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对 16S rRNA 基因测序和基于常规 PCR 的检测在诊断细菌病原体和发现新细菌方面的详细分析。

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

机构信息

International Joint Research Center for Microbiology and Infectious Diseases, Wohua Biotech, Binzhou, 256600, Shandong, China.

Department of Basic and Forensic Medicine, North Sichuan Medical College, Nanchong, 637100, Sichuan, China.

出版信息

Antonie Van Leeuwenhoek. 2024 Jul 16;117(1):102. doi: 10.1007/s10482-024-01999-1.

DOI:10.1007/s10482-024-01999-1
PMID:39012584
Abstract

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.

摘要

本研究利用 16S rRNA 基因测序首次分析了患有肿头综合征的鸡的细菌群落。从临床产蛋鸡中采集样本,并用常规聚合酶链反应 (PCR) 检测有无禽败血支原体 (APG) 和鹦鹉热衣原体 (ORT)。从这些样本中,选择了五个 APG 阳性 (APG) 和 APG 阴性 (N-APG) 样本,以及五个无特定病原体鸡 (SPF) 进行 16S rRNA 基因测序。结果表明,APG 和 ORT 在患有肿头综合征 (SHS) 的鸡样本中广泛存在 (10/10),而在所有五个 SPF 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 的灵敏度不足以用于诊断,APG 和 ORT 的灵敏度分别仅为 35.7% (5/14) 和 11.1% (1/9)。此外,16S rRNA 基因测序能够定量样本中的细菌,结果显示 APG 组中 APG 的相对丰度范围为 2.7%至 81.3%,而 N-APG 组中 APG 的相对丰度范围为 0.1%至 21.0%。值得注意的是,所有 5 个 SPF 样本中也检测到低水平的 APG。该研究还鉴定了大量动物和人类常见的细菌病原体,包括但不限于鸡败血支原体、哥伦比亚鹦鹉热衣原体、肠球菌、滑液支原体、肝螺杆菌和迟缓葡萄球菌。总之,16S rRNA 基因测序是一种用于细菌病原体诊断和发现新型细菌病原体的有价值的工具,而常规 PCR 用于诊断不可靠。

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