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Differential Expression Profiles in the Midgut of Triatoma infestans Infected with Trypanosoma cruzi

Chagas disease, or American trypanosomiasis, is a parasitic disease caused by the protozoan Trypanosoma cruzi and is transmitted by insects from the Triatominae subfamily. To identify components involved in the protozoan-vector relationship, we constructed and analyzed cDNA libraries from RNA isolat...

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Autores principales: Buarque, Diego S., Braz, Glória R. C., Martins, Rafael M., Tanaka-Azevedo, Anita M., Gomes, Cícera M., Oliveira, Felipe A. A., Schenkman, Sergio, Tanaka, Aparecida S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642171/
https://www.ncbi.nlm.nih.gov/pubmed/23658688
http://dx.doi.org/10.1371/journal.pone.0061203
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author Buarque, Diego S.
Braz, Glória R. C.
Martins, Rafael M.
Tanaka-Azevedo, Anita M.
Gomes, Cícera M.
Oliveira, Felipe A. A.
Schenkman, Sergio
Tanaka, Aparecida S.
author_facet Buarque, Diego S.
Braz, Glória R. C.
Martins, Rafael M.
Tanaka-Azevedo, Anita M.
Gomes, Cícera M.
Oliveira, Felipe A. A.
Schenkman, Sergio
Tanaka, Aparecida S.
author_sort Buarque, Diego S.
collection PubMed
description Chagas disease, or American trypanosomiasis, is a parasitic disease caused by the protozoan Trypanosoma cruzi and is transmitted by insects from the Triatominae subfamily. To identify components involved in the protozoan-vector relationship, we constructed and analyzed cDNA libraries from RNA isolated from the midguts of uninfected and T. cruzi-infected Triatoma infestans, which are major vectors of Chagas disease. We generated approximately 440 high-quality Expressed Sequence Tags (ESTs) from each T. infestans midgut cDNA library. The sequences were grouped in 380 clusters, representing an average length of 664.78 base pairs (bp). Many clusters were not classified functionally, representing unknown transcripts. Several transcripts involved in different processes (e.g., detoxification) showed differential expression in response to T. cruzi infection. Lysozyme, cathepsin D, a nitrophorin-like protein and a putative 14 kDa protein were significantly upregulated upon infection, whereas thioredoxin reductase was downregulated. In addition, we identified several transcripts related to metabolic processes or immunity with unchanged expressions, including infestin, lipocalins and defensins. We also detected ESTs encoding juvenile hormone binding protein (JHBP), which seems to be involved in insect development and could be a target in control strategies for the vector. This work demonstrates differential gene expression upon T. cruzi infection in the midgut of T. infestans. These data expand the current knowledge regarding vector-parasite interactions for Chagas disease.
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spelling pubmed-36421712013-05-08 Differential Expression Profiles in the Midgut of Triatoma infestans Infected with Trypanosoma cruzi Buarque, Diego S. Braz, Glória R. C. Martins, Rafael M. Tanaka-Azevedo, Anita M. Gomes, Cícera M. Oliveira, Felipe A. A. Schenkman, Sergio Tanaka, Aparecida S. PLoS One Research Article Chagas disease, or American trypanosomiasis, is a parasitic disease caused by the protozoan Trypanosoma cruzi and is transmitted by insects from the Triatominae subfamily. To identify components involved in the protozoan-vector relationship, we constructed and analyzed cDNA libraries from RNA isolated from the midguts of uninfected and T. cruzi-infected Triatoma infestans, which are major vectors of Chagas disease. We generated approximately 440 high-quality Expressed Sequence Tags (ESTs) from each T. infestans midgut cDNA library. The sequences were grouped in 380 clusters, representing an average length of 664.78 base pairs (bp). Many clusters were not classified functionally, representing unknown transcripts. Several transcripts involved in different processes (e.g., detoxification) showed differential expression in response to T. cruzi infection. Lysozyme, cathepsin D, a nitrophorin-like protein and a putative 14 kDa protein were significantly upregulated upon infection, whereas thioredoxin reductase was downregulated. In addition, we identified several transcripts related to metabolic processes or immunity with unchanged expressions, including infestin, lipocalins and defensins. We also detected ESTs encoding juvenile hormone binding protein (JHBP), which seems to be involved in insect development and could be a target in control strategies for the vector. This work demonstrates differential gene expression upon T. cruzi infection in the midgut of T. infestans. These data expand the current knowledge regarding vector-parasite interactions for Chagas disease. Public Library of Science 2013-05-02 /pmc/articles/PMC3642171/ /pubmed/23658688 http://dx.doi.org/10.1371/journal.pone.0061203 Text en © 2013 Buarque et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Buarque, Diego S.
Braz, Glória R. C.
Martins, Rafael M.
Tanaka-Azevedo, Anita M.
Gomes, Cícera M.
Oliveira, Felipe A. A.
Schenkman, Sergio
Tanaka, Aparecida S.
Differential Expression Profiles in the Midgut of Triatoma infestans Infected with Trypanosoma cruzi
title Differential Expression Profiles in the Midgut of Triatoma infestans Infected with Trypanosoma cruzi
title_full Differential Expression Profiles in the Midgut of Triatoma infestans Infected with Trypanosoma cruzi
title_fullStr Differential Expression Profiles in the Midgut of Triatoma infestans Infected with Trypanosoma cruzi
title_full_unstemmed Differential Expression Profiles in the Midgut of Triatoma infestans Infected with Trypanosoma cruzi
title_short Differential Expression Profiles in the Midgut of Triatoma infestans Infected with Trypanosoma cruzi
title_sort differential expression profiles in the midgut of triatoma infestans infected with trypanosoma cruzi
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642171/
https://www.ncbi.nlm.nih.gov/pubmed/23658688
http://dx.doi.org/10.1371/journal.pone.0061203
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