Cadnum Jennifer L, Hurless Kelly N, Deshpande Abhishek, Nerandzic Michelle M, Kundrapu Sirisha, Donskey Curtis J
Division of Infectious Diseases, Department of Medicine, Case Western Reserve University, Cleveland, Ohio, USA.
Research Service, Cleveland VA Medical Center, Cleveland, Ohio, USA.
J Clin Microbiol. 2014 Sep;52(9):3259-63. doi: 10.1128/JCM.00793-14. Epub 2014 Jun 23.
Effective and easy-to-use methods for detecting Clostridium difficile spore contamination would be useful for identifying environmental reservoirs and monitoring the effectiveness of room disinfection. Culture-based detection methods are sensitive for detecting C. difficile, but their utility is limited due to the requirement of anaerobic culture conditions and microbiological expertise. We developed a low-cost selective broth medium containing thioglycolic acid and l-cystine, termed C. difficile brucella broth with thioglycolic acid and l-cystine (CDBB-TC), for the detection of C. difficile from environmental specimens under aerobic culture conditions. The sensitivity and specificity of CDBB-TC (under aerobic culture conditions) were compared to those of CDBB (under anaerobic culture conditions) for the recovery of C. difficile from swabs collected from hospital room surfaces. CDBB-TC was significantly more sensitive than CDBB for recovering environmental C. difficile (36/41 [88%] versus 21/41 [51%], respectively; P = 0.006). C. difficile latex agglutination, an enzyme immunoassay for toxins A and B or glutamate dehydrogenase, and a PCR for toxin B genes were all effective as confirmatory tests. For 477 total environmental cultures, the specificity of CDBB-TC versus that of CDBB based upon false-positive yellow-color development of the medium without recovery of C. difficile was 100% (0 false-positive results) versus 96% (18 false-positive results), respectively. False-positive cultures for CDBB were attributable to the growth of anaerobic non-C. difficile organisms that did not grow in CDBB-TC. Our results suggest that CDBB-TC provides a sensitive and selective medium for the recovery of C. difficile organisms from environmental samples, without the need for anaerobic culture conditions.
有效的、易于使用的艰难梭菌孢子污染检测方法,对于识别环境储库以及监测病房消毒效果将很有用。基于培养的检测方法对艰难梭菌的检测很敏感,但由于需要厌氧培养条件和微生物学专业知识,其应用受到限制。我们开发了一种低成本的选择性肉汤培养基,含有巯基乙酸和L-胱氨酸,称为含巯基乙酸和L-胱氨酸的艰难梭菌布鲁氏菌肉汤(CDBB-TC),用于在需氧培养条件下从环境标本中检测艰难梭菌。将CDBB-TC(在需氧培养条件下)与CDBB(在厌氧培养条件下)从医院病房表面采集的拭子中回收艰难梭菌的敏感性和特异性进行了比较。CDBB-TC在回收环境中的艰难梭菌方面比CDBB明显更敏感(分别为36/41 [88%] 对21/41 [51%];P = 0.006)。艰难梭菌乳胶凝集试验、毒素A和B或谷氨酸脱氢酶的酶免疫测定以及毒素B基因的PCR作为确证试验均有效。对于总共477份环境培养物,基于培养基出现假阳性黄色显色但未回收艰难梭菌,CDBB-TC与CDBB的特异性分别为100%(0例假阳性结果)对96%(18例假阳性结果)。CDBB的假阳性培养物归因于厌氧非艰难梭菌生物体的生长,这些生物体在CDBB-TC中不生长。我们的结果表明,CDBB-TC为从环境样本中回收艰难梭菌生物体提供了一种敏感且具选择性的培养基,无需厌氧培养条件。