Literature DB >> 3379524

Ultrastructure of the encapsulation of Plasmodium cynomolgi (B strain) on the midgut of a refractory strain of Anopheles gambiae.

S M Paskewitz1, M R Brown, A O Lea, F H Collins.   

Abstract

Using transmission electron microscopy, we investigated the encapsulation of the simian malaria parasite, Plasmodium cynomolgi, in a refractory strain of the mosquito, Anopheles gambiae. After the ookinete penetrates the mosquito midgut epithelium and lodges between the basal membrane and the basal lamina, an electron-dense, melanin-like substance begins to coalesce around the parasite. Completely encapsulated parasites were found as early as 16 hr after the blood meal. Granules of the melanin-like substance often appeared to condense onto the parasite from the fluid in the extracellular spaces of the basal membrane labyrinth. Melanin granules also appeared to condense from the hemolymph onto the basal lamina underlying the parasite. In addition, groups of tubules, vesicles, and membranous whorls often were found in midgut cells that were located next to or were enclosing parasites. These structures were unusually electron-dense, and may have been associated with melanization. Hemocytes rarely were observed near completed capsules and neither hemocytes nor their remnants were components of the capsules. During later stages of encapsulation, parasites appeared abnormal and often were infiltrated with melanin. Although late-stage capsules were usually located basally, completed capsules enclosed by membranes were occasionally observed near the apical border of the midgut. Other capsules associated with cellular debris, were found in the lumen of the midgut from 1 to 6 days after the blood meal.

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Year:  1988        PMID: 3379524

Source DB:  PubMed          Journal:  J Parasitol        ISSN: 0022-3395            Impact factor:   1.276


  20 in total

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Journal:  EMBO J       Date:  2001-08-01       Impact factor: 11.598

3.  Comparative genomic analysis in the region of a major Plasmodium-refractoriness locus of Anopheles gambiae.

Authors:  Dana Thomasova; Lucas Q Ton; Richard R Copley; Evgeny M Zdobnov; Xuelan Wang; Young S Hong; Cheolho Sim; Peer Bork; Fotis C Kafatos; Frank H Collins
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-11       Impact factor: 11.205

4.  Molecular immune responses of the mosquito Anopheles gambiae to bacteria and malaria parasites.

Authors:  G Dimopoulos; A Richman; H M Müller; F C Kafatos
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-14       Impact factor: 11.205

5.  Silencing the genes for dopa decarboxylase or dopachrome conversion enzyme reduces melanization of foreign targets in Anopheles gambiae.

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Review 6.  Genetic variation in arthropod vectors of disease-causing organisms: obstacles and opportunities.

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7.  Anopheles gambiae hemocytes exhibit transient states of activation.

Authors:  William B Bryant; Kristin Michel
Journal:  Dev Comp Immunol       Date:  2015-10-26       Impact factor: 3.636

8.  Some strains of Plasmodium falciparum, a human malaria parasite, evade the complement-like system of Anopheles gambiae mosquitoes.

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9.  Mosquito transcriptome profiles and filarial worm susceptibility in Armigeres subalbatus.

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10.  An immune response-dependent mechanism for the vertical transmission of an entomopathogen.

Authors:  A Warburg; K Ostrovska
Journal:  Experientia       Date:  1989-08-15
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