Literature DB >> 8961639

Developmental studies of Anaplasma marginale (Rickettsiales:Anaplasmataceae) in male Dermacentor andersoni (Acari:Ixodidae) infected as adults by using nonradioactive in situ hybridization and microscopy.

N L Ge1, K M Kocan, E F Blouin, G L Murphy.   

Abstract

The development of Anaplasma marginale Theiler was studied in ticks using a nonradioactive in situ hybridization method developed in our laboratory. Male Rocky Mountain wood ticks, Dermacentor andersoni Stiles, were infected intrastadially by allowing them to feed for 7 d on an infected calf (acquisition feeding). The ticks were then removed and held in a humidity chamber for 5 d before being fed on a 2nd susceptible call for 10 d (transmission feeding). Two groups of 10 ticks were collected daily during the 22-d experiment. In one group one-half of each tick was processed and embedded in paraffin and in the other group one-half of each tick was embedded in LR White for in situ hybridization. The companion tick halves from each group were fixed and embedded in Dow Epoxy Resin resin for routine light and electron microscopy. As detected by in situ hybridization on LR White- and paraffin-embedded sections and by microscopy, initial infection of A. marginale in ticks occurred in gut tissues either on the 7th d of acquisition feeding or the 1st d of the held period and infection persisted throughout transmission feeding. The highest number of ticks with gut infection was observed on the 5th d of transmission feeding. Salivary glands became infected with A. marginale on the 1st day of transmission feeding and remained infected throughout the transmission feeding period. Peak infection was observed on day 4 of transmission feeding. After the beginning of transmission feeding, A. marginale infection was also observed in interstitial, reproductive, skeletal muscle, fat body, and Malpighian tubule tissues. Although A. marginale infection of ticks clearly originates in midgut epithelial cells, many tissues eventually become infected during transmission feeding, resulting in a generalized infection. The infection of multiple tissues may contribute to the ability of A. marginale infection to persist in intrastadially infected male ticks.

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Year:  1996        PMID: 8961639     DOI: 10.1093/jmedent/33.6.911

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


  13 in total

1.  Expression of Anaplasma marginale major surface protein 2 variants in persistently infected ticks.

Authors:  J de la Fuente; K M Kocan
Journal:  Infect Immun       Date:  2001-08       Impact factor: 3.441

2.  Comparison of surface proteins of Anaplasma marginale grown in tick cell culture, tick salivary glands, and cattle.

Authors:  A F Barbet; R Blentlinger; J Yi; A M Lundgren; E F Blouin; K M Kocan
Journal:  Infect Immun       Date:  1999-01       Impact factor: 3.441

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.  Infection of tick cells and bovine erythrocytes with one genotype of the intracellular ehrlichia Anaplasma marginale excludes infection with other genotypes.

Authors:  José de la Fuente; Jose C Garcia-Garcia; Edmour F Blouin; Jeremiah T Saliki; Katherine M Kocan
Journal:  Clin Diagn Lab Immunol       Date:  2002-05

5.  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

6.  African swine fever virus infection in the argasid host, Ornithodoros porcinus porcinus.

Authors:  S B Kleiboeker; T G Burrage; G A Scoles; D Fish; D L Rock
Journal:  J Virol       Date:  1998-03       Impact factor: 5.103

7.  Differential expression and sequence conservation of the Anaplasma marginale msp2 gene superfamily outer membrane proteins.

Authors:  Susan M Noh; Kelly A Brayton; Donald P Knowles; Joseph T Agnes; Michael J Dark; Wendy C Brown; Timothy V Baszler; Guy H Palmer
Journal:  Infect Immun       Date:  2006-06       Impact factor: 3.441

8.  Antigenic variation of Anaplasma marginale by expression of MSP2 mosaics.

Authors:  A F Barbet; A Lundgren; J Yi; F R Rurangirwa; G H Palmer
Journal:  Infect Immun       Date:  2000-11       Impact factor: 3.441

Review 9.  Antigens and alternatives for control of Anaplasma marginale infection in cattle.

Authors:  Katherine M Kocan; José de la Fuente; Alberto A Guglielmone; Roy D Meléndez
Journal:  Clin Microbiol Rev       Date:  2003-10       Impact factor: 26.132

Review 10.  Adaptations of the tick-borne pathogen, Anaplasma marginale, for survival in cattle and ticks.

Authors:  Katherine M Kocan; Jose De La Fuente; Edmour F Blouin; Jose Carlos Garcia-Garcia
Journal:  Exp Appl Acarol       Date:  2002       Impact factor: 2.132

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