Variation in germination of Clostridium difficile clinical isolates correlates to disease severity
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作者:
Carlson, Paul E., Jr.
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Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USA
Carlson, Paul E., Jr.
[1
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Kaiser, Alyssa M.
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Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USA
Kaiser, Alyssa M.
[1
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McColm, Sarah A.
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Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USA
McColm, Sarah A.
[1
]
Bauer, Jessica M.
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Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USA
Bauer, Jessica M.
[1
]
Young, Vincent B.
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Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USA
Univ Michigan, Dept Internal Med, Div Infect Dis, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USA
Young, Vincent B.
[1
,2
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Aronoff, David M.
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Vanderbilt Univ, Sch Med, Dept Pathol Microbiol & Immunol, Div Infect Dis,Dept Med, Nashville, TN 37232 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USA
Aronoff, David M.
[3
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Hanna, Philip C.
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Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USA
Hanna, Philip C.
[1
]
机构:
[1] Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48104 USA
[2] Univ Michigan, Dept Internal Med, Div Infect Dis, Ann Arbor, MI 48109 USA
[3] Vanderbilt Univ, Sch Med, Dept Pathol Microbiol & Immunol, Div Infect Dis,Dept Med, Nashville, TN 37232 USA
Over the past two decades, Clostridium difficile infections have been increasing in both number and severity throughout the world. As with other spore forming bacteria, germination is a vital step in the life cycle of this pathogen. Studies have examined differences in sporulation and toxin production among a number of C difficile clinical isolates; however, few have examined differences in germination and the relationship between this phenotype and disease severity. Here, over 100 C difficile isolates from the University of Michigan Health System were examined for overall germination in response to various combinations of known germinants (taurocholate) and co-germinants (glycine and histidine). Significant variation was observed among isolates under all conditions tested. Isolates representing ribotype 014020, which was the most frequently isolated ribotype at our hospital, exhibited increased germination in the presence of taurocholate and glycine when compared to isolates representing other ribotypes. Interestingly, isolates that caused severe disease exhibited significantly lower germination in response to minimal germination conditions (taurocholate only), indicating increased control over germination in these isolates. These data provide a broad picture of C difficile isolate germination and indicate a role for precise control of germination in disease severity. (C) 2015 Elsevier Ltd. All rights reserved.
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Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Carlson, Paul E., Jr.
Walk, Seth T.
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Univ Michigan, Dept Internal Med, Div Infect Dis, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Walk, Seth T.
Bourgis, Alexandra E. T.
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Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Bourgis, Alexandra E. T.
Liu, Melissa W.
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Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Liu, Melissa W.
Kopliku, Fatos
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Univ Michigan, Dept Internal Med, Div Infect Dis, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Kopliku, Fatos
Lo, Eugene
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Univ Michigan, Dept Internal Med, Div Infect Dis, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Lo, Eugene
Young, Vincent B.
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机构:
Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Internal Med, Div Infect Dis, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Young, Vincent B.
Aronoff, David M.
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h-index: 0
机构:
Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Internal Med, Div Infect Dis, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Aronoff, David M.
Hanna, Philip C.
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机构:
Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USAUniv Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
机构:
Mem Sloan Kettering Canc Ctr, Immunol Programs, Sloan Kettering Inst, Infect Dis Serv,Dept Med, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Immunol Programs, Sloan Kettering Inst, Infect Dis Serv,Dept Med, New York, NY 10065 USA
Lewis, Brittany B.
Carter, Rebecca A.
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Mem Sloan Kettering Canc Ctr, Immunol Programs, Sloan Kettering Inst, Infect Dis Serv,Dept Med, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Immunol Programs, Sloan Kettering Inst, Infect Dis Serv,Dept Med, New York, NY 10065 USA
Carter, Rebecca A.
Pamer, Eric G.
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Mem Sloan Kettering Canc Ctr, Immunol Programs, Sloan Kettering Inst, Infect Dis Serv,Dept Med, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Immunol Programs, Sloan Kettering Inst, Infect Dis Serv,Dept Med, New York, NY 10065 USA