Lehane, M. J. Biology of Blood-Sucking Bugs 2d edn (ed M. J. Lehane) (Cambridge College Press, 2005).
WHO. Reality Sheet: Vector-Borne Illnesses, https://www.who.int/news-room/fact-sheets/element/vector-borne-diseases (2020).
Müller, R. R. F., Kendrovski, V. & Montag, D. Biodiversity and Well being within the Face of Local weather Exchange (eds Marselle, R., Stadler, J., Korn, H., Irvine, Ok. & Bonn, A.) (Springer, 2019).
Hotez, P. J., Aksoy, S., Brindley, P. J. & Kamhawi, S. What constitutes a left out tropical illness? PLoS Negl. Trop. Dis. 14, e0008001 (2020).
Alvarez-Hernandez, D. A., Rivero-Zambrano, L., Martinez-Juarez, L. A. & Garcia-Rodriguez-Arana, R. Overcoming the worldwide burden of left out tropical illnesses. Ther. Adv. Infect. Dis. 7, 2049936120966449 (2020).
Herricks, J. R. et al. The worldwide burden of illness learn about 2013: What does it imply for the NTDs? PLoS Negl. Trop. Dis. 11, e0005424 (2017).
Akhoundi, M. et al. A Ancient Evaluation of the Classification, Evolution, and Dispersion of Leishmania Parasites and Sandflies. PLoS Negl. Trop. Dis. 10, e0004349 (2016).
Bates, P. A. Transmission of Leishmania metacyclic promastigotes through phlebotomine sand flies. Int. J. Parasitol. 37, 1097–1106 (2007).
Burza, S., Croft, S. L. & Boelaert, M. Leishmaniasis. Lancet 392, 951–970 (2018).
Cunha, J. et al. Characterization of the biology and infectivity of Leishmania infantum viscerotropic and dermotropic lines remoted from HIV+ and HIV− sufferers within the murine type of visceral Leishmaniasis. Parasit. Vectors 6, 122 (2013).
Ranasinghe, S. et al. Leishmania donovani zymodeme MON-37 remoted from an autochthonous visceral Leishmaniasis affected person in Sri Lanka. Pathog. Glob. Well being 106, 421–424 (2012).
Weiss, F., Vogenthaler, N., Franco-Paredes, C. & Parker, S. R. Leishmania tropica-induced cutaneous and presumptive concomitant viscerotropic Leishmaniasis with extended incubation. Arch. Dermatol. 145, 1023–1026 (2009).
Cecilio, P. et al. Deception and manipulation: the fingers of Leishmania, a a success parasite. Entrance. Immunol. 5, 480 (2014).
Belli, A. et al. Well-liked abnormal cutaneous Leishmaniasis brought about through Leishmania (L.) Chagasi in Nicaragua. Am. J. Trop. Med. Hyg. 61, 380–385 (1999).
Clemente, W. T., Couto, C. A., Ribeiro, D. D., de Medeiros Chaves Franca, M. & Sanches, M. D. An abnormal process visceral Leishmaniasis (Kala-azar) in a liver transplant recipient. Transplantation 83, 368–369 (2007).
Diro, E. et al. Peculiar manifestations of visceral Leishmaniasis in sufferers with HIV in north Ethiopia: An opening in pointers for the control of opportunistic infections in useful resource deficient settings. Lancet Infect. Dis. 15, 122–129 (2015).
van Griensven, J., Carrillo, E., Lopez-Velez, R., Lynen, L. & Moreno, J. Leishmaniasis in immunosuppressed people. Clin. Microbiol. Infect. 20, 286–299 (2014).
Jambulingam, P., Pradeep Kumar, N., Nandakumar, S., Paily, Ok. P. & Srinivasan, R. Home canine as reservoir hosts for Leishmania donovani within the southernmost Western Ghats in India. Acta Trop. 171, 64–67 (2017).
Dereure, J. et al. Visceral Leishmaniasis in japanese Sudan: Parasite id in people and canine; host−parasite relationships. Microbes Infect. 5, 1103–1108 (2003).
Elnaiem, D. A. et al. The Egyptian mongoose, Herpestes ichneumon, is a conceivable reservoir host of visceral Leishmaniasis in japanese Sudan. Parasitology 122, 531–536 (2001).
Gradoni, L. The Leishmaniases: Previous Omitted Tropical Illnesses (eds Bruschi, F. & Gradoni, L.) 1–13 (Springer World Publishing, 2018).
Kamhawi, S. The yin and yang of Leishmaniasis regulate. PLoS Negl. Trop. Dis. 11, e0005529 (2017).
Oryan, A. & Akbari, M. International chance elements in Leishmaniasis. Asian Percent. J. Trop. Med. 9, 925–932 (2016).
