Real-time quantitative PCR method for detection and quantification of Clostridioides difficile cells and spores
Author:
Publisher
Elsevier BV
Subject
Microbiology (medical),Molecular Biology,Microbiology
Reference9 articles.
1. Development of cpn60-based real-time quantitative PCR assays for the detection of 14 Campylobacter species and application to screening of canine fecal samples;Chaban;Appl. Environ. Microbiol.,2009
2. Enumeration of specific bacterial populations in complex intestinal communities using quantitative PCR based on the chaperonin-60 target;Dumonceaux;J. Microbiol. Methods,2006
3. Isolating and purifying Clostridium difficile spores;Edwards,2016
4. Development and evaluation of a PCR method for detection of the Clostridium difficile toxin B gene in stool specimens;Guilbault;J. Clin. Microbiol.,2002
5. cpnDB: a chaperonin sequence database;Hill;Genome Res.,2004
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1. Clostridioides difficile detection and infection in children: are they just small adults?;Journal of Medical Microbiology;2024-03-25
2. Molecular epidemiology of Clostridioides difficile obtained from fecal samples of wild animals in Brazil;Pesquisa Veterinária Brasileira;2024
3. Prevalence, Antimicrobial Resistance and Toxin-Encoding Genes of Clostridioides difficile from Environmental Sources Contaminated by Feces;Antibiotics;2023-01-12
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