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      New Insights into the Evolution of Wolbachia Infections in Filarial Nematodes Inferred from a Large Range of Screened Species

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          Abstract

          Background

          Wolbachia are intriguing symbiotic endobacteria with a peculiar host range that includes arthropods and a single nematode family, the Onchocercidae encompassing agents of filariases. This raises the question of the origin of infection in filariae. Wolbachia infect the female germline and the hypodermis. Some evidences lead to the theory that Wolbachia act as mutualist and coevolved with filariae from one infection event: their removal sterilizes female filariae; all the specimens of a positive species are infected; Wolbachia are vertically inherited; a few species lost the symbiont. However, most data on Wolbachia and filaria relationships derive from studies on few species of Onchocercinae and Dirofilariinae, from mammals.

          Methodology/Principal Findings

          We investigated the Wolbachia distribution testing 35 filarial species, including 28 species and 7 genera and/or subgenera newly screened, using PCR, immunohistochemical staining, whole mount fluorescent analysis, and cocladogenesis analysis. (i) Among the newly screened Onchocercinae from mammals eight species harbour Wolbachia but for some of them, bacteria are absent in the hypodermis, or in variable density. (ii) Wolbachia are not detected in the pathological model Monanema martini and in 8, upon 9, species of Cercopithifilaria. (iii) Supergroup F Wolbachia is identified in two newly screened Mansonella species and in Cercopithifilaria japonica. (iv) Type F Wolbachia infect the intestinal cells and somatic female genital tract. (v) Among Oswaldofilariinae, Waltonellinae and Splendidofilariinae, from saurian, anuran and bird respectively, Wolbachia are not detected.

          Conclusions/Significance

          The absence of Wolbachia in 63% of onchocercids, notably in the ancestral Oswaldofilariinae estimated 140 mya old, the diverse tissues or specimens distribution, and a recent lateral transfer in supergroup F Wolbachia, modify the current view on the role and evolution of the endosymbiont and their hosts. Further genomic analyses on some of the newly sampled species are welcomed to decipher the open questions.

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          Analyzing the mosaic structure of genes.

          Some genes in prokaryotes consist of a mosaic of regions derived from different ancestors by horizontal gene transfer. A method is described for demonstrating the statistical significance of such mosaic structure and for locating the crossover points separating different regions.
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            A modified bootscan algorithm for automated identification of recombinant sequences and recombination breakpoints.

            We have developed a modified BOOTSCAN algorithm that may be used to screen nucleotide sequence alignments for evidence of recombination without prior identification of nonrecombinant reference sequences. The algorithm is fast and includes a Bonferroni corrected statistical test of recombination to circumvent the multiple testing problems encountered when using the BOOTSCAN method to explore alignments for evidence of recombination. Using both simulated and real datasets we demonstrate that the modified algorithm is more powerful than other phylogenetic recombination detection methods and performs almost as well as one of the best substitution distribution recombination detection methods.
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              Widespread lateral gene transfer from intracellular bacteria to multicellular eukaryotes.

              Although common among bacteria, lateral gene transfer-the movement of genes between distantly related organisms-is thought to occur only rarely between bacteria and multicellular eukaryotes. However, the presence of endosymbionts, such as Wolbachia pipientis, within some eukaryotic germlines may facilitate bacterial gene transfers to eukaryotic host genomes. We therefore examined host genomes for evidence of gene transfer events from Wolbachia bacteria to their hosts. We found and confirmed transfers into the genomes of four insect and four nematode species that range from nearly the entire Wolbachia genome (>1 megabase) to short (<500 base pairs) insertions. Potential Wolbachia-to-host transfers were also detected computationally in three additional sequenced insect genomes. We also show that some of these inserted Wolbachia genes are transcribed within eukaryotic cells lacking endosymbionts. Therefore, heritable lateral gene transfer occurs into eukaryotic hosts from their prokaryote symbionts, potentially providing a mechanism for acquisition of new genes and functions.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2011
                22 June 2011
                : 6
                : 6
                : e20843
                Affiliations
                [1 ]Dipartimento di Biotecnologie e Bioscienze, Università degli Studi di Milano Bicocca, Milano, Italy
                [2 ]Parasitologie Comparée UMR 7205 CNRS & UMR 7245 CNRS, Muséum National d'Histoire Naturelle, Paris, France
                [3 ]School of Biological Sciences, University of Sydney, Sidney, Australia
                [4 ]Department of Medical Zoology, Osaka City University Medical School, Osaka, Japan
                [5 ]Department of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, United States of America
                [6 ]Instituto de Zoologia Tropical, Universidad Central de Venezuela, Caracas, Venezuela
                [7 ]Departamento de Zoologia, Universidade Federal de Juiz de Fora, Minas Geraes, Brasil
                [8 ]Dipartimento di Patologia Animale, Igiene e Sanità Pubblica Veterinaria, Università degli Studi di Milano, Milano, Italy
                [9 ]Research Foundation in Tropical Diseases and Environment, Buea, Cameroun
                [10 ]Département de Biologie Animale, Université Cheikh Anta Diop de Dakar, Dakar, Sénégal
                Agency for Science, Technology and Research - Singapore Immunology Network, Singapore
                Author notes

                Conceived and designed the experiments: MC OB. Performed the experiments: EF OB MB CM SU FL SGB RG SdSL SW MD MC. Analyzed the data: EF OB MB CM NL SU FL RG SdSL CB MC. Contributed reagents/materials/analysis tools: EF OB MB CM NL SU FL SGB RG CB SW MD. Wrote the paper: EF OB FL CB MC.

                Article
                PONE-D-11-03688
                10.1371/journal.pone.0020843
                3120775
                21731626
                7306e0be-936c-44db-a9d8-cb3a016df1a5
                Ferri et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 22 February 2011
                : 10 May 2011
                Page count
                Pages: 17
                Categories
                Research Article
                Biology
                Evolutionary Biology
                Evolutionary Processes
                Coevolution
                Organismal Evolution
                Animal Evolution
                Microbial Evolution
                Evolutionary Ecology
                Evolutionary Genetics

                Uncategorized
                Uncategorized

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