A comparison of culture methods and polymerase chain reaction in detecting Clostridioides difficile from hospital surfaces

被引:0
作者
Grainger, Rachel J. [1 ]
Kearney, Aoife [1 ]
Humphreys, Hilary [1 ,2 ]
Stevens, Niall T. [1 ]
机构
[1] Beaumont Hosp, Royal Coll Surg Ireland, Dept Clin Microbiol, RCSI Educ & Res Ctr, Dublin, Ireland
[2] Beaumont Hosp, Dept Clin Microbiol, Dublin, Ireland
关键词
Clostridioides difficile; cross infection; environment; polymerase chain reaction; CONTAMINATION; SPORES; PCR;
D O I
10.1099/jmm.0.001636
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Introduction. Environmental surveillance for Clostridioides difficile is challenging. There are no internationally agreed recommendations on which method should be used when environmental surveillance is undertaken. Aim. To compare the detection of C. difficile by RT-PCR to culture-based methods and to determine which is more sensitive and specific in the clinical environment. Methods. Forty-four near-patient areas of C. difficile-positive patients were sampled using contact plates and moistened flocked swabs. Results. Detection using moistened flocked swabs followed by RT-PCR or culture detected more C. difficile than contact plates. The sensitivity and specificity of a RT-PCR assay for tcdB compared to the culture methods was 76 and 91 %, respectively. Conclusion. Despite the lower sensitivity and specificity, RT-PCR could potentially offer a more rapid and practical alternative.
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共 11 条
[1]   A Novel Quantitative Sampling Technique for Detection and Monitoring of Clostridium difficile Contamination in the Clinical Environment [J].
Ali, Shanom ;
Muzslay, Monika ;
Wilson, Peter .
JOURNAL OF CLINICAL MICROBIOLOGY, 2015, 53 (08) :2570-2574
[2]   Consequences of Clostridium difficile infection: understanding the healthcare burden [J].
Bouza, E. .
CLINICAL MICROBIOLOGY AND INFECTION, 2012, 18 :5-12
[3]   Increased environmental sample area and recovery of Clostridium difficile spores from hospital surfaces by quantitative PCR and enrichment culture [J].
Brown, Kevin Antoine ;
MacDougall, Laura K. ;
Valenta, Kim ;
Simor, Andrew ;
Johnstone, Jennie ;
Mubareka, Samira ;
Broukhanski, George ;
Garber, Gary ;
McGeer, Allison ;
Daneman, Nick .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2018, 39 (08) :917-923
[4]   Evaluation of a commercial real-time polymerase chain reaction assay for detection of environmental contamination with Clostridium difficile [J].
Deshpande, A. ;
Kundrapu, S. ;
Sunkesula, V. C. K. ;
Cadnum, J. L. ;
Fertelli, D. ;
Donskey, C. J. .
JOURNAL OF HOSPITAL INFECTION, 2013, 85 (01) :76-78
[5]   Comparison of two environmental sampling tools for the detection of Clostridium difficile spores on hard bathroom surfaces in the hospital setting [J].
Engelhardt, N. E. P. ;
Foster, N. F. ;
Hong, S. ;
Riley, T. V. ;
McGechie, D. B. .
JOURNAL OF HOSPITAL INFECTION, 2017, 96 (03) :295-296
[6]   Approaches to the detection of Clostridioides difficile in the healthcare environment [J].
Grainger, R. J. ;
Stevens, N. T. ;
Humphreys, H. .
JOURNAL OF HOSPITAL INFECTION, 2019, 103 (04) :375-381
[7]   Comparison of qPCR versus culture for the detection and quantification of Clostridium difficile environmental contamination [J].
MacDougall, Laura K. ;
Broukhanski, George ;
Simor, Andrew ;
Johnstone, Jennie ;
Mubareka, Samira ;
McGeer, Allison ;
Daneman, Nick ;
Garber, Gary ;
Brown, Kevin A. .
PLOS ONE, 2018, 13 (08)
[8]   Quantitative detection of Clostridium difficile in hospital environmental samples by real-time polymerase chain reaction [J].
Mutters, R. ;
Nonnenmacher, C. ;
Susin, C. ;
Albrecht, U. ;
Kropatsch, R. ;
Schumacher, S. .
JOURNAL OF HOSPITAL INFECTION, 2009, 71 (01) :43-48
[9]   Development of a rapid-viability PCR method for detection of Clostridioides difficile spores from environmental samples [J].
Shams, Alicia M. ;
Rose, Laura J. ;
Noble-Wang, Judith A. .
ANAEROBE, 2020, 61
[10]   Prospective multicenter evaluation of a new immunoassay and real-time PCR for rapid diagnosis of Clostridium difficile-associated diarrhea in hospitalized patients [J].
van den Berg, RJ ;
van Coppenraet, LSB ;
Gerritsen, HJ ;
Endtz, HP ;
van der Vorm, ER ;
Kuijper, EJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (10) :5338-5340