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      Cospeciation of Psyllids and Their Primary Prokaryotic Endosymbionts

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      Applied and Environmental Microbiology
      American Society for Microbiology

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          Abstract

          Psyllids are plant sap-feeding insects that harbor prokaryotic endosymbionts in specialized cells within the body cavity. Four-kilobase DNA fragments containing 16S and 23S ribosomal DNA (rDNA) were amplified from the primary (P) endosymbiont of 32 species of psyllids representing three psyllid families and eight subfamilies. In addition, 0.54-kb fragments of the psyllid nuclear gene wingless were also amplified from 26 species. Phylogenetic trees derived from 16S-23S rDNA and from the host wingless gene are very similar, and tests of compatibility of the data sets show no significant conflict between host and endosymbiont phylogenies. This result is consistent with a single infection of a shared psyllid ancestor and subsequent cospeciation of the host and the endosymbiont. In addition, the phylogenies based on DNA sequences generally agreed with psyllid taxonomy based on morphology. The 3' end of the 16S rDNA of the P endosymbionts differs from that of other members of the domain Bacteria in the lack of a sequence complementary to the mRNA ribosome binding site. The rate of sequence change in the 16S-23S rDNA of the psyllid P endosymbiont was considerably higher than that of other bacteria, including other fast-evolving insect endosymbionts. The lineage consisting of the P endosymbionts of psyllids was given the designation Candidatus Carsonella (gen. nov.) with a single species, Candidatus Carsonella ruddii (sp. nov.).

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          Author and article information

          Journal
          Applied and Environmental Microbiology
          Applied and Environmental Microbiology
          American Society for Microbiology
          0099-2240
          July 01 2000
          July 01 2000
          : 66
          : 7
          : 2898-2905
          Article
          10.1128/AEM.66.7.2898-2905.2000
          92089
          10877784
          a6ede749-60ad-445d-ae04-2ab7457bc597
          © 2000
          History

          Molecular medicine,Neurosciences
          Molecular medicine, Neurosciences

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