Woo P C, Leung P K, Leung K W, Yuen K Y
Department of Microbiology, University of Hong Kong, Queen Mary Hospital, People's Republic of China.
Mol Pathol. 2000 Aug;53(4):211-5. doi: 10.1136/mp.53.4.211.
To ascertain the clinical relevance of a strain of Enterobacteriaceae isolated from the stool of a bone marrow transplant recipient with diarrhoea. The isolate could not be identified to the genus level by conventional phenotypic methods and required 16S ribosomal RNA (rRNA) gene sequencing for full identification.
The isolate was investigated phenotypically by standard biochemical methods using conventional biochemical tests and two commercially available systems, the Vitek (GNI+) and API (20E) systems. Genotypically, the 16S bacterial rRNA gene was amplified by the polymerase chain reaction (PCR) and sequenced. The sequence of the PCR product was compared with known 16S rRNA gene sequences in the GenBank database by multiple sequence alignment.
Conventional biochemical tests did not reveal a pattern resembling any known member of the Enterobacteriaceae family. The isolate was identified as Salmonella arizonae (73%) and Escherichia coli (76%) by the Vitek (GNI+) and API (20E) systems, respectively. 16S rRNA sequencing showed that there was only one base difference between the isolate and E coli K-12, but 48 and 47 base differences between the isolate and S typhimurium (NCTC 8391) and S typhi (St111), respectively, showing that it was an E coli strain. The patient did not require any specific treatment and the diarrhoea subsided spontaneously.
16S rRNA gene sequencing was useful in ascertaining the clinical relevance of the strain of Enterobacteriaceae isolated from the stool of the bone marrow transplant recipient with diarrhoea.
确定从一名患有腹泻的骨髓移植受者粪便中分离出的一株肠杆菌科细菌的临床相关性。通过传统表型方法无法将该分离株鉴定到属水平,需要进行16S核糖体RNA(rRNA)基因测序才能完全鉴定。
使用传统生化试验以及两种市售系统Vitek(GNI+)和API(20E)系统,通过标准生化方法对该分离株进行表型研究。在基因层面,通过聚合酶链反应(PCR)扩增细菌16S rRNA基因并进行测序。通过多重序列比对,将PCR产物的序列与GenBank数据库中已知的16S rRNA基因序列进行比较。
传统生化试验未显示出与肠杆菌科家族任何已知成员相似的模式。Vitek(GNI+)系统和API(20E)系统分别将该分离株鉴定为亚利桑那沙门氏菌(73%)和大肠杆菌(76%)。16S rRNA测序表明,该分离株与大肠杆菌K-12之间仅有一个碱基差异,但与鼠伤寒沙门氏菌(NCTC 8391)和伤寒沙门氏菌(St111)之间分别有48个和47个碱基差异,表明它是一株大肠杆菌菌株。患者无需任何特殊治疗,腹泻自行消退。
16S rRNA基因测序有助于确定从患有腹泻的骨髓移植受者粪便中分离出的肠杆菌科菌株的临床相关性。