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Identification of Virulence-Associated Characteristics in Clinical Isolates of Yersinia enterocolitica Lacking Classical Virulence Markers

机译:缺乏经典毒力标记的小肠结肠炎耶尔森氏菌临床分离株中毒力相关特征的鉴定

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摘要

Yersinia enterocolitica is an important enteric pathogen which has well-defined virulence determinants that allow the bacteria to become established in their hosts and overcome host defenses. A number of strains obtained from patients with diarrhea, however, lack these genes. Accordingly, the mechanisms by which they cause disease are uncertain. Most of these isolates belong to biotype 1A. Strains of this biotype are also frequently isolated from a variety of nonclinical sources, such as food, soil, water, and healthy animals, and there is evidence that some of these strains are avirulent. In this study we investigated 111 strains of Y. enterocolitica biotype 1A, 79 from symptomatic humans and 32 from nonclinical sources, for virulence-associated characteristics. DNA hybridization studies showed that none of the strains carried sequences homologous with pYV, the ∼70-kb Yersinia virulence plasmid. Some strains hybridized with DNA probes for one of the following chromosomal virulence-associated genes: ail (7.2%), myfA (11.7%), ystA (0.9%), and ystB (85%). In addition, 33 strains (29.7%) produced an enterotoxin that was reactive in infant mice. However, the frequencies of these virulence-associated properties in clinical and nonclinical isolates were similar. Clinical isolates invaded HEp-2 cells and Chinese hamster ovary cells to a significantly greater extent than nonclinical strains (P ≤ 0.002). In addition, clinical strains colonized the intestinal tracts of perorally inoculated mice for significantly longer periods than nonclinical isolates (P ≤ 0.01). Light and electron microscopic examination of tissue culture cells incubated with invasive yersiniae revealed that the bacteria invaded selected cells in large numbers but spared others, suggesting that biotype-1A strains of Y. enterocolitica may invade cells by a novel mechanism. These results indicate that some clinical isolates of Y. enterocolitica which lack classical virulence markers may be able to cause disease via virulence mechanisms which differ from those previously characterized in enteropathogenic Yersinia species.
机译:小肠结肠炎耶尔森菌是一种重要的肠道病原体,具有明确的毒力决定因素,可以使细菌在其宿主中建立并克服宿主防御能力。然而,从腹泻患者获得的许多菌株缺乏这些基因。因此,它们引起疾病的机制尚不确定。这些分离物大多数属于生物型1A。也经常从各种非临床来源(例如食物,土壤,水和健康的动物)中分离出这种生物型菌株,并且有证据表明其中某些菌株是无毒的。在这项研究中,我们调查了111株小肠结肠炎耶尔森菌菌株,79例有症状人类和32例非临床来源的毒力相关特征。 DNA杂交研究表明,这些菌株均未携带与pYV(约70 kb耶尔森菌毒力质粒)同源的序列。一些菌株与DNA探针杂交后出现以下与染色体毒力相关的基因之一:ail(7.2%),myfA(11.7%),ystA(0.9%)和ystB(85%)。此外,有33株(29.7%)产生的肠毒素对婴儿小鼠具有反应性。但是,在临床和非临床分离物中,这些与毒力相关的特性的频率相似。与非临床菌株相比,临床分离株侵袭HEp-2细胞和中国仓鼠卵巢细胞的程度要大得多(P≤0.002)。此外,与非临床分离株相比,临床菌株在经口接种的小鼠的肠道中定植的时间要长得多(P≤0.01)。用侵入性耶尔森氏菌培养的组织培养细胞的光镜和电镜观察表明,该细菌大量侵袭了选定的细胞,但幸免了其他细菌,这表明小肠结肠炎耶尔森氏菌的1A型生物菌株可以通过一种新的机制侵袭细胞。这些结果表明,缺乏经典毒力标记物的一些小肠结肠炎耶尔森氏菌临床分离株可能能够通过毒力机制引起疾病,这种机制不同于先前在肠道致病性耶尔森氏菌中表征的那些。

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