Literature DB >> 25467266

Description of microsporidia in simulids: molecular and morphological characterization of microsporidia in the larvae of Simulium pertinax Kollar (Diptera: Simuliidae).

Isabel Maria Vicente Guedes de Carvalho1, Artur Trancoso Lopo de Queiroz2, Rosiane Brito de Moraes3, Helio Benites Gil4, Rafael Alves5, Andréa de Barros Pinto Viviani6, James John Becnel7, Carlos José Pereira da Cunha de Araujo-Coutinho3.   

Abstract

INTRODUCTION: Microsporidia constitute the most common black fly pathogens, although the species' diversity, seasonal occurrence and transmission mechanisms remain poorly understood. Infections by this agent are often chronic and non-lethal, but they can cause reduced fecundity and decreased longevity. The objective of this study was to identify microsporidia infecting Simulium (Chirostilbia) pertinax (Kollar, 1832) larvae from Caraguatatuba, State of São Paulo, Brazil, by molecular and morphological characterization.
METHODS: Larvae were collected at a single point in a stream in a rural area of the city and were kept under artificial aeration until analysis. Polydispyrenia spp. infection was characterized by the presence of at least 32 mononuclear spores measuring 6.9 ± 1.0 × 5.0 ± 0.7 µm in persistent sporophorous vesicles. Similarly, Amblyospora spp. were characterized by the presence of eight uninucleate spores measuring 4.5 × 3.5 µm in sporophorous vesicles.
RESULTS: The molecular analysis confirmed the presence of microsporidian DNA in the 8 samples (prevalence of 0.51%). Six samples (Brazilian larvae) were related to Polydispyrenia simulii and Caudospora palustris reference sequences but in separate clusters. One sample was clustered with Amblyospora spp. Edhazardia aedis was the positive control taxon.
CONCLUSIONS: Samples identified as Polydispyrenia spp. and Amblyospora spp. were grouped with P. simulii and Amblyospora spp., respectively, corroborating previous results. However, the 16S gene tree showed a considerable distance between the black fly-infecting Amblyospora spp. and the mosquito-infecting spp. This distance suggests that these two groups are not congeneric. Additional genomic region evaluation is necessary to obtain a coherent phylogeny for this group.

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Year:  2014        PMID: 25467266     DOI: 10.1590/0037-8682-0165-2014

Source DB:  PubMed          Journal:  Rev Soc Bras Med Trop        ISSN: 0037-8682            Impact factor:   1.581


  3 in total

1.  Ultrastructural characterization of Pleistophora macrozoarcidis Nigerelli 1946 (Microsporidia) infecting the ocean pout Macrozoarces americanus (Perciformes, Zoarcidae) from the gulf of Maine, MA, USA.

Authors:  Manal El-Garhy; Ann Cali; Kareem Morsy; Abdel-Rahman Bashtar; Saleh Al Quraishy
Journal:  Parasitol Res       Date:  2016-09-24       Impact factor: 2.289

2.  Ultrastructure, molecular phylogeny, and prevalence rates of Alternosema bostrichidis gen. nov. sp. nov. (Microsporidia, Terresporidia), a parasite of Prostephanus truncatus and Dinoderus spp. (Coleoptera, Bostrichidae).

Authors:  Jerzy J Lipa; Yuri S Tokarev; Irma V Issi
Journal:  Parasitol Res       Date:  2020-01-22       Impact factor: 2.289

3.  Molecular phylogeny of heritable symbionts and microbiota diversity analysis in phlebotominae sand flies and Culex nigripalpus from Colombia.

Authors:  Rafael J Vivero-Gomez; Víctor A Castañeda-Monsalve; María Claudia Atencia; Richard Hoyos-Lopez; Gregory D Hurst; Gloria Cadavid-Restrepo; Claudia Ximena Moreno-Herrera
Journal:  PLoS Negl Trop Dis       Date:  2021-12-20
  3 in total

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