Role in virulence of phospholipases, listeriolysin O and listeriolysin S from epidemic Listeria monocytogenes using the chicken embryo infection model

被引:24
|
作者
Quereda, Juan J. [1 ,2 ,3 ,7 ]
Andersson, Christopher [4 ,5 ,6 ]
Cossart, Pascale [1 ,2 ,3 ]
Johansson, Jorgen [4 ,5 ,6 ]
Pizarro-Cerda, Javier [1 ,2 ,3 ,8 ,9 ,10 ]
机构
[1] Inst Pasteur, Dept Biol Cellulaire & Infect, Unite Interact Bacteries Cellules, F-75015 Paris, France
[2] INSERM, U604, F-75015 Paris, France
[3] INRA, USC2020, F-75015 Paris, France
[4] Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden
[5] Umea Univ, Lab Mol Infect Med Sweden MIMS, S-90187 Umea, Sweden
[6] Umea Univ, UCMR, S-90187 Umea, Sweden
[7] CEU Univ, Univ Cardenal Herrera CEU, Dept Prod & Sanidad Anim Salud Publ Vet & Ciencia, Grp Fisiopatol Reprod,Fac Vet, Valencia, Spain
[8] Inst Pasteur, Unite Rech Yersinia, Dept Microbiol, F-75015 Paris, France
[9] Inst Pasteur, Ctr Natl Reference Peste & Autres Yersinioses, F-75015 Paris, France
[10] Inst Pasteur, Ctr Collaborateur OMS Reference & Rech Yersinia, F-75015 Paris, France
基金
欧洲研究理事会; 瑞典研究理事会;
关键词
GENE-EXPRESSION; PATHOGEN; PROTEIN; CELLS; PRFA;
D O I
10.1186/s13567-017-0496-4
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Most human listeriosis outbreaks are caused by Listeria monocytogenes evolutionary lineage I strains which possess four exotoxins: a phosphatidylinositol-specific phospholipase C (PlcA), a broad-range phospholipase C (PlcB), listeriolysin O (LLO) and listeriolysin S (LLS). The simultaneous contribution of these molecules to virulence has never been explored. Here, the importance of these four exotoxins of an epidemic lineage I L. monocytogenes strain (F2365) in virulence was assessed in chicken embryos infected in the allantoic cavity. We show that LLS does not play a role in virulence while LLO is required to infect and kill chicken embryos both in wild type transcriptional regulator of virulence PrfA -(PrfAWT) and constitutively active PrfA (PrfA*) backgrounds. We demonstrate that PlcA, a toxin previously considered as a minor virulence factor, played a major role in virulence in a PrfA* background. Interestingly, GFP transcriptional fusions show that the plcA promoter is less active than the hly promoter in vitro, explaining why the contribution of PlcA to virulence could be observed more importantly in a PrfA* background. Together, our results suggest that PlcA might play a more important role in the infectious lifecycle of L. monocytogenes than previously thought, explaining why all the strains of L. monocytogenes have conserved an intact copy of plcA in their genomes.
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页数:9
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