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Zoonotic Transfer of Clostridium difficile Harboring Antimicrobial Resistance between Farm Animals and Humans

Journal of clinical microbiology, 2018-03, Vol.56 (3)

2018

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Comparison of Whole-Genome Sequence-Based Methods and PCR Ribotyping for Subtyping of Clostridioides difficile

Journal of clinical microbiology, 2022-02, Vol.60 (2), p.e0173721-e0173721

2022

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Relatedness of Human and Animal Clostridium difficile PCR Ribotype 078 Isolates Determined on the Basis of Multilocus Variable-Number Tandem-Repeat Analysis and Tetracycline Resistance

Journal of Clinical Microbiology, 2010-10, Vol.48 (10), p.3744-3749

2010

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Emergence of reduced susceptibility to metronidazole in Clostridium difficile

Journal of antimicrobial chemotherapy, 2008-11, Vol.62 (5), p.1046-1052

2008

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Spread and Epidemiology of Clostridium difficile Polymerase Chain Reaction Ribotype 027/Toxinotype III in The Netherlands

Clinical infectious diseases, 2007-09, Vol.45 (6), p.695-703

2007

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Application of multiple-locus variable-number tandem-repeat analysis to determine clonal spread of toxin A-negative Clostridium difficile in a general hospital in Buenos Aires, Argentina

Clinical microbiology and infection, 2009-12, Vol.15 (12), p.1080-1086

2009

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Clostridium difficile in Dutch animals: their presence, characteristics and similarities with human isolates

Clinical microbiology and infection, 2012-08, Vol.18 (8), p.778-784

2012

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Clostridium difficile in wild rodents and insectivores in the Netherlands

Letters in applied microbiology, 2019-07, Vol.69 (1), p.35-40

2019

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Type-Specific Risk Factors and Outcome in an Outbreak With 2 Different Clostridium difficile Types Simultaneously in 1 Hospital

Clinical infectious diseases, 2011-11, Vol.53 (9), p.860-869

2011

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Wild mice in and around the city of Utrecht, the Netherlands, are carriers of Clostridium difficile but not ESBL‐producing Enterobacteriaceae, Salmonella spp. or MRSA

Letters in applied microbiology, 2018-11, Vol.67 (5), p.513-519

2018

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An outbreak of Clostridium difficile infections due to new PCR ribotype 826: epidemiologic and microbiologic analyses

Clinical microbiology and infection, 2018-03, Vol.24 (3), p.309.e1-309.e4

2018

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Identification and validation of two peptide markers for the recognition of Clostridioides difficile MLST-1 and MLST-11 by MALDI-MS

Clinical microbiology and infection, 2019-07, Vol.25 (7), p.904.e1-904.e7

2019

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Acquisition of Clostridium difficile by piglets

Veterinary microbiology, 2011-04, Vol.149 (1-2), p.186-192

2011

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Use of Highly Discriminatory Fingerprinting to Analyze Clusters of Clostridium difficile Infection Cases Due to Epidemic Ribotype 027 Strains

Journal of Clinical Microbiology, 2008-03, Vol.46 (3), p.954-960

2008

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Emergence of Clostridium difficile infection in tuberculosis patients due to a highly rifampicin-resistant PCR ribotype 046 clone in Poland

European journal of clinical microbiology & infectious diseases, 2013-08, Vol.32 (8), p.1027-1030

2013

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Faecal shedding of antimicrobial-resistant Clostridium difficile strains by dogs

Journal of small animal practice, 2015-03, Vol.56 (3), p.190-195

2015

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Increased incidence of Clostridium difficile PCR ribotype 027 in Hesse, Germany, 2011 to 2013

Euro surveillance : bulletin européen sur les maladies transmissibles, 2014-03, Vol.19 (10), p.1

2014

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Community-Onset Clostridioides Difficile Infection in Hospitalized Patients in The Netherlands

Open forum infectious diseases, 2019-12, Vol.6 (12), p.ofz501-ofz501

2019

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Molecular typing and antimicrobial susceptibility testing to six antimicrobials of Clostridium difficile isolates from three Czech hospitals in Eastern Bohemia in 2011–2012

