Comparison of PCR‐based methods for the diagnosis of cutaneous leishmaniasis in two different epidemiological scenarios: Spain and Morocco

Background Cutaneous leishmaniasis (CL) is a disfiguring and stigmatising disease occurring in more than 70 countries across the world including Spain and Morocco. The use of sensitive tests that can differentiate Leishmania species is advised. Objective To evaluate the influence of the epidemiologi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the European Academy of Dermatology and Venereology 2018-11, Vol.32 (11), p.1999-2003
Hauptverfasser: Merino‐Espinosa, G., Rodríguez‐Granger, J., Morillas‐Márquez, F., Tercedor, J., Corpas‐López, V., Chiheb, S., Alcalde‐Alonso, M., Azaña‐Defez, J.M., Riyad, M., Díaz‐Sáez, V., Martín‐Sánchez, J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2003
container_issue 11
container_start_page 1999
container_title Journal of the European Academy of Dermatology and Venereology
container_volume 32
creator Merino‐Espinosa, G.
Rodríguez‐Granger, J.
Morillas‐Márquez, F.
Tercedor, J.
Corpas‐López, V.
Chiheb, S.
Alcalde‐Alonso, M.
Azaña‐Defez, J.M.
Riyad, M.
Díaz‐Sáez, V.
Martín‐Sánchez, J.
description Background Cutaneous leishmaniasis (CL) is a disfiguring and stigmatising disease occurring in more than 70 countries across the world including Spain and Morocco. The use of sensitive tests that can differentiate Leishmania species is advised. Objective To evaluate the influence of the epidemiological scenario on the reliability of the PCR techniques and contribute to the selection of the most efficient one for CL diagnosis. Methods The sensitivities of parasitological methods and four PCRs were compared in cutaneous samples from 77 patients from Spanish (PSH) and Moroccan hospitals (PMH). Exudates and fresh or paraffin‐embedded tissue biopsies were used. Results None of the PCRs used in this study allowed the diagnosis of all CL cases, showing also some drawbacks. Lmj4/Uni21‐PCR displayed the best sensitivity with PMH, but it did not provide positive results in PSH with CL confirmed by other PCRs. Conversely, JW13/JW14‐PCR and L. infantum‐PCR‐ELISA displayed good sensitivities with PSH that were not achieved with PMH. Nested‐ITS‐1‐PCR did not show enough sensitivity with paraffin‐embedded tissue biopsies. False‐negative results were obtained in 19% of PSH due to unspecific hybridizations of ITS‐1 primers with human chromosome1. Conclusions PCR should be routinely used in patients with cutaneous lesions compatible with CL and furthermore, the combination of two PCR techniques is advisable. The selection of these PCRs will be influenced by the epidemiological scenario: In areas where L. infantum is endemic, the use of the PCR‐ELISA joint with JW13/JW14‐PCR seems an appropriate choice, whereas in areas such as Morocco, Lmj4/Uni21 and ITS‐1 provide satisfactory results.
