Cargando…
A Tangled Web: Origins of Reproductive Parasitism
While typically a flea parasite and opportunistic human pathogen, the presence of Rickettsia felis (strain LSU-Lb) in the non-blood-feeding, parthenogenetically reproducing booklouse, Liposcelis bostrychophila, provides a system to ascertain factors governing not only host transitions but also oblig...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133264/ https://www.ncbi.nlm.nih.gov/pubmed/30060072 http://dx.doi.org/10.1093/gbe/evy159 |
_version_ | 1783354484841250816 |
---|---|
author | Gillespie, Joseph J Driscoll, Timothy P Verhoeve, Victoria I Rahman, Mohammed Sayeedur Macaluso, Kevin R Azad, Abdu F |
author_facet | Gillespie, Joseph J Driscoll, Timothy P Verhoeve, Victoria I Rahman, Mohammed Sayeedur Macaluso, Kevin R Azad, Abdu F |
author_sort | Gillespie, Joseph J |
collection | PubMed |
description | While typically a flea parasite and opportunistic human pathogen, the presence of Rickettsia felis (strain LSU-Lb) in the non-blood-feeding, parthenogenetically reproducing booklouse, Liposcelis bostrychophila, provides a system to ascertain factors governing not only host transitions but also obligate reproductive parasitism (RP). Analysis of plasmid pLbAR, unique to R. felis str. LSU-Lb, revealed a toxin–antitoxin module with similar features to prophage-encoded toxin–antitoxin modules utilized by parasitic Wolbachia strains to induce another form of RP, cytoplasmic incompatibility, in their arthropod hosts. Curiously, multiple deubiquitinase and nuclease domains of the large (3,841 aa) pLbAR toxin, as well the entire antitoxin, facilitated the detection of an assortment of related proteins from diverse intracellular bacteria, including other reproductive parasites. Our description of these remarkable components of the intracellular mobilome, including their presence in certain arthropod genomes, lends insight on the evolution of RP, while invigorating research on parasite-mediated biocontrol of arthropod-borne viral and bacterial pathogens. |
format | Online Article Text |
id | pubmed-6133264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61332642018-09-14 A Tangled Web: Origins of Reproductive Parasitism Gillespie, Joseph J Driscoll, Timothy P Verhoeve, Victoria I Rahman, Mohammed Sayeedur Macaluso, Kevin R Azad, Abdu F Genome Biol Evol Research Article While typically a flea parasite and opportunistic human pathogen, the presence of Rickettsia felis (strain LSU-Lb) in the non-blood-feeding, parthenogenetically reproducing booklouse, Liposcelis bostrychophila, provides a system to ascertain factors governing not only host transitions but also obligate reproductive parasitism (RP). Analysis of plasmid pLbAR, unique to R. felis str. LSU-Lb, revealed a toxin–antitoxin module with similar features to prophage-encoded toxin–antitoxin modules utilized by parasitic Wolbachia strains to induce another form of RP, cytoplasmic incompatibility, in their arthropod hosts. Curiously, multiple deubiquitinase and nuclease domains of the large (3,841 aa) pLbAR toxin, as well the entire antitoxin, facilitated the detection of an assortment of related proteins from diverse intracellular bacteria, including other reproductive parasites. Our description of these remarkable components of the intracellular mobilome, including their presence in certain arthropod genomes, lends insight on the evolution of RP, while invigorating research on parasite-mediated biocontrol of arthropod-borne viral and bacterial pathogens. Oxford University Press 2018-07-27 /pmc/articles/PMC6133264/ /pubmed/30060072 http://dx.doi.org/10.1093/gbe/evy159 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Gillespie, Joseph J Driscoll, Timothy P Verhoeve, Victoria I Rahman, Mohammed Sayeedur Macaluso, Kevin R Azad, Abdu F A Tangled Web: Origins of Reproductive Parasitism |
title | A Tangled Web: Origins of Reproductive Parasitism |
title_full | A Tangled Web: Origins of Reproductive Parasitism |
title_fullStr | A Tangled Web: Origins of Reproductive Parasitism |
title_full_unstemmed | A Tangled Web: Origins of Reproductive Parasitism |
title_short | A Tangled Web: Origins of Reproductive Parasitism |
title_sort | tangled web: origins of reproductive parasitism |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133264/ https://www.ncbi.nlm.nih.gov/pubmed/30060072 http://dx.doi.org/10.1093/gbe/evy159 |
work_keys_str_mv | AT gillespiejosephj atangledweboriginsofreproductiveparasitism AT driscolltimothyp atangledweboriginsofreproductiveparasitism AT verhoevevictoriai atangledweboriginsofreproductiveparasitism AT rahmanmohammedsayeedur atangledweboriginsofreproductiveparasitism AT macalusokevinr atangledweboriginsofreproductiveparasitism AT azadabduf atangledweboriginsofreproductiveparasitism AT gillespiejosephj tangledweboriginsofreproductiveparasitism AT driscolltimothyp tangledweboriginsofreproductiveparasitism AT verhoevevictoriai tangledweboriginsofreproductiveparasitism AT rahmanmohammedsayeedur tangledweboriginsofreproductiveparasitism AT macalusokevinr tangledweboriginsofreproductiveparasitism AT azadabduf tangledweboriginsofreproductiveparasitism |