Cargando…

Comparative proteomics of the vector Dermacentor reticulatus revealed differentially regulated proteins associated with pathogen transmission in response to laboratory infection with Rickettsia slovaca

BACKGROUND: Tick-borne rickettsial diseases are caused by pathogens acquired from hard ticks. In particular, Rickettsia slovaca, a zoonotic infectious bacterium causing tick-borne lymphadenopathy (TIBOLA), is transmitted by the vectors Dermacentor spp. that can be found all over Europe. Although rec...

Descripción completa

Detalles Bibliográficos
Autores principales: Flores-Ramirez, Gabriela, Sallay, Balázs, Danchenko, Maksym, Lakhneko, Olha, Špitalská, Eva, Skultety, Ludovit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591964/
https://www.ncbi.nlm.nih.gov/pubmed/31234913
http://dx.doi.org/10.1186/s13071-019-3564-y
_version_ 1783429816824889344
author Flores-Ramirez, Gabriela
Sallay, Balázs
Danchenko, Maksym
Lakhneko, Olha
Špitalská, Eva
Skultety, Ludovit
author_facet Flores-Ramirez, Gabriela
Sallay, Balázs
Danchenko, Maksym
Lakhneko, Olha
Špitalská, Eva
Skultety, Ludovit
author_sort Flores-Ramirez, Gabriela
collection PubMed
description BACKGROUND: Tick-borne rickettsial diseases are caused by pathogens acquired from hard ticks. In particular, Rickettsia slovaca, a zoonotic infectious bacterium causing tick-borne lymphadenopathy (TIBOLA), is transmitted by the vectors Dermacentor spp. that can be found all over Europe. Although recent studies point out the extreme complexity of bacteria-induced effects in these blood-feeding vectors, the knowledge of individual molecules involved in the preservation and transmission of the pathogen is still limited. System biology tools, including proteomics, may contribute greatly to the understanding of pathogen-tick-host interactions. METHODS: Herein, we performed a comparative proteomics study of the tick vector Dermacentor reticulatus that was experimentally infected with the endosymbiotic bacterium R. slovaca. Rickettsia-free ticks, collected in the southern region of Slovakia, were infected with the bacterium by a capillary tube-feeding system, and the dynamics of infection was assessed by quantitative PCR method after 5, 10, 15 and 27 days. RESULTS: At the stage of controlled proliferation (at 27 dpi), 33 (from 481 profiled) differentially abundant protein spots were detected on a two-dimensional gel. From the aforementioned protein spots, 21 were successfully identified by tandem mass spectrometry. CONCLUSIONS: Although a few discovered proteins were described as having structural or housekeeping functions, the vast majority of the affected proteins were suggested to be essential for tick attachment and feeding on the host, host immune system evasion and defensive response modulation to ensure successful pathogen transmission. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-019-3564-y) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6591964
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-65919642019-07-08 Comparative proteomics of the vector Dermacentor reticulatus revealed differentially regulated proteins associated with pathogen transmission in response to laboratory infection with Rickettsia slovaca Flores-Ramirez, Gabriela Sallay, Balázs Danchenko, Maksym Lakhneko, Olha Špitalská, Eva Skultety, Ludovit Parasit Vectors Research BACKGROUND: Tick-borne rickettsial diseases are caused by pathogens acquired from hard ticks. In particular, Rickettsia slovaca, a zoonotic infectious bacterium causing tick-borne lymphadenopathy (TIBOLA), is transmitted by the vectors Dermacentor spp. that can be found all over Europe. Although recent studies point out the extreme complexity of bacteria-induced effects in these blood-feeding vectors, the knowledge of individual molecules involved in the preservation and transmission of the pathogen is still limited. System biology tools, including proteomics, may contribute greatly to the understanding of pathogen-tick-host interactions. METHODS: Herein, we performed a comparative proteomics study of the tick vector Dermacentor reticulatus that was experimentally