doi_str_mv 10.1111/jdv.15034
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2032412747</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2032412747</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3254-e03937901093f2aa9e5b542946d822b1398821b687d86a675d93cb5255560ce13</originalsourceid><addsrcrecordid>eNp10LtO5DAUBmALLYJZoOAFkEsoAr7ESUyHBpYFgUDc2sixTxijJA52BkTHA1DwjDzJegjQrRsX_vSf4x-hTUp2aTx7D-ZplwrC0yU0oWlWJJwU_BeaEMmyREohV9HvEB4IIZSKYgWtMpmTlGVigt6mru2Vt8F12NX4cnr18fpeqQAGtzDMnAm4dh4PM8DGqvvOBRsWUM8H1YGbB9yADbNWdVYtnmyHh2cXbV2Dh27A0FsDrXWNu7daNTho6OI8F_bxda8iV53B5847rd06Wq5VE2Dj615Dt3-ObqZ_k7OL45PpwVmiORNpAoRLnktCieQ1U0qCqETKZJqZgrGKclkUjFZZkZsiU1kujOS6EkwIkRENlK-h7TG39-5xDmEoWxv3aprxSyUjnKWU5Wke6c5ItXcheKjL3ttW-ZeSknJRfhnLLz_Lj3brK3ZetWB-5HfbEeyN4Nk28PL_pPL08G6M_AeYpo_7</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2032412747</pqid></control><display><type>article</type><title>Comparison of PCR‐based methods for the diagnosis of cutaneous leishmaniasis in two different epidemiological scenarios: Spain and Morocco</title><source>Wiley-Blackwell Journals</source><source>MEDLINE</source><creator>Merino‐Espinosa, G. ; Rodríguez‐Granger, J. ; Morillas‐Márquez, F. ; Tercedor, J. ; Corpas‐López, V. ; Chiheb, S. ; Alcalde‐Alonso, M. ; Azaña‐Defez, J.M. ; Riyad, M. ; Díaz‐Sáez, V. ; Martín‐Sánchez, J.</creator><creatorcontrib>Merino‐Espinosa, G. ; Rodríguez‐Granger, J. ; Morillas‐Márquez, F. ; Tercedor, J. ; Corpas‐López, V. ; Chiheb, S. ; Alcalde‐Alonso, M. ; Azaña‐Defez, J.M. ; Riyad, M. ; Díaz‐Sáez, V. ; Martín‐Sánchez, J.</creatorcontrib><description>Background Cutaneous leishmaniasis (CL) is a disfiguring and stigmatising disease occurring in more than 70 countries across the world including Spain and Morocco. The use of sensitive tests that can differentiate Leishmania species is advised. Objective To evaluate the influence of the epidemiological scenario on the reliability of the PCR techniques and contribute to the selection of the most efficient one for CL diagnosis. Methods The sensitivities of parasitological methods and four PCRs were compared in cutaneous samples from 77 patients from Spanish (PSH) and Moroccan hospitals (PMH). Exudates and fresh or paraffin‐embedded tissue biopsies were used. Results None of the PCRs used in this study allowed the diagnosis of all CL cases, showing also some drawbacks. Lmj4/Uni21‐PCR displayed the best sensitivity with PMH, but it did not provide positive results in PSH with CL confirmed by other PCRs. Conversely, JW13/JW14‐PCR and L. infantum‐PCR‐ELISA displayed good sensitivities with PSH that were not achieved with PMH. Nested‐ITS‐1‐PCR did not show enough sensitivity with paraffin‐embedded tissue biopsies. False‐negative results were obtained in 19% of PSH due to unspecific hybridizations of ITS‐1 primers with human chromosome1. Conclusions PCR should be routinely used in patients with cutaneous lesions compatible with CL and furthermore, the combination of two PCR techniques is advisable. The selection of these PCRs will be influenced by the epidemiological scenario: In areas where L. infantum is endemic, the use of the PCR‐ELISA joint with JW13/JW14‐PCR seems an appropriate choice, whereas in areas such as Morocco, Lmj4/Uni21 and ITS‐1 provide satisfactory results.