| Literature DB >> 25126781 |
Beatrice Claudi1, Petra Spröte2, Anna Chirkova1, Nicolas Personnic1, Janine Zankl3, Nura Schürmann1, Alexander Schmidt4, Dirk Bumann5.
Abstract
Antibiotic therapy often fails to eliminate a fraction of transiently refractory bacteria, causing relapses and chronic infections. Multiple mechanisms can induce such persisters with high antimicrobial tolerance in vitro, but their in vivo relevance remains unclear. Using a fluorescent growth rate reporter, we detected extensive phenotypic variation of Salmonella in host tissues. This included slow-growing subsets as well as well-nourished fast-growing subsets driving disease progression. Monitoring of Salmonella growth and survival during chemotherapy revealed that antibiotic killing correlated with single-cell division rates. Nondividing Salmonella survived best but were rare, limiting their impact. Instead, most survivors originated from abundant moderately growing, partially tolerant Salmonella. These data demonstrate that host tissues diversify pathogen physiology, with major consequences for disease progression and control.Entities:
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Year: 2014 PMID: 25126781 DOI: 10.1016/j.cell.2014.06.045
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582