharma, H | en_US |
dc.contributor.author | Smith, H | en_US |
dc.contributor.author | Unicomb, L | en_US |
dc.contributor.author | Valcanis, M | en_US |
dc.date.issued | 2008-01-01 | en_US |
dc.identifier.citation | Epidemiology and Infection, 2008, 136 (11), pp. 1480 - 1491 | en_US |
dc.identifier.issn | 0950-2688 | en_US |
dc.identifier.uri | http://hdl.handle.net/10453/12111 | |
dc.description.abstract | We aimed to explore Campylobacter genotype-specific risk factors in Australia. Isolates collected prospectively from cases recruited into a case-control study were genotyped using flaA restriction fragment-length polymorphism typing ( flaA genotyping). Exposure information for cases and controls was collected by telephone interview. Risk factors were examined for major flaA genotypes using logistic and multinomial regression. Five flaA genotypes accounted for 325 of 590 (55%) cases - flaA-6b (n=129), flaA-6 (n=70), flaA-10 (n=48), flaA-2 (n=43), flaA-131 (n=35). In Australia, infections due to flaA-10 and flaA-2 were found to be significantly associated with eating non-poultry meat (beef and ham, respectively) in both case-control and inter-genotype comparisons. All major genotypes apart from flaA-10 were associated with chicken consumption in the case-control comparisons. Based on several clinical criteria, infections due to flaA-2 were more severe than those due to other genotypes. Thus genotype analysis may reveal genotype-specific niches and differences in virulence and transmission routes. © 2008 Cambridge University Press. | en_US |
dc.relation.ispartof | Epidemiology and Infection | en_US |
dc.relation.isbasedon | 10.1017/S0950268807000246 | en_US |
dc.subject.classification | Epidemiology | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Campylobacter jejuni | en_US |
dc.subject.mesh | Campylobacter Infections | en_US |
dc.subject.mesh | Flagellin | en_US |
dc.subject.mesh | DNA, Bacterial | en_US |
dc.subject.mesh | Bacterial Typing Techniques | en_US |
dc.subject.mesh | Multivariate Analysis | en_US |
dc.subject.mesh | Logistic Models | en_US |
dc.subject.mesh | Risk Factors | en_US |
dc.subject.mesh | Case-Control Studies | en_US |
dc.subject.mesh | Prospective Studies | en_US |
dc.subject.mesh | DNA Fingerprinting | en_US |
dc.subject.mesh | Genotype | en_US |
dc.subject.mesh | Polymorphism, Restriction Fragment Length | en_US |
dc.subject.mesh | Meat Products | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Aged, 80 and over | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Child | en_US |
dc.subject.mesh | Child, Preschool | en_US |
dc.subject.mesh | Infant | en_US |
dc.subject.mesh | Infant, Newborn | en_US |
dc.subject.mesh | Australia | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Male | en_US |
dc.title | Risk factors for infection with Campylobacter jejuni flaA genotypes | en_US |
dc.type | Journal Article | |
utslib.citation.volume | 11 | en_US |
utslib.citation.volume | 136 | en_US |
utslib.for | 111706 Epidemiology | en_US |
utslib.for | 1117 Public Health and Health Services | en_US |
pubs.embargo.period | Not known | en_US |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Strength - ithree - Institute of Infection, Immunity and Innovation | |
utslib.copyright.status | open_access | |
pubs.issue | 11 | en_US |
pubs.publication-status | Published | en_US |
pubs.volume | 136 | en_US |
Abstract:
We aimed to explore Campylobacter genotype-specific risk factors in Australia. Isolates collected prospectively from cases recruited into a case-control study were genotyped using flaA restriction fragment-length polymorphism typing ( flaA genotyping). Exposure information for cases and controls was collected by telephone interview. Risk factors were examined for major flaA genotypes using logistic and multinomial regression. Five flaA genotypes accounted for 325 of 590 (55%) cases - flaA-6b (n=129), flaA-6 (n=70), flaA-10 (n=48), flaA-2 (n=43), flaA-131 (n=35). In Australia, infections due to flaA-10 and flaA-2 were found to be significantly associated with eating non-poultry meat (beef and ham, respectively) in both case-control and inter-genotype comparisons. All major genotypes apart from flaA-10 were associated with chicken consumption in the case-control comparisons. Based on several clinical criteria, infections due to flaA-2 were more severe than those due to other genotypes. Thus genotype analysis may reveal genotype-specific niches and differences in virulence and transmission routes. © 2008 Cambridge University Press.
Please use this identifier to cite or link to this item:
Download statistics for the last 12 months
Not enough data to produce graph