TY - JOUR
T1 - Genetic diversity and phylogenetic relationships between Leishmania infantum from dogs, humans and wildlife in south-east Spain
AU - Ortuño, María
AU - Latrofa, Maria S
AU - Iborra, María A
AU - Pérez-Cutillas, Pedro
AU - Bernal, Luis J
AU - Risueño, José
AU - Muñoz, Clara
AU - Bernal, Ana
AU - Sánchez-Lopez, Pedro F
AU - Segovia, Manuel
AU - Annoscia, Giada
AU - Maia, Carla
AU - Cortes, Sofia
AU - Campino, Lenea
AU - Otranto, Domenico
AU - Berriatua, Eduardo
N1 - Funding Information:
Financial support to carry out this study was provided by the Spanish Ministry of Science and Innovation (Pr. Ref: AGL2013‐46981‐R) and the Instituto de Salud Carlos III within the Network of Tropical Diseases Research (RICET RD06/0021/1007). María Ortuño was granted a Short‐Term Scientific Mission by COST Action TD1303 (European Network for Neglected Vectors and Vector‐borne infections) to do some of the present work, and she and Clara Muñoz hold a “Contrato Predoctoral FPU” from the Universidad de Murcia. Samples from zoo animals were obtained thanks to collaboration with Terra Natura zoological and its veterinarian Ricardo Navarro López. Sofia Cortes has the support of the Fundação para a Ciência e Tecnologia/Ministério da Ciência, Tecnologia e Ensino Superior (Investigator Starting Grant IF/0773/2015).
Publisher Copyright:
© 2019 Blackwell Verlag GmbH
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Leishmania infantum causes human and canine leishmaniosis. The parasite, transmitted by phlebotomine sand flies, infects species other than dogs and people, including wildlife, although their role as reservoirs of infection remains unknown for most species. Molecular typing of parasites to investigate genetic variability and evolutionary proximity can help understand transmission cycles and designing control strategies. We investigated Leishmania DNA variability in kinetoplast (kDNA) and internal transcribed spacer 2 (ITS2) sequences in asymptomatically infected wildlife (n = 58) and symptomatically and asymptomatically infected humans (n = 38) and dogs (n = 15) from south-east Spain, using single nucleotide polymorphisms (SNPs) and in silico restriction fragment length polymorphism (RFLP) analyses. All ITS2 sequences (n = 76) displayed a 99%-100% nucleotide identity with a L. infantum reference sequence, except one with a 98% identity to a reference Leishmania panamensis sequence, from an Ecuadorian patient. No heterogeneity was recorded in the 73 L. infantum ITS2 sequences except for one SNP in a human parasite sequence. In contrast, kDNA analysis of 44 L. infantum sequences revealed 11 SNP genotypes (nucleotide variability up to 4.3%) and four RFLP genotypes including B, F and newly described S and T genotypes. Genotype frequency was significantly greater in symptomatic compared to asymptomatic individuals. Both methods similarly grouped parasites as predominantly or exclusively found in humans, in dogs, in wildlife or in all three of them. Accordingly, the phylogenetic analysis of kDNA sequences revealed three main clusters, two as a paraphyletic human parasites clade and a third including dogs, people and wildlife parasites. Results suggest that Leishmania infantum genetics is complex even in small geographical areas and that, probably, several independent transmission cycles take place simultaneously including some connecting animals and humans. Investigating these transmission networks may be useful in understanding the transmission dynamics, infection risk and therefore in planning L. infantum control strategies.
AB - Leishmania infantum causes human and canine leishmaniosis. The parasite, transmitted by phlebotomine sand flies, infects species other than dogs and people, including wildlife, although their role as reservoirs of infection remains unknown for most species. Molecular typing of parasites to investigate genetic variability and evolutionary proximity can help understand transmission cycles and designing control strategies. We investigated Leishmania DNA variability in kinetoplast (kDNA) and internal transcribed spacer 2 (ITS2) sequences in asymptomatically infected wildlife (n = 58) and symptomatically and asymptomatically infected humans (n = 38) and dogs (n = 15) from south-east Spain, using single nucleotide polymorphisms (SNPs) and in silico restriction fragment length polymorphism (RFLP) analyses. All ITS2 sequences (n = 76) displayed a 99%-100% nucleotide identity with a L. infantum reference sequence, except one with a 98% identity to a reference Leishmania panamensis sequence, from an Ecuadorian patient. No heterogeneity was recorded in the 73 L. infantum ITS2 sequences except for one SNP in a human parasite sequence. In contrast, kDNA analysis of 44 L. infantum sequences revealed 11 SNP genotypes (nucleotide variability up to 4.3%) and four RFLP genotypes including B, F and newly described S and T genotypes. Genotype frequency was significantly greater in symptomatic compared to asymptomatic individuals. Both methods similarly grouped parasites as predominantly or exclusively found in humans, in dogs, in wildlife or in all three of them. Accordingly, the phylogenetic analysis of kDNA sequences revealed three main clusters, two as a paraphyletic human parasites clade and a third including dogs, people and wildlife parasites. Results suggest that Leishmania infantum genetics is complex even in small geographical areas and that, probably, several independent transmission cycles take place simultaneously including some connecting animals and humans. Investigating these transmission networks may be useful in understanding the transmission dynamics, infection risk and therefore in planning L. infantum control strategies.
KW - Leishmania infantum
KW - Dog
KW - Genetic diversity
KW - Human
KW - Phylogeny
KW - Wildlife
UR - https://onlinelibrary.wiley.com/doi/full/10.1111/zph.12646
UR - http://www.scopus.com/inward/record.url?scp=85070879725&partnerID=8YFLogxK
U2 - 10.1111/zph.12646
DO - 10.1111/zph.12646
M3 - Article
C2 - 31512370
SN - 1863-1959
VL - 66
SP - 961
EP - 973
JO - Zoonoses And Public Health
JF - Zoonoses And Public Health
IS - 8
ER -