Literature DB >> 19811876

The natural history of Anaplasma marginale.

Katherine M Kocan1, José de la Fuente, Edmour F Blouin, Johann F Coetzee, S A Ewing.   

Abstract

The intracellular pathogen Anaplasma marginale (Rickettsiales: Anaplasmataceae), described by Sir Arnold Theiler in 1910, is endemic worldwide in tropical and subtropical areas. Infection of cattle with A. marginale causes bovine anaplasmosis, a mild to severe hemolytic disease that results in considerable economic loss to both dairy and beef industries. Transmission of A. marginale to cattle occurs biologically by ticks and mechanically by biting flies and by blood-contaminated fomites. Both male ticks and cattle hosts become persistently infected with A. marginale and serve as reservoirs of infection. While erythrocytes are the major site of infection in cattle, A. marginale undergoes a complex developmental cycle in ticks that begins by infection of gut cells, and transmission to susceptible hosts occurs from salivary glands during feeding. Major surface proteins (MSPs) play a crucial role in the interaction of A. marginale with host cells, and include adhesion proteins and MSPs from multigene families that undergo antigenic change and selection in cattle, thus contributing to maintenance of persistent infections. Many geographic strains of A. marginale have been identified worldwide, which vary in genotype, antigenic composition, morphology and infectivity for ticks. Isolates of A. marginale may be maintained by independent transmission events and a mechanism of infection/exclusion in cattle and ticks. The increasing numbers of A. marginale genotypes identified in some geographic regions most likely resulted from intensive cattle movement. However, concurrent A. marginale strain infections in cattle was reported, but these strains were more distantly related. Phylogenetic studies of selected geographic isolates of A. marginale, using msp4 and msp1alpha, provided information about the biogeography and evolution of A. marginale, and msp1alpha genotypes appear to have evolved under positive selection pressure. Live and killed vaccines have been used for control of anaplasmosis and both types of vaccines have advantages and disadvantages. Vaccines have effectively prevented clinical anaplasmosis in cattle but have failed to block A. marginale infection. Vaccines are needed that can prevent clinical disease and, simultaneously, prevent infection in cattle and ticks, thus eliminating these hosts as reservoirs of infection. Advances in genomics, proteomics, immunology and biochemical and molecular technologies during the last decade have been applied to research on A. marginale and related organisms, and the recent development of a cell culture system for A. marginale has provided a format for studying the pathogen/tick interface. Recent advancements and new research methodologies should provide additional opportunities for development of new strategies for control and prevention of bovine anaplasmosis.

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Year:  2009        PMID: 19811876     DOI: 10.1016/j.vetpar.2009.09.012

Source DB:  PubMed          Journal:  Vet Parasitol        ISSN: 0304-4017            Impact factor:   2.738


  91 in total

Review 1.  The role of CD8 T lymphocytes in rickettsial infections.

Authors:  David H Walker; J Stephen Dumler
Journal:  Semin Immunopathol       Date:  2015-04-01       Impact factor: 9.623

2.  Anaplasma spp. in dairy ruminants in Jordan: high individual and herd-level seroprevalence and association with abortions.

Authors:  Mohammad M Obaidat; Alaa E Bani Salman
Journal:  J Vet Diagn Invest       Date:  2019-04-11       Impact factor: 1.279

3.  Development and evaluation of a double-antigen sandwich ELISA to identify Anaplasma marginale-infected and A. centrale-vaccinated cattle.

Authors:  Macarena Sarli; Carolina S Thompson; María B Novoa; Beatriz S Valentini; Mariano Mastropaolo; Ignacio E Echaide; Susana T de Echaide; María E Primo
Journal:  J Vet Diagn Invest       Date:  2019-11-28       Impact factor: 1.279

4.  Ixodes scapularis does not harbor a stable midgut microbiome.

Authors:  Benjamin D Ross; Beth Hayes; Matthew C Radey; Xia Lee; Tanya Josek; Jenna Bjork; David Neitzel; Susan Paskewitz; Seemay Chou; Joseph D Mougous
Journal:  ISME J       Date:  2018-06-26       Impact factor: 10.302

5.  Seroprevalence of Anaplasma marginale and Babesia bigemina infections and associated risk factors in Machakos County, Kenya.

Authors:  F D Wesonga; J M Gachohi; P M Kitala; J M Gathuma; M J Njenga
Journal:  Trop Anim Health Prod       Date:  2016-11-22       Impact factor: 1.559

6.  Identification of a T-Cell Epitope That Is Globally Conserved among Outer Membrane Proteins (OMPs) OMP7, OMP8, and OMP9 of Anaplasma marginale Strains and with OMP7 from the A. marginale subsp. centrale Vaccine Strain.

Authors:  James R Deringer; Elkin G Forero-Becerra; Massaro W Ueti; Joshua E Turse; James E Futse; Susan M Noh; Guy H Palmer; Wendy C Brown
Journal:  Clin Vaccine Immunol       Date:  2017-01-05

7.  First Survey on the Presence and Distribution of Oxytetracycline-Resistance Genes in Anaplasma Species.

Authors:  Parisa Shahbazi; Sahar Nouri Gharajalar; Kolsoum Mohebbi; Jafar Taeb; Hosein Hashemzadeh Farhang; Ali Abbas Nikvand; Roghayeh Norouzi
Journal:  Acta Parasitol       Date:  2020-11-12       Impact factor: 1.440

8.  High co-infection rates of Babesia bovis, Babesia bigemina, and Anaplasma marginale in water buffalo in Western Cuba.

Authors:  Dasiel Obregón; Alejandro Cabezas-Cruz; Yasmani Armas; Jenevaldo B Silva; Adivaldo H Fonseca; Marcos R André; Pastor Alfonso; Márcia C S Oliveira; Rosangela Z Machado; Belkis Corona-González
Journal:  Parasitol Res       Date:  2019-01-28       Impact factor: 2.289

9.  Detection of Anaplasma marginale and A. phagocytophilum in bovine peripheral blood samples by duplex real-time reverse transcriptase PCR assay.

Authors:  James B Reinbold; Johann F Coetzee; Kamesh R Sirigireddy; Roman R Ganta
Journal:  J Clin Microbiol       Date:  2010-05-12       Impact factor: 5.948

10.  Active surveillance of Anaplasma marginale in populations of arthropod vectors (Acari: Ixodidae; Diptera: Tabanidae) during and after an outbreak of bovine anaplasmosis in southern Manitoba, Canada.

Authors:  Matthew E M Yunik; Terry D Galloway; L Robbin Lindsay
Journal:  Can J Vet Res       Date:  2016-04       Impact factor: 1.310

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