Abstract

The molecular evolution of virulence factors is a central theme in our understanding of bacterial pathogenesis and host-microbe interactions. Using bioinformatics and genome data mining, recent studies have shed light on the evolution of important virulence factor families and the mechanisms by which they have adapted and diversified in function. This perspective highlights three complementary approaches useful for studying the molecular evolution of virulence factors: identification and analysis of virulence factor homologs, detection of adaptations or functional shifts, and computational prediction of novel virulence factor families. Each of these research directions is associated with distinct questions, approaches, and challenges for future work. Moving forward, bioinformatics will continue to play a critical role in exploring the evolution of virulence factors, including those that target humans. By reconstructing past processes and events, we will be able to better interpret newly sequenced microbial genomes and detect future pathoadaptations.

Highlights

  • The molecular evolution of virulence factors is a central theme in our understanding of bacterial pathogenesis and host-microbe interactions

  • Pathogenic microorganisms interact with hosts by producing specialized virulence factor (VF) proteins that are capable of interacting with or disrupting host processes

  • How do virulence factors originate, diversify, and adapt over time? How can we use this knowledge of virulence factor evolution to discover novel virulence factors within the vast and growing collection of sequenced microbial genomes?

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Summary

Introduction

The molecular evolution of virulence factors is a central theme in our understanding of bacterial pathogenesis and host-microbe interactions. Exploring virulence factor evolution and diversity using bioinformatics: A perspective on our work mining genomic databases for homologs, adaptions, and new virulence factor families. Identifying VF homologs: exploring the sequence space near characterized VFs. New virulence factors are typically predicted based on detectable homology to previously characterized VF sequences.

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