Mucosal leishmaniasis is associated with the Leishmania RNA virus and inappropriate cutaneous leishmaniasis treatment
Mucosal leishmaniasis (ML) is a severe clinical form of leishmaniasis that is characterized by the destruction of the nasal and/or the oral mucosae and appears as a late complication in 5% to 10% of cutaneous leishmaniasis (CL) cases produced by species belonging to Leishmania (Viannia) subgenus. So...
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description | Mucosal leishmaniasis (ML) is a severe clinical form of leishmaniasis that is characterized by the destruction of the nasal and/or the oral mucosae and appears as a late complication in 5% to 10% of cutaneous leishmaniasis (CL) cases produced by species belonging to Leishmania (Viannia) subgenus. Some strains of Leishmania spp. carry an RNA virus known as Leishmania RNA virus (LRV) that may contribute to the appearance of ML.
To examine the role of LRV type 1 (LRV1) as a risk factor associated with ML, a retrospective case-control study involving 103 patients was conducted. Cases were defined as patients with ML (n = 33), and controls corresponded to patients with CL and without mucosal lesions (n = 70). Clinical data were recorded from the patient's medical records. Cryopreserved biopsies were used to detect LRV1 and identify Leishmania species.
The frequency of LRV1 in the 103 patients was 16.5% (95% CI,10.4-25.12) being higher in samples from cases [33.33% (95% CI,18.89-51.76) than from controls [8.57% (95% CI, 3.82-18.10)]. L. (V.) braziliensis was identified in 63.6% of cases and 55.7% of the controls. Multivariate logistic regression indicated that infection with Leishmania spp. carrying LRV1 (OR = 6.30; 95% CI,1.52-26.10, p = 0.011) acts as risk factors for ML occurrence, while the completed treatment for the cutaneous event decreases the risk of ML (OR = 0.039; 95% CI, 0.01-0.12, p < 0.0001).
Our data support the association between LRV1 and ML occurrence and emphasize the effect of completed treatment for CL in preventing ML. |
doi_str_mv | 10.1371/journal.pone.0317221 |
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To examine the role of LRV type 1 (LRV1) as a risk factor associated with ML, a retrospective case-control study involving 103 patients was conducted. Cases were defined as patients with ML (n = 33), and controls corresponded to patients with CL and without mucosal lesions (n = 70). Clinical data were recorded from the patient's medical records. Cryopreserved biopsies were used to detect LRV1 and identify Leishmania species.
The frequency of LRV1 in the 103 patients was 16.5% (95% CI,10.4-25.12) being higher in samples from cases [33.33% (95% CI,18.89-51.76) than from controls [8.57% (95% CI, 3.82-18.10)]. L. (V.) braziliensis was identified in 63.6% of cases and 55.7% of the controls. Multivariate logistic regression indicated that infection with Leishmania spp. carrying LRV1 (OR = 6.30; 95% CI,1.52-26.10, p = 0.011) acts as risk factors for ML occurrence, while the completed treatment for the cutaneous event decreases the risk of ML (OR = 0.039; 95% CI, 0.01-0.12, p < 0.0001).
Our data support the association between LRV1 and ML occurrence and emphasize the effect of completed treatment for CL in preventing ML.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0317221</identifier><identifier>PMID: 39854299</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adolescent ; Adult ; Aged ; Biology and Life Sciences ; Biopsy ; Care and treatment ; Case-Control Studies ; Causes of ; Cryopreservation ; Cutaneous leishmaniasis ; Ethics ; Female ; Genetic aspects ; Health aspects ; Health services ; Humans ; Infections ; Informed consent ; Leishmania ; Leishmania - genetics ; Leishmaniasis ; Leishmaniasis, Cutaneous - drug therapy ; Leishmaniasis, Cutaneous - parasitology ; Leishmaniasis, Mucocutaneous - drug therapy ; Leishmaniavirus - genetics ; Male ; Medical records ; Medicine and Health Sciences ; Middle Aged ; Mucosa ; Parasites ; Parasitic diseases ; Patients ; Protozoa ; Retrospective Studies ; Risk Factors ; RNA viruses ; Sample size ; Statistical analysis ; Ulcers ; Variables ; Vector-borne diseases ; Viruses ; Young Adult</subject><ispartof>PloS one, 2025, Vol.20 (1), p.e0317221</ispartof><rights>Copyright: © 2025 Pazmiño et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2025 Public Library of Science</rights><rights>2025 Pazmiño et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2025 Pazmiño et al 2025 Pazmiño et al</rights><rights>2025 Pazmiño et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3801-fc1ec8c49d5436db9db9420f62ac15fe50a214ed570a006e837e553598b8c0ce3</cites><orcidid>0000-0002-2669-0025 ; 0000-0002-5590-6470</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11759362/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11759362/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,4010,23845,27900,27901,27902,53766,53768,79569,79570</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39854299$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pazmiño, Fredy A</creatorcontrib><creatorcontrib>Parra-Muñoz, Marcela</creatorcontrib><creatorcontrib>Saavedra, Carlos H</creatorcontrib><creatorcontrib>Muvdi-Arenas, Sandra</creatorcontrib><creatorcontrib>Ovalle-Bracho, Clemencia</creatorcontrib><creatorcontrib>Echeverry, María C</creatorcontrib><title>Mucosal leishmaniasis is associated with the Leishmania RNA virus and inappropriate cutaneous leishmaniasis treatment</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Mucosal leishmaniasis (ML) is a severe clinical form of leishmaniasis that is characterized by the destruction of the nasal and/or the oral mucosae and appears as a late complication in 5% to 10% of cutaneous leishmaniasis (CL) cases produced by species belonging to Leishmania (Viannia) subgenus. Some strains of Leishmania spp. carry an RNA virus known as Leishmania RNA virus (LRV) that may contribute to the appearance of ML.