infected with the endosymbiotic bacterium R. slovaca. Rickettsia-free ticks, collected in the southern region of Slovakia, were infected with the bacterium by a capillary tube-feeding system, and the dynamics of infection was assessed by quantitative PCR method after 5, 10, 15 and 27 days. RESULTS: At the stage of controlled proliferation (at 27 dpi), 33 (from 481 profiled) differentially abundant protein spots were detected on a two-dimensional gel. From the aforementioned protein spots, 21 were successfully identified by tandem mass spectrometry. CONCLUSIONS: Although a few discovered proteins were described as having structural or housekeeping functions, the vast majority of the affected proteins were suggested to be essential for tick attachment and feeding on the host, host immune system evasion and defensive response modulation to ensure successful pathogen transmission. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-019-3564-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-24 /pmc/articles/PMC6591964/ /pubmed/31234913 http://dx.doi.org/10.1186/s13071-019-3564-y Text en © The Author(s) 2019 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
Flores-Ramirez, Gabriela
Sallay, Balázs
Danchenko, Maksym
Lakhneko, Olha
Špitalská, Eva
Skultety, Ludovit
Comparative proteomics of the vector Dermacentor reticulatus revealed differentially regulated proteins associated with pathogen transmission in response to laboratory infection with Rickettsia slovaca
title Comparative proteomics of the vector Dermacentor reticulatus revealed differentially regulated proteins associated with pathogen transmission in response to laboratory infection with Rickettsia slovaca
title_full Comparative proteomics of the vector Dermacentor reticulatus revealed differentially regulated proteins associated with pathogen transmission in response to laboratory infection with Rickettsia slovaca
title_fullStr Comparative proteomics of the vector Dermacentor reticulatus revealed differentially regulated proteins associated with pathogen transmission in response to laboratory infection with Rickettsia slovaca
title_full_unstemmed Comparative proteomics of the vector Dermacentor reticulatus revealed differentially regulated proteins associated with pathogen transmission in response to laboratory infection with Rickettsia slovaca
title_short Comparative proteomics of the vector Dermacentor reticulatus revealed differentially regulated proteins associated with pathogen transmission in response to laboratory infection with Rickettsia slovaca
title_sort comparative proteomics of the vector dermacentor reticulatus revealed differentially regulated proteins associated with pathogen transmission in response to laboratory infection with rickettsia slovaca
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591964/
https://www.ncbi.nlm.nih.gov/pubmed/31234913
http://dx.doi.org/10.1186/s13071-019-3564-y
work_keys_str_mv AT floresramirezgabriela comparativeproteomicsofthevectordermacentorreticulatusrevealeddifferentiallyregulatedproteinsassociatedwithpathogentransmissioninresponsetolaboratoryinfectionwithrickettsiaslovaca
AT sallaybalazs comparativeproteomicsofthevectordermacentorreticulatusrevealeddifferentiallyregulatedproteinsassociatedwithpathogentransmissioninresponsetolaboratoryinfectionwithrickettsiaslovaca
AT danchenkomaksym comparativeproteomicsofthevectordermacentorreticulatusrevealeddifferentiallyregulatedproteinsassociatedwithpathogentransmissioninresponsetolaboratoryinfectionwithrickettsiaslovaca
AT lakhnekoolha comparativeproteomicsofthevectordermacentorreticulatusrevealeddifferentiallyregulatedproteinsassociatedwithpathogentransmissioninresponsetolaboratoryinfectionwithrickettsiaslovaca
AT spitalskaeva comparativeproteomicsofthevectordermacentorreticulatusrevealeddifferentiallyregulatedproteinsassociatedwithpathogentransmissioninresponsetolaboratoryinfectionwithrickettsiaslovaca
AT skultetyludovit comparativeproteomicsofthevectordermacentorreticulatusrevealeddifferentiallyregulatedproteinsassociatedwithpathogentransmissioninresponsetolaboratoryinfectionwithrickettsiaslovaca