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Tissue-specific transcriptomics and proteomics of a filarial nematode and its Wolbachia endosymbiont

BACKGROUND: Filarial nematodes cause debilitating human diseases. While treatable, recent evidence suggests drug resistance is developing, necessitating the development of novel targets and new treatment options. Although transcriptomic and proteomic studies around the nematode life cycle have great...

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Autores principales: Luck, Ashley N., Anderson, Kathryn G., McClung, Colleen M., VerBerkmoes, Nathan C., Foster, Jeremy M., Michalski, Michelle L., Slatko, Barton E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642636/
https://www.ncbi.nlm.nih.gov/pubmed/26559510
http://dx.doi.org/10.1186/s12864-015-2083-2
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author Luck, Ashley N.
Anderson, Kathryn G.
McClung, Colleen M.
VerBerkmoes, Nathan C.
Foster, Jeremy M.
Michalski, Michelle L.
Slatko, Barton E.
author_facet Luck, Ashley N.
Anderson, Kathryn G.
McClung, Colleen M.
VerBerkmoes, Nathan C.
Foster, Jeremy M.
Michalski, Michelle L.
Slatko, Barton E.
author_sort Luck, Ashley N.
collection PubMed
description BACKGROUND: Filarial nematodes cause debilitating human diseases. While treatable, recent evidence suggests drug resistance is developing, necessitating the development of novel targets and new treatment options. Although transcriptomic and proteomic studies around the nematode life cycle have greatly enhanced our knowledge, whole organism approaches have not provided spatial resolution of gene expression, which can be gained by examining individual tissues. Generally, due to their small size, tissue dissection of human-infecting filarial nematodes remains extremely challenging. However, canine heartworm disease is caused by a closely related and much larger filarial nematode, Dirofilaria immitis. As with many other filarial nematodes, D. immitis contains Wolbachia, an obligate bacterial endosymbiont present in the hypodermis and developing oocytes within the uterus. Here, we describe the first concurrent tissue-specific transcriptomic and proteomic profiling of a filarial nematode (D. immitis) and its Wolbachia (wDi) in order to better understand tissue functions and identify tissue-specific antigens that may be used for the development of new diagnostic and therapeutic tools. METHODS: Adult D. immitis worms were dissected into female body wall (FBW), female uterus (FU), female intestine (FI), female head (FH), male body wall (MBW), male testis (MT), male intestine (MI), male head (MH) and 10.1186/s12864-015-2083-2 male spicule (MS) and used to prepare transcriptomic and proteomic libraries. RESULTS: Transcriptomic and proteomic analysis of several D. immitis tissues identified many biological functions enriched within certain tissues. Hierarchical clustering of the D. immitis tissue transcriptomes, along with the recently published whole-worm adult male and female D. immitis transcriptomes, revealed that the whole-worm transcriptome is typically dominated by transcripts originating from reproductive tissue. The uterus appeared to have the most variable transcriptome, possibly due to age. Although many functions are shared between the reproductive tissues, the most significant differences in gene expression were observed between the uterus and testis. Interestingly, wDi gene expression in the male and female body wall is fairly similar, yet slightly different to that of Wolbachia gene expression in the uterus. Proteomic methods verified 32 % of the predicted D. immitis proteome, including over 700 hypothetical proteins of D. immitis. Of note, hypothetical proteins were among some of the most abundant Wolbachia proteins identified, which may fulfill some important yet still uncharacterized biological function. CONCLUSIONS: The spatial resolution gained from this parallel transcriptomic and proteomic analysis adds to our understanding of filarial biology and serves as a resource with which to develop future therapeutic strategies against filarial nematodes and their Wolbachia endosymbionts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2083-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-46426362015-11-13 Tissue-specific transcriptomics and proteomics of a filarial nematode and its Wolbachia endosymbiont Luck, Ashley N. Anderson, Kathryn