To examine the role of LRV type 1 (LRV1) as a risk factor associated with ML, a retrospective case-control study involving 103 patients was conducted. Cases were defined as patients with ML (n = 33), and controls corresponded to patients with CL and without mucosal lesions (n = 70). Clinical data were recorded from the patient's medical records. Cryopreserved biopsies were used to detect LRV1 and identify Leishmania species.
The frequency of LRV1 in the 103 patients was 16.5% (95% CI,10.4-25.12) being higher in samples from cases [33.33% (95% CI,18.89-51.76) than from controls [8.57% (95% CI, 3.82-18.10)]. L. (V.) braziliensis was identified in 63.6% of cases and 55.7% of the controls. Multivariate logistic regression indicated that infection with Leishmania spp. carrying LRV1 (OR = 6.30; 95% CI,1.52-26.10, p = 0.011) acts as risk factors for ML occurrence, while the completed treatment for the cutaneous event decreases the risk of ML (OR = 0.039; 95% CI, 0.01-0.12, p < 0.0001).
Our data support the association between LRV1 and ML occurrence and emphasize the effect of completed treatment for CL in preventing ML.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biology and Life Sciences</subject><subject>Biopsy</subject><subject>Care and treatment</subject><subject>Case-Control Studies</subject><subject>Causes of</subject><subject>Cryopreservation</subject><subject>Cutaneous leishmaniasis</subject><subject>Ethics</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Health services</subject><subject>Humans</subject><subject>Infections</subject><subject>Informed consent</subject><subject>Leishmania</subject><subject>Leishmania - genetics</subject><subject>Leishmaniasis</subject><subject>Leishmaniasis, Cutaneous - drug therapy</subject><subject>Leishmaniasis, Cutaneous - parasitology</subject><subject>Leishmaniasis, Mucocutaneous - drug therapy</subject><subject>Leishmaniavirus - genetics</subject><subject>Male</subject><subject>Medical records</subject><subject>Medicine and Health Sciences</subject><subject>Middle Aged</subject><subject>Mucosa</subject><subject>Parasites</subject><subject>Parasitic diseases</subject><subject>Patients</subject><subject>Protozoa</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>RNA viruses</subject><subject>Sample size</subject><subject>Statistical analysis</subject><subject>Ulcers</subject><subject>Variables</subject><subject>Vector-borne diseases</subject><subject>Viruses</subject><subject>Young Adult</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNptkl2LEzEUhgdR3HX1H4gOCLI3rfmYzCRXUhZ1F6qC6HVIk5NOSjqpSWbFf29qZ0srQiAh5znv-eCtqpcYzTHt8LtNGOOg_HwXBpgjijtC8KPqEgtKZi1B9PHJ-6J6ltIGIUZ52z6tLqjgrCFCXFbj51GHpHztwaV-qwankkt1OSqloJ3KYOpfLvd17qFeHqH625dFfe_iWMDB1G5Qu10Mu7hPqPWY1QChxM5VcwSVtzDk59UTq3yCF9N9Vf34-OH7ze1s-fXT3c1iOdOUIzyzGoPmuhGGNbQ1K1FOQ5BtidKYWWBIEdyAYR1SCLXAaQeMUSb4imukgV5Vrw-6Ox-SnDaWJMVMtEQwwgpxdyBMUBtZ-t-q-FsG5eTfjxDXUsXstAe5stZ2xBirEG9a0okV59AyMIZbI9S-2vup2rjagtFl0Kj8meh5ZHC9XId7iXHHBG1JUbieFGL4OULKcuuSBu8P6zw0LhqMaEHf_IP-f7yJWqsygRtsKIX1XlQuOGk6whnnhXp7QvWgfO5T8GN2YUjnYHMAdQwpRbDH4TCSe1c-NCH3rpSTK0vaq9PFHJMebEj_AOCH4dw</recordid><startdate>2025</startdate><enddate>2025</enddate><creator>Pazmiño, Fredy A</creator><creator>Parra-Muñoz, Marcela</creator><creator>Saavedra, Carlos H</creator><creator>Muvdi-Arenas, Sandra</creator><creator>Ovalle-Bracho, Clemencia</creator><creator>Echeverry, María C</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-2669-0025</orcidid><orcidid>https://orcid.org/0000-0002-5590-6470</orcidid></search><sort><creationdate>2025</creationdate><title>Mucosal leishmaniasis is associated with the Leishmania RNA virus and inappropriate cutaneous leishmaniasis treatment</title><author>Pazmiño, Fredy A ; Parra-Muñoz, Marcela ; Saavedra, Carlos H ; Muvdi-Arenas, Sandra ; Ovalle-Bracho, Clemencia ; Echeverry, María