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评估新型显色培养基CHROMagar金黄色葡萄球菌培养基用于从人类临床标本中分离和初步鉴定金黄色葡萄球菌的性能。

Evaluation of CHROMagar Staph. aureus, a new chromogenic medium, for isolation and presumptive identification of Staphylococcus aureus from human clinical specimens.

作者信息

Gaillot O, Wetsch M, Fortineau N, Berche P

机构信息

Laboratoire de Bactériologie-Virologie, Hôpital Necker-Enfants Malades, Paris, France.

出版信息

J Clin Microbiol. 2000 Apr;38(4):1587-91. doi: 10.1128/JCM.38.4.1587-1591.2000.

Abstract

CHROMagar Staph. aureus (CSA) is a new chromogenic medium for presumptive identification of Staphylococcus aureus as mauve colonies after 24 h of incubation. We conducted a preliminary study with 100 S. aureus and 45 coagulase-negative Staphylococcus (CoNS) stock isolates plated on CSA. All S. aureus isolates yielded mauve colonies after 24 h of incubation at 37 degrees C, while CoNS isolates grew as blue, white, or beige colonies. Culture on CSA was then prospectively compared to a conventional laboratory method, i.e. , culture on 5% horse blood agar (HBA), catalase test, and latex agglutination test (HBA-catalase-latex), for isolation and presumptive identification of S. aureus from 2,000 consecutive clinical samples. Among the 310 S. aureus isolates recovered by at least one of the two methods, 296 grew as typical mauve colonies on CSA, while only 254 yielded catalase-positive, latex-positive colonies on HBA. The sensitivity of CSA was significantly higher than that of the conventional method (95.5 and 81.9%, respectively; P < 0.001) and allowed the recovery of important clinical isolates that were undetected on blood agar. The specificities of the two methods were not significantly different, although that of CSA was slightly higher (99.4% versus 98.9% for HBA-catalase-latex; P = 0. 08). On the basis of its excellent sensitivity and specificity, ease of identification of positive colonies, and absence of complementary testing, CSA can be recommended as a routine plating medium for presumptive identification of S. aureus in clinical specimens.

摘要

CHROMagar金黄色葡萄球菌培养基(CSA)是一种新型显色培养基,用于在孵育24小时后初步鉴定金黄色葡萄球菌为紫红色菌落。我们对接种在CSA上的100株金黄色葡萄球菌和45株凝固酶阴性葡萄球菌(CoNS)菌株进行了初步研究。所有金黄色葡萄球菌菌株在37℃孵育24小时后均产生紫红色菌落,而CoNS菌株生长为蓝色、白色或米色菌落。然后前瞻性地将CSA上的培养与传统实验室方法,即5%马血琼脂(HBA)培养、过氧化氢酶试验和乳胶凝集试验(HBA-过氧化氢酶-乳胶)进行比较,以从2000份连续临床样本中分离和初步鉴定金黄色葡萄球菌。在通过两种方法中的至少一种回收的310株金黄色葡萄球菌菌株中,296株在CSA上生长为典型的紫红色菌落,而只有254株在HBA上产生过氧化氢酶阳性、乳胶阳性菌落。CSA的敏感性显著高于传统方法(分别为95.5%和81.9%;P<0.001),并能回收在血琼脂上未检测到的重要临床分离株。两种方法的特异性没有显著差异,尽管CSA的特异性略高(HBA-过氧化氢酶-乳胶为98.9%,CSA为99.4%;P = 0.08)。基于其优异的敏感性和特异性、阳性菌落易于鉴定以及无需补充检测,CSA可推荐作为临床标本中金黄色葡萄球菌初步鉴定的常规接种培养基。

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