Folia microbiologica, 2017-09, Vol.62 (5), p.445-451

2017

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Clostridium difficile infection in an endemic setting in the Netherlands

European journal of clinical microbiology & infectious diseases, 2011-04, Vol.30 (4), p.587-593

2011

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Erratum to: Emergence of Clostridium difficile infection in tuberculosis patients due to a highly rifampicin-resistant PCR ribotype 046 clone in Poland

European journal of clinical microbiology & infectious diseases, 2013-10, Vol.32 (10), p.1359-1359

2013

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Emergence of Clostridium difficile Infection Due to a New Hypervirulent Strain, Polymerase Chain Reaction Ribotype 078

Clinical infectious diseases, 2008-11, Vol.47 (9), p.1162-1170

2008

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First cluster of clindamycin-resistant Clostridium difficile PCR ribotype 027 in Switzerland

Clinical microbiology and infection, 2008-05, Vol.14 (5), p.514-515

2008

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Isolation of the first three cases of Clostridium difficile polymerase chain reaction ribotype 027 in Singapore

Singapore medical journal, 2011-05, Vol.52 (5), p.361-364

2011

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Clostridium difficile infection in Europe: a hospital-based survey

The Lancet (British edition), 2011, Vol.377 (9759), p.63-73

2011

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Zoonotic Transfer of Clostridium difficile Harboring Antimicrobial Resistance between Farm Animals and Humans

Comparison of Whole-Genome Sequence-Based Methods and PCR Ribotyping for Subtyping of Clostridioides difficile

Relatedness of Human and Animal Clostridium difficile PCR Ribotype 078 Isolates Determined on the Basis of Multilocus Variable-Number Tandem-Repeat Analysis and Tetracycline Resistance

Emergence of reduced susceptibility to metronidazole in Clostridium difficile

Spread and Epidemiology of Clostridium difficile Polymerase Chain Reaction Ribotype 027/Toxinotype III in The Netherlands

Application of multiple-locus variable-number tandem-repeat analysis to determine clonal spread of toxin A-negative Clostridium difficile in a general hospital in Buenos Aires, Argentina

Clostridium difficile in Dutch animals: their presence, characteristics and similarities with human isolates

Clostridium difficile in wild rodents and insectivores in the Netherlands

Type-Specific Risk Factors and Outcome in an Outbreak With 2 Different Clostridium difficile Types Simultaneously in 1 Hospital

Wild mice in and around the city of Utrecht, the Netherlands, are carriers of Clostridium difficile but not ESBL‐producing Enterobacteriaceae, Salmonella spp. or MRSA

An outbreak of Clostridium difficile infections due to new PCR ribotype 826: epidemiologic and microbiologic analyses

Identification and validation of two peptide markers for the recognition of Clostridioides difficile MLST-1 and MLST-11 by MALDI-MS

Acquisition of Clostridium difficile by piglets

Use of Highly Discriminatory Fingerprinting to Analyze Clusters of Clostridium difficile Infection Cases Due to Epidemic Ribotype 027 Strains

Emergence of Clostridium difficile infection in tuberculosis patients due to a highly rifampicin-resistant PCR ribotype 046 clone in Poland

Faecal shedding of antimicrobial-resistant Clostridium difficile strains by dogs

Increased incidence of Clostridium difficile PCR ribotype 027 in Hesse, Germany, 2011 to 2013

Community-Onset Clostridioides Difficile Infection in Hospitalized Patients in The Netherlands

Molecular typing and antimicrobial susceptibility testing to six antimicrobials of Clostridium difficile isolates from three Czech hospitals in Eastern Bohemia in 2011–2012

Clostridium difficile infection in an endemic setting in the Netherlands

Erratum to: Emergence of Clostridium difficile infection in tuberculosis patients due to a highly rifampicin-resistant PCR ribotype 046 clone in Poland

Emergence of Clostridium difficile Infection Due to a New Hypervirulent Strain, Polymerase Chain Reaction Ribotype 078

First cluster of clindamycin-resistant Clostridium difficile PCR ribotype 027 in Switzerland

Isolation of the first three cases of Clostridium difficile polymerase chain reaction ribotype 027 in Singapore

Clostridium difficile infection in Europe: a hospital-based survey

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