</description><identifier>ISSN: 0926-9959</identifier><identifier>EISSN: 1468-3083</identifier><identifier>DOI: 10.1111/jdv.15034</identifier><identifier>PMID: 29704265</identifier><language>eng</language><publisher>England</publisher><subject>Adult ; Age Factors ; Aged ; Cohort Studies ; DNA Primers - genetics ; Enzyme-Linked Immunosorbent Assay - methods ; Female ; Humans ; Leishmania - pathogenicity ; Leishmaniasis, Cutaneous - diagnosis ; Leishmaniasis, Cutaneous - epidemiology ; Male ; Middle Aged ; Morocco - epidemiology ; Polymerase Chain Reaction - methods ; Prevalence ; Retrospective Studies ; Risk Assessment ; Sensitivity and Specificity ; Severity of Illness Index ; Sex Factors ; Spain - epidemiology ; Young Adult</subject><ispartof>Journal of the European Academy of Dermatology and Venereology, 2018-11, Vol.32 (11), p.1999-2003</ispartof><rights>2018 European Academy of Dermatology and Venereology</rights><rights>2018 European Academy of Dermatology and Venereology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3254-e03937901093f2aa9e5b542946d822b1398821b687d86a675d93cb5255560ce13</citedby><cites>FETCH-LOGICAL-c3254-e03937901093f2aa9e5b542946d822b1398821b687d86a675d93cb5255560ce13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjdv.15034$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjdv.15034$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29704265$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Merino‐Espinosa, G.</creatorcontrib><creatorcontrib>Rodríguez‐Granger, J.</creatorcontrib><creatorcontrib>Morillas‐Márquez, F.</creatorcontrib><creatorcontrib>Tercedor, J.</creatorcontrib><creatorcontrib>Corpas‐López, V.</creatorcontrib><creatorcontrib>Chiheb, S.</creatorcontrib><creatorcontrib>Alcalde‐Alonso, M.</creatorcontrib><creatorcontrib>Azaña‐Defez, J.M.</creatorcontrib><creatorcontrib>Riyad, M.</creatorcontrib><creatorcontrib>Díaz‐Sáez, V.</creatorcontrib><creatorcontrib>Martín‐Sánchez, J.</creatorcontrib><title>Comparison of PCR‐based methods for the diagnosis of cutaneous leishmaniasis in two different epidemiological scenarios: Spain and Morocco</title><title>Journal of the European Academy of Dermatology and Venereology</title><addtitle>J Eur Acad Dermatol Venereol</addtitle><description>Background Cutaneous leishmaniasis (CL) is a disfiguring and stigmatising disease occurring in more than 70 countries across the world including Spain and Morocco. The use of sensitive tests that can differentiate Leishmania species is advised. Objective To evaluate the influence of the epidemiological scenario on the reliability of the PCR techniques and contribute to the selection of the most efficient one for CL diagnosis. Methods The sensitivities of parasitological methods and four PCRs were compared in cutaneous samples from 77 patients from Spanish (PSH) and Moroccan hospitals (PMH). Exudates and fresh or paraffin‐embedded tissue biopsies were used. Results None of the PCRs used in this study allowed the diagnosis of all CL cases, showing also some drawbacks. Lmj4/Uni21‐PCR displayed the best sensitivity with PMH, but it did not provide positive results in PSH with CL confirmed by other PCRs. Conversely, JW13/JW14‐PCR and L. infantum‐PCR‐ELISA displayed good sensitivities with PSH that were not achieved with PMH. Nested‐ITS‐1‐PCR did not show enough sensitivity with paraffin‐embedded tissue biopsies. False‐negative results were obtained in 19% of PSH due to unspecific hybridizations of ITS‐1 primers with human chromosome1. Conclusions PCR should be routinely used in patients with cutaneous lesions compatible with CL and furthermore, the combination of two PCR techniques is advisable. The selection of these PCRs will be influenced by the epidemiological scenario: In areas where L. infantum is endemic, the use of the PCR‐ELISA joint with JW13/JW14‐PCR seems an appropriate choice, whereas in areas such as Morocco, Lmj4/Uni21 and ITS‐1 provide satisfactory results.