Cargando…
Concurrent transcriptional profiling of Dirofilaria immitis and its Wolbachia endosymbiont throughout the nematode life cycle reveals coordinated gene expression
BACKGROUND: Dirofilaria immitis, or canine heartworm, is a filarial nematode parasite that infects dogs and other mammals worldwide. Current disease control relies on regular administration of anthelmintic preventives, however, relatively poor compliance and evidence of developing drug resistance co...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289336/ https://www.ncbi.nlm.nih.gov/pubmed/25433394 http://dx.doi.org/10.1186/1471-2164-15-1041 |
_version_ | 1782352096373243904 |
---|---|
author | Luck, Ashley N Evans, Christopher C Riggs, Molly D Foster, Jeremy M Moorhead, Andrew R Slatko, Barton E Michalski, Michelle L |
author_facet | Luck, Ashley N Evans, Christopher C Riggs, Molly D Foster, Jeremy M Moorhead, Andrew R Slatko, Barton E Michalski, Michelle L |
author_sort | Luck, Ashley N |
collection | PubMed |
description | BACKGROUND: Dirofilaria immitis, or canine heartworm, is a filarial nematode parasite that infects dogs and other mammals worldwide. Current disease control relies on regular administration of anthelmintic preventives, however, relatively poor compliance and evidence of developing drug resistance could warrant alternative measures against D. immitis and related human filarial infections be taken. As with many other filarial nematodes, D. immitis contains Wolbachia, an obligate bacterial endosymbiont thought to be involved in providing certain critical metabolites to the nematode. Correlations between nematode and Wolbachia transcriptomes during development have not been examined. Therefore, we detailed the developmental transcriptome of both D. immitis and its Wolbachia (wDi) in order to gain a better understanding of parasite-endosymbiont interactions throughout the nematode life cycle. RESULTS: Over 215 million single-end 50 bp reads were generated from total RNA from D. immitis adult males and females, microfilariae (mf) and third and fourth-stage larvae (L3 and L4). We critically evaluated the transcriptomes of the various life cycle stages to reveal sex-biased transcriptional patterns, as well as transcriptional differences between larval stages that may be involved in larval maturation. Hierarchical clustering revealed both D. immitis and wDi transcriptional activity in the L3 stage is clearly distinct from other life cycle stages. Interestingly, a large proportion of both D. immitis and wDi genes display microfilarial-biased transcriptional patterns. Concurrent transcriptome sequencing identified potential molecular interactions between parasite and endosymbiont that are more prominent during certain life cycle stages. In support of metabolite provisioning between filarial nematodes and Wolbachia, the synthesis of the critical metabolite, heme, by wDi appears to be synchronized in a stage-specific manner (mf-specific) with the production of heme-binding proteins in D. immitis. CONCLUSIONS: Our integrated transcriptomic study has highlighted interesting correlations between Wolbachia and D. immitis transcription throughout the life cycle and provided a resource that may be used for the development of novel intervention strategies, not only for the treatment and prevention of D. immitis infections, but of other closely related human parasites as well. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-1041) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4289336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42893362015-01-11 Concurrent transcriptional profiling of Dirofilaria immitis and its Wolbachia endosymbiont throughout the nematode life cycle reveals coordinated gene expression Luck, Ashley N Evans, Christopher C Riggs, Molly D Foster, Jeremy M Moorhead, Andrew R Slatko, Barton E Michalski, Michelle L BMC Genomics Research Article BACKGROUND: Dirofilaria immitis, or canine heartworm, is a filarial nematode parasite that infects dogs and other mammals worldwide. Current disease control relies on regular administration of anthelmintic preventives, however, relatively poor compliance and evidence of developing drug resistance could warrant alternative measures against D. immitis and related human filarial infections be taken. As with many other filarial nematodes, D. immitis contains Wolbachia, an obligate bacterial endosymbiont thought to be involved in providing certain critical metabolites to the nematode. Correlations between nematode and Wolbachia transcriptomes during development have not been examined. Therefore, we