Blood meals from ‘dead-end’ vertebrate hosts enhance transmission potential of malaria-infected mosquitoes

Author:

Pathak Ashutosh K.ORCID,Shiau Justine C.ORCID,de Freitas Cury Rafael Sadock,Kyle Dennis E.ORCID

Abstract

ABSTRACTIngestion of an additional blood meal(s) by mosquitoes can accelerate parasite migration to the salivary glands in infected mosquitoes. Most studies, however, offer blood from the same vertebrate host species as the original challenge (for e.g., human for primary and additional blood meals). Here, we show a second blood meal from bovine and canine hosts can also enhance sporozoite migration inAnopheles stephensimosquitoes infected with the human- and rodent-restrictedPlasmodium falciparumandP. bergheirespectively. The extrinsic incubation period (time to sporozoite appearance in salivary glands) showed more consistent reductions with blood from human and bovine donors than canine blood, although the latter’s effect may be confounded by the toxicity, albeit non-specific, associated with the anticoagulant used to collect whole blood from donors. The complex patterns of enhancement highlight the limitations of a laboratory system but are nonetheless reminiscent of parasite host-specificity and mosquito adaptations, and the genetic predisposition ofAn. stephensifor bovine blood. We suggest that in natural settings, a blood meal from any vertebrate host could accentuate the risk of human infections byP. falciparum, although our observations should also be applicable to other species ofPlasmodiumand indeed other vector-borne diseases such as arboviruses for instance.Graphical AbstractHIGHLIGHTSPlasmodium falciparumandP. bergheicause malaria in humans and rodents, respectively.They are vectored byAnophelesspecies that can also imbibe blood from other vertebrate species.Parasite development is enhanced after another blood meal, usually from the same host (e.g., human).Here, bovine, and canine blood also enhanced development ofPlasmodiumspecies inAn. stephensi.In natural settings, blood from any host could enhance development of vector transmitted parasites.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3