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通过细胞介导免疫反应、传统及分子诊断技术诊断山羊副结核病

Diagnosis of paratuberculosis in goats by cell mediated immune response, conventional and molecular diagnostic techniques.

作者信息

Rawther Sulficar Shamsudeen, Saseendranath Mapranath Raghavan, Nair Govinda Pilla Krishnan, Tresamol Palathingal Vareid, Pillai Usha Narayana, Abraham John, Senthilkumar Tuticorin Maragatham Alagesan, Nagalakshmy Shrine, Nimisha Krishna Kripa Narayanan

机构信息

Department of Veterinary Epidemiology and Preventive Medicine, College of Veterinary and Animal Sciences, Mannuthy, Trichur, Kerala, India.

出版信息

Trop Anim Health Prod. 2012 Apr;44(4):911-4. doi: 10.1007/s11250-011-9986-y. Epub 2011 Sep 29.

DOI:10.1007/s11250-011-9986-y
PMID:21956142
Abstract

In the present study efficacy of single intradermal Johnin test, acid fast staining of faecal smear and IS 900 faecal polymerase chain reaction tests was evaluated in 200 goats for detection of Mycobacterium avium subsp paratuberculosis. Two hundred goats comprising 150 goats from an organised farm in Trichur district and 50 goats reared under field condition at farmers premise from Malappuram district of Kerala state formed the study population. Faecal smear from all the 200 goats was stained by Ziehl-Neelsen acid fast stain and faecal polymerase chain reaction (PCR) specific for M. avium subsp paratuberculosis (MAP); IS 900 was performed on all samples. All the animals were subjected to single intradermal Johnin test. Out of 200 goats screened for paratuberculosis, six goats (3%), 11 goats (5.5%) and 42 goats (21%) were found positive by Ziehl-Neelsen acid fast staining of faecal smear, single intradermal Johnin test and IS 900 PCR respectively. Results of the present study indicate that amplification of IS 900 insertion element was the most specific and sensitive diagnostic detection method. Single intradermal Johnin test and Ziehl-Neelsen acid fast staining did not show any significant difference.

摘要

在本研究中,对200只山羊进行了皮内注射琼宁试验、粪便涂片抗酸染色和IS 900粪便聚合酶链反应检测,以检测副结核分枝杆菌。200只山羊组成了研究群体,其中150只来自特里丘尔区一个有组织的农场,50只在喀拉拉邦马拉普拉姆区农民家中的田间条件下饲养。对所有200只山羊的粪便涂片进行齐-尼抗酸染色,并对副结核分枝杆菌(MAP)进行粪便聚合酶链反应(PCR);对所有样本进行IS 900检测。所有动物均接受皮内注射琼宁试验。在筛查副结核的200只山羊中,粪便涂片齐-尼抗酸染色、皮内注射琼宁试验和IS 900 PCR分别检测出6只山羊(3%)、11只山羊(5.5%)和42只山羊(21%)呈阳性。本研究结果表明,IS 900插入元件的扩增是最特异、最敏感的诊断检测方法。皮内注射琼宁试验和齐-尼抗酸染色未显示出任何显著差异。

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本文引用的文献

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Diagnostic Application of IS900 PCR Using Blood as a Source Sample for the Detection of Mycobacterium avium Subspecies Paratuberculosis in Early and Subclinical Cases of Caprine Paratuberculosis.以血液为样本来源的IS900聚合酶链反应在山羊副结核病早期及亚临床病例中检测鸟分枝杆菌副结核亚种的诊断应用
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Incidence of Mycobacterium avium subspecies paratuberculosis in a population-based cohort of patients with Crohn's disease and control subjects.基于人群的克罗恩病患者队列和对照受试者中副结核分枝杆菌亚种的发病率。
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Comparative evaluation of positive tests to Mycobacterium avium subsp. paratuberculosis in clinically healthy sheep and goats in south-west Greece using molecular techniques, serology, and culture.
使用分子技术、血清学和培养方法对希腊西南部临床健康绵羊和山羊中禽分枝杆菌副结核亚种阳性检测的比较评估
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Evaluation of the gamma interferon ELISA in sheep subclinically infected with Mycobacterium avium subspecies paratuberculosis using a whole-cell sonicate or a johnin purified-protein derivative.使用全细胞超声裂解物或副结核菌素纯化蛋白衍生物对亚临床感染鸟分枝杆菌副结核亚种的绵羊进行γ干扰素酶联免疫吸附测定的评估。
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The association of sub-clinical paratuberculosis with the fertility of Greek dairy ewes and goats varies with parity.亚临床型副结核病与希腊奶用母羊和母山羊繁殖力之间的关联因胎次而异。
Prev Vet Med. 2006 May 17;74(2-3):226-38. doi: 10.1016/j.prevetmed.2005.12.001. Epub 2006 Jan 9.
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Comparison of diagnostic detection methods for Mycobacterium avium subsp. paratuberculosis in North American bison.北美野牛副结核分枝杆菌诊断检测方法的比较。
Vet Pathol. 2005 Jan;42(1):42-51. doi: 10.1354/vp.42-1-42.
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Detection of Mycobacterium avium subsp. paratuberculosis by buoyant density centrifugation, sequence capture PCR and dot blot hybridisation.
Vet Microbiol. 2002 Jul 22;87(4):327-40. doi: 10.1016/s0378-1135(02)00082-2.
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Mycobacterium avium subsp. paratuberculosis: pathogen, pathogenesis and diagnosis.副结核分枝杆菌:病原体、发病机制与诊断
Rev Sci Tech. 2001 Apr;20(1):133-50. doi: 10.20506/rst.20.1.1275.
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Comparison of immunohistochemistry, acid-fast staining, and cultivation for detection of Mycobacterium paratuberculosis in goats.
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