Literature DB >> 11118656

Infection of Vero cells with Coxiella burnetii phase II: relative intracellular bacterial load and distribution estimated by confocal laser scanning microscopy and morphometry.

D S Zamboni1, R A Mortara, M Rabinovitch.   

Abstract

Coxiella burnetii, the agent of Q fever in man and of coxiellosis in other species, is an intracellular pathogen not yet grown axenically. Confocal laser fluorescence microscopy and morphometry were used to measure relative C. burnetii phase II loads and their intracellular distribution in aldehyde fixed and DAPI stained Vero cell monolayers. The fluorescence of single horizontal optical sections provided useful information on relative loads of bacteria in cells and vacuoles. The relative density of the bacteria in the vacuoles was inferred from ratios of fluorescence to vacuolar section areas. Relative bacterial loads, bacterial densities and section areas of large vacuoles increased exponentially between days 2 and 4 of the infection of gamma-irradiated host cells, stabilized between days 4 and 6, and decreased thereafter. Estimated minimum doubling times were higher for the overall complement of the intracellular organisms (about 12 h) than for bacteria that were confined to larger vacuoles (about 10 h).

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Mesh:

Year:  2001        PMID: 11118656     DOI: 10.1016/s0167-7012(00)00223-2

Source DB:  PubMed          Journal:  J Microbiol Methods        ISSN: 0167-7012            Impact factor:   2.363


  15 in total

1.  The early secretory pathway contributes to the growth of the Coxiella-replicative niche.

Authors:  Emanuel Martín Campoy; Felipe Carlos Martín Zoppino; María Isabel Colombo
Journal:  Infect Immun       Date:  2010-10-11       Impact factor: 3.441

2.  Coxiella burnetii type IVB secretion system region I genes are expressed early during the infection of host cells.

Authors:  John K Morgan; Brandon E Luedtke; Herbert A Thompson; Edward I Shaw
Journal:  FEMS Microbiol Lett       Date:  2010-08-18       Impact factor: 2.742

3.  Temporal analysis of Coxiella burnetii morphological differentiation.

Authors:  Sherry A Coleman; Elizabeth R Fischer; Dale Howe; David J Mead; Robert A Heinzen
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

4.  Growth of Coxiella burnetii in the Ixodes scapularis-derived IDE8 tick cell line.

Authors:  Brian Herrin; Saugata Mahapatra; Edmour F Blouin; Edward I Shaw
Journal:  Vector Borne Zoonotic Dis       Date:  2011-01-22       Impact factor: 2.133

5.  Nitric oxide partially controls Coxiella burnetii phase II infection in mouse primary macrophages.

Authors:  Dario S Zamboni; Michel Rabinovitch
Journal:  Infect Immun       Date:  2003-03       Impact factor: 3.441

6.  Coxiella burnetii localizes in a Rab7-labeled compartment with autophagic characteristics.

Authors:  Walter Berón; Maximiliano G Gutierrez; Michel Rabinovitch; Maria I Colombo
Journal:  Infect Immun       Date:  2002-10       Impact factor: 3.441

7.  Coxiella burnetii inhibits activation of host cell apoptosis through a mechanism that involves preventing cytochrome c release from mitochondria.

Authors:  Anja Lührmann; Craig R Roy
Journal:  Infect Immun       Date:  2007-08-20       Impact factor: 3.441

8.  Murine Alveolar Macrophages Are Highly Susceptible to Replication of Coxiella burnetii Phase II In Vitro.

Authors:  Talita D Fernandes; Larissa D Cunha; Juliana M Ribeiro; Liliana M Massis; Djalma S Lima-Junior; Hayley J Newton; Dario S Zamboni
Journal:  Infect Immun       Date:  2016-08-19       Impact factor: 3.441

9.  Growth and maintenance of Vero cell lines.

Authors:  Nicole C Ammerman; Magda Beier-Sexton; Abdu F Azad
Journal:  Curr Protoc Microbiol       Date:  2008-11

10.  Phagocytosis of apoptotic cells increases the susceptibility of macrophages to infection with Coxiella burnetii phase II through down-modulation of nitric oxide production.

Authors:  Dario S Zamboni; Michel Rabinovitch
Journal:  Infect Immun       Date:  2004-04       Impact factor: 3.441

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