生物技术进展 ›› 2024, Vol. 14 ›› Issue (4): 631-639.DOI: 10.19586/j.2095-2341.2024.0019

• 研究论文 • 上一篇    

云南蚕区家蚕微孢子虫遗传多样性分析

张永红1(), 苏振国1, 罗家福1, 李春峰2(), 敖宝林3   

  1. 1.云南省农业科学院蚕桑蜜蜂研究所,云南 蒙自 661101
    2.西南大学,微孢子虫感染与防控重庆市重点实验室,重庆 400715
    3.陆良县蚕桑服务中心,云南 陆良 655600
  • 收稿日期:2024-02-04 接受日期:2024-04-24 出版日期:2024-07-25 发布日期:2024-08-07
  • 通讯作者: 李春峰
  • 作者简介:张永红 E-mail: zhang200503@126.com
  • 基金资助:
    云南省农业科学院预研项目(2024KYZX-01);重庆市重点实验室开放课题项目(CKMIC202102)

Analysis of Genetic Diversity of Nosema bombycis in Yunnan Sericulture Region

Yonghong ZHANG1(), Zhenguo SU1, Jiafu LUO1, Chunfeng LI2(), Baolin AO3   

  1. 1.Institute of Sericulture and Apiculture,Yunnan Academy of Agricultural Science,Yunnan Mengzi 661101,China
    2.Chongqing Key Laboratory of Microsporidia Infection and Control,Southwest University,Chongqing 400715,China
    3.Mulberry-silkworm Service Center of Luliang County,Yunnan Luliang 655600,China
  • Received:2024-02-04 Accepted:2024-04-24 Online:2024-07-25 Published:2024-08-07
  • Contact: Chunfeng LI

摘要:

家蚕微孢子虫(Nosema bombycis)是蚕业生产上一种重要病害——微粒子病的病原体。探讨家蚕微孢子虫种内的遗传多样性,可为云南蚕区家蚕微粒子病的防控提供参考依据。从云南省不同养蚕地区收集了感染微孢子虫的病蚕样品,分离纯化家蚕微孢子虫并提取基因组,克隆SSU rDNA(small subunit ribosomal DNA)和ITS(internal transcribed spacer)序列并进行生物信息学分析。结果发现,云南蚕区Nosema bombycis 分离株SSU rDNA序列同源性高达99%以上,遗传距离小于0.006,它们在长度和多个位点存在差异,呈现不同程度的多态性;ITS遗传差异较为显著,序列中存在多碱基的插入或缺失、单碱基的转换和颠换。基于SSU rDNA和rDNA-ITS序列构建系统发生树,结果显示,云南蚕区家蚕微孢子虫分离株系间存在遗传分化,种群间亲缘关系与地理位置无直接联系。研究结果丰富了云南蚕区家蚕微孢子虫的种内遗传多样性。

关键词: 家蚕微孢子虫, 遗传多样性, 核糖体小亚基, 转录间隔区

Abstract:

Nosema bombycis, a crucial pathogen causing silkworm pebrin, poses a significant threat to sericulture production. This study aimed to investigate the genetic diversity within N. bombycis species, providing valuable insights for the prevention and control of silkworm pebrin in the Yunnan sericultural region. We collected infected silkworm samples from diverse rearing areas in Yunnan Province, isolated and purified the Bombyx mori larvae, extracted their genomes, cloned the small subunit ribosomal DNA (SSU rDNA) and internal transcribed spacer (ITS) sequences, and conducted comprehensive bioinformatics analyses. Results revealed that the SSU rDNA sequences of N. bombycis isolated in the Yunnan silkworm region exhibit over 99% homology, with a genetic distance of less than 0.006. However, these isolates displayed variations in length and multiple loci, indicating varying degrees of polymorphism. In contrast, the rDNA-ITS sequences exhibited significant genetic differences, characterized by multiple base insertions or deletions, as well as single base substitutions and inversions. Utilizing the SSU rDNA and ITS sequences, we constructed a phylogenetic tree, which revealed genetic differentiation among the isolated strains of N. bombycis in the Yunnan sericultural region. Notably, the results indicated no direct correlation between the genetic relationships of these populations and their geographical locations. This study has significantly enriched our understanding of the intra-species genetic diversity of N. bombycis in the Yunnan silkworm-raising region, providing a valuable foundation for further research on silkworm pebrin prevention and control strategies.

Key words: Nosema bombycis, genetic diversity, ribosomal small subunit, transcribed spacer

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