Department of Microbiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi UP 221005, India.
World J Gastroenterol. 2013 Feb 21;19(7):1056-67. doi: 10.3748/wjg.v19.i7.1056.
To characterize oxidase- and urease-producing bacterial isolates, grown aerobically, that originated from antral biopsies of patients suffering from acid peptic diseases.
A total of 258 antral biopsy specimens were subjected to isolation of bacteria followed by tests for oxidase and urease production, acid tolerance and aerobic growth. The selected isolates were further characterized by molecular techniques viz. amplifications for 16S rRNA using universal eubacterial and HSP60 gene specific primers. The amplicons were subjected to restriction analysis and partial sequencing. A phylogenetic tree was generated using unweighted pair group method with arithmetic mean (UPGMA) from evolutionary distance computed with bootstrap test of phylogeny. Assessment of acidity tolerance of bacteria isolated from antrum was performed using hydrochloric acid from 10(-7) mol/L to 10(-1) mol/L.
Of the 258 antral biopsy specimens collected from patients, 179 (69.4%) were positive for urease production by rapid urease test and 31% (80/258) yielded typical Helicobacter pylori (H. pylori) after 5-7 d of incubation under a microaerophilic environment. A total of 240 (93%) antral biopsies yielded homogeneous semi-translucent and small colonies after overnight incubation. The partial 16S rRNA sequences revealed that the isolates had 99% similarity with Pseudomonas species. A phylogenetic tree on the basis of 16S rRNA sequences denoted that JQ927226 and JQ927227 were likely to be related to Pseudomonas fluorescens (P. fluorescens). On the basis of HSP60 sequences applied to the UPGMA phylogenetic tree, it was observed that isolated strains in an aerobic environment were likely to be P. fluorescens, and HSP60 sequences had more discriminatory potential rather than 16S rRNA sequences. Interestingly, this bacterium was acid tolerant for hours at low pH. Further, a total of 250 (96.9%) genomic DNA samples of 258 biopsy specimens and DNA from 240 bacterial isolates were positive for the 613 bp amplicons by targeting P. fluorescens-specific conserved putative outer membrane protein gene sequences.
This study indicates that bacterial isolates from antral biopsies grown aerobically were P. fluorescens, and thus acid-tolerant bacteria other than H. pylori can also colonize the stomach and may be implicated in pathogenesis/protection.
鉴定从患有酸相关消化性疾病患者的胃窦活检中分离得到的、需氧生长且产氧化酶和脲酶的细菌。
对 258 份胃窦活检标本进行细菌分离,然后检测氧化酶和脲酶的产生、耐酸能力和需氧生长情况。使用通用细菌 16S rRNA 扩增和 HSP60 基因特异性引物,通过分子技术进一步鉴定所选分离株。扩增产物进行限制性分析和部分测序。使用基于非加权配对组算术平均(UPGMA)的系统发育树,从基于进化距离的系统发育 bootstrap 检验中生成。使用 10(-7)mol/L 至 10(-1)mol/L 的盐酸评估从胃窦分离的细菌的耐酸性。
从患者的 258 份胃窦活检标本中,179 份(69.4%)快速脲酶试验呈脲酶阳性,31%(80/258)在微需氧环境下孵育 5-7 天后产生典型的幽门螺杆菌(H. pylori)。240 份(93%)胃窦活检标本在过夜孵育后产生均匀的半透明、小菌落。部分 16S rRNA 序列显示分离株与假单胞菌属具有 99%的相似性。基于 16S rRNA 序列的系统发育树表明,JQ927226 和 JQ927227 可能与荧光假单胞菌(P. fluorescens)有关。基于 HSP60 序列的 UPGMA 系统发育树表明,在需氧环境中分离的菌株可能是荧光假单胞菌,HSP60 序列比 16S rRNA 序列具有更高的鉴别潜力。有趣的是,这种细菌在低 pH 值下能耐受数小时的酸性。此外,对 258 份活检标本中的 250 份(96.9%)基因组 DNA 样本和 240 株细菌分离株进行检测,结果显示靶向荧光假单胞菌特异性保守假定外膜蛋白基因序列的 613 bp 扩增子均为阳性。
本研究表明,从需氧生长的胃窦活检中分离的细菌为荧光假单胞菌,因此除幽门螺杆菌外,耐酸细菌也可以定植于胃,并可能与发病机制/保护有关。