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首页> 外文期刊>Journal of Clinical Microbiology >Detection and Verification of Mycobacterium avium subsp. paratuberculosis in Fresh Ileocolonic Mucosal Biopsy Specimens from Individuals with and without Crohn's Disease
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Detection and Verification of Mycobacterium avium subsp. paratuberculosis in Fresh Ileocolonic Mucosal Biopsy Specimens from Individuals with and without Crohn's Disease

机译:禽分枝杆菌亚种的检测和验证。患有和不患有克罗恩病的个体的新鲜结肠结肠黏膜活检标本中的副结核病

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摘要

Mycobacterium avium subsp. paratuberculosis is a robust and phenotypically versatile pathogen which causes chronic inflammation of the intestine in many species, including primates. M. avium subsp. paratuberculosis infection is widespread in domestic livestock and is present in retail pasteurized cows' milk in the United Kingdom and, potentially, elsewhere. Water supplies are also at risk. The involvement of M. avium subsp. paratuberculosis in Crohn's disease (CD) in humans has been uncertain because of the substantial difficulties in detecting this pathogen. In its Ziehl-Neelsen staining-negative form, M. avium subsp. paratuberculosis is highly resistant to chemical and enzymatic lysis. The present study describes the development of optimized sample processing and DNA extraction procedures with fresh human intestinal mucosal biopsy specimens which ensure access to M. avium subsp. paratuberculosis DNA and maximize detection of these low-abundance pathogens. Also described are two nested PCR methodologies targeted at IS900, designated IS900[L/AV] and IS900[TJ1-4], which are uniquely specific for IS900. Detection of M. avium subsp. paratuberculosis in mucosal biopsy specimens was also evaluated by using mycobacterial growth indicator tube (MGIT) cultures (Becton Dickinson). IS900[L/AV] PCR detected M. avium subsp. paratuberculosis in 34 of 37 (92%) patients with CD and in 9 of 34 (26%) controls without CD (noninflammatory bowel disease [nIBD] controls) (P = 0.0002; odds ratio = 3.47). M. avium subsp. paratuberculosis was detected by IS900[L/AV] PCR in MGIT cultures after 14 to 88 weeks of incubation in 14 of 33 (42%) CD patients and 3 of 33 (9%) nIBD controls (P = 0.0019; odds ratio = 4.66). Nine of 15 (60%) MGIT cultures of specimens from CD patients incubated for more than 38 weeks were positive for M. avium subsp. paratuberculosis. In each case the identity of IS900 from M. avium subsp. paratuberculosis was verified by amplicon sequencing. The rate of detection of M. avium subsp. paratuberculosis in individuals with CD is highly significant and implicates this chronic enteric pathogen in disease causation.
机译:鸟分枝杆菌子亚种。 肺结核是一种健壮且具有表型用途的病原体,可导致包括灵长类在内的许多物种的肠道慢性炎症。 M。 avium 子空间肺结核感染在家畜中普遍存在,在英国以及可能在其他地方存在于零售巴氏杀菌牛奶中。供水也有危险。 M的参与。 avium 子空间人类克罗恩病(CD)中的肺结核尚不确定,因为很难检测到这种病原体。 Zemhl-Neelsen染色阴性形式, M。 avium 子空间肺结核对化学和酶促裂解具有高度抵抗力。本研究描述了使用新鲜的人肠道粘膜活检标本进行优化的样品处理和DNA提取程序的开发,这些标本可确保获得 M。 avium 子空间肺结核 DNA并最大限度地检测这些低丰度病原体。还介绍了针对IS 900 的两种嵌套式PCR方法,称为IS 900 [L / AV]和IS 900 [TJ1-4],专门针对IS 900 。检测 M。 avium 子空间还使用分枝杆菌生长指示管(MGIT)培养物(Becton Dickinson)评估了粘膜活检标本中的肺结核。 IS 900 [L / AV] PCR检测到 M。 avium 子空间37名患有CD的患者中的34名肺结核和无CD的34名对照中的9名(26%)(非炎性肠病[nIBD]对照)( P = 0.0002;优势比= 3.47)。 M。 avium 子空间33名(42%)CD患者中的14名和33名中的3名在培养14至88周后,通过IS 900 [L / AV] PCR在MGIT培养物中检测到肺结核 (9%)nIBD对照( P = 0.0019;优势比= 4.66)。来自CD患者的15个MGIT培养物样本中有9个(60%)培养了38周以上,它们的 M呈阳性。 avium 子空间肺结核。在每种情况下, M的IS 900 的身份。 avium 子空间通过扩增子测序证实了肺结核 M的检出率。 avium 子空间患有CD的个体中的肺结核高度重要,并且提示这种慢性肠病原体与疾病成因有关。

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