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溶藻弧菌16S-23S基因间隔区分析及用于鉴定珊瑚致病菌株XSBZ03的PCR检测

Vibrio alginolyticus 16S-23S intergenic spacer region analysis, and PCR assay for identification of coral pathogenic strain XSBZ03.

作者信息

Li Hongyue, Zhang Xiang, Long Hao, Hu Chaoqun, Zhou Yongcan, Wang Shifeng, Ke Shaowen, Xie Zhenyu

机构信息

State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan University, Haikou 570228, PR China.

出版信息

Dis Aquat Organ. 2018 Jun 19;129(1):71-83. doi: 10.3354/dao03233.

Abstract

Porites andrewsi white syndrome (PAWS), caused by Vibrio alginolyticus strains XSBZ03 and XSBZ14, poses a serious threat to corals in the South China Sea. To obtain a specific target against which to develop a rapid PCR detection method for the coral pathogenic strain XSBZ03, the 16S-23S rRNA gene intergenic spacer (IGS) region of 4 strains of V. alginolyticus, including the XSBZ03 and XSBZ14 strains, was amplified, sequenced and analyzed. Six types of IGS were found: IGS0, IGSG, IGSIA, IGSAG, IGSGLV, and IGSGLAV. IGS0, IGSG, IGSIA, IGSAG and IGSGLV appeared to be the most prevalent forms in the 4 strains and the percentage identity range within each type was 91.4-100%, 89.3-98.5%, 83.0-99.8%, 91.5-95.6%, and 88.7-99.3%, respectively. IGSGLAV was found only in the HN08155 strain, a causative agent of fish disease. IGSGLAV, IGSGLV and IGSAG are reported here for the first time in V. alginolyticus. An IGS sequence specific to the XSBZ03 strain was identified following alignment of the homologous IGSs, and used to design strain-specific primers for its rapid identification by PCR. The results from PCR analysis suggest that the method is a rapid, practical, and reliable tool for the identification of the XSBZ03 strain in samples of isolated bacteria, as well as seawater and coral samples spiked with the bacterial strain. This is the first report of a rapid diagnostic assay for a causative agent of PAWS, based on PCR detection of a coral pathogen at the strain level. After applying this assay in coral transplantation, the survival rates of transplanted corals were significantly increased. This diagnostic assay should aid with both the elucidation of the cause of the disease, and transplantation of PAWS-free P. andrewsi in the South China Sea.

摘要

溶藻弧菌XSBZ03和XSBZ14菌株引起的安德鲁氏滨珊瑚白色综合征(PAWS),对中国南海的珊瑚构成严重威胁。为了获得一个特定靶点,以便开发针对珊瑚致病菌株XSBZ03的快速PCR检测方法,对包括XSBZ03和XSBZ14菌株在内的4株溶藻弧菌的16S - 23S rRNA基因间隔区(IGS)进行了扩增、测序和分析。发现了6种类型的IGS:IGS0、IGSG、IGSIA、IGSAG、IGSGLV和IGSGLAV。IGS0、IGSG、IGSIA、IGSAG和IGSGLV似乎是这4株菌中最常见的形式,每种类型内的百分比一致性范围分别为91.4 - 100%、89.3 - 98.5%、83.0 - 99.8%、91.5 - 95.6%和88.7 - 99.3%。IGSGLAV仅在鱼类疾病病原体HN08155菌株中发现。IGSGLAV、IGSGLV和IGSAG在溶藻弧菌中首次在此报道。通过同源IGS比对鉴定出XSBZ03菌株特异性的IGS序列,并用于设计菌株特异性引物,通过PCR对其进行快速鉴定。PCR分析结果表明,该方法是一种快速、实用且可靠的工具,可用于鉴定分离细菌样本以及添加了该菌株的海水和珊瑚样本中的XSBZ03菌株。这是基于菌株水平上对珊瑚病原体的PCR检测,首次报道针对PAWS病原体的快速诊断检测方法。在珊瑚移植中应用该检测方法后,移植珊瑚的存活率显著提高。这种诊断检测方法应有助于阐明疾病病因以及在中国南海移植无PAWS的安德鲁氏滨珊瑚。

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