Romina Manfrino , Alejandra Gutierrez , Haifa Ben Gharsa , Christina Schuster , Claudia López Lastra , Andreas Leclerque
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引用次数: 0
摘要
本研究的目的是对从阿根廷不同地理区域和昆虫寄主收集到的 15 株巴维氏菌进行分子分类鉴定,并研究这些分离株之间和分离株内部的多样性水平。根据 EF1A-RPB1-RPB2 连接基因和 BLOC 标记的系统进化分析,所有 Beauveria 菌株均被鉴定为 Beauveria bassiana。在这两个系统发育的 B. bassiana 支系中,来自阿根廷的分离株并没有根据地理来源或寄主进行聚类。通过 PCR 扩增核 28S rRNA 编码序列的内含子插入热点区,对这 15 个真菌分离物进行了进一步分析。根据内含子序列和位置,在研究的 15 个分离物中发现了 7 个不同的 I 组内含子组合,分别称为变体 A、B1、B2、C、D、E 和 F。在 10 个分离株中发现了由单个 28Si2 内含子组成的变异体 B1/B2,而变异体 A 出现了两次,变异体 C 至 F 在所研究的分离株中是唯一的。确定 28S rRNA 基因中的不同内含子和内含子组合是实现阿根廷 B. bassiana 分离物种下区分的有力工具。
Molecular taxonomic characterization and infra-specific diversity of entomopathogenic Beauveria bassiana fungi from Argentina
It has been the aim of this study to molecular-taxonomically identify 15 Beauveria isolates collected from different geographical regions and insect hosts in Argentina and to investigate the levels of inter- and intra-specific diversity across this set of isolates. Based on phylogenetic analyses of EF1A-RPB1-RPB2 concatenated genes and BLOC markers, all Beauveria strains were identify as Beauveria bassiana. Within the B. bassiana clades of both phylogenies, isolates from Argentina were not clustered according to geographic origin or host. The 15 fungal isolates were further analyzed by PCR amplification of the intron insertion hot spot region of the nuclear 28S rRNA encoding sequence. By intron sequence and position, seven different group-I intron combinations termed variants A, B1, B2, C, D, E and F were found in the 15 isolates under study. Variants B1/B2 consisting of a single 28Si2 intron were found in ten isolates, whereas variant A occurred twice and variants C through F were unique across the set of isolates under study. The determination of the different introns and intron combinations in the 28S rRNA gene is a powerful tool for achieving infraspecific differentiation of B. bassiana isolates from Argentina.