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Plasmodium berghei PIMMS2 Promotes Ookinete Invasion of the Anopheles gambiae Mosquito Midgut

Mosquito midgut stages of the malaria parasite present an attractive biological system to study host-parasite interactions and develop interventions to block disease transmission. Mosquito infection ensues upon oocyst development that follows ookinete invasion and traversal of the mosquito midgut ep...

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Autores principales: Ukegbu, Chiamaka V., Akinosoglou, Karolina A., Christophides, George K., Vlachou, Dina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520436/
https://www.ncbi.nlm.nih.gov/pubmed/28559405
http://dx.doi.org/10.1128/IAI.00139-17
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author Ukegbu, Chiamaka V.
Akinosoglou, Karolina A.
Christophides, George K.
Vlachou, Dina
author_facet Ukegbu, Chiamaka V.
Akinosoglou, Karolina A.
Christophides, George K.
Vlachou, Dina
author_sort Ukegbu, Chiamaka V.
collection PubMed
description Mosquito midgut stages of the malaria parasite present an attractive biological system to study host-parasite interactions and develop interventions to block disease transmission. Mosquito infection ensues upon oocyst development that follows ookinete invasion and traversal of the mosquito midgut epithelium. Here, we report the characterization of PIMMS2 (Plasmodium invasion of mosquito midgut screen candidate 2), a Plasmodium berghei protein with structural similarities to subtilisin-like proteins. PIMMS2 orthologs are present in the genomes of all plasmodia and are mapped between the subtilisin-encoding genes SUB1 and SUB3. P. berghei PIMMS2 is specifically expressed in zygotes and ookinetes and is localized on the ookinete surface. Loss of PIMMS2 function through gene disruption by homologous recombination leads to normal development of motile ookinetes that exhibit a severely impaired capacity to traverse the mosquito midgut and transform to oocysts. Genetic complementation of the disrupted locus with a mutated PIMMS2 allele reveals that amino acid residues corresponding to the putative subtilisin-like catalytic triad are important but not essential for protein function. Our data demonstrate that PIMMS2 is a novel ookinete-specific protein that promotes parasite traversal of the mosquito midgut epithelium and establishment of mosquito infection.
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spelling pubmed-55204362017-07-31 Plasmodium berghei PIMMS2 Promotes Ookinete Invasion of the Anopheles gambiae Mosquito Midgut Ukegbu, Chiamaka V. Akinosoglou, Karolina A. Christophides, George K. Vlachou, Dina Infect Immun Cellular Microbiology: Pathogen-Host Cell Molecular Interactions Mosquito midgut stages of the malaria parasite present an attractive biological system to study host-parasite interactions and develop interventions to block disease transmission. Mosquito infection ensues upon oocyst development that follows ookinete invasion and traversal of the mosquito midgut epithelium. Here, we report the characterization of PIMMS2 (Plasmodium invasion of mosquito midgut screen candidate 2), a Plasmodium berghei protein with structural similarities to subtilisin-like proteins. PIMMS2 orthologs are present in the genomes of all plasmodia and are mapped between the subtilisin-encoding genes SUB1 and SUB3. P. berghei PIMMS2 is specifically expressed in zygotes and ookinetes and is localized on the ookinete surface. Loss of PIMMS2 function through gene disruption by homologous recombination leads to normal development of motile ookinetes that exhibit a severely impaired capacity to traverse the mosquito midgut and transform to oocysts. Genetic complementation of the disrupted locus with a mutated PIMMS2 allele reveals that amino acid residues corresponding to the putative subtilisin-like catalytic triad are important but not essential for protein function. Our data demonstrate that PIMMS2 is a novel ookinete-specific protein that promotes parasite traversal of the mosquito midgut epithelium and establishment of mosquito infection. American Society for Microbiology 2017-07-19 /pmc/articles/PMC5520436/ /pubmed/28559405 http://dx.doi.org/10.1128/IAI.00139-17 Text en Copyright © 2017 Ukegbu et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Cellular Microbiology: Pathogen-Host Cell Molecular Interactions
Ukegbu, Chiamaka V.
Akinosoglou, Karolina A.
Christophides, George K.
Vlachou, Dina
Plasmodium berghei PIMMS2 Promotes Ookinete Invasion of the Anopheles gambiae Mosquito Midgut
title Plasmodium berghei PIMMS2 Promotes Ookinete Invasion of the Anopheles gambiae Mosquito Midgut
title_full Plasmodium berghei PIMMS2 Promotes Ookinete Invasion of the Anopheles gambiae Mosquito Midgut
title_fullStr Plasmodium berghei PIMMS2 Promotes Ookinete Invasion of the Anopheles gambiae Mosquito Midgut
title_full_unstemmed Plasmodium berghei PIMMS2 Promotes Ookinete Invasion of the Anopheles gambiae Mosquito Midgut
title_short Plasmodium berghei PIMMS2 Promotes Ookinete Invasion of the Anopheles gambiae Mosquito Midgut
title_sort plasmodium berghei pimms2 promotes ookinete invasion of the anopheles gambiae mosquito midgut
topic Cellular Microbiology: Pathogen-Host Cell Molecular Interactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520436/
https://www.ncbi.nlm.nih.gov/pubmed/28559405
http://dx.doi.org/10.1128/IAI.00139-17
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