Literature DB >> 17420231

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

Massaro W Ueti1, James O Reagan, Donald P Knowles, Glen A Scoles, Varda Shkap, Guy H Palmer.   

Abstract

Understanding the determinants of efficient tick-borne microbial transmission is needed to better predict the emergence of highly transmissible pathogen strains and disease outbreaks. Although the basic developmental cycle of Anaplasma and Ehrlichia spp. within the tick has been delineated, there are marked differences in the ability of specific strains to be efficiently tick transmitted. Using the highly transmissible St. Maries strain of Anaplasma marginale in Dermacentor andersoni as a positive control and two unrelated nontransmissible strains, we identified distinct barriers to efficient transmission within the tick. The Mississippi strain was unable to establish infection at the level of the midgut epithelium despite successful ingestion of infected blood following acquisition feeding on a bacteremic animal host. This inability to colonize the midgut epithelium prevented subsequent development within the salivary glands and transmission. In contrast, A. marginale subsp. centrale colonized the midgut and then the salivary glands, replicating to a titer indistinguishable from that of the highly transmissible St. Maries strain and at least 100 times greater than that previously associated with successful transmission. Nonetheless, A. marginale subsp. centrale was not transmitted, even when a large number of infected ticks was used for transmission feeding. These results establish that there are at least two specific barriers to efficient tick-borne transmission, the midgut and salivary glands, and highlight the complexity of the pathogen-tick interaction.

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Year:  2007        PMID: 17420231      PMCID: PMC1932854          DOI: 10.1128/IAI.00284-07

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  27 in total

1.  Differential adhesion of major surface proteins 1a and 1b of the ehrlichial cattle pathogen Anaplasma marginale to bovine erythrocytes and tick cells.

Authors:  J de la Fuente; J C Garcia-Garcia; E F Blouin; K M Kocan
Journal:  Int J Parasitol       Date:  2001-02       Impact factor: 3.981

2.  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

3.  Development of colonies of Anaplasma marginale in the gut of incubated Dermacentor andersoni.

Authors:  K M Kocan; D Holbert; S A Ewing; J A Hair; S J Barron
Journal:  Am J Vet Res       Date:  1983-09       Impact factor: 1.156

4.  Major surface protein 1a effects tick infection and transmission of Anaplasma marginale.

Authors:  J de la Fuente; J C Garcia-Garcia; E F Blouin; B R McEwen; D Clawson; K M Kocan
Journal:  Int J Parasitol       Date:  2001-12       Impact factor: 3.981

5.  Reorganization of genera in the families Rickettsiaceae and Anaplasmataceae in the order Rickettsiales: unification of some species of Ehrlichia with Anaplasma, Cowdria with Ehrlichia and Ehrlichia with Neorickettsia, descriptions of six new species combinations and designation of Ehrlichia equi and 'HGE agent' as subjective synonyms of Ehrlichia phagocytophila.

Authors:  J S Dumler; A F Barbet; C P Bekker; G A Dasch; G H Palmer; S C Ray; Y Rikihisa; F R Rurangirwa
Journal:  Int J Syst Evol Microbiol       Date:  2001-11       Impact factor: 2.747

6.  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

7.  Expression of equi merozoite antigen 2 during development of Babesia equi in the midgut and salivary gland of the vector tick Boophilus microplus.

Authors:  Massaro W Ueti; Guy H Palmer; Lowell S Kappmeyer; Glen A Scoles; Donald P Knowles
Journal:  J Clin Microbiol       Date:  2003-12       Impact factor: 5.948

8.  Molecular conservation of MSP4 and MSP5 in Anaplasma marginale and A. centrale vaccine strain.

Authors:  T Molad; K A Brayton; G H Palmer; S Michaeli; V Shkap
Journal:  Vet Microbiol       Date:  2004-05-20       Impact factor: 3.293

Review 9.  Lyme borreliosis.

Authors:  Gerold Stanek; Franc Strle
Journal:  Lancet       Date:  2003-11-15       Impact factor: 79.321

10.  Transmission of Anaplasma marginale by Boophilus microplus: retention of vector competence in the absence of vector-pathogen interaction.

Authors:  James E Futse; Massaro W Ueti; Donald P Knowles; Guy H Palmer
Journal:  J Clin Microbiol       Date:  2003-08       Impact factor: 5.948

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  39 in total

1.  Efficacy of a doxycycline treatment regimen initiated during three different phases of experimental ehrlichiosis.

Authors:  Jennifer C McClure; Michelle L Crothers; John J Schaefer; Patrick D Stanley; Glen R Needham; S A Ewing; Roger W Stich
Journal:  Antimicrob Agents Chemother       Date:  2010-10-04       Impact factor: 5.191

2.  Dermacentor andersoni transmission of Francisella tularensis subsp. novicida reflects bacterial colonization, dissemination, and replication coordinated with tick feeding.

Authors:  Kathryn E Reif; Guy H Palmer; Massaro W Ueti; Glen A Scoles; J J Margolis; D M Monack; Susan M Noh
Journal:  Infect Immun       Date:  2011-09-19       Impact factor: 3.441

3.  Association of pathogen strain-specific gene transcription and transmission efficiency phenotype of Anaplasma marginale.

Authors:  Joseph T Agnes; David Herndon; Massaro W Ueti; Solomon S Ramabu; Marc Evans; Kelly A Brayton; Guy H Palmer
Journal:  Infect Immun       Date:  2010-03-22       Impact factor: 3.441

4.  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

5.  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

6.  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

7.  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

8.  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

9.  Subolesin expression in response to pathogen infection in ticks.

Authors:  Zorica Zivkovic; Alessandra Torina; Ruchira Mitra; Angela Alongi; Salvatore Scimeca; Katherine M Kocan; Ruth C Galindo; Consuelo Almazán; Edmour F Blouin; Margarita Villar; Ard M Nijhof; Rinosh Mani; Giuseppa La Barbera; Santo Caracappa; Frans Jongejan; José de la Fuente
Journal:  BMC Immunol       Date:  2010-02-19       Impact factor: 3.615

10.  Characterization of Anaplasma marginale subsp. centrale Strains by Use of msp1aS Genotyping Reveals a Wildlife Reservoir.

Authors:  Zamantungwa T H Khumalo; Helen N Catanese; Nicole Liesching; Paidashe Hove; Nicola E Collins; Mamohale E Chaisi; Assefaw H Gebremedhin; Marinda C Oosthuizen; Kelly A Brayton
Journal:  J Clin Microbiol       Date:  2016-07-20       Impact factor: 5.948

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