Literature DB >> 17060466

Differential clearance and immune responses to tick cell-derived versus macrophage culture-derived Ehrlichia chaffeensis in mice.

Roman R Ganta1, Chuanmin Cheng, Elizabeth C Miller, Bridget L McGuire, Lalitha Peddireddi, Kamesh R Sirigireddy, Stephen K Chapes.   

Abstract

Human monocytic ehrlichiosis is caused by a tick-transmitted rickettsia, Ehrlichia chaffeensis. We recently reported that E. chaffeensis grown in tick cells expresses different proteins than bacteria grown in macrophages. Therefore, we tested the hypothesis that immune responses against E. chaffeensis would be different if the mice are challenged with bacteria grown in macrophages or tick cells. We assessed the E. chaffeensis clearance from the peritoneum, spleen, and liver by C57BL/6J mice using a TaqMan-based real-time reverse transcription-PCR assay. Macrophage-grown E. chaffeensis was cleared in 2 weeks from the peritoneum, whereas the pathogen from tick cells persisted for nine additional days and included three relapses of increasing bacterial load separated by three-day intervals. Tick cell-grown bacteria also persisted in the livers and spleens with higher bacterial loads compared to macrophage-grown bacteria and fluctuated over a period of 35 days. Three-day periodic cycles were detected in T-cell CD62L/CD44 ratios in the spleen and bone marrow in response to infections with both tick cell- and macrophage-grown bacteria and were accompanied by similar periodic cycles of spleen cell cytokine secretions and nitric oxide and interleukin-6 by peritoneal macrophages. The E. chaffeensis-specific immunoglobulin G response was considerably higher and steadily increased in mice infected with the tick cell-derived E. chaffeensis compared to DH82-grown bacteria. In addition, antigens detected by the immunoglobulins were significantly different between mice infected with the E. chaffeensis originating from tick cells or macrophages. The differences in the immune response to tick cell-grown bacteria compared to macrophage-grown bacteria reflected a delay in the shift of gene expression from the tick cell-specific Omp 14 gene to the macrophage-specific Omp 19 gene. These data suggest that the host response to E. chaffeensis depends on the source of the bacteria and that this experimental model requires the most natural inoculum possible to allow for a realistic understanding of host resistance.

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Year:  2006        PMID: 17060466      PMCID: PMC1828415          DOI: 10.1128/IAI.01127-06

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  55 in total

1.  Antibody-mediated elimination of the obligate intracellular bacterial pathogen Ehrlichia chaffeensis during active infection.

Authors:  G M Winslow; E Yager; K Shilo; E Volk; A Reilly; F K Chu
Journal:  Infect Immun       Date:  2000-04       Impact factor: 3.441

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Journal:  Nature       Date:  1999-10-14       Impact factor: 49.962

3.  Persistence of Ehrlichia phagocytophila infection in lambs in relation to clinical parameters and antibody responses.

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Journal:  Vet Rec       Date:  1998-11-14       Impact factor: 2.695

4.  Cyclic rickettsemia during persistent Anaplasma marginale infection of cattle.

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Journal:  Infect Immun       Date:  1990-04       Impact factor: 3.441

5.  The carrier status of sheep, cattle and African buffalo recovered from heartwater.

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Journal:  Vet Parasitol       Date:  1989-12       Impact factor: 2.738

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Journal:  J Infect Dis       Date:  1978-02       Impact factor: 5.226

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Journal:  Clin Microbiol Rev       Date:  1991-07       Impact factor: 26.132

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Journal:  J Clin Microbiol       Date:  1991-12       Impact factor: 5.948

9.  Differential expression of the msp1alpha gene of Anaplasma marginale occurs in bovine erythrocytes and tick cells.

Authors:  Jose C Garcia-Garcia; José de la Fuente; Edmour F Blouin; Todd J Johnson; Thomas Halbur; Virginia C Onet; Jeremiah T Saliki; Katherine M Kocan
Journal:  Vet Microbiol       Date:  2004-03-05       Impact factor: 3.293

10.  Nitric oxide. A macrophage product responsible for cytostasis and respiratory inhibition in tumor target cells.

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Journal:  J Exp Med       Date:  1989-05-01       Impact factor: 14.307

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  31 in total

1.  Cloning of the major outer membrane protein expression locus in Anaplasma platys and seroreactivity of a species-specific antigen.

Authors:  Tzung-Huei Lai; Nelson G Orellana; Yumi Yuasa; Yasuko Rikihisa
Journal:  J Bacteriol       Date:  2011-04-15       Impact factor: 3.490

2.  Immunization with Ehrlichia P28 outer membrane proteins confers protection in a mouse model of ehrlichiosis.

Authors:  Patricia A Crocquet-Valdes; Nagaraja R Thirumalapura; Nahed Ismail; Xuejie Yu; Tais B Saito; Heather L Stevenson; Colette A Pietzsch; Sunil Thomas; David H Walker
Journal:  Clin Vaccine Immunol       Date:  2011-10-26

3.  Virulence potential of Ehrlichia chaffeensis strains of distinct genome sequences.

Authors:  Koshiro Miura; Yasuko Rikihisa
Journal:  Infect Immun       Date:  2007-04-16       Impact factor: 3.441

Review 4.  Progress and obstacles in vaccine development for the ehrlichioses.

Authors:  Jere W McBride; David H Walker
Journal:  Expert Rev Vaccines       Date:  2010-09       Impact factor: 5.217

5.  Ehrlichia chaffeensis infections in Drosophila melanogaster.

Authors:  Alison Luce-Fedrow; Tonia Von Ohlen; Stephen K Chapes
Journal:  Infect Immun       Date:  2009-08-17       Impact factor: 3.441

6.  Composition of the surface proteome of Anaplasma marginale and its role in protective immunity induced by outer membrane immunization.

Authors:  Susan M Noh; Kelly A Brayton; Wendy C Brown; Junzo Norimine; Gerhard R Munske; Christine M Davitt; Guy H Palmer
Journal:  Infect Immun       Date:  2008-03-03       Impact factor: 3.441

7.  Laboratory maintenance of Ehrlichia chaffeensis and Ehrlichia canis and recovery of organisms for molecular biology and proteomics studies.

Authors:  Chuanmin Cheng; Roman R Ganta
Journal:  Curr Protoc Microbiol       Date:  2008-05

8.  Total, membrane, and immunogenic proteomes of macrophage- and tick cell-derived Ehrlichia chaffeensis evaluated by liquid chromatography-tandem mass spectrometry and MALDI-TOF methods.

Authors:  Gwi-Moon Seo; Chuanmin Cheng; John Tomich; Roman R Ganta
Journal:  Infect Immun       Date:  2008-08-18       Impact factor: 3.441

9.  Use of Drosophila S2 cells as a model for studying Ehrlichia chaffeensis infections.

Authors:  Alison Luce-Fedrow; Tonia Von Ohlen; Daniel Boyle; Roman R Ganta; Stephen K Chapes
Journal:  Appl Environ Microbiol       Date:  2008-02-01       Impact factor: 4.792

10.  Defining the immune response to Ehrlichia species using murine models.

Authors:  Stephen K Chapes; Roman R Ganta
Journal:  Vet Parasitol       Date:  2008-10-17       Impact factor: 2.738

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