Jin-Ho Yun, Jongsun Park, Hong Xi, Sangjune Nam, Wonhoon Lee, Seong-Ki Kim
{"title":"Comprehensive Analysis of the Fourteen Complete Genome Sequences of <i>Buchnera aphidicola</i> Isolated from <i>Aphis</i> Species.","authors":"Jin-Ho Yun, Jongsun Park, Hong Xi, Sangjune Nam, Wonhoon Lee, Seong-Ki Kim","doi":"10.4014/jmb.2409.09004","DOIUrl":null,"url":null,"abstract":"<p><p>Endosymbionts are important for insect species as they provide essential substances to the host. Due to the technical advance of NGS technology and <i>de novo</i> assemblers, many endosymbionts bacterial genomes are available now. Here, we analysed fourteen endosymbiont bacterial genomes of <i>Aphis</i> genius, one of notorious pest species. Fourteen genomes displayed the length between 628,098 bp to 634,931 bp; GC ratio was from 24.2 % to 25.6 % with no structural variation found. The nucleotide diversity distribution across the 14 endosymbiont genomes revealed three distinct regions, each separated by varying levels of nucleotide diversity. Intraspecific variations identified from endosymbiont bacterial genomes of the same host species revealed numbers of SNPs ranging from 31 (0.0049%) to 1,652 (0.26%) and those of INDELs ranging from 7 (21 bp; 0.0033%) to 104 (285 bp; 0.0045%). 250 unique SSRs, 28 different common SSR groups, and one different SSR group in two genomes were identified and used as a potential molecular marker to distinguish intraspecific population. Phylogenetic analysis further showed congruence between the endosymbiont bacterial genomes and the host species phylogeny, except <i>Aphis nasturtii</i>, <i>Aphis helianth</i>, and <i>Aphis auranti</i>, which require additional endosymbiont genomes for clarification. This comparative analysis result could serve as a cornerstone for understanding the relationship between host and endosymbiont species from a genomic perspective.</p>","PeriodicalId":16481,"journal":{"name":"Journal of microbiology and biotechnology","volume":"35 ","pages":"e2409004"},"PeriodicalIF":2.5000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of microbiology and biotechnology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.4014/jmb.2409.09004","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Endosymbionts are important for insect species as they provide essential substances to the host. Due to the technical advance of NGS technology and de novo assemblers, many endosymbionts bacterial genomes are available now. Here, we analysed fourteen endosymbiont bacterial genomes of Aphis genius, one of notorious pest species. Fourteen genomes displayed the length between 628,098 bp to 634,931 bp; GC ratio was from 24.2 % to 25.6 % with no structural variation found. The nucleotide diversity distribution across the 14 endosymbiont genomes revealed three distinct regions, each separated by varying levels of nucleotide diversity. Intraspecific variations identified from endosymbiont bacterial genomes of the same host species revealed numbers of SNPs ranging from 31 (0.0049%) to 1,652 (0.26%) and those of INDELs ranging from 7 (21 bp; 0.0033%) to 104 (285 bp; 0.0045%). 250 unique SSRs, 28 different common SSR groups, and one different SSR group in two genomes were identified and used as a potential molecular marker to distinguish intraspecific population. Phylogenetic analysis further showed congruence between the endosymbiont bacterial genomes and the host species phylogeny, except Aphis nasturtii, Aphis helianth, and Aphis auranti, which require additional endosymbiont genomes for clarification. This comparative analysis result could serve as a cornerstone for understanding the relationship between host and endosymbiont species from a genomic perspective.
期刊介绍:
The Journal of Microbiology and Biotechnology (JMB) is a monthly international journal devoted to the advancement and dissemination of scientific knowledge pertaining to microbiology, biotechnology, and related academic disciplines. It covers various scientific and technological aspects of Molecular and Cellular Microbiology, Environmental Microbiology and Biotechnology, Food Biotechnology, and Biotechnology and Bioengineering (subcategories are listed below). Launched in March 1991, the JMB is published by the Korean Society for Microbiology and Biotechnology (KMB) and distributed worldwide.