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将C(18)-羧丙基甜菜碱标本处理方法应用于从反刍动物组织标本中回收副结核分枝杆菌。

Application of the C(18)-carboxypropylbetaine specimen processing method to recovery of Mycobacterium avium subsp. paratuberculosis from ruminant tissue specimens.

作者信息

Thornton Charles G, MacLellan Kerry M, Stabel Judith R, Carothers Christine, Whitlock Robert H, Passen Selvin

机构信息

Integrated Research Technology, LLC, c/o Quest Diagnostics Incorporated, 1901 Sulfur Spring Road, Baltimore, MD 21227, USA.

出版信息

J Clin Microbiol. 2002 May;40(5):1783-90. doi: 10.1128/JCM.40.5.1783-1790.2002.

Abstract

The causative agent of Johne's disease is Mycobacterium avium subsp. paratuberculosis. This is a chronic, debilitating gastrointestinal disorder that affects ruminants and is responsible for significant economic loss. The specimen processing method that combines C(18)-carboxypropylbetaine (CB-18) treatment and lytic enzyme decontamination has been shown to improve the diagnosis of mycobacterioses. This processing method was applied to the isolation of M. avium subsp. paratuberculosis from ruminant tissue samples. The BACTEC 12B liquid culture system was used but was supplemented with 1% egg yolk emulsion, 4 microg of mycobactin J, and 0.5% pyruvate (12B/EMP) for use in conjunction with this method. The final concentration of antibiotics used was 10 microg of vancomycin, 30 microg of amphotericin B, and 20 microg of nalidixic acid (VAN) per ml. A 7H10-based solid medium was also used that included mycobactin J, pyruvate, and VAN but excluded the egg yolk emulsion (7H10/MPV). Several M. avium subsp. paratuberculosis isolates were examined during the evaluation of this processing method. It was observed that treatment with lytic enzymes stimulated the growth of M. avium subsp. paratuberculosis; however, the growth of one isolate was markedly inhibited due to the presence of vancomycin. Subsequently, the vancomycin concentration in the VAN formulation was reduced to 2 microg/ml. A blinded panel of 60 previously characterized tissue samples from bovine and bison were then processed and analyzed by smear and culture. Historically, 31 and 37 specimens were classified as positive by histology and culture, respectively. The overall sensitivity and specificity of smear relative to culture following CB-18 processing were 97.6 and 89.5%, respectively. The 12B/EMP/VAN liquid culture system recovered M. avium subsp. paratuberculosis from 39 specimens, whereas 7H10/MPV and Herrold's egg yolk media recovered M. avium subsp. paratuberculosis from 26 and 16 specimens, respectively. The average times to positive were 7.4 +/- 8.3, 29.9 +/- 2.6, and 24 +/- 0 days, respectively. The contamination rates were 4.8, 22.6, and 20.0%, respectively.

摘要

约内氏病的病原体是副结核分枝杆菌鸟型亚种。这是一种影响反刍动物的慢性、使人衰弱的胃肠道疾病,会造成重大经济损失。已证明,结合使用C(18)-羧丙基甜菜碱(CB-18)处理和溶菌酶去污的标本处理方法可改善分枝杆菌病的诊断。该处理方法应用于从反刍动物组织样本中分离副结核分枝杆菌鸟型亚种。使用了BACTEC 12B液体培养系统,但补充了1%蛋黄乳剂、4微克分枝杆菌素J和0.5%丙酮酸盐(12B/EMP)以便与该方法联合使用。所用抗生素的终浓度为每毫升10微克万古霉素、30微克两性霉素B和20微克萘啶酸(VAN)。还使用了一种基于7H10的固体培养基,其中包括分枝杆菌素J、丙酮酸盐和VAN,但不含蛋黄乳剂(7H10/MPV)。在评估该处理方法期间,检测了几株副结核分枝杆菌鸟型亚种分离株。观察到用溶菌酶处理可刺激副结核分枝杆菌鸟型亚种的生长;然而,由于存在万古霉素,一株分离株的生长受到明显抑制。随后,将VAN配方中的万古霉素浓度降至2微克/毫升。然后对一组来自牛和野牛的60份先前已鉴定的组织样本进行盲法处理,并通过涂片和培养进行分析。从历史数据来看,分别有31份和37份标本经组织学和培养分类为阳性。经CB-18处理后,涂片相对于培养的总体敏感性和特异性分别为97.6%和89.5%。12B/EMP/VAN液体培养系统从39份标本中分离出副结核分枝杆菌鸟型亚种,而7H10/MPV和赫罗尔德蛋黄培养基分别从26份和16份标本中分离出副结核分枝杆菌鸟型亚种。阳性平均时间分别为7.4±8.3、29.9±2.6和24±0天。污染率分别为4.8%、22.6%和20.0%。

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