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首页> 外文期刊>Indian Journal of Animal Research >Detection of Mycoplasma gallinaceum by PCR amplification of the 16S rRNA gene from respiratory disease in village chickens
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Detection of Mycoplasma gallinaceum by PCR amplification of the 16S rRNA gene from respiratory disease in village chickens

机译:PCR扩增来自村鸡呼吸道疾病的16S rRNA基因的PCR扩增检测

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摘要

In the present study, Mycoplasma gallinaceum w as detected by PCR amplification of 16S rRNA gene from chronic respiratory disease in village chickens of Cauvery delta region of Tamil Nadu. Necropsy was performed to find out the etiological agent in desi birds mortality. At necropsy, airsacculitis with caseous exudate were found in the thoracic and abdominal cavity. Caseous material from airsacs was collected aseptically from dead birds for detection of Mycoplasma species. DNA was extracted from caseous material by using tissue DNA extraction kit. PCR was carried out using primers to amplify 16S rRNA gene belonging to Mycoplasma species. The amplified product yielded approximately 700-bp length (703 to 713 bp) of the 16S rRNA gene specific for Mycoplasma species. Further, it was subjected to sequence analysis and confirmed as Mycoplasma gallinaceum by NCBI blast analysis. In the present communication, detection of M. gallinaceum by PCR amplification of 16S rRNA gene provides a powerful tool for rapid diagnosis.
机译:在本研究中,PCR扩增来自泰米尔纳德岛Cauvery Delta地区村鸡的慢性呼吸道疾病的PCR扩增的支原体Gallinaeum W.进行了尸检,以了解Desi鸟死亡率的病因。在尸检时,在胸腔和腹腔中发现了患有盲骨渗出物的空气抗炎。从死鸟中无菌收集来自Airsacs的骨架材料,以检测支原体。通过使用组织DNA提取试剂盒从勾壳材料中提取DNA。使用引物进行PCR以扩增属于支原体物种的16S rRNA基因。扩增产物产生约700磅的长度(703至713bp),其用于支原体物种特异性。此外,通过NCBI Blast分析对其进行序列分析并确认为支原体Gallina身材。在本通信中,通过PCR扩增的M. Gallinaceum的检测为16S rRNA基因提供了一种快速诊断的强大工具。

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