Literature DB >> 24317079

Carriage of Clostridium difficile by wild urban Norway rats (Rattus norvegicus) and black rats (Rattus rattus).

Chelsea G Himsworth1, David M Patrick, Sunny Mak, Claire M Jardine, Patrick Tang, J Scott Weese.   

Abstract

Clostridium difficile is an important cause of enteric infections in humans. Recently, concerns have been raised regarding whether animals could be a source of C. difficile spores. Although colonization has been identified in a number of domestic species, the ability of commensal pests to serve as a reservoir for C. difficile has not been well investigated. The objective of this study was to determine whether urban rats (Rattus spp.) from Vancouver, Canada, carry C. difficile. Clostridium difficile was isolated from the colon contents of trapped rats and was characterized using ribotyping, toxinotyping, and toxin gene identification. Generalized linear mixed models and spatial analysis were used to characterize the ecology of C. difficile in rats. Clostridium difficile was isolated from 95 of 724 (13.1%) rats, although prevalence differed from 0% to 46.7% among city blocks. The odds of being C. difficile positive decreased with increasing weight (odds ratio [OR], 0.67; 95% confidence interval [CI], 0.53 to 0.87), suggesting that carriage is more common in younger animals. The strains isolated included 9 ribotypes that matched recognized international designations, 5 identified by our laboratory in previous studies, and 21 "novel" ribotypes. Some strains were clustered geographically; however, the majority were dispersed throughout the study area, supporting environmental sources of exposure and widespread environmental contamination with a variety of C. difficile strains. Given that urban rats are the source of a number of other pathogens responsible for human morbidity and mortality, the potential for rats to be a source of C. difficile for humans deserves further consideration.

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Year:  2013        PMID: 24317079      PMCID: PMC3911036          DOI: 10.1128/AEM.03609-13

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  35 in total

1.  The characteristics of rat populations.

Authors:  D E DAVIS
Journal:  Q Rev Biol       Date:  1953-12       Impact factor: 4.875

2.  Production of actin-specific ADP-ribosyltransferase (binary toxin) by strains of Clostridium difficile.

Authors:  S Stubbs; M Rupnik; M Gibert; J Brazier; B Duerden; M Popoff
Journal:  FEMS Microbiol Lett       Date:  2000-05-15       Impact factor: 2.742

3.  Development of a new PCR-ribotyping method for Clostridium difficile based on ribosomal RNA gene sequencing.

Authors:  P Bidet; F Barbut; V Lalande; B Burghoffer; J C Petit
Journal:  FEMS Microbiol Lett       Date:  1999-06-15       Impact factor: 2.742

4.  Vermin on pig farms are vectors for Clostridium difficile PCR ribotypes 078 and 045.

Authors:  S A Burt; L Siemeling; E J Kuijper; L J A Lipman
Journal:  Vet Microbiol       Date:  2012-05-18       Impact factor: 3.293

5.  Longitudinal study of Clostridium difficile and antimicrobial susceptibility of Escherichia coli in healthy horses in a community setting.

Authors:  A Schoster; H R Staempfli; L G Arroyo; R J Reid-Smith; N Janecko; P E Shewen; J S Weese
Journal:  Vet Microbiol       Date:  2012-04-17       Impact factor: 3.293

6.  Multiplex PCR targeting tpi (triose phosphate isomerase), tcdA (Toxin A), and tcdB (Toxin B) genes for toxigenic culture of Clostridium difficile.

Authors:  Ludovic Lemee; Anne Dhalluin; Sabrina Testelin; Marie-Andre Mattrat; Karine Maillard; Jean-François Lemeland; Jean-Louis Pons
Journal:  J Clin Microbiol       Date:  2004-12       Impact factor: 5.948

7.  Clostridium difficile carriage in healthy infants in the community: a potential reservoir for pathogenic strains.

Authors:  Clotilde Rousseau; Isabelle Poilane; Loic De Pontual; Anne-Claire Maherault; Alban Le Monnier; Anne Collignon
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8.  Prevalence and distribution of Clostridium difficile PCR ribotypes in cats and dogs from animal shelters in Thuringia, Germany.

