Standing genetic variation in contingency loci drives the rapid adaptation of Campylobacter jejuni to a novel host

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Standing genetic variation in contingency loci drives the rapid adaptation of Campylobacter jejuni to a novel host

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Title: Standing genetic variation in contingency loci drives the rapid adaptation of Campylobacter jejuni to a novel host
Author: Jerome, John P.; Bell, Julia A.; Plovanich-Jones, Anne E.; Barrick, Jeffrey E.; Brown, C. Titus; Mansfield, Linda S.
Abstract: The genome of the food-borne pathogen Campylobacter jejuni contains multiple highly mutable sites, or contingency loci. It has been suggested that standing variation at these loci is a mechanism for rapid adaptation to a novel environment, but this phenomenon has not been shown experimentally. In previous work we showed that the virulence of C. jejuni NCTC11168 increased after serial passage through a C57BL/6 IL-10-/- mouse model of campylobacteriosis. Here we sought to determine the genetic basis of this adaptation during passage. Re-sequencing of the 1.64Mb genome to 200-500X coverage allowed us to define variation in 23 contingency loci to an unprecedented depth both before and after in vivo adaptation. Mutations in the mouse-adapted C. jejuni were largely restricted to the homopolymeric tracts of thirteen contingency loci. These changes cause significant alterations in open reading frames of genes in surface structure biosynthesis loci and in genes with only putative functions. Several loci with open reading frame changes also had altered transcript abundance. The increase in specific phases of contingency loci during in vivo passage of C. jejuni, coupled with the observed virulence increase and the lack of other types of genetic changes, is the first experimental evidence that these variable regions play a significant role in C. jejuni adaptation and virulence in a novel host.
Description: John P. Jerome is with Michigan State University, Julia A. Bell is with Michigan State University, Anne E. Plovanich-Jones is with Michigan State University, Jeffrey E. Barrick is with UT Austin, C. Titus Brown is with Michigan State University, Linda S. Mansfield is with Michigan State University.
Department: Biochemistry
Subject: Campylobacter jejuni genetics and genomics microbiology contingency loci adaptation mutation virulence genetic variation
URI: http://hdl.handle.net/2152/13658
Date: 2011-01

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