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四种致病性禽支原体诊断实时TaqMan PCR检测方法的开发。

The development of diagnostic real-time TaqMan PCRs for the four pathogenic avian mycoplasmas.

作者信息

Raviv Ziv, Kleven Stanley H

机构信息

Department of Population Health, Poultry Diagnostic and Research Center, University of Georgia, Athens, GA 30602-4875, USA.

出版信息

Avian Dis. 2009 Mar;53(1):103-7. doi: 10.1637/8469-091508-Reg.1.

Abstract

Four avian mycoplasmas are commonly recognized as poultry pathogens: Mycoplasma gallisepticum (MG), Mycoplasma synoviae (MS), Mycoplasma meleagridis (MM), and Mycoplasma iowae (MI). The avian mycoplasmas are associated with respiratory disease, synovitis and arthritis, poor performance, skeletal deformities, and embryo mortality. Three main approaches are used for the diagnosis of avian mycoplasmosis: isolation and identification, detection of antibodies, and molecular detection of the organism's nucleic acid by PCR. In recent years real-time PCR technology has revolutionized the way clinical microbiology laboratories diagnose infectious diseases, but so far only a limited number of diagnostic real-time PCRs have been proposed for avian mycoplasma diagnostics. We developed a complete set of reliable diagnostic real-time TaqMan PCR assays for the four pathogenic avian mycoplasmas. The selected genomic targets of the developed assays were species specific and intraspecifically conserved and included the 16S-23S intergenic spacer region of MS and MM, the upstream region to the 16S ribosomal DNA of MI, and highly conserved foci of the mgc2 gene of MG. The four assays were demonstrated to be highly specific and sensitive to their target avian mycoplasma, with detection limits of one copy per reaction mix for the MG assay and 10 copies per reaction mix for the MS, MM, and MI assays. We believe that the incorporation of the developed assays in avian mycoplasma diagnostics will contribute to the accuracy, efficiency, and feasibility of diagnosis of these pathogens.

摘要

四种禽支原体通常被认为是家禽病原体

鸡毒支原体(MG)、滑液支原体(MS)、火鸡支原体(MM)和衣阿华支原体(MI)。禽支原体与呼吸道疾病、滑膜炎和关节炎、生产性能不佳、骨骼畸形以及胚胎死亡有关。诊断禽支原体病主要有三种方法:分离鉴定、抗体检测以及通过聚合酶链反应(PCR)对病原体核酸进行分子检测。近年来,实时PCR技术彻底改变了临床微生物实验室诊断传染病的方式,但到目前为止,针对禽支原体诊断提出的诊断性实时PCR数量有限。我们开发了一套完整可靠的针对四种致病性禽支原体的诊断性实时TaqMan PCR检测方法。所开发检测方法选定的基因组靶点具有种特异性且在种内保守,包括MS和MM的16S - 23S基因间隔区、MI的16S核糖体DNA上游区域以及MG的mgc2基因高度保守位点。这四种检测方法被证明对其目标禽支原体具有高度特异性和敏感性,MG检测方法的检测限为每个反应混合物1个拷贝,MS、MM和MI检测方法的检测限为每个反应混合物10个拷贝。我们相信,将所开发的检测方法纳入禽支原体诊断将有助于提高这些病原体诊断的准确性、效率和可行性。

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