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肠道病原体检测、鉴定及药敏试验的快速方法。

Rapid method for detection, identification, and susceptibility testing of enteric pathogens.

作者信息

Stager C E, Erikson E, Davis J R

出版信息

J Clin Microbiol. 1983 Jan;17(1):79-84. doi: 10.1128/jcm.17.1.79-84.1983.

Abstract

Three hundred and seven colonies believed to be enteric pathogens were selected from primary plates of MacConkey, xylose desoxycholate, or salmonella-shigella agar for inoculation to lactose-sucrose broth, urea-41 motility medium, modified Andrade glucose broth with inverted Durham tube, pregrowth broth, triple sugar iron agar, lysine iron agar (LIA), and Christensen urea agar. The rapid screen consisted of interpreting the lactose-sucrose, urea-41 motility, and modified Andrade glucose broth gas reactions after 4 to 6 h at 35 degrees C. These rapid screening biochemicals plus LIA were incubated for 24 h if further interpretation was required. Reference biochemicals (triple sugar iron, LIA, and Christensen urea agars) were interpreted at 24 h. Of 307 isolates, 49 (16%) were reported as negative for enteric pathogens after 4 to 6 h because their biochemical profiles were not compatible with those for enteric pathogens. A total of 87 (28.3%) isolates produced biochemical profiles at 4 to 6 h that were presumptive for enteric pathogens. The 87 presumptive pathogens were inoculated into the AutoMicrobic system Gram-Negative General Susceptibility Card and the AutoMicrobic system Enterobacteriaceae-Plus Biochemical Card (AMS-EBC+) after 4 to 6 h of growth in pregrowth broth. Of these isolates, 63 were confirmed to be enteric pathogens, of which 61 (96.8%) were correctly identified by the AMS-EBC+. One isolate was identified as Shigella dysenteriae by AMS-EBC+ but confirmed as Shigella flexneri biotype 6 by a reference laboratory. The other isolate was identified as Arizona hinshawii by AMS-EBC+ but was confirmed as Salmonella enteritidis. Of the 307 isolates, 166 (54.1%) required further interpretation of the rapid screening biochemicals plus LIA at 24 h; 5 of these were detected as enteric pathogens. The same 68 enteric pathogens were detected by both the rapid method and the reference method. The results from the general susceptibility card agreed with agar diffusion results at 99.2%. One Salmonella enteritidis and four Shigella spp. showed minor discrepancies with tetracycline. No very major or major discrepancies were observed.

摘要

从麦康凯、木糖脱氧胆酸盐或沙门菌 - 志贺菌琼脂的原始平板中挑选出307个被认为是肠道病原体的菌落,接种到乳糖 - 蔗糖肉汤、尿素 - 41动力培养基、带有倒置德汉氏小管的改良安德拉德葡萄糖肉汤、预增菌肉汤、三糖铁琼脂、赖氨酸铁琼脂(LIA)和克里斯滕森尿素琼脂中。快速筛选包括在35℃下培养4至6小时后解读乳糖 - 蔗糖、尿素 - 41动力和改良安德拉德葡萄糖肉汤的气体反应。如果需要进一步解读,这些快速筛选生化指标加上LIA需培养24小时。参考生化指标(三糖铁、LIA和克里斯滕森尿素琼脂)在24小时解读。在307个分离株中,49个(16%)在4至6小时后被报告为肠道病原体阴性,因为它们的生化特征与肠道病原体不相符。共有87个(28.3%)分离株在4至6小时产生了疑似肠道病原体的生化特征。在预增菌肉汤中生长4至6小时后,将这87个疑似病原体接种到自动微生物系统革兰氏阴性通用药敏卡和自动微生物系统肠杆菌科加生化卡(AMS - EBC +)中。在这些分离株中,63个被确认为肠道病原体,其中61个(96.8%)被AMS - EBC +正确鉴定。一个分离株被AMS - EBC +鉴定为痢疾志贺菌,但参考实验室确认为福氏志贺菌6型。另一个分离株被AMS - EBC +鉴定为欣氏亚利桑那菌,但被确认为肠炎沙门菌。在307个分离株中,166个(54.1%)需要在24小时对快速筛选生化指标加上LIA进行进一步解读;其中5个被检测为肠道病原体。快速方法和参考方法检测到相同的68个肠道病原体。通用药敏卡的结果与琼脂扩散结果的一致性为99.2%。一株肠炎沙门菌和四株志贺菌属在四环素检测上存在微小差异。未观察到非常重大或重大差异。

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