Pavli, A. & Maltezou, H. C. Leishmaniasis, an rising an infection in vacationers. Int. J. Infect. Dis. 14, e1032–e1039 (2010).
Berry, I. & Berrang-Ford, L. Leishmaniasis, warfare, and political terror: A spatio-temporal research. Soc. Sci. Med. 167, 140–149 (2016).
Dujardin, J. C. et al. Unfold of vector-borne illnesses and overlook of Leishmaniasis, Europe. Emerg. Infect. Dis. 14, 1013–1018 (2008).
Kholoud, Ok., Denis, S., Lahouari, B., El Hidan, M. A. & Souad, B. Control of Leishmaniases within the generation of weather trade in Morocco. Int. J. Environ. Res. Public Well being https://doi.org/10.3390/ijerph15071542 (2018).
Shimabukuro, P. H. F., de Andrade, A. J. & Galati, E. A. B. Tick list of American sand flies (Diptera, Psychodidae, Phlebotominae): genera, species, and their distribution. Zookeys 660, 67–106 (2017).
Lane, R. P. Clinical Bugs and Arachnids (Springer, 1993).
Dvorak, V., Shaw, J. & Volf, P. The Leishmaniases: Previous Omitted Tropical Illnesses (eds Bruschi, F. & Gradoni, F.) 31–77 (Springer World Publishing, 2018).
Maroli, M., Feliciangeli, M. D., Bichaud, L., Charrel, R. N. & Gradoni, L. Phlebotomine sandflies and the spreading of Leishmaniases and different illnesses of public well being fear. Med. Vet. Entomol. 27, 123–147 (2013).
ECDC. Phlebotomine sand flies—factsheet for mavens, https://www.ecdc.europa.european/en/disease-vectors/details/phlebotomine-sand-flies (2014).
Benkova, I. & Volf, P. Impact of temperature on metabolism of Phlebotomus papatasi (Diptera: Psychodidae). J. Med. Entomol. 44, 150–154 (2007).
Erguler, Ok. et al. A climate-driven and box data-assimilated inhabitants dynamics type of sand flies. Sci. Rep. 9, 2469 (2019).
Kasap, O. E. & Alten, B. Laboratory estimation of degree-day developmental necessities of Phlebotomus papatasi (Diptera: Psychodidae). J. Vector Ecol. 30, 328–333 (2005).
Killick-Kendrick, R. The biology and regulate of phlebotomine sand flies. Clin. Dermatol. 17, 279–289 (1999).
Killick-Kendrick, R. Global Elegance Parasites: Leishmania (ed Farrell, J. P.) (Springer, 2001).
Carrier, M. Clinical Entomology for Scholars (Cambridge College Press, 2012).
Legal professional, P., Killick-Kendrick, M., Rowland, T., Rowton, E. & Volf, P. Laboratory colonization and mass rearing of phlebotomine sand flies (Diptera, Psychodidae). Parasite 24, 42 (2017).
Volf, P. & Volfova, V. Established order and upkeep of sand fly colonies. J. Vector Ecol. 36, S1–S9 (2011).
Rutledge, L. C. & Gupta, R. Ok. Clinical and Veterinary Entomology (eds Mullen, G. & Durden, L.) (Instructional Press, 2002).
Gebresilassie, A. et al. Host-feeding choice of Phlebotomus orientalis (Diptera: Psychodidae) in a virulent disease focal point of visceral Leishmaniasis in northern Ethiopia. Parasit. Vectors 8, 270 (2015).
Handman, E. & Bullen, D. V. Interplay of Leishmania with the host macrophage. Developments Parasitol. 18, 332–334 (2002).
Quinnell, R. J. & Courtenay, O. Transmission, reservoir hosts and regulate of zoonotic visceral Leishmaniasis. Parasitology 136, 1915–1934 (2009).
USA_Department_of_Defense. Sand Flies – Importance, Surveillance, and Keep an eye on in ContingencyOperations (Armed Forces Pest Control Board, 2015).
Abdeladhim, M., Kamhawi, S. & Valenzuela, J. G. What’s at the back of a sand fly chunk? The profound impact of sand fly saliva on host hemostasis, irritation, and immunity. Infect. Genet. Evol. 28, 691–703 (2014).
Minnick, M. F. et al. Oroya fever and verruga peruana: bartonelloses distinctive to South The united states. PLoS Negl. Trop. Dis. 8, e2919 (2014).
Pons, M. J., Gomes, C., Del Valle-Mendoza, J. & Ruiz, J. Carrion’s illness: Greater than a sand fly-vectored sickness. PLoS Pathog. 12, e1005863 (2016).
Moriconi, M. et al. Phlebotomine sand fly-borne pathogens within the Mediterranean Basin: Human Leishmaniasis and phlebovirus infections. PLoS Negl. Trop. Dis. 11, e0005660 (2017).
