Literature DB >> 2724178

Development of Edhazardia aedis (Kudo, 1930) n. g., n. comb. (Microsporida: Amblyosporidae) in the mosquito Aedes aegypti (L.) (Diptera: Culicidae).

J J Becnel1, V Sprague, T Fukuda, E I Hazard.   

Abstract

A microsporidium of the mosquito Aedes aegypti (L.), identified as Nosema aedis Kudo, 1930, was found to be a heterosporous species with 3 sporulation sequences. Usually, 1 sequence developed in a parental generation host individual that was infected per os as a larva and the other 2 developed concurrently in a filial host larva that was infected transovarially. Under some conditions there were deviations from the parental host-filial host alternation. The 1st sporulation sequence was diplokaryotic (diploid in a particular sense) throughout; the other 2 arose from diplokaryotic meronts, developed concurrently and ended with haploid spores. Haplosis in 1 case was by means of dissociation of the diplokaryon. In the other case it was by meiosis. Conflicting reports about whether the members of the diplokaryon in the latter sequence separate and undergo meiosis individually or coalesce and undergo meiosis as 1 nucleus were resolved in favor of the latter idea. A new genus in family Amblyosporidae was created to contain this species, which then became Edhazardia aedis (Kudo, 1930) n. g., n. comb.

Entities:  

Mesh:

Year:  1989        PMID: 2724178     DOI: 10.1111/j.1550-7408.1989.tb01057.x

Source DB:  PubMed          Journal:  J Protozool        ISSN: 0022-3921


  10 in total

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Authors:  Jamie Bojko; Grant D Stentiford
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3.  Contrasting host-pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes.

Authors:  Christopher A Desjardins; Neil D Sanscrainte; Jonathan M Goldberg; David Heiman; Sarah Young; Qiandong Zeng; Hiten D Madhani; James J Becnel; Christina A Cuomo
Journal:  Nat Commun       Date:  2015-05-13       Impact factor: 14.919

4.  3-Dimensional organization and dynamics of the microsporidian polar tube invasion machinery.

Authors:  Pattana Jaroenlak; Michael Cammer; Alina Davydov; Joseph Sall; Mahrukh Usmani; Feng-Xia Liang; Damian C Ekiert; Gira Bhabha
Journal:  PLoS Pathog       Date:  2020-09-18       Impact factor: 6.823

5.  Proteome of Aedes aegypti in response to infection and coinfection with microsporidian parasites.

Authors:  Alison B Duncan; Philip Agnew; Valérie Noel; Edith Demettre; Martial Seveno; Jean-Paul Brizard; Yannis Michalakis
Journal:  Ecol Evol       Date:  2012-04       Impact factor: 2.912

6.  ESTs from the microsporidian Edhazardia aedis.

Authors:  Erin E Gill; James J Becnel; Naomi M Fast
Journal:  BMC Genomics       Date:  2008-06-20       Impact factor: 3.969

7.  Genetic diversity of two Daphnia-infecting microsporidian parasites, based on sequence variation in the internal transcribed spacer region.

Authors:  Enrique González-Tortuero; Jakub Rusek; Inbar Maayan; Adam Petrusek; Lubomír Piálek; Stefan Laurent; Justyna Wolinska
Journal:  Parasit Vectors       Date:  2016-05-20       Impact factor: 3.876

8.  Host genotype and environment affect the trade-off between horizontal and vertical transmission of the parasite Edhazardia aedis.

Authors:  Giacomo Zilio; Kevin Thiévent; Jacob C Koella
Journal:  BMC Evol Biol       Date:  2018-04-24       Impact factor: 3.260

9.  Microsporidia with Vertical Transmission Were Likely Shaped by Nonadaptive Processes.

Authors:  Karen L Haag; Jean-François Pombert; Yukun Sun; Nathalia Rammé M de Albuquerque; Brendan Batliner; Peter Fields; Tiago Falcon Lopes; Dieter Ebert
Journal:  Genome Biol Evol       Date:  2020-01-01       Impact factor: 3.416

10.  A new method of metabarcoding Microsporidia and their hosts reveals high levels of microsporidian infections in mosquitoes (Culicidae).

Authors:  Artur Trzebny; Anna Slodkowicz-Kowalska; James J Becnel; Neil Sanscrainte; Miroslawa Dabert
Journal:  Mol Ecol Resour       Date:  2020-07-01       Impact factor: 7.090

  10 in total

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