Literature DB >> 15036535

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

Jose C Garcia-Garcia1, José de la Fuente, Edmour F Blouin, Todd J Johnson, Thomas Halbur, Virginia C Onet, Jeremiah T Saliki, Katherine M Kocan.   

Abstract

Major surface proteins (MSP) 1a and 1b of the tick-borne pathogen Anaplasma marginale (Rickettsiales: Anaplasmataceae) are conserved on A. marginale derived from bovine erythrocytes and tick cells. MSP1a and MSP1b form the MSP1 complex and are adhesins involved in infection of host cells. While both MSP1a and MSP1b are adhesins for bovine erythrocytes, only MSP1a is an adhesin for cultured and native tick cells. These studies were initiated because antibody responses to MSP1a and MSP1b differed in cattle immunized with killed A. marginale derived from bovine erythrocytes or cultured tick cells. A strong antibody response to MSP1a was observed in cattle immunized with erythrocyte-derived A. marginale, whereas cattle immunized with tick cell culture-derived A. marginale produced antibodies preferentially to MSP1b. The molecular basis of this differential antibody response was then studied using Western blot, confocal microscopy and reverse transcriptase (RT)-PCR. Whereas expression of MSP1b by A. marginale derived from both bovine and tick host cells was similar at the protein and RNA levels, expression of MSP1a by A. marginale in these cells differed. Low levels of MSP1a were observed in cultured tick cells and tick salivary glands, but high expression of MSP1a occurred on A. marginale derived from bovine erythrocytes. The analysis of the expression of the msp1alpha gene by RT-PCR suggests that the differential expression of MSP1a is regulated at the transcriptional level and may influence the infectivity of A. marginale for host cells. Variation in the expression of MSP1a may also contribute to phenotypic and antigenic changes in the pathogen.

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Year:  2004        PMID: 15036535     DOI: 10.1016/j.vetmic.2003.10.021

Source DB:  PubMed          Journal:  Vet Microbiol        ISSN: 0378-1135            Impact factor:   3.293


  10 in total

1.  Transcription analysis of the major antigenic protein 1 multigene family of three in vitro-cultured Ehrlichia ruminantium isolates.

Authors:  Cornelis P J Bekker; Milagros Postigo; Amar Taoufik; Lesley Bell-Sakyi; Conchita Ferraz; Dominique Martinez; Frans Jongejan
Journal:  J Bacteriol       Date:  2005-07       Impact factor: 3.490

2.  Identification of Anaplasma marginale proteins specifically upregulated during colonization of the tick vector.

Authors:  Solomon S Ramabu; Massaro W Ueti; Kelly A Brayton; Timothy V Baszler; Guy H Palmer
Journal:  Infect Immun       Date:  2010-05-03       Impact factor: 3.441

3.  Expression of Anaplasma marginale ankyrin repeat-containing proteins during infection of the mammalian host and tick vector.

Authors:  Solomon S Ramabu; David A Schneider; Kelly A Brayton; Massaro W Ueti; Telmo Graça; James E Futse; Susan M Noh; Timothy V Baszler; Guy H Palmer
Journal:  Infect Immun       Date:  2011-05-16       Impact factor: 3.441

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

Authors:  Roman R Ganta; Chuanmin Cheng; Elizabeth C Miller; Bridget L McGuire; Lalitha Peddireddi; Kamesh R Sirigireddy; Stephen K Chapes
Journal:  Infect Immun       Date:  2006-10-23       Impact factor: 3.441

Review 5.  Anaplasma marginale and Anaplasma phagocytophilum: Rickettsiales pathogens of veterinary and public health significance.

Authors:  Farhan Ahmad Atif
Journal:  Parasitol Res       Date:  2015-09-07       Impact factor: 2.289

6.  Global transcriptional analysis reveals surface remodeling of Anaplasma marginale in the tick vector.

Authors:  G Kenitra Hammac; Sebastián Aguilar Pierlé; Xiaoya Cheng; Glen A Scoles; Kelly A Brayton
Journal:  Parasit Vectors       Date:  2014-04-21       Impact factor: 3.876

7.  Phylogeographic analysis reveals association of tick-borne pathogen, Anaplasma marginale, MSP1a sequences with ecological traits affecting tick vector performance.

Authors:  Agustín Estrada-Peña; Victoria Naranjo; Karina Acevedo-Whitehouse; Atilio J Mangold; Katherine M Kocan; José de la Fuente
Journal:  BMC Biol       Date:  2009-09-01       Impact factor: 7.431

8.  Promoter analysis of macrophage- and tick cell-specific differentially expressed Ehrlichia chaffeensis p28-Omp genes.

Authors:  Lalitha Peddireddi; Chuanmin Cheng; Roman R Ganta
Journal:  BMC Microbiol       Date:  2009-05-19       Impact factor: 3.605

9.  Identification and Characterization of Anaplasma phagocytophilum Proteins Involved in Infection of the Tick Vector, Ixodes scapularis.

Authors:  Margarita Villar; Nieves Ayllón; Katherine M Kocan; Elena Bonzón-Kulichenko; Pilar Alberdi; Edmour F Blouin; Sabine Weisheit; Lourdes Mateos-Hernández; Alejandro Cabezas-Cruz; Lesley Bell-Sakyi; Marie Vancová; Tomáš Bílý; Damien F Meyer; Jan Sterba; Marinela Contreras; Nataliia Rudenko; Libor Grubhoffer; Jesús Vázquez; José de la Fuente
Journal:  PLoS One       Date:  2015-09-04       Impact factor: 3.240

10.  Anaplasma phagocytophilum MSP4 and HSP70 Proteins Are Involved in Interactions with Host Cells during Pathogen Infection.

Authors:  Marinela Contreras; Pilar Alberdi; Lourdes Mateos-Hernández; Isabel G Fernández de Mera; Ana L García-Pérez; Marie Vancová; Margarita Villar; Nieves Ayllón; Alejandro Cabezas-Cruz; James J Valdés; Snorre Stuen; Christian Gortazar; José de la Fuente
Journal:  Front Cell Infect Microbiol       Date:  2017-07-05       Impact factor: 5.293

  10 in total

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