Literature DB >> 15799524

Variation among geographically separated populations of Dermacentor andersoni (Acari: Ixodidae) in midgut susceptibility to Anaplasma marginale (Rickettsiales: Anaplasmataceae).

Glen A Scoles1, Massaro W Ueti, Guy H Palmer.   

Abstract

Anaplasma marginale is a tick-borne rickettsial pathogen of cattle that is endemic throughout large areas of the United States. Cattle that survive acute infection become life-long persistently infected carriers. In the intermountain west the Rocky Mountain wood tick, Dermacentor andersoni Stiles, is the most common vector of A. marginale. Male D. andersoni acquire A. marginale when feeding on persistently infected cattle and biologically transmit it when they transfer from infected to susceptible hosts. Host-seeking adult D. andersoni were collected from four widely separated natural populations and tested for susceptibility to midgut colonization with A. marginale. Male ticks were fed on calves persistently infected with a strain of A. marginale naturally transmitted by D. andersoni. Gut infection rates ranged from 12.5% of ticks collected from a mountain site near Hamilton, MT, to 62.5% of ticks from a rangeland site near Riley, OR. Sites near Miles City, MT, and Kamloops, British Columbia, Canada, had intermediate levels of susceptibility. The infection rates differed significantly among populations, and the same populations sampled in two consecutive years were not significantly different from one year to the next. Although there was variation among the populations in the size of ticks, size was unrelated to acquisition of gut infection. Quantitative polymerase chain reaction (PCR) demonstrated that there was no significant difference between populations in the mean number of genome copies in the guts of infected ticks. A. marginale from infected ticks was genotyped to confirm that they were all infected with the laboratory strain, and a sample of 682 field-collected D. andersoni was surveyed for A. marginale by nested PCR; none were found to be naturally infected. Infection of the gut is an essential constituent of vector competence for A. marginale; in this study, we have demonstrated significant variation among populations in this key component of vector competence.

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Year:  2005        PMID: 15799524     DOI: 10.1603/0022-2585(2005)042[0153:vagspo]2.0.co;2

Source DB:  PubMed          Journal:  J Med Entomol        ISSN: 0022-2585            Impact factor:   2.278


  19 in total

1.  Identification of multilocus genetic heterogeneity in Anaplasma marginale subsp. centrale and its restriction following tick-borne transmission.

Authors:  David R Herndon; Massaro W Ueti; Kathryn E Reif; Susan M Noh; Kelly A Brayton; Joseph T Agnes; Guy H Palmer
Journal:  Infect Immun       Date:  2013-03-18       Impact factor: 3.441

2.  Anaplasma marginale Actively Modulates Vacuolar Maturation during Intracellular Infection of Its Tick Vector, Dermacentor andersoni.

Authors:  Forgivemore Magunda; Chelsea Wright Thompson; David A Schneider; Susan M Noh
Journal:  Appl Environ Microbiol       Date:  2016-07-15       Impact factor: 4.792

3.  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

4.  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

5.  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

6.  Immunization-induced Anaplasma marginale-specific T-lymphocyte responses impaired by A. marginale infection are restored after eliminating infection with tetracycline.

Authors:  Joshua E Turse; Glen A Scoles; James R Deringer; Lindsay M Fry; Wendy C Brown
Journal:  Clin Vaccine Immunol       Date:  2014-07-09

7.  Generation of antigenic variants via gene conversion: Evidence for recombination fitness selection at the locus level in Anaplasma marginale.

Authors:  James E Futse; Kelly A Brayton; Seth D Nydam; Guy H Palmer
Journal:  Infect Immun       Date:  2009-06-01       Impact factor: 3.441

8.  Novel genetic variants of Anaplasma phagocytophilum, Anaplasma bovis, Anaplasma centrale, and a novel Ehrlichia sp. in wild deer and ticks on two major islands in Japan.

Authors:  Makoto Kawahara; Yasuko Rikihisa; Quan Lin; Emiko Isogai; Kenji Tahara; Asao Itagaki; Yoshimichi Hiramitsu; Tomoko Tajima
Journal:  Appl Environ Microbiol       Date:  2006-02       Impact factor: 4.792

9.  The bacterial microbiome of Dermacentor andersoni ticks influences pathogen susceptibility.

Authors:  Cory A Gall; Kathryn E Reif; Glen A Scoles; Kathleen L Mason; Michelle Mousel; Susan M Noh; Kelly A Brayton
Journal:  ISME J       Date:  2016-02-16       Impact factor: 10.302

10.  Anaplasma marginale superinfection attributable to pathogen strains with distinct genomic backgrounds.

Authors:  Eduardo Vallejo Esquerra; David R Herndon; Francisco Alpirez Mendoza; Juan Mosqueda; Guy H Palmer
Journal:  Infect Immun       Date:  2014-10-06       Impact factor: 3.441

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