详细分析 16S rRNA 基因测序和传统 PCR 检测在诊断细菌病原体和发现新型细菌方面的应用。

IF 1.8 3区 生物学 Q4 MICROBIOLOGY
Mei-Na Li, Ting Wang, Nan Wang, Qiang Han, Xue-Ming You, Shuai Zhang, Cui-Cui Zhang, Yong-Qiang Shi, Pei-Zhuang Qiao, Cheng-Lian Man, Teng Feng, Yue-Yue Li, Zhuang Zhu, Ke-Ji Quan, Teng-Lin Xu, George Fei Zhang
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引用次数: 0

摘要

本研究首次利用 16S rRNA 基因测序技术分析了受肿头症影响的鸡体内的细菌群落。样本取自临床产蛋鸡,采用传统聚合酶链式反应(PCR)检测是否存在副猪嗜血杆菌(APG)和鼻腔鸟杆菌(ORT)。从样本中选出 5 个 APG 阳性(APG)和 APG 阴性(N-APG)样本,以及 5 个特定的无病原体鸡样本,进行 16S rRNA 基因测序。结果显示,在患有肿头综合征(SHS,9/10)的鸡样本中广泛检测到 APG 和 ORT,而在所有五个无特定病原体(SPF)的样本中均检测到 APG。相比之下,根据 16S rRNA 基因测序数据,常规 PCR 的灵敏度不足以诊断 APG 和 ORT,灵敏度分别仅为 35.7%(5/14)和 11.1%(1/9)。此外,16S rRNA 基因测序还能对样本中的细菌进行定量分析,结果显示 APG 组中 APG 的相对丰度为 2.7% 至 81.3%,而 N-APG 组中 APG 的相对丰度为 0.1% 至 21.0%。值得注意的是,在所有 5 个 SPF 样品中也检测到了低浓度的 APG。研究还发现了大量动物和人类常见的细菌病原体,包括但不限于ananis Gallibacterium、Riemerella columbina、Enterococcus cecorum、Mycoplasma synoviae、Helicobacter hepaticus 和 Staphylococcus lentus。总之,16S rRNA 基因测序是诊断细菌病原体和发现新型细菌病原体的重要工具,而传统的 PCR 诊断方法并不可靠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A detailed analysis of 16S rRNA gene sequencing and conventional PCR-based testing for the diagnosis of bacterial pathogens and discovery of novel bacteria.

A detailed analysis of 16S rRNA gene sequencing and conventional PCR-based testing for the diagnosis of bacterial pathogens and discovery of novel bacteria.

This study represents the first analysis of the bacterial community in chickens affected by swollen head syndrome, utilizing 16S rRNA gene sequencing. Samples were obtained from clinical laying chickens and were examined for the presence of Avibacterium paragallinarum (APG) and Ornithobacterium rhinotracheale (ORT) using conventional polymerase chain reaction (PCR). From the samples, five APG-positive (APG) and APG-negative (N-APG) samples were chosen, along with five specific pathogen-free chickens, for 16S rRNA gene sequencing. Results showed that APG and ORT were widely detected in the chicken samples with swollen head syndrome (SHS, 9/10), while APG was detected in all five specific pathogen-free (SPF) samples. In contrast, conventional PCR sensitivity was found to be inadequate for diagnosis, with only 35.7% (5/14) and 11.1% (1/9) sensitivity for APG and ORT, respectively, based on 16S rRNA gene sequencing data. Furthermore, 16S rRNA gene sequencing was able to quantify the bacteria in the samples, revealing that the relative abundance of APG in the APG group ranged from 2.7 to 81.3%, while the relative abundance of APG in the N-APG group ranged from 0.1 to 21.0%. Notably, a low level of APG was also detected in all 5 SPF samples. The study also identified a significant number of animal and human common bacterial pathogens, including but not limited to Gallibacterium anatis, Riemerella columbina, Enterococcus cecorum, Mycoplasma synoviae, Helicobacter hepaticus, and Staphylococcus lentus. In conclusion, 16S rRNA gene sequencing is a valuable tool for bacterial pathogen diagnosis and the discovery of novel bacterial pathogens, while conventional PCR is not reliable for diagnosis.

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来源期刊
CiteScore
5.60
自引率
11.50%
发文量
104
审稿时长
3 months
期刊介绍: Antonie van Leeuwenhoek publishes papers on fundamental and applied aspects of microbiology. Topics of particular interest include: taxonomy, structure & development; biochemistry & molecular biology; physiology & metabolic studies; genetics; ecological studies; especially molecular ecology; marine microbiology; medical microbiology; molecular biological aspects of microbial pathogenesis and bioinformatics.
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