Literature DB >> 11162767

Intracellular passage within macrophages affects the trafficking of virulent tubercle bacilli upon reinfection of other macrophages in a serum-dependent manner.

K A McDonough1, M A Florczyk, Y Kress.   

Abstract

SETTING: The interaction of tubercle bacilli with macrophages is central to understanding of tuberculosis disease.
OBJECTIVE: The objective was to determine whether prior passage within macrophages affects the behavior of Mycobacterium tuberculosis (Mtb) upon re-entry into other macrophages.
DESIGN: Transmission electron microscopy was used to monitor fusion of bacterial phagosomes with late endosomal/lysosomal compartments using thoria as a fluid phase marker. Two-dimensional polyacrylamide gel electrophoresis was used to study bacterial protein expression within macrophages.
RESULTS: H37Rv and BCG expressed novel proteins within macrophages. H37Rv also underwent less fusion after intracellular (IC) (24.2+/-7.7%) than extracellular (XC) (67.4+/-5.5%) passage when the bacteria entered new macrophages in small clusters. These effects were inhibited by serum, and were not observed with H37Ra or BCG bacteria (78.9+/-1.6% fused for all conditions). In addition, vacuoles which contained single bacilli were less likely to acquire markers (26.9+/-2.6%) than those that contained multiple bacilli (77.3+/-2.8%).
CONCLUSION: These results indicate that phagolysosomal fusion patterns can be modulated by a variety of factors and that virulent Mtb bacteria may express proteins within macrophages that alter their interaction with these host cells. Copyright 2000 Harcourt Publishers Ltd.

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Year:  2000        PMID: 11162767     DOI: 10.1054/tuld.2000.0268

Source DB:  PubMed          Journal:  Tuber Lung Dis        ISSN: 0962-8479


  8 in total

1.  Acid stress response of a mycobacterial proteome: insight from a gene ontology analysis.

Authors:  Bryan Ap Roxas; Qingbo Li
Journal:  Int J Clin Exp Med       Date:  2009-11-10

2.  Identification and characterization of mycobacterial proteins differentially expressed under standing and shaking culture conditions, including Rv2623 from a novel class of putative ATP-binding proteins.

Authors:  M A Florczyk; L A McCue; R F Stack; C R Hauer; K A McDonough
Journal:  Infect Immun       Date:  2001-09       Impact factor: 3.441

3.  Dysregulation of serine biosynthesis contributes to the growth defect of a Mycobacterium tuberculosis crp mutant.

Authors:  Guangchun Bai; Damen D Schaak; Eric A Smith; Kathleen A McDonough
Journal:  Mol Microbiol       Date:  2011-09-08       Impact factor: 3.501

4.  Identification of a Mycobacterium tuberculosis putative classical nitroreductase gene whose expression is coregulated with that of the acr aene within macrophages, in standing versus shaking cultures, and under low oxygen conditions.

Authors:  Anjan Purkayastha; Lee Ann McCue; Kathleen A McDonough
Journal:  Infect Immun       Date:  2002-03       Impact factor: 3.441

5.  Regulation of the CRISPR-Associated Genes by Rv2837c (CnpB) via an Orn-Like Activity in Tuberculosis Complex Mycobacteria.

Authors:  Yang Zhang; Jun Yang; Guangchun Bai
Journal:  J Bacteriol       Date:  2018-03-26       Impact factor: 3.490

6.  A family of acr-coregulated Mycobacterium tuberculosis genes shares a common DNA motif and requires Rv3133c (dosR or devR) for expression.

Authors:  Matthew A Florczyk; Lee Ann McCue; Anjan Purkayastha; Egidio Currenti; Meyer J Wolin; Kathleen A McDonough
Journal:  Infect Immun       Date:  2003-09       Impact factor: 3.441

7.  Use of gene dosage effects for a whole-genome screen to identify Mycobacterium marinum macrophage infection loci.

Authors:  Bonggoo Park; Selvakumar Subbian; Sahar H El-Etr; Suat L G Cirillo; Jeffrey D Cirillo
Journal:  Infect Immun       Date:  2008-04-28       Impact factor: 3.441

8.  The Mycobacterium bovis BCG cyclic AMP receptor-like protein is a functional DNA binding protein in vitro and in vivo, but its activity differs from that of its M. tuberculosis ortholog, Rv3676.

Authors:  Guangchun Bai; Michaela A Gazdik; Damen D Schaak; Kathleen A McDonough
Journal:  Infect Immun       Date:  2007-09-04       Impact factor: 3.441

  8 in total

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