Killing ofMycobacterium aviumandMycobacterium tuberculosisby a Mycobacteriophage Delivered by a Nonvirulent Mycobacterium: A Model for Phage Therapy of Intracellular Bacterial Pathogens
Author(s) -
Lawrence Broxmeyer,
Danuta Sosnowska,
Elizabeth Miltner,
Ofelia Chacón,
Dirk Wagner,
Jeffery A. McGarvey,
Raúl G. Barletta,
Luiz E. Bermudez
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/343812
Subject(s) - microbiology and biotechnology , mycobacterium smegmatis , mycobacterium tuberculosis , lytic cycle , mycobacterium , biology , virology , intracellular parasite , tuberculosis , phage therapy , immune system , bacteria , bacteriophage , immunology , virus , medicine , biochemistry , genetics , pathology , escherichia coli , gene
Mycobacterium avium causes disseminated infection in patients with acquired immune deficiency syndrome. Mycobacterium tuberculosis is a pathogen associated with the deaths of millions of people worldwide annually. Effective therapeutic regimens exist that are limited by the emergence of drug resistance and the inability of antibiotics to kill dormant organisms. The present study describes a system using Mycobacterium smegmatis, an avirulent mycobacterium, to deliver the lytic phage TM4 where both M. avium and M. tuberculosis reside within macrophages. These results showed that treatment of M. avium-infected, as well as M. tuberculosis-infected, RAW 264.7 macrophages, with M. smegmatis transiently infected with TM4, resulted in a significant time- and titer-dependent reduction in the number of viable intracellular bacilli. In addition, the M. smegmatis vacuole harboring TM4 fuses with the M. avium vacuole in macrophages. These results suggest a potentially novel concept to kill intracellular pathogenic bacteria and warrant future development.
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