| Literature DB >> 24631574 |
Iyo Takemura-Uchiyama1, Jumpei Uchiyama2, Makoto Osanai3, Norihito Morimoto4, Tadashi Asagiri4, Takako Ujihara5, Masanori Daibata2, Tetsuro Sugiura4, Shigenobu Matsuzaki6.
Abstract
Nosocomial respiratory infections caused by methicillin-resistant Staphylococcus aureus (MRSA) can progress to lethal systemic infections. Bacteriophage (phage) therapy is expected to be effective against these critical infections. Previously, phage S13' was proposed as a potential therapeutic phage. We here examined phage treatment in a mouse model of lung-derived septicemia using phage S13'. Intraperitoneal phage administration at 6 h postinfection reduced the severity of infection and rescued the infected mice. Phage S13' can efficiently lyse hospital-acquired MRSA strains causing pneumonia-associated bacteremia in vitro. Thus, phage therapy may be a possible therapeutic intervention in staphylococcal lung-derived septicemia.Entities:
Keywords: Bacteriophage; Mouse; Podoviridae; Therapeutic; Therapy
Mesh:
Year: 2014 PMID: 24631574 DOI: 10.1016/j.micinf.2014.02.011
Source DB: PubMed Journal: Microbes Infect ISSN: 1286-4579 Impact factor: 2.700