Computerized complex typing of Escherichia coli strains from different clinical materials.

Acta microbiologica Hungarica Pub Date : 1993-01-01
E Czirók, M Herpay, H Milch
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引用次数: 0

Abstract

A multivariate analysis of 3334 Escherichia coli strains originating from different clinical materials revealed that 50.2% of isolates belonged to the most common 12 (O1, O2, O4, O6, O7, O8, O15, O18, O45, O75, O78, O83) out of 133 serogroups. Haemolysin (Hly) production, mannose resistant haemagglutinating activity for human erythrocytes (MRHA) and colicinogenicity (Col) were recorded in 30, 30 and 36%, respectively. Antigens K1 and K5 were present in 11% and 6.6%, respectively. Association were found among certain serotypes and virulence markers (O1, H-, H7, K1, MRHA, Col; O2, H-, Kl, Col; O4, H-, H5, MRHA, Hly; O6, H-, H1, MRHA, Hly; O6, K5, MRHA, Col; O7, H-, H4, K1, MRHA, Col; O18ac, H7, K1, Col; O18ac, H-, K5, MRHA, Hly; O78, H-, Col (V-type); O83, H-, K1, Col). There were associations among clinical specimens, age of patients, nosocomial group of diseases, serogroups and virulence markers, too (cerebrospinal fluid-CSF-O7, O18ac, O45, O83-K1-newborn meningitis; O78-ColV-meningitis, sepsis, inflammations diseases of premature babies; CFS-O6, MRHA, Hly-adult-meningitis, sepsis, urinary tract infection-UTI-, pneumonia, other inflammatory diseases; blood-O2, O4, O6, O18ac, ONT, K5, MRHA, Hly-sepsis, UTI, hepatic diseases; urine-O1, O2, O4, O6, O18ac, O75, virulence markers fall to differ among upper and lower UTI; faeces-O1, O4, O6, O18ac, O78, virulence markers rare). Associations were also found among animal pathogenicity tests, specimens, serogroups and virulence factors: highly virulent group strains (i.e. LD50 below 10(6)) belonged to serogroups O2, O6, O18ac, possessed antigen K1 (less frequently the presence of MRHA, Hly, K5) and originated mainly from CSF. With mouse lung toxicity test correlations of serogroups (O4, O6, O18ac), antigen K5, MRHA, Hly and specimens (blood) were also shown. However, association was found between the lack of virulence factors and phage insensitivity and also between K5 positivity and sensitivity to phages 16, 17, there were no correlations between serogroups and phage patterns. On the basis of the above-described associations one can find correlations among virulence markers, serotype, and nosological group of diseases. Animal pathogenicity tests give additional data in understanding the pathomechanism of diseases. Correlations between phage patterns and serogroups reveal certain epidemiological relatedness and also virulence of strains.

来自不同临床材料的大肠杆菌菌株的计算机复杂分型。
对来自不同临床材料的3334株大肠杆菌进行多因素分析,发现133个血清群中最常见的12个(O1、O2、O4、O6、O7、O8、O15、O18、O45、O75、O78、O83)占50.2%。溶血素(Hly)产量、甘露糖抗人红细胞血凝活性(MRHA)和大肠杆菌致病性(Col)分别为30%、30%和36%。抗原K1和K5分别占11%和6.6%。在某些血清型和毒力标记物(O1、H-、H7、K1、MRHA、Col;O2, H-, Kl, Col;O4, H-, H5, MRHA, Hly;O6, H-, H1, MRHA, Hly;O6, K5, MRHA, Col;O7, H-, H4, K1, MRHA, Col;O18ac, H7, K1, Col;O18ac, H-, K5, MRHA, Hly;O78, H-, Col (v型);O83, H-, K1, Col)。临床标本、患者年龄、医院疾病组、血清组和毒力标志物(脑脊液- csf - o7、O18ac、O45、o83 - k1 -新生儿脑膜炎;o78 - colv -脑膜炎、败血症、早产儿炎症性疾病;CFS-O6、MRHA、h成人-脑膜炎、败血症、尿路感染- uti、肺炎、其他炎症性疾病;血氧、O4、O6、O18ac、ONT、K5、MRHA、Hly-sepsis、UTI、肝病;尿中o1、O2、O4、O6、O18ac、O75等毒力指标在上下尿路感染中差异较大;粪便- o1, O4, O6, O18ac, O78,毒力标记罕见)。动物致病性试验、标本、血清组和毒力因子之间也存在相关性:高毒力组菌株(即LD50低于10(6))属于O2、O6、O18ac血清组,具有抗原K1(较少出现MRHA、Hly、K5),主要来源于CSF。小鼠肺毒性试验还显示了血清组(O4、O6、O18ac)、抗原K5、MRHA、Hly和标本(血)的相关性。然而,毒力因子的缺乏与噬菌体不敏感之间存在关联,K5阳性与噬菌体16、17的敏感性之间也存在关联,血清组与噬菌体模式之间没有相关性。在上述关联的基础上,人们可以发现毒力标记物、血清型和疾病分类学组之间的相关性。动物致病性试验为了解疾病的发病机制提供了额外的数据。噬菌体模式和血清群之间的相关性揭示了某些流行病学相关性以及菌株的毒力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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