Fallon D, Ackland G, Andrews N, Frodsham D, Howe S, Howells K, Nye K J, Warren R E
Public Health Laboratory Service (Midlands), Group Headquarters, The Royal Shrewsbury Hospital, Mytton Oak Road, Shrewsbury SY3 8XQ, UK. PHLS Statistics Unit, 61 Colindale Ave, London NW9 5EQ, UK.
J Clin Pathol. 2003 Aug;56(8):608-12. doi: 10.1136/jcp.56.8.608.
To compare four media-UTI medium, BBL CHROMagar, CPS ID2, and Harlequin CLED-using a collection of fully characterised organisms and subsequent "field trial".
Seven hundred and eighty seven fully characterised isolates (730 Gram negative bacteria, 47 Gram positive bacteria, and 10 yeasts) were used to test for accuracy of organism identification. To assess isolation rates and ability to detect mixed cultures, 1435 urine samples were cultured in the three best performing chromogenic media (UTI medium, BBL CHROMagar, and CPS ID2) and CLED.
The chromogenic agars differed in their accuracy of identification, with BBL CHROMagar performing best and Harlequin CLED performing least well. Similarly, BBL CHROMagar achieved a higher overall isolation rate than UTI medium and CPS ID2. When mixed growth was defined as greater than two organism types, BBL CHROMagar detected more mixed cultures than did UTI medium and CPS ID2, although the differences were not significant. When mixed growth was defined as greater than one organism type the increased number of mixed growths detected by BBL CHROMagar became significant, largely because of differences in enterococcal isolation rates.
The use of BBL CHROMagar, UTI medium, or CPS ID2 chromogenic agar as a replacement for CLED agar would improve the detection rate of contaminated urine samples. Enhanced identification helps to distinguish different species, facilitating the monitoring of bacterial resistance in support of the national antibiotic strategy. BBL CHROMagar gave the highest overall organism recovery rates, greatest ability to detect mixed cultures, and the most accurate identification of organisms.
使用一组特征明确的菌株并进行后续“现场试验”,比较四种培养基——泌尿道感染(UTI)培养基、BBL CHROMagar培养基、CPS ID2培养基和丑角CLED培养基。
使用787株特征明确的分离株(730株革兰氏阴性菌、47株革兰氏阳性菌和10株酵母菌)来测试菌株鉴定的准确性。为评估分离率和检测混合培养物的能力,将1435份尿液样本接种于三种表现最佳的显色培养基(UTI培养基、BBL CHROMagar培养基和CPS ID2培养基)和CLED培养基中进行培养。
显色琼脂在鉴定准确性方面存在差异,BBL CHROMagar培养基表现最佳,丑角CLED培养基表现最差。同样,BBL CHROMagar培养基的总体分离率高于UTI培养基和CPS ID2培养基。当将混合生长定义为两种以上菌株类型时,BBL CHROMagar培养基检测到的混合培养物比UTI培养基和CPS ID2培养基更多,尽管差异不显著。当将混合生长定义为一种以上菌株类型时,BBL CHROMagar培养基检测到的混合生长数量增加变得显著,这主要是由于肠球菌分离率的差异。
使用BBL CHROMagar培养基、UTI培养基或CPS ID2显色琼脂替代CLED琼脂可提高污染尿液样本的检测率。增强的鉴定有助于区分不同物种,便于监测细菌耐药性,以支持国家抗生素战略。BBL CHROMagar培养基的总体菌株回收率最高,检测混合培养物的能力最强,对菌株的鉴定最准确。