Abstract

BackgroundSequence mutations represent a driving force of adaptive evolution in bacterial pathogens. It is especially evident in reductive genome evolution where bacteria underwent lifestyles shifting from a free-living to a strictly intracellular or host-depending life. It resulted in loss-of-function mutations and/or the acquisition of virulence gene clusters. Bacillus anthracis shares a common soil bacterial ancestor with its closely related bacillus species but is the only obligate, causative agent of inhalation anthrax within the genus Bacillus. The anthrax-causing Bacillus anthracis experienced the similar lifestyle changes. We thus hypothesized that the bacterial pathogen would follow a compatible evolution path.ResultsIn this study, a cluster-based evolution scheme was devised to analyze genes that are gained by or lost from B. anthracis. The study detected gene losses/gains at two separate evolutionary stages. The stage I is when B. anthracis and its sister species within the Bacillus cereus group diverged from other species in genus Bacillus. The stage II is when B. anthracis differentiated from its two closest relatives: B. cereus and B. thuringiensis. Many genes gained at these stages are homologues of known pathogenic factors such those for internalin, B. anthracis-specific toxins and large groups of surface proteins and lipoproteins.ConclusionThe analysis presented here allowed us to portray a progressive evolutionary process during the lifestyle shift of B. anthracis, thus providing new insights into how B. anthracis had evolved and bore a promise of finding drug and vaccine targets for this strategically important pathogen.

Highlights

  • Sequence mutations represent a driving force of adaptive evolution in bacterial pathogens

  • With an E-value of 1e-4, the comparisons of target genomes (TG)-reference genome (RG) resulted in a gene absence/presence matrix

  • Genomes of B. anthracis, B. cereus, and B. thuringiensis, genomes of B. subtilis and B. licheniformis, and those of B. halodurans, and B. clausii were clustered in three separate phylogenetic clades (Fig. 1.I)

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Summary

Introduction

Sequence mutations represent a driving force of adaptive evolution in bacterial pathogens It is especially evident in reductive genome evolution where bacteria underwent lifestyles shifting from a free-living to a strictly intracellular or host-depending life. It resulted in lossof-function mutations and/or the acquisition of virulence gene clusters. Genome reduction and gene acquisition in adaptive bacterial evolution: Two sides of coins Sequence mutations represent a driving force of adaptive evolution in bacterial pathogens They allow the pathogens to survive and prosper within the host immune systems and to develop unique host specificity [1,2,3,4]. This study addressed questions on what occurred in gene content during the adaptive evolution and how they impacted on the pathogenesis of B. anthracis

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