TY - JOUR
T1 - Cross-talk among flesh-eating Aeromonas hydrophila strains in mixed infection leading to necrotizing fasciitis
AU - Ponnusamy, Duraisamy
AU - Kozlova, Elena V.
AU - Sha, Jian
AU - Erova, Tatiana E.
AU - Azar, Sasha R.
AU - Fitts, Eric C.
AU - Kirtley, Michelle L.
AU - Tiner, Bethany L.
AU - Andersson, Jourdan A.
AU - Grim, Christopher J.
AU - Isom, Richard P.
AU - Hasan, Nur A.
AU - Colwell, Rita R.
AU - Chopra, Ashok K.
N1 - Funding Information:
Financial support was provided to A.K.C. through Leon Bromberg and Robert E. Shope and John S. Dunn Distinguished Chair in Global Health endowments, University of Texas Medical Branch, and NIH Grant 2RO1A1039129 was awarded to R.R.C. D.P. was supported in part by the James W. McLaughlin Postdoctoral Fellowship. B.L.T. and J.A.A. were supported in part by theWHO Collaborating Center for Vaccine Development, UTMB. E.C.F. was supported in part by T32 Biodefense Training Grant AI060549.
PY - 2016/1/19
Y1 - 2016/1/19
N2 - Necrotizing fasciitis (NF) caused by flesh-eating bacteria is associated with high case fatality. In an earlier study, we reported infection of an immunocompetent individual with multiple strains of Aeromonas hydrophila (NF1-NF4), the latter three constituted a clonal group whereas NF1 was phylogenetically distinct. To understand the complex interactions of these strains in NF pathophysiology, a mouse model was used, whereby either single or mixed A. hydrophila strains were injected intramuscularly. NF2, which harbors exotoxin A (exoA) gene, was highly virulent when injected alone, but its virulence was attenuated in the presence of NF1 (exoA-minus). NF1 alone, although not lethal to animals, became highly virulent when combined with NF2, its virulence augmented by cis-exoA expression when injected alone in mice. Based on metagenomics and microbiological analyses, it was found that, in mixed infection, NF1 selectively disseminated to mouse peripheral organs, whereas the other strains (NF2, NF3, and NF4) were confined to the injection site and eventually cleared. In vitro studies showed NF2 to be more effectively phagocytized and killed by macrophages than NF1. NF1 inhibited growth of NF2 on solid media, but ExoA of NF2 augmented virulence of NF1 and the presence of NF1 facilitated clearance of NF2 from animals either by enhanced priming of host immune system or direct killing via a contact-dependent mechanism.
AB - Necrotizing fasciitis (NF) caused by flesh-eating bacteria is associated with high case fatality. In an earlier study, we reported infection of an immunocompetent individual with multiple strains of Aeromonas hydrophila (NF1-NF4), the latter three constituted a clonal group whereas NF1 was phylogenetically distinct. To understand the complex interactions of these strains in NF pathophysiology, a mouse model was used, whereby either single or mixed A. hydrophila strains were injected intramuscularly. NF2, which harbors exotoxin A (exoA) gene, was highly virulent when injected alone, but its virulence was attenuated in the presence of NF1 (exoA-minus). NF1 alone, although not lethal to animals, became highly virulent when combined with NF2, its virulence augmented by cis-exoA expression when injected alone in mice. Based on metagenomics and microbiological analyses, it was found that, in mixed infection, NF1 selectively disseminated to mouse peripheral organs, whereas the other strains (NF2, NF3, and NF4) were confined to the injection site and eventually cleared. In vitro studies showed NF2 to be more effectively phagocytized and killed by macrophages than NF1. NF1 inhibited growth of NF2 on solid media, but ExoA of NF2 augmented virulence of NF1 and the presence of NF1 facilitated clearance of NF2 from animals either by enhanced priming of host immune system or direct killing via a contact-dependent mechanism.
KW - Aeromonas hydrophila
KW - Intramuscular mouse model
KW - Metagenomics
KW - Mixed infections
KW - Necrotizing fasciitis
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U2 - 10.1073/pnas.1523817113
DO - 10.1073/pnas.1523817113
M3 - Article
C2 - 26733683
AN - SCOPUS:84955128448
SN - 0027-8424
VL - 113
SP - 722
EP - 727
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 3
ER -