Authors:  Alexander Schneeberg; Maja Rupnik; Heinrich Neubauer; Christian Seyboldt
Journal:  Anaerobe       Date:  2012-08-24       Impact factor: 3.331

9.  A novel toxinotyping scheme and correlation of toxinotypes with serogroups of Clostridium difficile isolates.

Authors:  M Rupnik; V Avesani; M Janc; C von Eichel-Streiber; M Delmée
Journal:  J Clin Microbiol       Date:  1998-08       Impact factor: 5.948

10.  Identification of toxin A-negative, toxin B-positive Clostridium difficile by PCR.

Authors:  H Kato; N Kato; K Watanabe; N Iwai; H Nakamura; T Yamamoto; K Suzuki; S M Kim; Y Chong; E B Wasito
Journal:  J Clin Microbiol       Date:  1998-08       Impact factor: 5.948

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Review 1.  Environmental Factors and Zoonotic Pathogen Ecology in Urban Exploiter Species.

Authors:  Jamie L Rothenburger; Chelsea H Himsworth; Nicole M Nemeth; David L Pearl; Claire M Jardine
Journal:  Ecohealth       Date:  2017-06-19       Impact factor: 3.184

Review 2.  Clostridium difficile in Food and Animals: A Comprehensive Review.

Authors:  C Rodriguez; B Taminiau; J Van Broeck; M Delmée; G Daube
Journal:  Adv Exp Med Biol       Date:  2016       Impact factor: 2.622

3.  Wildlife health: A foundation for preparedness for environmental change.

Authors:  Craig Stephen
Journal:  Can Vet J       Date:  2016-10       Impact factor: 1.008

4.  Environmental Factors Associated with the Carriage of Bacterial Pathogens in Norway Rats.

Authors:  Jamie L Rothenburger; Chelsea G Himsworth; Nicole M Nemeth; David L Pearl; Claire M Jardine
Journal:  Ecohealth       Date:  2018-02-09       Impact factor: 3.184

5.  Exposure to Rats and Rat-Associated Leptospira and Bartonella Species Among People Who Use Drugs in an Impoverished, Inner-City Neighborhood of Vancouver, Canada.

Authors:  David A McVea; Chelsea G Himsworth; David M Patrick; L Robbin Lindsay; Michael Kosoy; Thomas Kerr
Journal:  Vector Borne Zoonotic Dis       Date:  2018-01-03       Impact factor: 2.133

6.  Clostridioides difficile and multi-drug-resistant staphylococci in free-living rodents and marsupials in parks of Belo Horizonte, Brazil.

Authors:  Jordana Almeida Santana; Salene Angelini Colombo; Brendhal Almeida Silva; Amanda Nádia Diniz; Lara Ribeiro de Almeida; Carlos Augusto Oliveira Junior; Francisco Carlos Faria Lobato; Giliane de Souza Trindade; Adriano Pereira Paglia; Rodrigo Otávio Silveira Silva
Journal:  Braz J Microbiol       Date:  2021-11-11       Impact factor: 2.476

7.  Livestock-associated methicillin-resistant Staphylococcus aureus and Clostridium difficile in wild Norway rats (Rattus norvegicus) from Ontario swine farms.

Authors:  Jamie L Rothenburger; Joyce D Rousseau; J Scott Weese; Claire M Jardine
Journal:  Can J Vet Res       Date:  2018-01       Impact factor: 1.310

Review 8.  Clostridium (Clostridioides) difficile in animals.

Authors:  J Scott Weese
Journal:  J Vet Diagn Invest       Date:  2020-01-06       Impact factor: 1.279

9.  Whole genome sequencing reveals potential spread of Clostridium difficile between humans and farm animals in the Netherlands, 2002 to 2011.

Authors:  C W Knetsch; T R Connor; A Mutreja; S M van Dorp; I M Sanders; H P Browne; D Harris; L Lipman; E C Keessen; J Corver; E J Kuijper; T D Lawley
Journal:  Euro Surveill       Date:  2014-11-13

10.  Longitudinal study of Clostridium difficile shedding in raccoons on swine farms and conservation areas in Ontario, Canada.

Authors:  Kristin J Bondo; J Scott Weese; Joyce Rouseau; Claire M Jardine
Journal:  BMC Vet Res       Date:  2015-10-07       Impact factor: 2.741

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