Chemotherapy against babesiosis
Babesiosis is caused by a haemotropic protozoal parasite of the genus Babesia, member of the phylum Apicomplexa and transmitted by the bite of an infected tick. There are many Babesia species affecting livestock, dogs, horses and rodents which are of economic significance. Infections can occur witho...
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Published in: | Veterinary parasitology Vol. 138; no. 1; pp. 147 - 160 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Netherlands
Elsevier B.V
31-05-2006
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Subjects: | |
Online Access: | Get full text |
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Summary: | Babesiosis is caused by a haemotropic protozoal parasite of the genus
Babesia, member of the phylum Apicomplexa and transmitted by the bite of an infected tick. There are many
Babesia species affecting livestock, dogs, horses and rodents which are of economic significance. Infections can occur without producing symptoms, but babesiosis may also be severe and sometimes fatal caused by the intraerythrocytic parasite development. The disease can cause fever, fatigue and haemolytic anemia lasting from several days to several months. There are a number of effective babesiacides, but imidocarb dipropionate (which consistently clears the parasitaemia; often the only available drug on the market) and diminazene aceturate are the most widely used. Some
Babesia spp. can infect humans, particularly
Babesia microti and
Babesia divergens, and human babesiosis is a significant emerging tick-borne zoonotic disease. Clinical manifestations differ markedly between European and North American diseases. In clinical cases, a combination of clindamycin and quinine is administered as the standard treatment, but also administration of atovaquone–azithromycin is successful. Supportive therapy such as intravenous fluids and blood transfusions are employed when necessary. More specific fast-acting new treatments for babesiosis have now to be developed. This should be facilitated by the knowledge of the
Babesia spp. genome and increased interest for this malaria-like parasite. |
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Bibliography: | http://dx.doi.org/10.1016/j.vetpar.2006.01.048 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-3 ObjectType-Review-1 |
ISSN: | 0304-4017 1873-2550 |
DOI: | 10.1016/j.vetpar.2006.01.048 |