Abstract

Virulence factors generally enhance a pathogen's fitness and thereby foster transmission. However, most studies of pathogen fitness have been performed by averaging the phenotypes over large populations. Here, we have analyzed the fitness costs of virulence factor expression by Salmonella enterica subspecies I serovar Typhimurium in simple culture experiments. The type III secretion system ttss-1, a cardinal virulence factor for eliciting Salmonella diarrhea, is expressed by just a fraction of the S. Typhimurium population, yielding a mixture of cells that either express ttss-1 (TTSS-1+ phenotype) or not (TTSS-1− phenotype). Here, we studied in vitro the TTSS-1+ phenotype at the single cell level using fluorescent protein reporters. The regulator hilA controlled the fraction of TTSS-1+ individuals and their ttss-1 expression level. Strikingly, cells of the TTSS-1+ phenotype grew slower than cells of the TTSS-1− phenotype. The growth retardation was at least partially attributable to the expression of TTSS-1 effector and/or translocon proteins. In spite of this growth penalty, the TTSS-1+ subpopulation increased from <10% to approx. 60% during the late logarithmic growth phase of an LB batch culture. This was attributable to an increasing initiation rate of ttss-1 expression, in response to environmental cues accumulating during this growth phase, as shown by experimental data and mathematical modeling. Finally, hilA and hilD mutants, which form only fast-growing TTSS-1− cells, outcompeted wild type S. Typhimurium in mixed cultures. Our data demonstrated that virulence factor expression imposes a growth penalty in a non-host environment. This raises important questions about compensating mechanisms during host infection which ensure successful propagation of the genotype.

Highlights

  • The ability to infect a host and elicit disease is dictated by the virulence factors expressed by a given pathogen

  • Single cell analyses might be of significant interest, in particular if virulence factors, which are expressed in a bistable fashion by some but not all members of a pathogen population, e.g. the ttss-1 system of S

  • Single cell reporters for studying the type III secretion system 1 (TTSS-1)+ phenotype We started our analysis of the TTSS-1+ phenotype by probing ttss-1 expression at the single cell level

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Summary

Introduction

The ability to infect a host and elicit disease is dictated by the virulence factors expressed by a given pathogen. Single cell analyses might be of significant interest, in particular if virulence factors, which are expressed in a bistable fashion by some but not all members of a pathogen population, e.g. the ttss-1 system of S. In some cases, two different phenotypes are expressed by isogenic organisms living in the same environment. The response is driven by a dedicated (set of) regulator(s), which responds to environmental signals (operon model of Jacob [7]). This response is subject to stochastic fluctuations. Two models may explain the advantage of bistability: i. in ‘‘bet hedging’’, the

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