</description><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Cohort Studies</subject><subject>DNA Primers - genetics</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>Female</subject><subject>Humans</subject><subject>Leishmania - pathogenicity</subject><subject>Leishmaniasis, Cutaneous - diagnosis</subject><subject>Leishmaniasis, Cutaneous - epidemiology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Morocco - epidemiology</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Prevalence</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Sensitivity and Specificity</subject><subject>Severity of Illness Index</subject><subject>Sex Factors</subject><subject>Spain - epidemiology</subject><subject>Young Adult</subject><issn>0926-9959</issn><issn>1468-3083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10LtO5DAUBmALLYJZoOAFkEsoAr7ESUyHBpYFgUDc2sixTxijJA52BkTHA1DwjDzJegjQrRsX_vSf4x-hTUp2aTx7D-ZplwrC0yU0oWlWJJwU_BeaEMmyREohV9HvEB4IIZSKYgWtMpmTlGVigt6mru2Vt8F12NX4cnr18fpeqQAGtzDMnAm4dh4PM8DGqvvOBRsWUM8H1YGbB9yADbNWdVYtnmyHh2cXbV2Dh27A0FsDrXWNu7daNTho6OI8F_bxda8iV53B5847rd06Wq5VE2Dj615Dt3-ObqZ_k7OL45PpwVmiORNpAoRLnktCieQ1U0qCqETKZJqZgrGKclkUjFZZkZsiU1kujOS6EkwIkRENlK-h7TG39-5xDmEoWxv3aprxSyUjnKWU5Wke6c5ItXcheKjL3ttW-ZeSknJRfhnLLz_Lj3brK3ZetWB-5HfbEeyN4Nk28PL_pPL08G6M_AeYpo_7</recordid><startdate>201811</startdate><enddate>201811</enddate><creator>Merino‐Espinosa, G.</creator><creator>Rodríguez‐Granger, J.</creator><creator>Morillas‐Márquez, F.</creator><creator>Tercedor, J.</creator><creator>Corpas‐López, V.</creator><creator>Chiheb, S.</creator><creator>Alcalde‐Alonso, M.</creator><creator>Azaña‐Defez, J.M.</creator><creator>Riyad, M.</creator><creator>Díaz‐Sáez, V.</creator><creator>Martín‐Sánchez, J.</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201811</creationdate><title>Comparison of PCR‐based methods for the diagnosis of cutaneous leishmaniasis in two different epidemiological scenarios: Spain and Morocco</title><author>Merino‐Espinosa, G. ; Rodríguez‐Granger, J. ; Morillas‐Márquez, F. ; Tercedor, J. ; Corpas‐López, V. ; Chiheb, S. ; Alcalde‐Alonso, M. ; Azaña‐Defez, J.M. ; Riyad, M. ; Díaz‐Sáez, V. ; Martín‐Sánchez, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3254-e03937901093f2aa9e5b542946d822b1398821b687d86a675d93cb5255560ce13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adult</topic><topic>Age Factors</topic><topic>Aged</topic><topic>Cohort Studies</topic><topic>DNA Primers - genetics</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>Female</topic><topic>Humans</topic><topic>Leishmania - pathogenicity</topic><topic>Leishmaniasis, Cutaneous - diagnosis</topic><topic>Leishmaniasis, Cutaneous - epidemiology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Morocco - epidemiology</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Prevalence</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Sensitivity and Specificity</topic><topic>Severity of Illness Index</topic><topic>Sex Factors</topic><topic>Spain - epidemiology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Merino‐Espinosa, G.</creatorcontrib><creatorcontrib>Rodríguez‐Granger, J.</creatorcontrib><creatorcontrib>Morillas‐Márquez, F.</creatorcontrib><creatorcontrib>Tercedor, J.</creatorcontrib><creatorcontrib>Corpas‐López, V.</creatorcontrib><creatorcontrib>Chiheb, S.</creatorcontrib><creatorcontrib>Alcalde‐Alonso, M.</creatorcontrib><creatorcontrib>Azaña‐Defez, J.M.</creatorcontrib><creatorcontrib>Riyad, M.</creatorcontrib><creatorcontrib>Díaz‐Sáez, V.</creatorcontrib><creatorcontrib>Martín‐Sánchez, J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the European Academy of Dermatology and Venereology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Merino‐Espinosa, G.</au><au>Rodríguez‐Granger, J.</au><au>Morillas‐Márquez, F.</au><au>Tercedor, J.</au><au>Corpas‐López, V.</au><au>Chiheb, S.</au><au>Alcalde‐Alonso, M.</au><au>Azaña‐Defez, J.M.</au><au>Riyad, M.</au><au>Díaz‐Sáez, V.