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Evaluation of BBL CHROMagar orientation medium for detection and presumptive identification of urinary tract pathogens.

机译:评估BBL CHROMagar定向培养基对尿路病原体的检测和推定鉴定。

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摘要

The microbiological performance of BBL CHROMagar Orientation medium and CPS ID2 agar was compared to that of Columbia agar with 5% sheep blood and MacConkey agar without crystal violet for the enumeration and presumptive identification of bacteria responsible for urinary tract infections. Of a total of 658 clinical urine specimens, 118 specimens yielded no growth, 402 specimens yielded growth with cell counts of > or = 10(5) CFU/ml, and 138 specimens yielded growth with cell counts of < 10(5) CFU/ml. Of the specimens with cell counts of > or = 10(5) CFU/ml, 163 were pure cultures and 239 were mixed cultures. A total of 266 Escherichia coli organisms were isolated on both chromogenic media, 260 were isolated on blood agar, and 248 were isolated on MacConkey agar. One strain (0.4%) failed to develop the expected pink color on CHROMagar Orientation medium, and 23 strains (8.7%) failed to develop the expected pink color on CPS ID2 agar. Enterococci (CHROMagar Orientation medium, n = 266; CPS ID2 agar, n = 265) produced small blue-green colonies on both chromogenic media. Fifty of the mixed cultures contained enterococci that were detected only on the chromogenic media. The Klebsiella-Enterobacter-Serratia (KES) and the Proteus-Morganella-Providencia (PMP) groups could be identified on both chromogenic media. Of 66 isolates of the KES group, 63 grew with the expected color on CHROMagar Orientation medium and 58 of 64 isolates grew with the expected color on CPS ID2 agar. Other microorganisms required further identification. The use of chromogenic medium formulations offers a time-saving method for the reliable detection, enumeration, and presumptive identification of urinary tract pathogens. One of the greatest advantages of these media is the easy recognition of mixed cultures.
机译:将BBL CHROMagar定向培养基和CPS ID2琼脂的微生物学性能与含5%羊血的哥伦比亚琼脂和不含结晶紫的MacConkey琼脂的微生物学性能进行了比较,以进行细菌计数和推测性鉴定,这些细菌负责尿路感染。在总共658个临床尿液标本中,有118个标本没有生长,有402个标本在细胞计数>或= 10(5)CFU / ml的情况下生长,有138个标本在细胞计数<10(5)CFU / ml的情况下生长。毫升在细胞计数大于或等于10(5)CFU / ml的标本中,纯培养物为163个,混合培养物为239个。在两种显色培养基上共分离出266种大肠杆菌,在血琼脂上分离出260种,在MacConkey琼脂上分离出248种。 1株(0.4%)在CHROMagar定向培养基上未显示出预期的粉红色,23株(8.7%)在CPS ID2琼脂上未显示出预期的粉红色。肠球菌(CHROMagar定向培养基,n = 266; CPS ID2琼脂,n = 265)在两种生色培养基上均产生小的蓝绿色菌落。混合培养物中有五十种含有仅在生色培养基上检测到的肠球菌。克雷伯菌-肠炎沙雷氏菌(KES)和变形杆菌-摩根氏菌-普罗旺登氏菌(PMP)组可在两种生色培养基上鉴定。在KES组的66个分离株中,有63个在CHROMagar定向培养基上以预期的颜色生长,在64个分离株中有58个在CPS ID2琼脂上以预期的颜色生长。其他微生物需要进一步鉴定。发色培养基配方的使用提供了一种节省时间的方法,用于可靠地检测,枚举和推定性鉴定尿路病原体。这些媒体的最大优势之一是易于识别混合文化。

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