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Abstract. The malaria transmission potential of wild, infective Anopheles from western Kenya was evaluated by determining the number of sporozoites transmitted in vitro by salivation when their mouthparts were inserted into capillary tubes containing either sucrose or blood. With sucrose, 86.6% of 102 infective Anopheles transmitted a geometric mean (GM) of 3.84 sporozoites (range 1–34). With blood, 23.1% of 104 infective Anopheles , tested on the day of collection, transmitted a GM of 2.30 sporozoites (range 1–117). For Anopheles held 5 days postcapture before testing with blood, 53.6% of 56 transmitted a GM of 6.04 sporozoites (range 1–420). Transmitting Anopheles contained significantly more salivary gland sporozoites than non-transmitters. No significant differences were detected between Anopheles gambiae Giles sensu lato and Anopheles funestus Giles in sporozoite transmission by individuals with sporozoites in their salivary glands.
Sporozoites were detected microscopically in the salivary duct from heads in 80.3% of 117 infective Anopheles (GM=11.2, range 1–71). Sporozoite detection in mosquito heads by ELISA was 25% less efficient than microscopic detection.
Over 98% of the infective Anopheles transmitted less than twenty-five sporozoites. Transmitted sporozoites represented only about 3% of the total sporozoites in the salivary glands suggesting that sporozoite transmission may be restricted to sporozoites in the salivary duct at the time of feeding. Results are discussed in relation to anti-sporozoite vaccine development.  相似文献   
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IMMUNOGLOBULIN polypeptide chains consist of two well defined regions designated the “variable region” and the “constant region”. Whereas great diversity exists in amino-acid sequences of variable regions, the constant regions of a given subclass of heavy chains (CH)* are essentially invariant in sequence1, 2. Exceptions are the allelic forms, such as the rabbit allotypes A14 and A153, 4, where a threonine-alanine interchange occurs in the constant region of γ chains (Appella, Chersi, R. G. M. and Dubiski, in preparation). The markers unique to a chains (for example, A14-A15) are closely linked to allotypic markers at the a locus (a1, a2, a3)3, 4 which seem to be present on four different Ig heavy chain classes (α, γ, ε, µ)5–7. These puzzling observations can be explained if the a locus determinants are variable region markers which reflect genetically controlled differences in some relatively constant residues within the VH region sequences7.  相似文献   
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The following article from Medical and Veterinary Entomology, ‘Established and emerging pathogens in Ixodes ricinus ticks collected from birds on a conservation island in the Baltic Sea’ by J. Franke, F. Meier, A. Moledenhauer, E. Straube, W. Dorne and A. Hildebrandt, published online on 26 September 2010 in Wiley Online Library ( wileyonlinelibrary.com ), has been retracted by agreement between the journal Editors, Doug D. Colwell, Mary Cameron, Domenico Otranto and Hilary Ranson and Blackwell Publishing Ltd. and with the knowledge of the authors. The retraction has been agreed due to overlap between this article and the following articles published in the journal Ticks and Tick‐borne Diseases: ‘The potential role of migratory birds in transmission cycles of Babesia spp., Anaplasma phagocytophilum, and Rickettsia spp.’ by Anke Hildebrandt, Jan Franke, Frank Meier, Svea Sachse, Wolfram Dorn and Eberhard Straube. Ticks and Tick‐Bourne Diseases, Volume 1 Issue 2, 2010, pages 105–107 DOI: 10.1016/j.ttbdis.2009.12.003 http://www.sciencedirect.com/science/article/pii/S1877959X10000105 and Are birds reservoir hosts for Borrelia afzelii? By Jan Franke, Anja Moldenhauer, A., Anke Hildebrandt, Wolfram Dorn, Ticks and Tick‐Borne Diseases, Volume 1 Issue 2, 109–112 DOI: 10.1016/j.ttbdis.2010.03.001 http://www.sciencedirect.com/science/article/pii/S1877959X10000336  相似文献   
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