G. McClung, Colleen M. VerBerkmoes, Nathan C. Foster, Jeremy M. Michalski, Michelle L. Slatko, Barton E. BMC Genomics Research Article BACKGROUND: Filarial nematodes cause debilitating human diseases. While treatable, recent evidence suggests drug resistance is developing, necessitating the development of novel targets and new treatment options. Although transcriptomic and proteomic studies around the nematode life cycle have greatly enhanced our knowledge, whole organism approaches have not provided spatial resolution of gene expression, which can be gained by examining individual tissues. Generally, due to their small size, tissue dissection of human-infecting filarial nematodes remains extremely challenging. However, canine heartworm disease is caused by a closely related and much larger filarial nematode, Dirofilaria immitis. As with many other filarial nematodes, D. immitis contains Wolbachia, an obligate bacterial endosymbiont present in the hypodermis and developing oocytes within the uterus. Here, we describe the first concurrent tissue-specific transcriptomic and proteomic profiling of a filarial nematode (D. immitis) and its Wolbachia (wDi) in order to better understand tissue functions and identify tissue-specific antigens that may be used for the development of new diagnostic and therapeutic tools. METHODS: Adult D. immitis worms were dissected into female body wall (FBW), female uterus (FU), female intestine (FI), female head (FH), male body wall (MBW), male testis (MT), male intestine (MI), male head (MH) and 10.1186/s12864-015-2083-2 male spicule (MS) and used to prepare transcriptomic and proteomic libraries. RESULTS: Transcriptomic and proteomic analysis of several D. immitis tissues identified many biological functions enriched within certain tissues. Hierarchical clustering of the D. immitis tissue transcriptomes, along with the recently published whole-worm adult male and female D. immitis transcriptomes, revealed that the whole-worm transcriptome is typically dominated by transcripts originating from reproductive tissue. The uterus appeared to have the most variable transcriptome, possibly due to age. Although many functions are shared between the reproductive tissues, the most significant differences in gene expression were observed between the uterus and testis. Interestingly, wDi gene expression in the male and female body wall is fairly similar, yet slightly different to that of Wolbachia gene expression in the uterus. Proteomic methods verified 32 % of the predicted D. immitis proteome, including over 700 hypothetical proteins of D. immitis. Of note, hypothetical proteins were among some of the most abundant Wolbachia proteins identified, which may fulfill some important yet still uncharacterized biological function. CONCLUSIONS: The spatial resolution gained from this parallel transcriptomic and proteomic analysis adds to our understanding of filarial biology and serves as a resource with which to develop future therapeutic strategies against filarial nematodes and their Wolbachia endosymbionts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2083-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-11 /pmc/articles/PMC4642636/ /pubmed/26559510 http://dx.doi.org/10.1186/s12864-015-2083-2 Text en © Luck et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
Anderson, Kathryn G.
McClung, Colleen M.
VerBerkmoes, Nathan C.
Foster, Jeremy M.
Michalski, Michelle L.
Slatko, Barton E.
Tissue-specific transcriptomics and proteomics of a filarial nematode and its Wolbachia endosymbiont
title Tissue-specific transcriptomics and proteomics of a filarial nematode and its Wolbachia endosymbiont
title_full Tissue-specific transcriptomics and proteomics of a filarial nematode and its Wolbachia endosymbiont
title_fullStr Tissue-specific transcriptomics and proteomics of a filarial nematode and its Wolbachia endosymbiont
title_full_unstemmed Tissue-specific transcriptomics and proteomics of a filarial nematode and its Wolbachia endosymbiont
title_short Tissue-specific transcriptomics and proteomics of a filarial nematode and its Wolbachia endosymbiont
title_sort tissue-specific transcriptomics and proteomics of a filarial nematode and its wolbachia endosymbiont
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642636/
https://www.ncbi.nlm.nih.gov/pubmed/26559510
http://dx.doi.org/10.1186/s12864-015-2083-2
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