Toxinotype V Clostridium difficile in Humans and Food Animals
Clostridium difficile is a recognized pathogen in neonatal pigs and may contribute to enteritis in calves. Toxinotype V strains have been rare causes of human C. difficile–associated disease (CDAD). We examined toxinotype V in human disease, the genetic relationship of animal and human toxinotype V...
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Centers for Disease Control and Prevention
2008-07-01
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doaj-e630cb84c5c74a00ab2230c702f87c4a2020-11-25T01:02:57ZengCenters for Disease Control and PreventionEmerging Infectious Diseases1080-60401080-60592008-07-011471039104510.3201/eid1407.071641Toxinotype V Clostridium difficile in Humans and Food AnimalsMichael A. JhungAngela D. ThompsonGeorge E. KillgoreWalter E. ZukowskiGlenn SongerMichael WarnyStuart JohnsonDale N. GerdingL. Clifford McDonaldBrandi M. LimbagoClostridium difficile is a recognized pathogen in neonatal pigs and may contribute to enteritis in calves. Toxinotype V strains have been rare causes of human C. difficile–associated disease (CDAD). We examined toxinotype V in human disease, the genetic relationship of animal and human toxinotype V strains, and in vitro toxin production of these strains. From 2001 through 2006, 8 (1.3%) of 620 patient isolates were identified as toxinotype V; before 2001, 7 (<0.02%) of ≈6,000 isolates were identified as toxinotype V. Six (46.2%) of 13 case-patients for whom information was available had community-associated CDAD. Molecular characterization showed a high degree of similarity between human and animal toxinotype V isolates; all contained a 39-bp tcdC deletion and most produced binary toxin. Further study is needed to understand the epidemiology of CDAD caused by toxinotype V C. difficile, including the potential of foodborne transmission to humans.https://wwwnc.cdc.gov/eid/article/14/7/07-1641_articleClostridium difficileinterspecies transmissionmolecular epidemiologyresearchUnited States |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Michael A. Jhung Angela D. Thompson George E. Killgore Walter E. Zukowski Glenn Songer Michael Warny Stuart Johnson Dale N. Gerding L. Clifford McDonald Brandi M. Limbago |
spellingShingle |
Michael A. Jhung Angela D. Thompson George E. Killgore Walter E. Zukowski Glenn Songer Michael Warny Stuart Johnson Dale N. Gerding L. Clifford McDonald Brandi M. Limbago Toxinotype V Clostridium difficile in Humans and Food Animals Emerging Infectious Diseases Clostridium difficile interspecies transmission molecular epidemiology research United States |
author_facet |
Michael A. Jhung Angela D. Thompson George E. Killgore Walter E. Zukowski Glenn Songer Michael Warny Stuart Johnson Dale N. Gerding L. Clifford McDonald Brandi M. Limbago |
author_sort |
Michael A. Jhung |
title |
Toxinotype V Clostridium difficile in Humans and Food Animals |
title_short |
Toxinotype V Clostridium difficile in Humans and Food Animals |
title_full |
Toxinotype V Clostridium difficile in Humans and Food Animals |
title_fullStr |
Toxinotype V Clostridium difficile in Humans and Food Animals |
title_full_unstemmed |
Toxinotype V Clostridium difficile in Humans and Food Animals |
title_sort |
toxinotype v clostridium difficile in humans and food animals |
publisher |
Centers for Disease Control and Prevention |
series |
Emerging Infectious Diseases |
issn |
1080-6040 1080-6059 |
publishDate |
2008-07-01 |
description |
Clostridium difficile is a recognized pathogen in neonatal pigs and may contribute to enteritis in calves. Toxinotype V strains have been rare causes of human C. difficile–associated disease (CDAD). We examined toxinotype V in human disease, the genetic relationship of animal and human toxinotype V strains, and in vitro toxin production of these strains. From 2001 through 2006, 8 (1.3%) of 620 patient isolates were identified as toxinotype V; before 2001, 7 (<0.02%) of ≈6,000 isolates were identified as toxinotype V. Six (46.2%) of 13 case-patients for whom information was available had community-associated CDAD. Molecular characterization showed a high degree of similarity between human and animal toxinotype V isolates; all contained a 39-bp tcdC deletion and most produced binary toxin. Further study is needed to understand the epidemiology of CDAD caused by toxinotype V C. difficile, including the potential of foodborne transmission to humans. |
topic |
Clostridium difficile interspecies transmission molecular epidemiology research United States |
url |
https://wwwnc.cdc.gov/eid/article/14/7/07-1641_article |
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