Cargando…
Comparative Genomic Analyses of New and Old World Viscerotropic Leishmanine Parasites: Further Insights into the Origins of Visceral Leishmaniasis Agents
Visceral leishmaniasis (VL), also known as kala-azar, is an anthropozoonotic disease affecting human populations on five continents. Aetiologic agents belong to the Leishmania (L.) donovani complex. Until the 1990s, three leishmanine parasites comprised this complex: L. (L.) donovani Laveran & M...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865424/ https://www.ncbi.nlm.nih.gov/pubmed/36677318 http://dx.doi.org/10.3390/microorganisms11010025 |
_version_ | 1784875834713047040 |
---|---|
author | Silveira, Fernando Tobias Sousa Junior, Edivaldo Costa Silvestre, Rodrigo Vellasco Duarte Vasconcelos dos Santos, Thiago Sosa-Ochoa, Wilfredo Valeriano, Concepción Zúniga Ramos, Patrícia Karla Santos Casseb, Samir Mansour Moraes Lima, Luciana Vieira do Rêgo Campos, Marliane Batista da Matta, Vania Lucia Gomes, Claudia Maria Flores, Gabriela V. Araujo Sandoval Pacheco, Carmen M. Corbett, Carlos Eduardo Laurenti, Márcia Dalastra |
author_facet | Silveira, Fernando Tobias Sousa Junior, Edivaldo Costa Silvestre, Rodrigo Vellasco Duarte Vasconcelos dos Santos, Thiago Sosa-Ochoa, Wilfredo Valeriano, Concepción Zúniga Ramos, Patrícia Karla Santos Casseb, Samir Mansour Moraes Lima, Luciana Vieira do Rêgo Campos, Marliane Batista da Matta, Vania Lucia Gomes, Claudia Maria Flores, Gabriela V. Araujo Sandoval Pacheco, Carmen M. Corbett, Carlos Eduardo Laurenti, Márcia Dalastra |
author_sort | Silveira, Fernando Tobias |
collection | PubMed |
description | Visceral leishmaniasis (VL), also known as kala-azar, is an anthropozoonotic disease affecting human populations on five continents. Aetiologic agents belong to the Leishmania (L.) donovani complex. Until the 1990s, three leishmanine parasites comprised this complex: L. (L.) donovani Laveran & Mesnil 1903, L. (L.) infantum Nicolle 1908, and L. (L.) chagasi Lainson & Shaw 1987 (=L. chagasi Cunha & Chagas 1937). The VL causal agent in the New World (NW) was previously identified as L. (L.) chagasi. After the development of molecular characterization, however, comparisons between L. (L.) chagasi and L. (L.) infantum showed high similarity, and L. (L.) chagasi was then regarded as synonymous with L. (L.) infantum. It was, therefore, suggested that L. (L.) chagasi was not native to the NW but had been introduced from the Old World by Iberian colonizers. However, in light of ecological evidence from the NW parasite’s enzootic cycle involving a wild phlebotomine vector (Lutzomyia longipalpis) and a wild mammal reservoir (the fox, Cerdocyon thous), we have recently analyzed by molecular clock comparisons of the DNA polymerase alpha subunit gene the whole-genome sequence of L. (L.) infantum chagasi of the most prevalent clinical form, atypical dermal leishmaniasis (ADL), from Honduras (Central America) with that of the same parasite from Brazil (South America), as well as those of L. (L.) donovani (India) and L. (L.) infantum (Europe), which revealed that the Honduran parasite is older ancestry (382,800 ya) than the parasite from Brazil (143,300 ya), L. (L.) donovani (33,776 ya), or L. (L.) infantum (13,000 ya). In the present work, we have now amplified the genomic comparisons among these leishmanine parasites, exploring mainly the variations in the genome for each chromosome, and the number of genomic SNPs for each chromosome. Although the results of this new analysis have confirmed a high genomic similarity (~99%) among these parasites [except L. (L.) donovani], the Honduran parasite revealed a single structural variation on chromosome 17, and the highest frequency of genomic SNPs (more than twice the number seen in the Brazilian one), which together to its extraordinary ancestry (382,800 ya) represent strong evidence that L. (L.) chagasi/L. (L.) infantum chagasi is, in fact, native to the NW, and therefore with valid taxonomic status. Furthermore, the Honduran parasite, the most ancestral viscerotropic leishmanine parasite, showed genomic and clinical taxonomic characteristics compatible with a new Leishmania species causing ADL in Central America. |
format | Online Article Text |
id | pubmed-9865424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98654242023-01-22 Comparative Genomic Analyses of New and Old World Viscerotropic Leishmanine Parasites: Further Insights into the Origins of Visceral Leishmaniasis Agents Silveira, Fernando Tobias Sousa Junior, Edivaldo Costa Silvestre, Rodrigo Vellasco Duarte Vasconcelos dos Santos, Thiago Sosa-Ochoa, Wilfredo Valeriano, Concepción Zúniga Ramos, Patrícia Karla Santos Casseb, Samir Mansour Moraes Lima, Luciana Vieira do Rêgo Campos, Marliane Batista da Matta, Vania Lucia Gomes, Claudia Maria Flores, Gabriela V. Araujo Sandoval Pacheco, Carmen M. Corbett, Carlos Eduardo Laurenti, Márcia Dalastra Microorganisms Article Visceral leishmaniasis (VL), also known as kala-azar, is an anthropozoonotic disease affecting human populations on five continents. Aetiologic agents belong to the Leishmania (L.) donovani complex. Until the 1990s, three leishmanine parasites comprised this complex: L. (L.) donovani Laveran & Mesnil 1903, L. (L.) infantum Nicolle 1908, and L. (L.) chagasi Lainson & Shaw 1987 (=L. chagasi Cunha & Chagas 1937). The VL causal agent in the New World (NW) was previously identified