Journal of Bacteriology · 2013 · 66 citations · 78 references
Life SciencesInfectious DiseasesMicrobiologyBacteriologyHost-pathogen InteractionsMicrobial PathogenesisBacterial InfectionsBacterial PathogenesisBiofilm Formation In InfectionDisease Transmission In InsectsInsect PathogensVector-pathogen InteractionsBacterial Biofilm AccumulationBacterial Biofilm EffectsBiofilm InterferenceFlea Pathogen TransmissionFlea Transmission Of PathogensFlea-borne PathogensFlea-pathogen InteractionsHost Antimicrobial Peptides
Transmission of Yersinia pestis is greatly enhanced after it forms a bacterial biofilm in the foregut of the flea vector that interferes with normal blood feeding. Here we report that the ability to produce a normal foregut-blocking infection depends on induction of the Y. pestis PhoP-PhoQ two-component regulatory system in the flea. Y. pestis phoP-negative mutants achieved normal infection rates and bacterial loads in the flea midgut but produced a less cohesive biofilm both in vitro and in the flea and had a greatly reduced ability to localize to and block the flea foregut. Thus, not only is the PhoP-PhoQ system induced in the flea gut environment, but also this induction is required to produce a normal transmissible infection. The altered biofilm phenotype in the flea was not due to lack of PhoPQ-dependent or PmrAB-dependent addition of aminoarabinose to the Y. pestis lipid A, because an aminoarabinose-deficient mutant that is highly sensitive to cationic antimicrobial peptides had a normal phenotype in the flea digestive tract. In addition to enhancing transmissibility, induction of the PhoP-PhoQ system in the arthropod vector prior to transmission may preadapt Y. pestis to resist the initial encounter with the mammalian innate immune response.
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Genome sequence of Yersinia pestis, the causative agent of plague
Julian Parkhill, Brendan W. Wren, Nicholas R. Thomson et al. · Nature · 2001 · 1.2K citations · Full text