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Acquisition and transmission of Theileria parva by vector tick, Rhipicephalus appendiculatus

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Title: Acquisition and transmission of Theileria parva by vector tick, Rhipicephalus appendiculatus
Authors: Konnai, Satoru Browse this author →KAKEN DB
Imamura, Saiki Browse this author
Nakajima, Chie Browse this author →KAKEN DB
Witola, William Harold Browse this author
Yamada, Shinji Browse this author
Simuunza, Martin Browse this author
Nambota, Andrew Browse this author
Yasuda, Jun Browse this author
Ohashi, Kazuhiko Browse this author →KAKEN DB
Onuma, Misao Browse this author →KAKEN DB
Keywords: Theileria parva
Real-time PCR
Detection
Monitoring
Transmission
Issue Date: Aug-2006
Publisher: Elsevier B.V.
Journal Title: Acta Tropica
Volume: 99
Issue: 1
Start Page: 34
End Page: 41
Publisher DOI: 10.1016/j.actatropica.2006.06.008
PMID: 16899209
Abstract: In order to investigate the transmission dynamics of Theileria parva (T. parva) by the brown ear tick, Rhipicephalus appendiculatus (R. appendiculatus), under experimental conditions, detection of T. parva in ticks and cattle was performed by a quantitative real-time PCR assay. A calf inoculated with a T. parva mixture became PCR-positive for T. parva infection on day 8 post-inoculation, and subsequently, nymphal ticks were introduced and maintained to feed on the infected calf for 6 days. Engorged nymphs were collected daily and allowed to molt into adults, and overall, 70.8% (121/171) of the adult ticks acquired the T. parva infection. Furthermore, the T. parva infection rate in ticks under field conditions was monitored by real-time PCR in R. appendiculatus ticks collected from a traditionally managed pastoral land of Zambia, on which Sanga breed cattle are traditionally reared and the area has endemic East Coast fever (ECF). A total of 70 cattle were randomly selected in the same area and 67 (95.7%) were found to be serologically positive for R. appendiculatus tick antigen (RIM36). Twenty-nine (43.3%) of the 67 serologically positive cattle were real-time PCR-positive for T. parva, although no piroplasms could be detected in the blood smears. Unexpectedly, out of 614 R. appendiculatus nymphal and adult ticks collected by flagging vegetation, 4.1% were positive for T. parva DNA. However, since the rate of transmission of T. parva from infected cattle to ticks and vice versa and the serological evidence of exposure to R. appendiculatus ticks in naturally exposed cattle were relatively high, it would be wise in such a case to consider vector control as well as vaccination against ECF as control measures.
Relation: http://www.sciencedirect.com/science/journal/0001706X
Type: article (author version)
URI: http://hdl.handle.net/2115/15427
Appears in Collections:獣医学院・獣医学研究院 (Graduate School of Veterinary Medicine / Faculty of Veterinary Medicine) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 今内 覚

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