Literature DB >> 8427453

Development of Anaplasma marginale in salivary glands of male Dermacentor andersoni.

K M Kocan1, W L Goff, D Stiller, W Edwards, S A Ewing, P L Claypool, T C McGuire, J A Hair, S J Barron.   

Abstract

Development of the rickettsia, Anaplasma marginale, in salivary glands of male Dermacentor andersoni exposed as nymphs or adult ticks, was studied indirectly by inoculation of susceptible calves with homogenates and directly by examination, using light microscopy and a DNA probe; some unfed ticks were incubated before tissues were collected. Salivary gland homogenates made from ticks in every treatment group caused anaplasmosis when injected into susceptible calves; prepatent periods decreased as the time that ticks had fed increased. Colonies of A marginale were seen only in salivary glands of ticks exposed as adults and not in those exposed as nymphs; the percentage of salivary gland acini infected in these ticks increased linearly with feeding time. However, the probe detected A marginale DNA in salivary glands of ticks from both groups; the amount of DNA detected increased as feeding time was extended. The amount of A marginale DNA appeared to remain constant in gut tissues, but to increase in salivary glands. Salivary glands of adult-infected male ticks that were incubated, but did not feed a second time, became infected with A marginale, and the pattern of infection of acini varied with incubation temperature. Development of A marginale in salivary glands appears to be coordinated with the tick feeding cycle; highest infection rate was observed in ticks exposed as adults.

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Year:  1993        PMID: 8427453

Source DB:  PubMed          Journal:  Am J Vet Res        ISSN: 0002-9645            Impact factor:   1.156


  14 in total

1.  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

2.  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

3.  Specific expression of Anaplasma marginale major surface protein 2 salivary gland variants occurs in the midgut and is an early event during tick transmission.

Authors:  Christiane V Löhr; Fred R Rurangirwa; Terry F McElwain; David Stiller; Guy H Palmer
Journal:  Infect Immun       Date:  2002-01       Impact factor: 3.441

4.  Restriction of major surface protein 2 (MSP2) variants during tick transmission of the ehrlichia Anaplasma marginale.

Authors:  F R Rurangirwa; D Stiller; D M French; G H Palmer
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-16       Impact factor: 11.205

5.  Strain diversity in major surface protein 2 expression during tick transmission of Anaplasma marginale.

Authors:  F R Rurangirwa; D Stiller; G H Palmer
Journal:  Infect Immun       Date:  2000-05       Impact factor: 3.441

6.  Quantitative differences in salivary pathogen load during tick transmission underlie strain-specific variation in transmission efficiency of Anaplasma marginale.

Authors:  Massaro W Ueti; Donald P Knowles; Christine M Davitt; Glen A Scoles; Timothy V Baszler; Guy H Palmer
Journal:  Infect Immun       Date:  2008-10-27       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.  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

10.  Identification of midgut and salivary glands as specific and distinct barriers to efficient tick-borne transmission of Anaplasma marginale.

Authors:  Massaro W Ueti; James O Reagan; Donald P Knowles; Glen A Scoles; Varda Shkap; Guy H Palmer
Journal:  Infect Immun       Date:  2007-04-09       Impact factor: 3.441

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