Effects of octopamine, chlordimeform, and demethylchlordimeform on amine-controlled tick salivary glands isolated from feeding Amblyomma americanum (L.)

1983 ◽  
Vol 19 (2) ◽  
pp. 133-140 ◽  
Author(s):  
Glen R. Needham ◽  
Thomas L. Pannabecker
2001 ◽  
Vol 184 (8) ◽  
pp. 1056-1064 ◽  
Author(s):  
Subrata Das ◽  
Gautam Banerjee ◽  
Kathleen DePonte ◽  
Nancy Marcantonio ◽  
Fred S. Kantor ◽  
...  

1994 ◽  
Vol 24 (4) ◽  
pp. 563-567 ◽  
Author(s):  
William J. Lamoreaux ◽  
Glen R. Needham ◽  
Lewis B. Coons

2001 ◽  
Vol 69 (5) ◽  
pp. 3057-3066 ◽  
Author(s):  
A. F. Barbet ◽  
Jooyoung Yi ◽  
Anna Lundgren ◽  
B. R. McEwen ◽  
E. F. Blouin ◽  
...  

ABSTRACT The rickettsial pathogen Anaplasma marginale expresses a variable immunodominant outer membrane protein, major surface protein 2 (MSP2), involved in antigenic variation and long-term persistence of the organism in carrier animals. MSP2 contains a central hypervariable region of about 100 amino acids that encodes immunogenic B-cell epitopes that induce variant-specific antibodies during infection. Previously, we have shown that MSP2 is encoded on a polycistronic mRNA transcript in erythrocyte stages of A. marginale and defined the structure of the genomic expression site for this transcript. In this study, we show that the same expression site is utilized in stages of A. marginale infecting tick salivary glands. We also analyzed the variability of this genomic expression site in Oklahoma strain A. marginale transmitted from in vitro cultures to cattle and between cattle and ticks. The structure of the expression site and flanking regions was conserved except for sequence that encoded the MSP2 hypervariable region. At least three different MSP2 variants were encoded in each A. marginalepopulation. The major sequence variants did not change on passage ofA. marginale between culture, acute erythrocyte stage infections, and tick salivary glands but did change during persistent infections of cattle. The variant types found in tick salivary glands most closely resembled those present in bovine blood at the time of acquisition of infection, whether infection was acquired from an acute or from a persistent rickettsemia. These variations in structure of an expression site for a major, immunoprotective outer membrane protein have important implications for vaccine development and for obtaining an improved understanding of the mechanisms of persistence of ehrlichial infections in humans, domestic animals, and reservoir hosts.


1989 ◽  
Vol 19 (4) ◽  
pp. 343-349 ◽  
Author(s):  
Janis L. McSwain ◽  
James S. Tucker ◽  
Richard C. Essenberg ◽  
John R. Sauer

1989 ◽  
Vol 70 (7) ◽  
pp. 1895-1898 ◽  
Author(s):  
L. D. Jones ◽  
E. Hodgson ◽  
P. A. Nuttall

2019 ◽  
Vol 87 (4) ◽  
Author(s):  
Chanakan Suwanbongkot ◽  
Ingeborg M. Langohr ◽  
Emma K. Harris ◽  
Wellesley Dittmar ◽  
Rebecca C. Christofferson ◽  
...  

ABSTRACTTick vectors are capable of transmitting several rickettsial species to vertebrate hosts, resulting in various levels of disease. Studies have demonstrated the transmissibility of both rickettsial pathogens and novelRickettsiaspecies or strains with unknown pathogenicity to vertebrate hosts during tick blood meal acquisition; however, the quantitative nature of transmission remains unknown. We tested the hypothesis that if infection severity is a function of the rickettsial load delivered during tick transmission, then a more virulent spotted fever group (SFG)Rickettsiaspecies is transmitted at higher levels during tick feeding. UsingAmblyomma maculatumcohorts infected withRickettsia parkerior “CandidatusRickettsia andeanae,” a quantitative PCR (qPCR) assay was employed to quantify rickettsiae in tick salivary glands and saliva, as well as in the vertebrate hosts at the tick attachment site over the duration of tick feeding. Significantly greater numbers ofR. parkerithan of “Ca. Rickettsia andeanae” rickettsiae were present in tick saliva and salivary glands and in the vertebrate hosts at the feeding site during tick feeding. Microscopy demonstrated the presence of both rickettsial species in tick salivary glands, and immunohistochemical analysis of the attachment site identified localizedR. parkeri, but not “Ca. Rickettsia andeanae,” in the vertebrate host. Lesions were also distinct and more severe in vertebrate hosts exposed toR. parkerithan in those exposed to “Ca. Rickettsia andeanae.” The specific factors that contribute to the generation of a sustained rickettsial infection and subsequent disease have yet to be elucidated, but the results of this study suggest that the rickettsial load in ticks and during transmission may be an important element.


1995 ◽  
Vol 25 (2) ◽  
pp. 225-233 ◽  
Author(s):  
Alan S. Bowman ◽  
John R. Sauer ◽  
Paul A. Neese ◽  
Jack W. Dillwith

Author(s):  
Michael E. Hume ◽  
Richard C. Essenberg ◽  
Ronald W. McNew ◽  
John A. Bantle ◽  
John R. Sauer

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