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Multispacer typing of Rickettsia isolates from humans and ticks in Tunisia revealing new genotypes

BACKGROUND: Rickettsioses are important remerging vector born infections. In Tunisia, many species have been described in humans and vectors. Genotyping is important for tracking pathogen movement between hosts and vectors. In this study, we characterized Rickettsia species detected in patients and...

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Autores principales: Znazen, Abir, Khrouf, Fatma, Elleuch, Nihel, Lahiani, Dorra, Marrekchi, Chakib, M’Ghirbi, Youmna, Ben Jemaa, Mounir, Bouattour, Ali, Hammami, Adnene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883474/
https://www.ncbi.nlm.nih.gov/pubmed/24380581
http://dx.doi.org/10.1186/1756-3305-6-367
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author Znazen, Abir
Khrouf, Fatma
Elleuch, Nihel
Lahiani, Dorra
Marrekchi, Chakib
M’Ghirbi, Youmna
Ben Jemaa, Mounir
Bouattour, Ali
Hammami, Adnene
author_facet Znazen, Abir
Khrouf, Fatma
Elleuch, Nihel
Lahiani, Dorra
Marrekchi, Chakib
M’Ghirbi, Youmna
Ben Jemaa, Mounir
Bouattour, Ali
Hammami, Adnene
author_sort Znazen, Abir
collection PubMed
description BACKGROUND: Rickettsioses are important remerging vector born infections. In Tunisia, many species have been described in humans and vectors. Genotyping is important for tracking pathogen movement between hosts and vectors. In this study, we characterized Rickettsia species detected in patients and vectors using multispacer typing (MST), proposed by Founier et al. and based on three intergenic spacers (dksA-xerC, rmpE- tRNA(fMet), mppA-pruC) sequencing. METHODS: Our study included 25 patients hospitalized during 2009. Ticks and fleas were collected in the vicinity of confirmed cases. Serology was performed on serum samples by microimmunofluorescence using Rickettsia conorii and Rickettsia typhi antigens. To detect and identify Rickettsia species, PCR targeting ompA, ompB and gltA genes followed by sequencing was performed on 18 obtained skin biopsies and on all collected vectors. Rickettsia positive samples were further characterized using primers targeting three intergenic spacers (dksA-xerC, rmpE- tRNA(fMet) and mppA-purC). RESULTS: A rickettsial infection was confirmed in 15 cases (60%). Serology was positive in 13 cases (52%). PCR detected Rickettsia DNA in four biopsies (16%) allowing the identification of R. conorii subsp israelensis in three cases and R. conorii subsp conorii in one case. Among 380 collected ticks, nine presented positive PCR (2.4%) allowing the identification of six R. conorii subsp israelensis, two R. massiliae and one R. conorii subsp conorii. Among 322 collected fleas, only one was positive for R. felis. R. conorii subsp israelensis strains detected in humans and vectors clustered together and showed a new MST genotype. Similarly, R. conorii subsp conorii strains detected in a skin biopsy and a tick were genetically related and presented a new MST genotype. CONCLUSIONS: New Rickettsia spotted fever strain genotypes were found in Tunisia. Isolates detected in humans and vectors were genetically homogenous despite location differences in their original isolation suggesting epidemiologic circulation of these strains.
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spelling pubmed-38834742014-01-08 Multispacer typing of Rickettsia isolates from humans and ticks in Tunisia revealing new genotypes Znazen, Abir Khrouf, Fatma Elleuch, Nihel Lahiani, Dorra Marrekchi, Chakib M’Ghirbi, Youmna Ben Jemaa, Mounir Bouattour, Ali Hammami, Adnene Parasit Vectors Research BACKGROUND: Rickettsioses are important remerging vector born infections. In Tunisia, many species have been described in humans and vectors. Genotyping is important for tracking pathogen movement between hosts and vectors. In this study, we characterized Rickettsia species detected in patients and vectors using multispacer typing (MST), proposed by Founier et al. and based on three intergenic spacers (dksA-xerC, rmpE- tRNA(fMet), mppA-pruC) sequencing. METHODS: Our study included 25 patients hospitalized during 2009. Ticks and fleas were collected in the vicinity of confirmed cases. Serology was performed on serum samples by microimmunofluorescence using Rickettsia conorii and Rickettsia typhi antigens. To detect and identify Rickettsia species, PCR targeting ompA, ompB and gltA genes followed by sequencing was performed on 18 obtained skin biopsies and on all collected vectors. Rickettsia positive samples were further characterized using primers targeting three intergenic spacers (dksA-xerC, rmpE- tRNA(fMet) and mppA-purC). RESULTS: A rickettsial infection was confirmed in 15 cases (60%). Serology was positive in 13 cases (52%). PCR detected Rickettsia DNA in four biopsies (16%) allowing the identification of R. conorii subsp israelensis in three cases and R. conorii subsp conorii in one case. Among 380 collected ticks, nine presented positive PCR (2.4%) allowing the identification of six R. conorii subsp israelensis, two R. massiliae and one R. conorii subsp conorii. Among 322 collected fleas, only one was positive for R. felis. R. conorii subsp israelensis strains detected in humans and vectors clustered together and showed a new MST genotype. Similarly, R. conorii subsp conorii strains detected in a skin biopsy and a tick were genetically related and presented a new MST genotype. CONCLUSIONS: New Rickettsia spotted fever strain genotypes were found in Tunisia. Isolates detected in humans and vectors were genetically homogenous despite location differences in their original isolation suggesting epidemiologic circulation of these strains. BioMed Central 2013-12-31 /pmc/articles/PMC3883474/ /pubmed/24380581 http://dx.doi.org/10.1186/1756-3305-6-367 Text en Copyright © 2013 Znazen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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
Znazen, Abir
Khrouf, Fatma
Elleuch, Nihel
Lahiani, Dorra
Marrekchi, Chakib
M’Ghirbi, Youmna
Ben Jemaa, Mounir
Bouattour, Ali
Hammami, Adnene
Multispacer typing of Rickettsia isolates from humans and ticks in Tunisia revealing new genotypes
title Multispacer typing of Rickettsia isolates from humans and ticks in Tunisia revealing new genotypes
title_full Multispacer typing of Rickettsia isolates from humans and ticks in Tunisia revealing new genotypes
title_fullStr Multispacer typing of Rickettsia isolates from humans and ticks in Tunisia revealing new genotypes
title_full_unstemmed Multispacer typing of Rickettsia isolates from humans and ticks in Tunisia revealing new genotypes
title_short Multispacer typing of Rickettsia isolates from humans and ticks in Tunisia revealing new genotypes
title_sort multispacer typing of rickettsia isolates from humans and ticks in tunisia revealing new genotypes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883474/
https://www.ncbi.nlm.nih.gov/pubmed/24380581
http://dx.doi.org/10.1186/1756-3305-6-367
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