detailed the developmental transcriptome of both D. immitis and its Wolbachia (wDi) in order to gain a better understanding of parasite-endosymbiont interactions throughout the nematode life cycle. RESULTS: Over 215 million single-end 50 bp reads were generated from total RNA from D. immitis adult males and females, microfilariae (mf) and third and fourth-stage larvae (L3 and L4). We critically evaluated the transcriptomes of the various life cycle stages to reveal sex-biased transcriptional patterns, as well as transcriptional differences between larval stages that may be involved in larval maturation. Hierarchical clustering revealed both D. immitis and wDi transcriptional activity in the L3 stage is clearly distinct from other life cycle stages. Interestingly, a large proportion of both D. immitis and wDi genes display microfilarial-biased transcriptional patterns. Concurrent transcriptome sequencing identified potential molecular interactions between parasite and endosymbiont that are more prominent during certain life cycle stages. In support of metabolite provisioning between filarial nematodes and Wolbachia, the synthesis of the critical metabolite, heme, by wDi appears to be synchronized in a stage-specific manner (mf-specific) with the production of heme-binding proteins in D. immitis. CONCLUSIONS: Our integrated transcriptomic study has highlighted interesting correlations between Wolbachia and D. immitis transcription throughout the life cycle and provided a resource that may be used for the development of novel intervention strategies, not only for the treatment and prevention of D. immitis infections, but of other closely related human parasites as well. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-1041) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-29 /pmc/articles/PMC4289336/ /pubmed/25433394 http://dx.doi.org/10.1186/1471-2164-15-1041 Text en © Luck et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Luck, Ashley N Evans, Christopher C Riggs, Molly D Foster, Jeremy M Moorhead, Andrew R Slatko, Barton E Michalski, Michelle L Concurrent transcriptional profiling of Dirofilaria immitis and its Wolbachia endosymbiont throughout the nematode life cycle reveals coordinated gene expression |
title | Concurrent transcriptional profiling of Dirofilaria immitis and its Wolbachia endosymbiont throughout the nematode life cycle reveals coordinated gene expression |
title_full | Concurrent transcriptional profiling of Dirofilaria immitis and its Wolbachia endosymbiont throughout the nematode life cycle reveals coordinated gene expression |
title_fullStr | Concurrent transcriptional profiling of Dirofilaria immitis and its Wolbachia endosymbiont throughout the nematode life cycle reveals coordinated gene expression |
title_full_unstemmed | Concurrent transcriptional profiling of Dirofilaria immitis and its Wolbachia endosymbiont throughout the nematode life cycle reveals coordinated gene expression |
title_short | Concurrent transcriptional profiling of Dirofilaria immitis and its Wolbachia endosymbiont throughout the nematode life cycle reveals coordinated gene expression |
title_sort | concurrent transcriptional profiling of dirofilaria immitis and its wolbachia endosymbiont throughout the nematode life cycle reveals coordinated gene expression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289336/ https://www.ncbi.nlm.nih.gov/pubmed/25433394 http://dx.doi.org/10.1186/1471-2164-15-1041 |
work_keys_str_mv | AT luckashleyn concurrenttranscriptionalprofilingofdirofilariaimmitisanditswolbachiaendosymbiontthroughoutthenematodelifecyclerevealscoordinatedgeneexpression AT evanschristopherc concurrenttranscriptionalprofilingofdirofilariaimmitisanditswolbachiaendosymbiontthroughoutthenematodelifecyclerevealscoordinatedgeneexpression AT riggsmollyd concurrenttranscriptionalprofilingofdirofilariaimmitisanditswolbachiaendosymbiontthroughoutthenematodelifecyclerevealscoordinatedgeneexpression AT fosterjeremym concurrenttranscriptionalprofilingofdirofilariaimmitisanditswolbachiaendosymbiontthroughoutthenematodelifecyclerevealscoordinatedgeneexpression AT moorheadandrewr concurrenttranscriptionalprofilingofdirofilariaimmitisanditswolbachiaendosymbiontthroughoutthenematodelifecyclerevealscoordinatedgeneexpression AT slatkobartone concurrenttranscriptionalprofilingofdirofilariaimmitisanditswolbachiaendosymbiontthroughoutthenematodelifecyclerevealscoordinatedgeneexpression AT michalskimichellel concurrenttranscriptionalprofilingofdirofilariaimmitisanditswolbachiaendosymbiontthroughoutthenematodelifecyclerevealscoordinatedgeneexpression |