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The Transcriptome of Leishmania major Developmental Stages in Their Natural Sand Fly Vector

The life cycle of the Leishmania parasite in the sand fly vector involves differentiation into several distinctive forms, each thought to represent an adaptation to specific microenvironments in the midgut of the fly. Based on transcriptome sequencing (RNA-Seq) results, we describe the first high-re...

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Autores principales: Inbar, Ehud, Hughitt, V. Keith, Dillon, Laura A. L., Ghosh, Kashinath, El-Sayed, Najib M., Sacks, David L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380837/
https://www.ncbi.nlm.nih.gov/pubmed/28377524
http://dx.doi.org/10.1128/mBio.00029-17
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author Inbar, Ehud
Hughitt, V. Keith
Dillon, Laura A. L.
Ghosh, Kashinath
El-Sayed, Najib M.
Sacks, David L.
author_facet Inbar, Ehud
Hughitt, V. Keith
Dillon, Laura A. L.
Ghosh, Kashinath
El-Sayed, Najib M.
Sacks, David L.
author_sort Inbar, Ehud
collection PubMed
description The life cycle of the Leishmania parasite in the sand fly vector involves differentiation into several distinctive forms, each thought to represent an adaptation to specific microenvironments in the midgut of the fly. Based on transcriptome sequencing (RNA-Seq) results, we describe the first high-resolution analysis of the transcriptome dynamics of four distinct stages of Leishmania major as they develop in a natural vector, Phlebotomus duboscqi. The early transformation from tissue amastigotes to procyclic promastigotes in the blood-fed midgut was accompanied by the greatest number of differentially expressed genes, including the downregulation of amastins, and upregulation of multiple cell surface proteins, sugar and amino acid transporters, and genes related to glucose metabolism and cell cycle progression. The global changes accompanying post-blood meal differentiation of procyclic promastigotes to the nectomonad and metacyclic stages were less extensive, though each displayed a unique signature. The transcriptome of nectomonads, which has not been studied previously, revealed changes consistent with cell cycle arrest and the upregulation of genes associated with starvation and stress, including autophagic pathways of protein recycling. Maturation to the infective, metacyclic stage was accompanied by changes suggesting preadaptation to the intracellular environment of the mammalian host, demonstrated by the amastigote-like profiles of surface proteins and metabolism-related genes. Finally, a direct comparison between sand fly-derived and culture-derived metacyclics revealed a reassuring similarity between the two forms, with the in vivo forms distinguished mainly by a stronger upregulation of transcripts associated with nutrient stress.
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spelling pubmed-53808372017-04-12 The Transcriptome of Leishmania major Developmental Stages in Their Natural Sand Fly Vector Inbar, Ehud Hughitt, V. Keith Dillon, Laura A. L. Ghosh, Kashinath El-Sayed, Najib M. Sacks, David L. mBio Research Article The life cycle of the Leishmania parasite in the sand fly vector involves differentiation into several distinctive forms, each thought to represent an adaptation to specific microenvironments in the midgut of the fly. Based on transcriptome sequencing (RNA-Seq) results, we describe the first high-resolution analysis of the transcriptome dynamics of four distinct stages of Leishmania major as they develop in a natural vector, Phlebotomus duboscqi. The early transformation from tissue amastigotes to procyclic promastigotes in the blood-fed midgut was accompanied by the greatest number of differentially expressed genes, including the downregulation of amastins, and upregulation of multiple cell surface proteins, sugar and amino acid transporters, and genes related to glucose metabolism and cell cycle progression. The global changes accompanying post-blood meal differentiation of procyclic promastigotes to the nectomonad and metacyclic stages were less extensive, though each displayed a unique signature. The transcriptome of nectomonads, which has not been studied previously, revealed changes consistent with cell cycle arrest and the upregulation of genes associated with starvation and stress, including autophagic pathways of protein recycling. Maturation to the infective, metacyclic stage was accompanied by changes suggesting preadaptation to the intracellular environment of the mammalian host, demonstrated by the amastigote-like profiles of surface proteins and metabolism-related genes. Finally, a direct comparison between sand fly-derived and culture-derived metacyclics revealed a reassuring similarity between the two forms, with the in vivo forms distinguished mainly by a stronger upregulation of transcripts associated with nutrient stress. American Society for Microbiology 2017-04-04 /pmc/articles/PMC5380837/ /pubmed/28377524 http://dx.doi.org/10.1128/mBio.00029-17 Text en Copyright © 2017 Inbar et al. http://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 (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Inbar, Ehud
Hughitt, V. Keith
Dillon, Laura A. L.
Ghosh, Kashinath
El-Sayed, Najib M.
Sacks, David L.
The Transcriptome of Leishmania major Developmental Stages in Their Natural Sand Fly Vector
title The Transcriptome of Leishmania major Developmental Stages in Their Natural Sand Fly Vector
title_full The Transcriptome of Leishmania major Developmental Stages in Their Natural Sand Fly Vector
title_fullStr The Transcriptome of Leishmania major Developmental Stages in Their Natural Sand Fly Vector
title_full_unstemmed The Transcriptome of Leishmania major Developmental Stages in Their Natural Sand Fly Vector
title_short The Transcriptome of Leishmania major Developmental Stages in Their Natural Sand Fly Vector
title_sort transcriptome of leishmania major developmental stages in their natural sand fly vector
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380837/
https://www.ncbi.nlm.nih.gov/pubmed/28377524
http://dx.doi.org/10.1128/mBio.00029-17
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