Dipeptidyl peptidase III as a DNA marker to investigate epidemiology and taxonomy of Old World Leishmania species.

<h4>Background</h4>Dipeptidyl peptidase III (DPPIII) member of M49 peptidase family is a zinc-dependent metallopeptidase that cleaves dipeptides sequentially from the N-terminus of its substrates. In Leishmania, DPPIII, was reported with other peptidases to play a significant role in par...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Insaf Bel Hadj Ali, Hamed Chouaieb, Yusr Saadi Ben Aoun, Emna Harigua-Souiai, Hejer Souguir, Alia Yaacoub, Oussaïma El Dbouni, Zoubir Harrat, Maowia M Mukhtar, Moncef Ben Said, Nabil Haddad, Akila Fathallah-Mili, Ikram Guizani
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
Materias:
Acceso en línea:https://doaj.org/article/3f51e8a49a2c4c47bbf6a839aaee125f
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:3f51e8a49a2c4c47bbf6a839aaee125f
record_format dspace
spelling oai:doaj.org-article:3f51e8a49a2c4c47bbf6a839aaee125f2021-12-02T20:23:43ZDipeptidyl peptidase III as a DNA marker to investigate epidemiology and taxonomy of Old World Leishmania species.1935-27271935-273510.1371/journal.pntd.0009530https://doaj.org/article/3f51e8a49a2c4c47bbf6a839aaee125f2021-07-01T00:00:00Zhttps://doi.org/10.1371/journal.pntd.0009530https://doaj.org/toc/1935-2727https://doaj.org/toc/1935-2735<h4>Background</h4>Dipeptidyl peptidase III (DPPIII) member of M49 peptidase family is a zinc-dependent metallopeptidase that cleaves dipeptides sequentially from the N-terminus of its substrates. In Leishmania, DPPIII, was reported with other peptidases to play a significant role in parasites' growth and survival. In a previous study, we used a coding sequence annotated as DPPIII to develop and evaluate a PCR assay that is specific to dermotropic Old World (OW) Leishmania species. Thus, our objective was to further assess use of this gene for Leishmania species identification and for phylogeny, and thus for diagnostic and molecular epidemiology studies of Old World Leishmania species.<h4>Methodology</h4>Orthologous DDPIII genes were searched in all Leishmania genomes and aligned to design PCR primers and identify relevant restriction enzymes. A PCR assays was developed and seventy-two Leishmania fragment sequences were analyzed using MEGA X genetics software to infer evolution and phylogenetic relationships of studied species and strains. A PCR-RFLP scheme was also designed and tested on 58 OW Leishmania strains belonging to 8 Leishmania species and evaluated on 75 human clinical skin samples.<h4>Findings</h4>Sequence analysis showed 478 variable sites (302 being parsimony informative). Test of natural selection (dN-dS) (-0.164, SE = 0.013) inferred a negative selection, characteristic of essential genes, corroborating the DPPIII importance for parasite survival. Inter- and intra-specific genetic diversity was used to develop universal amplification of a 662bp fragment. Sequence analyses and phylogenies confirmed occurrence of 6 clusters congruent to L. major, L. tropica, L. aethiopica, L. arabica, L. turanica, L. tarentolae species, and one to the L. infantum and L. donovani species complex. A PCR-RFLP algorithm for Leishmania species identification was designed using double digestions with HaeIII and KpnI and with SacI and PvuII endonucleases. Overall, this PCR-RFLP yielded distinct profiles for each of the species L. major, L. tropica, L. aethiopica, L. arabica and L. turanica and the L. (Sauroleishmania) L. tarentolae. The species L. donovani, and L. infantum shared the same profile except for strains of Indian origin. When tested on clinical samples, the DPPIII PCR showed sensitivities of 82.22% when compared to direct examination and was able to identify 84.78% of the positive samples.<h4>Conclusion</h4>The study demonstrates that DPPIII gene is suitable to detect and identify Leishmania species and to complement other molecular methods for leishmaniases diagnosis and epidemiology. Thus, it can contribute to evidence-based disease control and surveillance.Insaf Bel Hadj AliHamed ChouaiebYusr Saadi Ben AounEmna Harigua-SouiaiHejer SouguirAlia YaacoubOussaïma El DbouniZoubir HarratMaowia M MukhtarMoncef Ben SaidNabil HaddadAkila Fathallah-MiliIkram GuizaniPublic Library of Science (PLoS)articleArctic medicine. Tropical medicineRC955-962Public aspects of medicineRA1-1270ENPLoS Neglected Tropical Diseases, Vol 15, Iss 7, p e0009530 (2021)
institution DOAJ
collection DOAJ
language EN
topic Arctic medicine. Tropical medicine
RC955-962
Public aspects of medicine
RA1-1270
spellingShingle Arctic medicine. Tropical medicine
RC955-962
Public aspects of medicine
RA1-1270
Insaf Bel Hadj Ali
Hamed Chouaieb
Yusr Saadi Ben Aoun
Emna Harigua-Souiai
Hejer Souguir
Alia Yaacoub
Oussaïma El Dbouni
Zoubir Harrat
Maowia M Mukhtar
Moncef Ben Said
Nabil Haddad
Akila Fathallah-Mili
Ikram Guizani
Dipeptidyl peptidase III as a DNA marker to investigate epidemiology and taxonomy of Old World Leishmania species.
