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应用环介导等温扩增技术检测中国南方地区副猪嗜血杆菌分离株及分离株特性分析

Detection of Haemophilus parasuis isolates from South China by loop-mediated isothermal amplification and isolate characterisation.

作者信息

Zhang Jian-Min, Shen Hai-Yan, Liao Ming, Ren Tao, Guo Li-Li, Xu Cheng-Gang, Feng Sai-Xiang, Fan Hui-Ying, Li Jing-Yi, Chen Ji-Dang, Zhang Bin

机构信息

The Key Laboratory of Animal Disease Control and Prevention of the Ministry of Agriculture, South China Agricultural University.

出版信息

Onderstepoort J Vet Res. 2012 Apr 24;79(1):E1-6. doi: 10.4102/ojvr.v79i1.383.

Abstract

Haemophilus parasuis is the etiological agent of Glässer's disease, which is characterised by fibrinous polyserositis, meningitis and polyarthritis, causing severe economic losses to the swine industry. In this study, a loop-mediated isothermal amplification (LAMP) test was developed to improve the specificity, facility and speed of diagnosis of H. parasuis isolates. The LAMP assay rapidly amplified the target gene within 50 min incubation at 63 °C in a laboratory water bath. The LAMP amplicon could be visualised directly in the reaction tubes following the addition of SYBR Green I dye. The detection limit of this LAMP method was 10 CFU/mL, which was 10 times more sensitive than the earlier 16S rRNA polymerase chain reaction (PCR) test conducted by Oliveira, Galina and Pijoan (2001), and no cross-reactivity was observed from other non-H. parasuis strains. This LAMP test was evaluated further on 187 clinical specimens from pigs suspected of being infected with H. parasuis. Forty-three were found positive by bacterial isolation of H. parasuis, as well as by the 16S rRNA PCR and LAMP tests. The 43 H. parasuis isolates were classified into 9 serovars and had 37 genetic patterns when analysed by pulsed-field gel electrophoresis (PFGE). This displayed that various H. parasuis serovars and genotypes were widely distributed in South China. Therefore, the speed, specificity and sensitivity of the LAMP test, the lack of a need for expensive equipment, and the visual readout showed great potential for a correct clinical diagnosis of H. parasuis in favour of controlling Glässer's disease.

摘要

副猪嗜血杆菌是格拉泽氏病的病原体,其特征为纤维素性多浆膜炎、脑膜炎和多关节炎,给养猪业造成严重经济损失。在本研究中,开发了一种环介导等温扩增(LAMP)检测方法,以提高副猪嗜血杆菌分离株诊断的特异性、便利性和速度。LAMP检测在实验室水浴中于63℃孵育50分钟内快速扩增目标基因。加入SYBR Green I染料后,LAMP扩增产物可直接在反应管中可视化。该LAMP方法的检测限为10 CFU/mL,比奥利维拉、加林娜和皮霍安(2001年)早期进行的16S rRNA聚合酶链反应(PCR)检测灵敏度高10倍,且未观察到与其他非副猪嗜血杆菌菌株的交叉反应。对187份疑似感染副猪嗜血杆菌的猪临床样本进一步评估了该LAMP检测。通过副猪嗜血杆菌的细菌分离以及16S rRNA PCR和LAMP检测,发现43份样本呈阳性。通过脉冲场凝胶电泳(PFGE)分析,这43株副猪嗜血杆菌分离株被分为9个血清型,具有37种基因模式。这表明不同的副猪嗜血杆菌血清型和基因型在中国南方广泛分布。因此,LAMP检测方法的速度、特异性和灵敏度,无需昂贵设备以及可视化读数显示出在副猪嗜血杆菌临床诊断中具有巨大潜力,有助于控制格拉泽氏病。

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