C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3801-fc1ec8c49d5436db9db9420f62ac15fe50a214ed570a006e837e553598b8c0ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Biology and Life Sciences</topic><topic>Biopsy</topic><topic>Care and treatment</topic><topic>Case-Control Studies</topic><topic>Causes of</topic><topic>Cryopreservation</topic><topic>Cutaneous leishmaniasis</topic><topic>Ethics</topic><topic>Female</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Health services</topic><topic>Humans</topic><topic>Infections</topic><topic>Informed consent</topic><topic>Leishmania</topic><topic>Leishmania - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pazmiño, Fredy A</au><au>Parra-Muñoz, Marcela</au><au>Saavedra, Carlos H</au><au>Muvdi-Arenas, Sandra</au><au>Ovalle-Bracho, Clemencia</au><au>Echeverry, María C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mucosal leishmaniasis is associated with the Leishmania RNA virus and inappropriate cutaneous leishmaniasis treatment</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2025</date><risdate>2025</risdate><volume>20</volume><issue>1</issue><spage>e0317221</spage><pages>e0317221-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Mucosal leishmaniasis (ML) is a severe clinical form of leishmaniasis that is characterized by the destruction of the nasal and/or the oral mucosae and appears as a late complication in 5% to 10% of cutaneous leishmaniasis (CL) cases produced by species belonging to Leishmania (Viannia) subgenus. Some strains of Leishmania spp. carry an RNA virus known as Leishmania RNA virus (LRV) that may contribute to the appearance of ML.
To examine the role of LRV type 1 (LRV1) as a risk factor associated with ML, a retrospective case-control study involving 103 patients was conducted. Cases were defined as patients with ML (n = 33), and controls corresponded to patients with CL and without mucosal lesions (n = 70). Clinical data were recorded from the patient's medical records. Cryopreserved biopsies were used to detect LRV1 and identify Leishmania species.
The frequency of LRV1 in the 103 patients was 16.5% (95% CI,10.4-25.12) being higher in samples from cases [33.33% (95% CI,18.89-51.76) than from controls [8.57% (95% CI, 3.82-18.10)]. L. (V.) braziliensis was identified in 63.6% of cases and 55.7% of the controls. Multivariate logistic regression indicated that infection with Leishmania spp. carrying LRV1 (OR = 6.30; 95% CI,1.52-26.10, p = 0.011) acts as risk factors for ML occurrence, while the completed treatment for the cutaneous event decreases the risk of ML (OR = 0.039; 95% CI, 0.01-0.12, p < 0.0001).
Our data support the association between LRV1 and ML occurrence and emphasize the effect of completed treatment for CL in preventing ML.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>39854299</pmid><doi>10.1371/journal.pone.0317221</doi><orcidid>https://orcid.org/0000-0002-2669-0025</orcidid><orcidid>https://orcid.org/0000-0002-5590-6470</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS) |
subjects | Adolescent Adult Aged Biology and Life Sciences Biopsy Care and treatment Case-Control Studies Causes of Cryopreservation Cutaneous leishmaniasis Ethics Female Genetic aspects Health aspects Health services Humans Infections Informed consent Leishmania Leishmania - genetics Leishmaniasis Leishmaniasis, Cutaneous - drug therapy Leishmaniasis, Cutaneous - parasitology Leishmaniasis, Mucocutaneous - drug therapy Leishmaniavirus - genetics Male Medical records Medicine and Health Sciences Middle Aged Mucosa Parasites Parasitic diseases Patients Protozoa Retrospective Studies Risk Factors RNA viruses Sample size Statistical analysis Ulcers Variables Vector-borne diseases Viruses Young Adult |
title | Mucosal leishmaniasis is associated with the Leishmania RNA virus and inappropriate cutaneous leishmaniasis treatment |
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