Literature DB >> 7858023

Molecular and biological characterization of a newly isolated Anaplasma marginale strain.

I S Eriks1, D Stiller, W L Goff, M Panton, S M Parish, T F McElwain, G H Palmer.   

Abstract

Anaplasma marginale, a rickettsial hemoparasite of cattle and other ruminants, results in significant economic losses worldwide. Distinct strains of A. marginale have been identified based on differences in tick transmissibility, molecular size of surface proteins and DNA restriction fragments, and reactivity to a panel of monoclonal antibodies. These different strains vary considerably in their virulence, antigenic composition, and ability to protect against heterologous challenge. In this paper, we report on the molecular characterization of a newly isolated strain of A. marginale, designated St. Maries, recovered from an acutely infected cow in northern Idaho. Dermacentor andersoni ticks taken from the infected animal were tested for infection by RNA probe analysis. The infection rate of male ticks (as determined by midgut infection) was 100%, and the infection rate of female ticks was 83%. Infected male ticks were able to transmit the St. Maries strain to a susceptible calf. The high infection rate in male ticks may be particularly relevant, given that male ticks are believed to be epidemiologically important in transmission of A. marginale because of their intermittent feeding behavior, which promotes interhost transfer. The newly isolated strain differs from other US strains, including strains previously isolated in Idaho and Washington, based on reactivity to a panel of monoclonal antibodies and restriction fragment length polymorphisms. These results imply that antigenically distinct strains of A. marginale may arise within the same region.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 7858023     DOI: 10.1177/104063879400600406

Source DB:  PubMed          Journal:  J Vet Diagn Invest        ISSN: 1040-6387            Impact factor:   1.279


  23 in total

1.  Complete genome sequencing of Anaplasma marginale reveals that the surface is skewed to two superfamilies of outer membrane proteins.

Authors:  Kelly A Brayton; Lowell S Kappmeyer; David R Herndon; Michael J Dark; David L Tibbals; Guy H Palmer; Travis C McGuire; Donald P Knowles
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-23       Impact factor: 11.205

2.  Identification of novel antigenic proteins in a complex Anaplasma marginale outer membrane immunogen by mass spectrometry and genomic mapping.

Authors:  Job E Lopez; William F Siems; Guy H Palmer; Kelly A Brayton; Travis C McGuire; Junzo Norimine; Wendy C Brown
Journal:  Infect Immun       Date:  2005-12       Impact factor: 3.441

3.  Strain composition of the ehrlichia Anaplasma marginale within persistently infected cattle, a mammalian reservoir for tick transmission.

Authors:  G H Palmer; F R Rurangirwa; T F McElwain
Journal:  J Clin Microbiol       Date:  2001-02       Impact factor: 5.948

4.  Stability and tick transmission phenotype of gfp-transformed Anaplasma marginale through a complete in vivo infection cycle.

Authors:  Susan M Noh; Massaro W Ueti; Guy H Palmer; Ulrike G Munderloh; Roderick F Felsheim; Kelly A Brayton
Journal:  Appl Environ Microbiol       Date:  2010-11-05       Impact factor: 4.792

5.  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

6.  Expression of major surface protein 2 antigenic variants during acute Anaplasma marginale rickettsemia.

Authors:  G Eid; D M French; A M Lundgren; A F Barbet; T F McElwain; G H Palmer
Journal:  Infect Immun       Date:  1996-03       Impact factor: 3.441

7.  Independence of Anaplasma marginale strains with high and low transmission efficiencies in the tick vector following simultaneous acquisition by feeding on a superinfected mammalian reservoir host.

Authors:  Maria F B M Galletti; Massaro W Ueti; Donald P Knowles; Kelly A Brayton; Guy H Palmer
Journal:  Infect Immun       Date:  2009-02-02       Impact factor: 3.441

8.  Experimental transmission of bovine anaplasmosis (caused by Anaplasma marginale) by means of Dermacentor variabilis and D. andersoni (Ixodidae) collected in western Canada.

Authors:  Murray W Lankester; W Brad Scandrett; Elizabeth J Golsteyn-Thomas; Neil C Chilton; Alvin A Gajadhar
Journal:  Can J Vet Res       Date:  2007-10       Impact factor: 1.310

9.  Glycosylation of Anaplasma marginale major surface protein 1a and its putative role in adhesion to tick cells.

Authors:  Jose C Garcia-Garcia; José de la Fuente; Gianna Bell-Eunice; Edmour F Blouin; Katherine M Kocan
Journal:  Infect Immun       Date:  2004-05       Impact factor: 3.441

10.  Tick-borne transmission of two genetically distinct Anaplasma marginale strains following superinfection of the mammalian reservoir host.

Authors:  Christina K Leverich; Guy H Palmer; Donald P Knowles; Kelly A Brayton
Journal:  Infect Immun       Date:  2008-06-23       Impact factor: 3.441

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