as L. (L.) chagasi. After the development of molecular characterization, however, comparisons between L. (L.) chagasi and L. (L.) infantum showed high similarity, and L. (L.) chagasi was then regarded as synonymous with L. (L.) infantum. It was, therefore, suggested that L. (L.) chagasi was not native to the NW but had been introduced from the Old World by Iberian colonizers. However, in light of ecological evidence from the NW parasite’s enzootic cycle involving a wild phlebotomine vector (Lutzomyia longipalpis) and a wild mammal reservoir (the fox, Cerdocyon thous), we have recently analyzed by molecular clock comparisons of the DNA polymerase alpha subunit gene the whole-genome sequence of L. (L.) infantum chagasi of the most prevalent clinical form, atypical dermal leishmaniasis (ADL), from Honduras (Central America) with that of the same parasite from Brazil (South America), as well as those of L. (L.) donovani (India) and L. (L.) infantum (Europe), which revealed that the Honduran parasite is older ancestry (382,800 ya) than the parasite from Brazil (143,300 ya), L. (L.) donovani (33,776 ya), or L. (L.) infantum (13,000 ya). In the present work, we have now amplified the genomic comparisons among these leishmanine parasites, exploring mainly the variations in the genome for each chromosome, and the number of genomic SNPs for each chromosome. Although the results of this new analysis have confirmed a high genomic similarity (~99%) among these parasites [except L. (L.) donovani], the Honduran parasite revealed a single structural variation on chromosome 17, and the highest frequency of genomic SNPs (more than twice the number seen in the Brazilian one), which together to its extraordinary ancestry (382,800 ya) represent strong evidence that L. (L.) chagasi/L. (L.) infantum chagasi is, in fact, native to the NW, and therefore with valid taxonomic status. Furthermore, the Honduran parasite, the most ancestral viscerotropic leishmanine parasite, showed genomic and clinical taxonomic characteristics compatible with a new Leishmania species causing ADL in Central America. MDPI 2022-12-21 /pmc/articles/PMC9865424/ /pubmed/36677318 http://dx.doi.org/10.3390/microorganisms11010025 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Silveira, Fernando Tobias Sousa Junior, Edivaldo Costa Silvestre, Rodrigo Vellasco Duarte Vasconcelos dos Santos, Thiago Sosa-Ochoa, Wilfredo Valeriano, Concepción Zúniga Ramos, Patrícia Karla Santos Casseb, Samir Mansour Moraes Lima, Luciana Vieira do Rêgo Campos, Marliane Batista da Matta, Vania Lucia Gomes, Claudia Maria Flores, Gabriela V. Araujo Sandoval Pacheco, Carmen M. Corbett, Carlos Eduardo Laurenti, Márcia Dalastra Comparative Genomic Analyses of New and Old World Viscerotropic Leishmanine Parasites: Further Insights into the Origins of Visceral Leishmaniasis Agents |
title | Comparative Genomic Analyses of New and Old World Viscerotropic Leishmanine Parasites: Further Insights into the Origins of Visceral Leishmaniasis Agents |
title_full | Comparative Genomic Analyses of New and Old World Viscerotropic Leishmanine Parasites: Further Insights into the Origins of Visceral Leishmaniasis Agents |
title_fullStr | Comparative Genomic Analyses of New and Old World Viscerotropic Leishmanine Parasites: Further Insights into the Origins of Visceral Leishmaniasis Agents |
title_full_unstemmed | Comparative Genomic Analyses of New and Old World Viscerotropic Leishmanine Parasites: Further Insights into the Origins of Visceral Leishmaniasis Agents |
title_short | Comparative Genomic Analyses of New and Old World Viscerotropic Leishmanine Parasites: Further Insights into the Origins of Visceral Leishmaniasis Agents |
title_sort | comparative genomic analyses of new and old world viscerotropic leishmanine parasites: further insights into the origins of visceral leishmaniasis agents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865424/ https://www.ncbi.nlm.nih.gov/pubmed/36677318 http://dx.doi.org/10.3390/microorganisms11010025 |
work_keys_str_mv | AT silveirafernandotobias comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT sousajunioredivaldocosta comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT silvestrerodrigovellascoduarte comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT vasconcelosdossantosthiago comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT sosaochoawilfredo comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT valerianoconcepcionzuniga comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT ramospatriciakarlasantos comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT cassebsamirmansourmoraes comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT limalucianavieiradorego comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT camposmarlianebatista comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT damattavanialucia comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT gomesclaudiamaria comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT floresgabrielavaraujo comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT sandovalpachecocarmenm comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT corbettcarloseduardo comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents AT laurentimarciadalastra comparativegenomicanalysesofnewandoldworldviscerotropicleishmanineparasitesfurtherinsightsintotheoriginsofvisceralleishmaniasisagents |