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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of Culture Methods and a DNA Probe-Based PCR Assay for Detection of Campylobacter Species in Clinical Specimens of Feces
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Evaluation of Culture Methods and a DNA Probe-Based PCR Assay for Detection of Campylobacter Species in Clinical Specimens of Feces

机译:粪便临床标本中弯曲杆菌属的培养方法和基于DNA探针的PCR检测方法的评估

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Campylobacter species are the leading agents of bacterial gastroenteritis in developed countries. In this study 320 specimens of feces from patients with symptoms of acute gastroenteritis were cultured for Campylobacter species by direct plating on modified charcoal cefoperazone deoxycholate agar and by enrichment in modified Preston broth, with or without blood added, for 48 h at 37°C prior to plating. A 16S/23S PCR/DNA probe membrane-based colorimetric detection assay was evaluated on a subset of the feces (n = 127), including 18 culture-positive and 109 culture-negative specimens. DNA was extracted directly from the fecal specimens by using the QIAamp DNA stool Minikit for the DNA probe-based PCR assay (PCR/DNA probe assay). A second PCR/DNA probe assay based on the 16S rRNA gene in Campylobacter spp. was applied to all specimens that were culture negative, PCR/DNA positive on initial analysis. Campylobacter species were cultured in 20 of the 320 specimens. The 16S/23S PCR/DNA probe assay detected campylobacter DNA in 17 of 18 (94% sensitivity) culture-positive specimens and in 41 (38%) culture-negative specimens. The presence of campylobacter DNA in 35 of 41 culture-negative specimens was confirmed by the 16S PCR/DNA probe assay. DNA sequence analysis of seven 16S/23S PCR products and five 16S PCR products amplified from a selection of these specimens confirmed the presence of campylobacter DNA and more specifically Campylobacter jejuni, C. concisus, C. curvus, and C. gracilis DNA in these specimens. The molecular assays described in this study are rapid methods for the detection and identification of Campylobacter species in fecal specimens. The finding of Campylobacter spp. DNA in a large number of specimens of feces from patients with no other identified cause of diarrhea may suggest that Campylobacter spp. other than C. jejuni and C. coli may account for a proportion of cases of acute gastroenteritis in which no etiological agent is currently identified.
机译:弯曲杆菌是发达国家细菌性肠胃炎的主要病原体。在这项研究中,通过直接在改良的木炭头孢哌酮脱氧胆酸盐琼脂上平板接种,并富集改良的普雷斯顿肉汤(添加或不添加血液)来培养320例患有急性胃肠炎症状的粪便标本中的弯曲杆菌属。电镀前在37°C下放置48小时。在粪便的一部分( n = 127)上评估了基于16S / 23S PCR / DNA探针膜的比色检测测定法,包括18个培养阳性和109个培养阴性标本。使用QIAamp DNA粪便Minikit直接从粪便标本中提取DNA,用于基于DNA探针的PCR测定(PCR / DNA探针测定)。基于C.emyampbacter spp中16S rRNA基因的第二次PCR / DNA探针检测。在最初分析时,将其用于所有培养阴性,PCR / DNA阳性的标本。在320个标本中的20个中培养了 Campylobacter 物种。 16S / 23S PCR / DNA探针检测在18份培养阳性样本中的17份(灵敏度为94%)和41份培养阴性样本(38%)中检测到弯曲杆菌DNA。通过16S PCR / DNA探针检测证实了41个培养阴性样品中的35个中存在弯曲杆菌DNA。从这些样本中扩增出的7种16S / 23S PCR产物和5种16S PCR产物的DNA序列分析证实了弯曲杆菌DNA的存在,更确切地说是空肠弯曲杆菌(empyC jejuni), C。谦虚 C。曲线 C。这些标本中的gracilis DNA。这项研究中描述的分子测定是快速检测和鉴定粪便标本中弯曲杆菌的方法。 <弯曲菌>弯曲杆菌的发现。大量未发现腹泻原因的患者粪便标本中的DNA可能表明 Campylobacter spp。除了 C。空肠 C。大肠杆菌可能是目前未发现病原体的急性胃肠炎病例的一部分。

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