Literature DB >> 8341579

Heterogeneity in patterns of malarial oocyst infections in the mosquito vector.

G F Medley1, R E Sinden, S Fleck, P F Billingsley, N Tirawanchai, M H Rodriguez.   

Abstract

Oocyst prevalence and intensity have been recorded in 349 laboratory infections of Anopheles stephensi with Plasmodium berghei. Intensity and prevalence of infection are shown to be predictably related. The structure and heterogeneity in the infections has been analysed with the objective of describing the biological mechanisms by which the observed negative binomial oocyst distributions are generated. The analysis has revealed that the most likely processes lie within the population dynamic events of malaria within the mosquito, namely gametogenesis, fertilization and mortality. The distribution is similar in all Plasmodium-mosquito combinations examined so far, whether they are of laboratory (P. gallinaceum in Aedes aegypti) or field (P. vivax in An. albimanus and P. falciparum in An. gambiae s.l. and An. funestus) origin. Further we conclude that there is competition between parasites in the vector. Oocyst frequency distribution analysis shows that under natural conditions of transmission intensity, and even under the best laboratory conditions, significant numbers (> 10%) of fully susceptible mosquitoes will not be infected under conditions where the mean infection is as high as 250 oocysts. Failure to infect is not therefore an absolute indicator of refractoriness. In assessing transmission data it is shown that sample sizes should not be less than 50, and ideally 100 mosquitoes, if reliable data are to be obtained. In field it is suggested that difficulties in determining the low natural intensity of oocyst infections indicate that prevalence estimates are a useful and accessible parameter to measure.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1993        PMID: 8341579     DOI: 10.1017/s0031182000076721

Source DB:  PubMed          Journal:  Parasitology        ISSN: 0031-1820            Impact factor:   3.234


  38 in total

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Authors:  A M Tomas; G Margos; G Dimopoulos; L H van Lin; T F de Koning-Ward; R Sinha; P Lupetti; A L Beetsma; M C Rodriguez; M Karras; A Hager; J Mendoza; G A Butcher; F Kafatos; C J Janse; A P Waters; R E Sinden
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2.  The IC(50) of anti-Pfs25 antibody in membrane-feeding assay varies among species.

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Journal:  Vaccine       Date:  2010-04-29       Impact factor: 3.641

3.  Leukocytes in a Plasmodium falciparum-infected blood meal reduce transmission of malaria to Anopheles mosquitoes.

Authors:  A H Lensen; M Bolmer-Van de Vegte; G J van Gemert; W M Eling; R W Sauerwein
Journal:  Infect Immun       Date:  1997-09       Impact factor: 3.441

4.  Population genetic structure of Plasmodium falciparum in the two main African vectors, Anopheles gambiae and Anopheles funestus.

Authors:  Zeinab Annan; Patrick Durand; Francisco J Ayala; Céline Arnathau; Parfait Awono-Ambene; Frédéric Simard; Fabien G Razakandrainibe; Jacob C Koella; Didier Fontenille; François Renaud
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-30       Impact factor: 11.205

5.  Evaluation of Plasmodium vivax HAP2 as a transmission-blocking vaccine candidate.

Authors:  Yue Qiu; Yan Zhao; Fei Liu; Bo Ye; Zhenjun Zhao; Sataporn Thongpoon; Wanlapa Roobsoong; Jetsumon Sattabongkot; Liwang Cui; Qi Fan; Yaming Cao
Journal:  Vaccine       Date:  2020-02-21       Impact factor: 3.641

6.  Suppressive effect of azithromycin on Plasmodium berghei mosquito stage development and apicoplast replication.

Authors:  Shoichi Shimizu; Yoshio Osada; Tamotsu Kanazawa; Yoshiya Tanaka; Meiji Arai
Journal:  Malar J       Date:  2010-03-10       Impact factor: 2.979

7.  Population biology of malaria within the mosquito: density-dependent processes and potential implications for transmission-blocking interventions.

Authors:  Thomas S Churcher; Emma J Dawes; Robert E Sinden; George K Christophides; Jacob C Koella; María-Gloria Basáñez
Journal:  Malar J       Date:  2010-11-04       Impact factor: 2.979

8.  Overexpression of phosphatase and tensin homolog improves fitness and decreases Plasmodium falciparum development in Anopheles stephensi.

Authors:  Eric S Hauck; Yevgeniya Antonova-Koch; Anna Drexler; Jose Pietri; Nazzy Pakpour; Darin Liu; Jacob Blacutt; Michael A Riehle; Shirley Luckhart
Journal:  Microbes Infect       Date:  2013-06-15       Impact factor: 2.700

9.  Anti-Pfs25 human plasma reduces transmission of Plasmodium falciparum isolates that have diverse genetic backgrounds.

Authors:  Dari F Da; Saurabh Dixit; Jetsumon Sattabonkot; Jianbing Mu; Luc Abate; Bhanumati Ramineni; Jean Bosco Ouedraogo; Nicholas J MacDonald; Michael P Fay; Xin-zhuan Su; Anna Cohuet; Yimin Wu
Journal:  Infect Immun       Date:  2013-03-18       Impact factor: 3.441

10.  Transmission-blocking activity is determined by transmission-reducing activity and number of control oocysts in Plasmodium falciparum standard membrane-feeding assay.

Authors:  Kazutoyo Miura; Bruce J Swihart; Bingbing Deng; Luwen Zhou; Thao P Pham; Ababacar Diouf; Timothy Burton; Michael P Fay; Carole A Long
Journal:  Vaccine       Date:  2016-06-29       Impact factor: 3.641

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