</au><au>Martín‐Sánchez, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of PCR‐based methods for the diagnosis of cutaneous leishmaniasis in two different epidemiological scenarios: Spain and Morocco</atitle><jtitle>Journal of the European Academy of Dermatology and Venereology</jtitle><addtitle>J Eur Acad Dermatol Venereol</addtitle><date>2018-11</date><risdate>2018</risdate><volume>32</volume><issue>11</issue><spage>1999</spage><epage>2003</epage><pages>1999-2003</pages><issn>0926-9959</issn><eissn>1468-3083</eissn><abstract>Background Cutaneous leishmaniasis (CL) is a disfiguring and stigmatising disease occurring in more than 70 countries across the world including Spain and Morocco. The use of sensitive tests that can differentiate Leishmania species is advised. Objective To evaluate the influence of the epidemiological scenario on the reliability of the PCR techniques and contribute to the selection of the most efficient one for CL diagnosis. Methods The sensitivities of parasitological methods and four PCRs were compared in cutaneous samples from 77 patients from Spanish (PSH) and Moroccan hospitals (PMH). Exudates and fresh or paraffin‐embedded tissue biopsies were used. Results None of the PCRs used in this study allowed the diagnosis of all CL cases, showing also some drawbacks. Lmj4/Uni21‐PCR displayed the best sensitivity with PMH, but it did not provide positive results in PSH with CL confirmed by other PCRs. Conversely, JW13/JW14‐PCR and L. infantum‐PCR‐ELISA displayed good sensitivities with PSH that were not achieved with PMH. Nested‐ITS‐1‐PCR did not show enough sensitivity with paraffin‐embedded tissue biopsies. False‐negative results were obtained in 19% of PSH due to unspecific hybridizations of ITS‐1 primers with human chromosome1. Conclusions PCR should be routinely used in patients with cutaneous lesions compatible with CL and furthermore, the combination of two PCR techniques is advisable. The selection of these PCRs will be influenced by the epidemiological scenario: In areas where L. infantum is endemic, the use of the PCR‐ELISA joint with JW13/JW14‐PCR seems an appropriate choice, whereas in areas such as Morocco, Lmj4/Uni21 and ITS‐1 provide satisfactory results.</abstract><cop>England</cop><pmid>29704265</pmid><doi>10.1111/jdv.15034</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0926-9959
ispartof Journal of the European Academy of Dermatology and Venereology, 2018-11, Vol.32 (11), p.1999-2003
issn 0926-9959
1468-3083
language eng
recordid cdi_proquest_miscellaneous_2032412747
source Wiley-Blackwell Journals; MEDLINE
subjects Adult
Age Factors
Aged
Cohort Studies
DNA Primers - genetics
Enzyme-Linked Immunosorbent Assay - methods
Female
Humans
Leishmania - pathogenicity
Leishmaniasis, Cutaneous - diagnosis
Leishmaniasis, Cutaneous - epidemiology
Male
Middle Aged
Morocco - epidemiology
Polymerase Chain Reaction - methods
Prevalence
Retrospective Studies
Risk Assessment
Sensitivity and Specificity
Severity of Illness Index
Sex Factors
Spain - epidemiology
Young Adult
title Comparison of PCR‐based methods for the diagnosis of cutaneous leishmaniasis in two different epidemiological scenarios: Spain and Morocco
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T09%3A58%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Comparison%20of%20PCR%E2%80%90based%20methods%20for%20the%20diagnosis%20of%20cutaneous%20leishmaniasis%20in%20two%20different%20epidemiological%20scenarios:%20Spain%20and%20Morocco&rft.jtitle=Journal%20of%20the%20European%20Academy%20of%20Dermatology%20and%20Venereology&rft.au=Merino%E2%80%90Espinosa,%20G.&rft.date=2018-11&rft.volume=32&rft.issue=11&rft.spage=1999&rft.epage=2003&rft.pages=1999-2003&rft.issn=0926-9959&rft.eissn=1468-3083&rft_id=info:doi/10.1111/jdv.15034&rft_dat=%3Cproquest_cross%3E2032412747%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2032412747&rft_id=info:pmid/29704265&rfr_iscdi=true