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Genomic analysis of two phlebotomine sand fly vectors of leishmania from the new and old World

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Genomic analysis of two phlebotomine sand fly vectors of leishmania from the new and old World. / Sandflies.
In: PLoS Neglected Tropical Diseases, Vol. 17, No. 4, e0010862, 12.04.2023.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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Sandflies. Genomic analysis of two phlebotomine sand fly vectors of leishmania from the new and old World. PLoS Neglected Tropical Diseases. 2023 Apr 12;17(4):e0010862. doi: 10.1371/journal.pntd.0010862

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Sandflies. / Genomic analysis of two phlebotomine sand fly vectors of leishmania from the new and old World. In: PLoS Neglected Tropical Diseases. 2023 ; Vol. 17, No. 4.

Bibtex

@article{38f238b9414043d68a77d90d0e14aabb,
title = "Genomic analysis of two phlebotomine sand fly vectors of leishmania from the new and old World",
abstract = "Phlebotomine sand flies are of global significance as important vectors of human disease, transmitting bacterial, viral, and protozoan pathogens, including the kinetoplastid parasites of the genus Leishmania, the causative agents of devastating diseases collectively termed leishmaniasis. More than 40 pathogenic Leishmania species are transmitted to humans by approximately 35 sand fly species in 98 countries with hundreds of millions of people at risk around the world. No approved efficacious vaccine exists for leishmaniasis and available therapeutic drugs are either toxic and/or expensive, or the parasites are becoming resistant to the more recently developed drugs. Therefore, sand fly and/or reservoir control are currently the most effective strategies to break transmission. To better understand the biology of sand flies, including the mechanisms involved in their vectorial capacity, insecticide resistance, and population structures we sequenced the genomes of two geographically widespread and important sand fly vector species: Phlebotomus papatasi, a vector of Leishmania parasites that cause cutaneous leishmaniasis, (distributed in Europe, the Middle East and North Africa) and Lutzomyia longipalpis, a vector of Leishmania parasites that cause visceral leishmaniasis (distributed across Central and South America). We categorized and curated genes involved in processes important to their roles as disease vectors, including chemosensation, blood feeding, circadian rhythm, immunity, and detoxification, as well as mobile genetic elements. We also defined gene orthology and observed micro-synteny among the genomes. Finally, we present the genetic diversity and population structure of these species in their respective geographical areas. These genomes will be a foundation on which to base future efforts to prevent vector-borne transmission of Leishmania parasites.",
keywords = "Animals, Genomics, Humans, Leishmania/genetics, Leishmaniasis, Cutaneous, Phlebotomus/parasitology, Psychodidae/parasitology",
author = "Sandflies and Fr{\'e}d{\'e}ric Labb{\'e} and Maha Abdeladhim and Jenica Abrudan and Araki, {Alejandra Saori} and Araujo, {Ricardo N} and Peter Arensburger and Benoit, {Joshua B} and Brazil, {Reginaldo Pecanha} and Bruno, {Rafaela V} and {Bueno da Silva Rivas}, Gustavo and {Carvalho de Abreu}, Vinicius and Jason Charamis and Coutinho-Abreu, {Iliano V} and {da Costa-Latg{\'e}}, {Samara G} and Alistair Darby and Dillon, {Viv M} and Emrich, {Scott J} and Daniela Fernandez-Medina and {Figueiredo Gontijo}, Nelder and Flanley, {Catherine M} and Derek Gatherer and Genta, {Fernando A} and Sandra Gesing and Giraldo-Calder{\'o}n, {Gloria I} and Bruno Gomes and Aguiar, {Eric Roberto Guimaraes Rocha} and Hamilton, {James G C} and Omar Hamarsheh and Mallory Hawksworth and Hendershot, {Jacob M} and Hickner, {Paul V} and Jean-Luc Imler and Panagiotis Ioannidis and Jennings, {Emily C} and Shaden Kamhawi and Charikleia Karageorgiou and Kennedy, {Ryan C} and Andreas Krueger and Latorre-Estivalis, {Jos{\'e} M} and Petros Ligoxygakis and Meireles-Filho, {Antonio Carlos A} and Patrick Minx and Miranda, {Jose Carlos} and Montague, {Michael J} and Nowling, {Ronald J} and Fabiano Oliveira and Jo{\~a}o Ortig{\~a}o-Farias and Pavan, {Marcio G} and Sant'Anna, {Mauricio R V} and Dillon, {Rod J}",
year = "2023",
month = apr,
day = "12",
doi = "10.1371/journal.pntd.0010862",
language = "English",
volume = "17",
journal = "PLoS Neglected Tropical Diseases",
issn = "1935-2727",
publisher = "Public Library of Science",
number = "4",

}

RIS

TY - JOUR

T1 - Genomic analysis of two phlebotomine sand fly vectors of leishmania from the new and old World

