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Title[redir]:
Vancomycin-resistant enterococci exploit antibiotic-induced innate immune deficits | Nature
Description:
Why antibiotic-resistant bacteria are so successful at causing infections in patients being treated with antibiotics is a something of a mystery. One previously unrecognized factor is reported in this issue: treatment with the broad-spectrum antibiotic vancomycin increases infection with resistant bacteria by compromising intestinal innate immunity. In mice receiving the antibiotic, intestinal expression of the antimicrobial protein, RegIIIγ was suppressed. RegIIIγ is notably effective against vancomycin-resistant Enterococcus (VRE), a common infection in hospitalized patients. Therapies that increase levels of this protein, such as orally administered lipopolysaccharide, may therefore be of use in patients receiving broad-spectrum antibiotics. Infection with antibiotic-resistant bacteria, such as vancomycin-resistant Enterococcus (VRE), is a dangerous and costly complication of broad-spectrum antibiotic therapy1,2. How antibiotic-mediated elimination of commensal bacteria promotes infection by antibiotic-resistant bacteria is a fertile area for speculation with few defined mechanisms. Here we demonstrate that antibiotic treatment of mice notably downregulates intestinal expression of RegIIIγ (also known as Reg3g), a secreted C-type lectin that kills Gram-positive bacteria, including VRE. Downregulation of RegIIIγ markedly decreases in vivo killing of VRE in the intestine of antibiotic-treated mice. Stimulation of intestinal Toll-like receptor 4 by oral administration of lipopolysaccharide re-induces RegIIIγ, thereby boosting innate immune resistance of antibiotic-treated mice against VRE. Compromised mucosal innate immune defence, as induced by broad-spectrum antibiotic therapy, can be corrected by selectively stimulating mucosal epithelial Toll-like receptors, providing a potential therapeutic approach to reduce colonization and infection by antibiotic-resistant microbes.
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article, google, scholar, nature, cas, intestinal, vancomycinresistant, access, antibiotic, innate, bacteria, mice, med, enterococci, research, content, enterococcus, tolllike, gut, infect, cookies, immune, pamer, infection, regiiiγ, colonization, usa, department, privacy, data, information, brandl, antibioticresistant, vre, epithelial, open, patients, immunity, author, york, powerpoint, plitas, mihu, schnabl, eric, broadspectrum, treatment, receptor, lipopolysaccharide, dis,
Topics {✒️}
nature portfolio permissions reprints privacy policy advertising scripps research institute social media infectious diseases service nature immunol nature med myd88-mediated signals induce broad-spectrum antibiotic therapy1 nature 446 nature 455 nature broad-spectrum antibiotic therapy vancomycin-resistant enterococcal infections supplementary figures s1-s8 secreted c-type lectin vancomycin-resistant enterococcus research vancomycin-resistant enterococci kills gram-positive bacteria anti-anaerobic antibiotic treatment innate immune recognition springerlink instant access permissions antibiotic-mediated elimination author contributions author correspondence antibiotic-resistant bacteria katharina brandl personal data development antibiotic-resistant microbes sloan-kettering institute data protection intestinal epithelial cells potential therapeutic approach gram-positive bacteria privacy article brandl intestinal bactericidal lectin model gut symbiont managing antibiotic resistance microbicidal proteins involved anaerobic microbiota inhibit explore content subscription content chronic intestinal inflammation institutional subscriptions read
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headline:Vancomycin-resistant enterococci exploit antibiotic-induced innate immune deficits
description:Why antibiotic-resistant bacteria are so successful at causing infections in patients being treated with antibiotics is a something of a mystery. One previously unrecognized factor is reported in this issue: treatment with the broad-spectrum antibiotic vancomycin increases infection with resistant bacteria by compromising intestinal innate immunity. In mice receiving the antibiotic, intestinal expression of the antimicrobial protein, RegIIIγ was suppressed. RegIIIγ is notably effective against vancomycin-resistant Enterococcus (VRE), a common infection in hospitalized patients. Therapies that increase levels of this protein, such as orally administered lipopolysaccharide, may therefore be of use in patients receiving broad-spectrum antibiotics. Infection with antibiotic-resistant bacteria, such as vancomycin-resistant Enterococcus (VRE), is a dangerous and costly complication of broad-spectrum antibiotic therapy1,2. How antibiotic-mediated elimination of commensal bacteria promotes infection by antibiotic-resistant bacteria is a fertile area for speculation with few defined mechanisms. Here we demonstrate that antibiotic treatment of mice notably downregulates intestinal expression of RegIIIγ (also known as Reg3g), a secreted C-type lectin that kills Gram-positive bacteria, including VRE. Downregulation of RegIIIγ markedly decreases in vivo killing of VRE in the intestine of antibiotic-treated mice. Stimulation of intestinal Toll-like receptor 4 by oral administration of lipopolysaccharide re-induces RegIIIγ, thereby boosting innate immune resistance of antibiotic-treated mice against VRE. Compromised mucosal innate immune defence, as induced by broad-spectrum antibiotic therapy, can be corrected by selectively stimulating mucosal epithelial Toll-like receptors, providing a potential therapeutic approach to reduce colonization and infection by antibiotic-resistant microbes.
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name:Eric G. Pamer
affiliation:
name:Infectious Diseases Service, Immunology Program, Sloan-Kettering Institute
address:
name:Department of Medicine, Infectious Diseases Service, Immunology Program, Sloan-Kettering Institute,
type:PostalAddress
type:Organization
name:Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, New York 10021, USA
address:
name:Department of Clinical Laboratories, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, New York 10021, USA,
type:PostalAddress
type:Organization
email:[email protected]
PostalAddress:
name:Department of Medicine, Infectious Diseases Service, Immunology Program, Sloan-Kettering Institute,
name:Present addresses: Department of Genetics, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA (K.B.); Department of Infectious Diseases, MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA (C.N.M.); Department of Medicine, University of California San Diego, La Jolla, California 92093, USA (B.S.).,
name:Hepatobiliary Service,,
name:Department of Medicine, Infectious Diseases Service, Immunology Program, Sloan-Kettering Institute,
name:Present addresses: Department of Genetics, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA (K.B.); Department of Infectious Diseases, MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA (C.N.M.); Department of Medicine, University of California San Diego, La Jolla, California 92093, USA (B.S.).,
name:Department of Medicine, Infectious Diseases Service, Immunology Program, Sloan-Kettering Institute,
name:Department of Medicine, Infectious Diseases Service, Immunology Program, Sloan-Kettering Institute,
name:Department of Clinical Laboratories, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, New York 10021, USA,
name:Department of Medicine, Columbia University, New York, New York 10032, USA,
name:Present addresses: Department of Genetics, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA (K.B.); Department of Infectious Diseases, MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA (C.N.M.); Department of Medicine, University of California San Diego, La Jolla, California 92093, USA (B.S.).,
name:Hepatobiliary Service,,
name:Department of Medicine, Infectious Diseases Service, Immunology Program, Sloan-Kettering Institute,
name:Department of Clinical Laboratories, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, New York 10021, USA,
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