Wang Sibao, Miao Xuexia, Zhao Weiguo, Huang Bo, Fan Meizhen, Li Zengzhi, Huang Yongping
Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 300 Fenglin Road, Shanghai 200032, Peoples' Republic of China.
Mycol Res. 2005 Dec;109(Pt 12):1364-72. doi: 10.1017/s0953756205003709.
Inter-simple sequence repeat (ISSR) markers were used to investigate genetic diversity among 39 isolates of Beauveria spp. (36 B. bassiana, one B. brongniartii, one B. amorpha, and one B. velata) isolated from different insect hosts and geographical origins. Eighteen among 33 primers that contained different simple sequence repeats (SSR) were chosen for their reproducibility and high polymorphism. Considerable intraspecific and interspecific variability among the isolates of Beauveria spp. was revealed. One hundred sixty-eight highly reproducible fragments were amplified in all 39 isolates with an average of 9.3 markers per primer; among these, 161 (95.8%) were polymorphic. For 36 B. bassiana isolates, 8.9 (1-13) markers per primer were scored, and a total of 123 fragments were amplified, in which 102 (82.9%) were polymorphic. Among the 168 polymorphic bands, 7 bands were considered to be specific for B. brongniartii isolate Bbr06, 14 bands for B. amorpha isolate Ba08, and 18 bands for B. velata isolate Bv0. Within 36 B. bassiana isolates, genetic similarity ranged from 0.651 to 0.972. However, the genetic similarity values among different Beauveria species ranged from 0.411 to 0.720, suggesting that ISSR technique was successful in differentiating the three closely related species from B. bassiana. The results also indicated that there was a certain association between B. bassiana isolates and their geographical origins, but no clear correlation between those isolates and their insect hosts. The present study suggested that ISSR markers can be used as robust molecular markers for the population genetics, epidemiological and ecological studies of entomopathogenic fungi.
利用简单序列重复区间(ISSR)标记对39株球孢白僵菌属菌株(36株球孢白僵菌、1株布氏白僵菌、1株拟青霉和1株绿僵菌)的遗传多样性进行了研究,这些菌株分离自不同的昆虫宿主和地理来源。从33个含有不同简单序列重复(SSR)的引物中选择了18个,因其具有可重复性和高多态性。结果显示球孢白僵菌属菌株种内和种间存在显著变异。在所有39株菌株中扩增出168个高度可重复的片段,每个引物平均有9.3个标记;其中,161个(95.8%)是多态性的。对于36株球孢白僵菌菌株,每个引物有8.9个(1 - 13个)标记,共扩增出123个片段,其中102个(82.9%)是多态性的。在168个多态性条带中,7个条带被认为是布氏白僵菌菌株Bbr06特有的,14个条带是拟青霉菌株Ba08特有的,18个条带是绿僵菌菌株Bv0特有的。在36株球孢白僵菌菌株中,遗传相似性范围为0.651至0.972。然而,不同球孢白僵菌物种之间的遗传相似性值范围为0.411至0.720,这表明ISSR技术成功地区分了与球孢白僵菌密切相关的三个物种。结果还表明,球孢白僵菌菌株与其地理来源之间存在一定关联,但这些菌株与其昆虫宿主之间没有明显相关性。本研究表明,ISSR标记可作为昆虫病原真菌群体遗传学、流行病学和生态学研究的可靠分子标记。