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首页> 外文期刊>Iranian journal of clinical infectious diseases >First Real-Time PCR in Morocco for Human Leptospirosis Using TaqMan Probes Targeting the LipL32 Gene
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First Real-Time PCR in Morocco for Human Leptospirosis Using TaqMan Probes Targeting the LipL32 Gene

机译:使用TaqMan探针靶向LipL32基因在摩洛哥进行人类钩端螺旋体病的首次实时PCR

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摘要

Currently, qPCR has been used as a rapid diagnostic method for human leptospirosis. Previous studies have indicated that qPCR has high sensitivity in the early days of the illness.The aim of this study was to evaluate qPCR as a diagnostic method for human leptospirosis in the National Institute of Hygiene, Rabat, Morocco.From 2004 to 2016, 67 sera related to 67 patients with clinical signs mimic to leptospirosis were sent to the laboratory of Bacteriology for routine diagnosis and confirmation. SAT, ELISA IgM, ELISA IgG, and qPCR were used for the diagnosis.High positivity was observed by SAT (88.24%), ELISA IgM (58.82%), and real-time PCR (17.64%), in sequence. No negative results by serological tests had positive results by real-time PCR. Forty-six patients were males (68.68%) and 21 were females (31.34%). The high incidence observed was from Sidi Qacem (40%).SAT and ELISA IgM are useful for the diagnosis of human leptospirosis in Morocco and they can provide prompt and low-cost diagnosis, especially when resources are limited.
机译:目前,qPCR已被用作人类钩端螺旋体病的快速诊断方法。先前的研究表明qPCR在疾病的早期具有很高的敏感性,这项研究的目的是评估摩洛哥国家拉美卫生研究院(National Institute of Hygiene)的qPCR作为人类钩端螺旋体病的诊断方法.2004年至2016年,67与67例临床表现类似钩端螺旋体病的患者相关的血清被送至细菌学实验室进行常规诊断和确诊。采用SAT,ELISA IgM,ELISA IgG和qPCR进行诊断,依次检测SAT(88.24%),ELISA IgM(58.82%)和实时PCR(17.64%)的阳性率。血清学检测没有阴性结果,实时荧光定量PCR没有阳性结果。男性46例(68.68%),女性21例(31.34%)。观察到的高发病率来自Sidi Qacem(40%)。SAT和ELISA IgM可用于摩洛哥人钩端螺旋体病的诊断,并且可以提供快速,低成本的诊断,尤其是在资源有限的情况下。

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