AU - Sandflies

AU - Labbé, Frédéric

AU - Abdeladhim, Maha

AU - Abrudan, Jenica

AU - Araki, Alejandra Saori

AU - Araujo, Ricardo N

AU - Arensburger, Peter

AU - Benoit, Joshua B

AU - Brazil, Reginaldo Pecanha

AU - Bruno, Rafaela V

AU - Bueno da Silva Rivas, Gustavo

AU - Carvalho de Abreu, Vinicius

AU - Charamis, Jason

AU - Coutinho-Abreu, Iliano V

AU - da Costa-Latgé, Samara G

AU - Darby, Alistair

AU - Dillon, Viv M

AU - Emrich, Scott J

AU - Fernandez-Medina, Daniela

AU - Figueiredo Gontijo, Nelder

AU - Flanley, Catherine M

AU - Gatherer, Derek

AU - Genta, Fernando A

AU - Gesing, Sandra

AU - Giraldo-Calderón, Gloria I

AU - Gomes, Bruno

AU - Aguiar, Eric Roberto Guimaraes Rocha

AU - Hamilton, James G C

AU - Hamarsheh, Omar

AU - Hawksworth, Mallory

AU - Hendershot, Jacob M

AU - Hickner, Paul V

AU - Imler, Jean-Luc

AU - Ioannidis, Panagiotis

AU - Jennings, Emily C

AU - Kamhawi, Shaden

AU - Karageorgiou, Charikleia

AU - Kennedy, Ryan C

AU - Krueger, Andreas

AU - Latorre-Estivalis, José M

AU - Ligoxygakis, Petros

AU - Meireles-Filho, Antonio Carlos A

AU - Minx, Patrick

AU - Miranda, Jose Carlos

AU - Montague, Michael J

AU - Nowling, Ronald J

AU - Oliveira, Fabiano

AU - Ortigão-Farias, João

AU - Pavan, Marcio G

AU - Sant'Anna, Mauricio R V

AU - Dillon, Rod J

PY - 2023/4/12

Y1 - 2023/4/12

N2 - Phlebotomine sand flies are of global significance as important vectors of human disease, transmitting bacterial, viral, and protozoan pathogens, including the kinetoplastid parasites of the genus Leishmania, the causative agents of devastating diseases collectively termed leishmaniasis. More than 40 pathogenic Leishmania species are transmitted to humans by approximately 35 sand fly species in 98 countries with hundreds of millions of people at risk around the world. No approved efficacious vaccine exists for leishmaniasis and available therapeutic drugs are either toxic and/or expensive, or the parasites are becoming resistant to the more recently developed drugs. Therefore, sand fly and/or reservoir control are currently the most effective strategies to break transmission. To better understand the biology of sand flies, including the mechanisms involved in their vectorial capacity, insecticide resistance, and population structures we sequenced the genomes of two geographically widespread and important sand fly vector species: Phlebotomus papatasi, a vector of Leishmania parasites that cause cutaneous leishmaniasis, (distributed in Europe, the Middle East and North Africa) and Lutzomyia longipalpis, a vector of Leishmania parasites that cause visceral leishmaniasis (distributed across Central and South America). We categorized and curated genes involved in processes important to their roles as disease vectors, including chemosensation, blood feeding, circadian rhythm, immunity, and detoxification, as well as mobile genetic elements. We also defined gene orthology and observed micro-synteny among the genomes. Finally, we present the genetic diversity and population structure of these species in their respective geographical areas. These genomes will be a foundation on which to base future efforts to prevent vector-borne transmission of Leishmania parasites.

AB - Phlebotomine sand flies are of global significance as important vectors of human disease, transmitting bacterial, viral, and protozoan pathogens, including the kinetoplastid parasites of the genus Leishmania, the causative agents of devastating diseases collectively termed leishmaniasis. More than 40 pathogenic Leishmania species are transmitted to humans by approximately 35 sand fly species in 98 countries with hundreds of millions of people at risk around the world. No approved efficacious vaccine exists for leishmaniasis and available therapeutic drugs are either toxic and/or expensive, or the parasites are becoming resistant to the more recently developed drugs. Therefore, sand fly and/or reservoir control are currently the most effective strategies to break transmission. To better understand the biology of sand flies, including the mechanisms involved in their vectorial capacity, insecticide resistance, and population structures we sequenced the genomes of two geographically widespread and important sand fly vector species: Phlebotomus papatasi, a vector of Leishmania parasites that cause cutaneous leishmaniasis, (distributed in Europe, the Middle East and North Africa) and Lutzomyia longipalpis, a vector of Leishmania parasites that cause visceral leishmaniasis (distributed across Central and South America). We categorized and curated genes involved in processes important to their roles as disease vectors, including chemosensation, blood feeding, circadian rhythm, immunity, and detoxification, as well as mobile genetic elements. We also defined gene orthology and observed micro-synteny among the genomes. Finally, we present the genetic diversity and population structure of these species in their respective geographical areas. These genomes will be a foundation on which to base future efforts to prevent vector-borne transmission of Leishmania parasites.

KW - Animals

KW - Genomics

KW - Humans

KW - Leishmania/genetics

KW - Leishmaniasis, Cutaneous

KW - Phlebotomus/parasitology

KW - Psychodidae/parasitology

U2 - 10.1371/journal.pntd.0010862

DO - 10.1371/journal.pntd.0010862

M3 - Journal article

C2 - 37043542

VL - 17

JO - PLoS Neglected Tropical Diseases

JF - PLoS Neglected Tropical Diseases

SN - 1935-2727

IS - 4

M1 - e0010862

ER -