Bull Tim J, McMinn Elizabeth J, Sidi-Boumedine Karim, Skull Angela, Durkin Damien, Neild Penny, Rhodes Glenn, Pickup Roger, Hermon-Taylor John
Department of Surgery, St. George's Hospital Medical School, London SW17 0RE, United Kingdom.
J Clin Microbiol. 2003 Jul;41(7):2915-23. doi: 10.1128/JCM.41.7.2915-2923.2003.
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.
副结核分枝杆菌鸟型亚种是一种生命力顽强且表型多样的病原体,可在包括灵长类动物在内的多种物种中引发肠道慢性炎症。副结核分枝杆菌鸟型亚种感染在家畜中广泛存在,在英国的零售巴氏杀菌牛奶中也有发现,其他地方可能也存在。水源也面临风险。由于检测这种病原体存在很大困难,副结核分枝杆菌鸟型亚种与人类克罗恩病(CD)的关联一直不明确。在其齐-尼氏染色阴性形态下,副结核分枝杆菌鸟型亚种对化学和酶解具有高度抗性。本研究描述了针对新鲜人肠道黏膜活检标本优化样本处理和DNA提取程序的开发,这确保了能够获取副结核分枝杆菌鸟型亚种的DNA,并最大限度地检测这些低丰度病原体。还描述了两种针对IS900的巢式PCR方法,分别命名为IS900[L/AV]和IS900[TJ1-4],它们对IS900具有独特的特异性。还使用分枝杆菌生长指示管(MGIT)培养法(BD公司)评估了黏膜活检标本中副结核分枝杆菌鸟型亚种的检测情况。IS900[L/AV] PCR在37例CD患者中的34例(92%)以及34例无CD的对照(非炎症性肠病[nIBD]对照)中的9例(26%)检测到副结核分枝杆菌鸟型亚种(P = 0.0002;优势比 = 3.47)。在33例CD患者中的14例(42%)以及33例nIBD对照中的3例(9%)经14至88周培养后的MGIT培养物中,通过IS900[L/AV] PCR检测到副结核分枝杆菌鸟型亚种(P = 0.0019;优势比 = 4.66)。15例培养时间超过38周的CD患者标本的MGIT培养物中有9例(60%)副结核分枝杆菌鸟型亚种呈阳性。在每种情况下,通过扩增子测序验证了来自副结核分枝杆菌鸟型亚种的IS900的身份。CD患者中副结核分枝杆菌鸟型亚种的检测率非常显著,表明这种慢性肠道病原体与疾病病因有关。