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Jpn J Infect Dis ; 57(3): 107-9, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15218219

ABSTRACT

Ticks were collected from ruminants in various areas of Sudan in 1998 and 2000. Primer pairs of rickettsial citrate synthase gene (gltA) and a spotted fever group (SFG) rickettsial 190-kDa surface antigen gene (rompA), respectively, were used for identification. Polymerase chain reaction (PCR)-positive products were used for DNA sequencing. The gltA gene was detected in 55% of the ticks examined (57/104). Among the 57 ticks studied, 19 were positive for the rompA gene. Thus, 18% of the ticks examined were found to be infected with SFG rickettsiae. The nucleotide sequences of the amplified rompA gene fragment of Hyalomma spp. and Amblyomma spp. were similar to those of Rickettsia aeschlimannii and Rickettsia africae, respectively. In this study, we succeeded in detecting the SFG rickettsiae gene in ticks, and established that there were at least two species of SFG rickettsiae in field ticks in Sudan.


Subject(s)
Arachnid Vectors/microbiology , Boutonneuse Fever/veterinary , Rickettsia conorii/isolation & purification , Ruminants/parasitology , Tick Infestations/veterinary , Ticks/microbiology , Animals , Bacterial Outer Membrane Proteins/genetics , Boutonneuse Fever/epidemiology , Boutonneuse Fever/transmission , Gene Amplification , Phylogeny , Polymerase Chain Reaction , Rickettsia conorii/classification , Ruminants/microbiology , Species Specificity , Sudan/epidemiology , Tick Infestations/epidemiology
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