description <h4>Background</h4>Dipeptidyl peptidase III (DPPIII) member of M49 peptidase family is a zinc-dependent metallopeptidase that cleaves dipeptides sequentially from the N-terminus of its substrates. In Leishmania, DPPIII, was reported with other peptidases to play a significant role in parasites' growth and survival. In a previous study, we used a coding sequence annotated as DPPIII to develop and evaluate a PCR assay that is specific to dermotropic Old World (OW) Leishmania species. Thus, our objective was to further assess use of this gene for Leishmania species identification and for phylogeny, and thus for diagnostic and molecular epidemiology studies of Old World Leishmania species.<h4>Methodology</h4>Orthologous DDPIII genes were searched in all Leishmania genomes and aligned to design PCR primers and identify relevant restriction enzymes. A PCR assays was developed and seventy-two Leishmania fragment sequences were analyzed using MEGA X genetics software to infer evolution and phylogenetic relationships of studied species and strains. A PCR-RFLP scheme was also designed and tested on 58 OW Leishmania strains belonging to 8 Leishmania species and evaluated on 75 human clinical skin samples.<h4>Findings</h4>Sequence analysis showed 478 variable sites (302 being parsimony informative). Test of natural selection (dN-dS) (-0.164, SE = 0.013) inferred a negative selection, characteristic of essential genes, corroborating the DPPIII importance for parasite survival. Inter- and intra-specific genetic diversity was used to develop universal amplification of a 662bp fragment. Sequence analyses and phylogenies confirmed occurrence of 6 clusters congruent to L. major, L. tropica, L. aethiopica, L. arabica, L. turanica, L. tarentolae species, and one to the L. infantum and L. donovani species complex. A PCR-RFLP algorithm for Leishmania species identification was designed using double digestions with HaeIII and KpnI and with SacI and PvuII endonucleases. Overall, this PCR-RFLP yielded distinct profiles for each of the species L. major, L. tropica, L. aethiopica, L. arabica and L. turanica and the L. (Sauroleishmania) L. tarentolae. The species L. donovani, and L. infantum shared the same profile except for strains of Indian origin. When tested on clinical samples, the DPPIII PCR showed sensitivities of 82.22% when compared to direct examination and was able to identify 84.78% of the positive samples.<h4>Conclusion</h4>The study demonstrates that DPPIII gene is suitable to detect and identify Leishmania species and to complement other molecular methods for leishmaniases diagnosis and epidemiology. Thus, it can contribute to evidence-based disease control and surveillance.
format article
author Insaf Bel Hadj Ali
Hamed Chouaieb
Yusr Saadi Ben Aoun
Emna Harigua-Souiai
Hejer Souguir
Alia Yaacoub
Oussaïma El Dbouni
Zoubir Harrat
Maowia M Mukhtar
Moncef Ben Said
Nabil Haddad
Akila Fathallah-Mili
Ikram Guizani
author_facet Insaf Bel Hadj Ali
Hamed Chouaieb
Yusr Saadi Ben Aoun
Emna Harigua-Souiai
Hejer Souguir
Alia Yaacoub
Oussaïma El Dbouni
Zoubir Harrat
Maowia M Mukhtar
Moncef Ben Said
Nabil Haddad
Akila Fathallah-Mili
Ikram Guizani
author_sort Insaf Bel Hadj Ali
title Dipeptidyl peptidase III as a DNA marker to investigate epidemiology and taxonomy of Old World Leishmania species.
title_short Dipeptidyl peptidase III as a DNA marker to investigate epidemiology and taxonomy of Old World Leishmania species.
title_full Dipeptidyl peptidase III as a DNA marker to investigate epidemiology and taxonomy of Old World Leishmania species.
title_fullStr Dipeptidyl peptidase III as a DNA marker to investigate epidemiology and taxonomy of Old World Leishmania species.
title_full_unstemmed Dipeptidyl peptidase III as a DNA marker to investigate epidemiology and taxonomy of Old World Leishmania species.
title_sort dipeptidyl peptidase iii as a dna marker to investigate epidemiology and taxonomy of old world leishmania species.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/3f51e8a49a2c4c47bbf6a839aaee125f
work_keys_str_mv AT insafbelhadjali dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT hamedchouaieb dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT yusrsaadibenaoun dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT emnahariguasouiai dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT hejersouguir dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT aliayaacoub dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT oussaimaeldbouni dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT zoubirharrat dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT maowiammukhtar dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT moncefbensaid dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT nabilhaddad dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT akilafathallahmili dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
AT ikramguizani dipeptidylpeptidaseiiiasadnamarkertoinvestigateepidemiologyandtaxonomyofoldworldleishmaniaspecies
_version_ 1718374101488238592