Literature DB >> 29467241

Polar cell fate stimulates Wolbachia intracellular growth.

Ajit D Kamath1, Mark A Deehan1, Horacio M Frydman2,3.   

Abstract

Bacteria are crucial partners in the development and evolution of vertebrates and invertebrates. A large fraction of insects harbor Wolbachia, bacterial endosymbionts that manipulate host reproduction to favor their spreading. Because they are maternally inherited, Wolbachia are under selective pressure to reach the female germline and infect the offspring. However, Wolbachia infection is not limited to the germline. Somatic cell types, including stem cell niches, have higher Wolbachia loads compared with the surrounding tissue. Here, we show a novel Wolbachia tropism to polar cells (PCs), specialized somatic cells in the Drosophila ovary. During oogenesis, all stages of PC development are easily visualized, facilitating the investigation of the kinetics of Wolbachia intracellular growth. Wolbachia accumulation is triggered by particular events of PC morphogenesis, including differentiation from progenitors and between stages 8 and 9 of oogenesis. Moreover, induction of ectopic PC fate is sufficient to promote Wolbachia accumulation. We found that Wolbachia PC tropism is evolutionarily conserved across most Drosophila species, but not in Culex mosquitos. These findings highlight the coordination of endosymbiont tropism with host development and cell differentiation.
© 2018. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Drosophila oogenesis; Endosymbiont; Polar cell; Wolbachia

Mesh:

Year:  2018        PMID: 29467241      PMCID: PMC5897597          DOI: 10.1242/dev.158097

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  72 in total

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Authors:  Efrat Assa-Kunik; Isabel L Torres; Eyal D Schejter; Daniel St Johnston; Ben-Zion Shilo
Journal:  Development       Date:  2007-03       Impact factor: 6.868

4.  Polarization of both major body axes in Drosophila by gurken-torpedo signalling.

Authors:  A González-Reyes; H Elliott; D St Johnston
Journal:  Nature       Date:  1995-06-22       Impact factor: 49.962

5.  Tissue distribution and prevalence of Wolbachia infections in tsetse flies, Glossina spp.

Authors:  Q Cheng; T D Ruel; W Zhou; S K Moloo; P Majiwa; S L O'Neill; S Aksoy
Journal:  Med Vet Entomol       Date:  2000-03       Impact factor: 2.739

6.  Jak-STAT regulation of male germline stem cell establishment during Drosophila embryogenesis.

Authors:  X Rebecca Sheng; Trevor Posenau; Juliann J Gumulak-Smith; Erika Matunis; Mark Van Doren; Matthew Wawersik
Journal:  Dev Biol       Date:  2009-07-28       Impact factor: 3.582

7.  Genetic analysis of Drosophila sechellia specialization: oviposition behavior toward the major aliphatic acids of its host plant.

Authors:  M Amlou; B Moreteau; J R David
Journal:  Behav Genet       Date:  1998-11       Impact factor: 2.805

8.  Eyes absent, a key repressor of polar cell fate during Drosophila oogenesis.

Authors:  Jianwu Bai; Denise Montell
Journal:  Development       Date:  2002-12       Impact factor: 6.868

9.  Extreme divergence of Wolbachia tropism for the stem-cell-niche in the Drosophila testis.

Authors:  Michelle E Toomey; Horacio M Frydman
Journal:  PLoS Pathog       Date:  2014-12-18       Impact factor: 6.823

10.  A cellular basis for Wolbachia recruitment to the host germline.

Authors:  Laura R Serbus; William Sullivan
Journal:  PLoS Pathog       Date:  2007-12       Impact factor: 6.823

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  1 in total

1.  Wolbachia and host germline components compete for kinesin-mediated transport to the posterior pole of the Drosophila oocyte.

Authors:  Shelbi L Russell; Nassim Lemseffer; Pamela M White; William T Sullivan
Journal:  PLoS Pathog       Date:  2018-08-15       Impact factor: 6.823

  1 in total

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