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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of CHROMagar Staph. aureus, a New Chromogenic Medium, for Isolation and Presumptive Identification ofStaphylococcus aureus from Human Clinical Specimens
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Evaluation of CHROMagar Staph. aureus, a New Chromogenic Medium, for Isolation and Presumptive Identification ofStaphylococcus aureus from Human Clinical Specimens

机译:CHROMagar葡萄球菌的评估。金黄色葡萄球菌,一种新的生色培养基,用于从人类临床标本中分离和推测性鉴定金黄色葡萄球菌

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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°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. aureusin clinical specimens.
机译:CHROMagar葡萄球菌。金黄色葡萄球菌(CSA)是一种新的生色培养基,用于在孵育24小时后推定将金黄色葡萄球菌鉴定为淡紫色菌落。我们对100个 S进行了初步研究。接种在CSA上的金黄色葡萄球菌和45个凝固酶阴性的金黄色葡萄球菌(CoNS)分离株。所有 S。在37°C孵育24小时后,金黄色葡萄球菌分离出淡紫色菌落,而CoNS菌株则以蓝色,白色或米色菌落生长。然后将CSA上的培养物与常规实验室方法进行前瞻性比较,即在5%马血琼脂(HBA)上培养,过氧化氢酶试验和乳胶凝集试验(HBA-过氧化氢酶-乳胶),以分离和推定 S.从2,000个连续的临床样本中提取金黄色葡萄球菌。在310个 S中。通过两种方法中至少一种回收的金黄色葡萄球菌,在CSA上有296个典型的紫红色菌落生长,而在HBA上只有254个产生过氧化氢酶阳性,乳胶阳性菌落。 CSA的敏感性显着高于常规方法(分别为95.5%和81.9%; P <0.001),并且可以回收血琼脂中未检测到的重要临床分离株。两种方法的特异性没有显着差异,尽管CSA的特异性略高(HBA-过氧化氢酶-胶乳的99.4%比98.9%; P = 0.08)。基于其优异的敏感性和特异性,易于鉴定阳性菌落,并且无需进行补充检测,可以推荐CSA作为常规平板培养基,用于推定鉴定 S。临床标本中的金黄色葡萄球菌。

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