Elliott, R. M. & Brennan, B. Rising phleboviruses. Curr. Opin. Virol. 5, 50–57 (2014).
Alkan, C. et al. Sandfly-borne phleboviruses of Eurasia and Africa: Epidemiology, genetic variety, geographic vary, regulate measures. Antivir. Res. 100, 54–74 (2013).
Howell, B. A., Azar, M. M., Landry, M. L. & Shaw, A. C. Toscana virus encephalitis in a traveler returning to the US. J. Clin. Microbiol. 53, 1445–1447 (2015).
Peyrefitte, C. N. et al. Toscana virus and acute meningitis, France. Emerg. Infect. Dis. 11, 778–780 (2005).
Bates, P. A. Leishmania sand fly interplay: Development and demanding situations. Curr. Opin. Microbiol. 11, 340–344 (2008).
Killick-Kendrick, R. Phlebotomine vectors of the Leishmaniases: a evaluation. Med. Vet. Entomol. 4, 1–24 (1990).
WHO. Keep an eye on of the Leishmaniases. Global Well being Organ Tech Rep Ser xii-xiii, 1–186 (Global Well being Group (WHO), 2010).
Volf, P. & Myskova, J. Sand flies and Leishmania: Particular as opposed to permissive vectors. Developments Parasitol. 23, 91–92 (2007).
Cecilio, P. et al. Exploring Lutzomyia longipalpis sand fly vector competence for Leishmania primary parasites. J. Infect. Dis. 222, 1199–1203 (2020).
Dostalova, A. & Volf, P. Leishmania construction in sand flies: Parasite–vector interactions assessment. Parasit. Vectors 5, 276 (2012).
Kamhawi, S. Phlebotomine sand flies and Leishmania parasites: Buddies or foes? Developments Parasitol. 22, 439–445 (2006).
Kamhawi, S. et al. A job for insect galectins in parasite survival. Cellular 119, 329–341 (2004).
Forestier, C. L., Gao, Q. & Boons, G. J. Leishmania lipophosphoglycan: How you can determine structure-activity relationships for this extremely advanced and multifunctional glycoconjugate? Entrance. Cellular Infect. Microbiol. 4, 193 (2014).
Myskova, J. et al. Characterization of a midgut mucin-like glycoconjugate of Lutzomyia longipalpis with a possible function in Leishmania attachment. Parasit. Vectors 9, 413 (2016).
Ramalho-Ortigao, M., Saraiva, E. M. & Traub-Cseko, Y. M. Sand fly-Leishmania interactions: lengthy relationships don’t seem to be essentially simple. Open Parasitol. J. 4, 195–204 (2010).
Nieves, E. & Pimenta, P. F. Construction of Leishmania (Viannia) braziliensis and Leishmania (Leishmania) amazonensis within the sand fly Lutzomyia migonei (Diptera: Psychodidae). J. Med. Entomol. 37, 134–140 (2000).
Legal professional, P. G. et al. Construction of Leishmania primary in Phlebotomus duboscqi and Sergentomyia schwetzi (Diptera: Psychodidae). Am. J. Trop. Med. Hyg. 43, 31–43 (1990).
Rogers, M. E. The function of leishmania proteophosphoglycans in sand fly transmission and an infection of the Mammalian host. Entrance. Microbiol. 3, 223 (2012).
Pimenta, P. F., Modi, G. B., Pereira, S. T., Shahabuddin, M. & Sacks, D. L. A singular function for the peritrophic matrix in protective Leishmania from the hydrolytic actions of the sand fly midgut. Parasitology 115, 359–369 (1997).
Pruzinova, Ok. et al. Leishmania mortality in sand fly blood meal isn’t species-specific and does no longer consequence from direct impact of proteinases. Parasit. Vectors 11, 37 (2018).
Rego, F. D. & Soares, R. P. Lutzomyia longipalpis: An replace in this sand fly vector. Acad. Bras. Cienc. 93, e20200254 (2021).
Sant’anna, M. R., Diaz-Albiter, H., Mubaraki, M., Dillon, R. J. & Bates, P. A. Inhibition of trypsin expression in Lutzomyia longipalpis the usage of RNAi complements the survival of Leishmania. Parasit. Vectors 2, 62 (2009).
Silva Fernandes, T. L. et al. Galactosamine reduces sandfly intestine protease exercise thru TOR downregulation and will increase Lutzomyia susceptibility to Leishmania. Insect Biochem. Mol. Biol. 122, 103393 (2020).
Secundino, N. F., Eger-Mangrich, I., Braga, E. M., Santoro, M. M. & Pimenta, P. F. Lutzomyia longipalpis peritrophic matrix: formation, constitution, and chemical composition. J. Med. Entomol. 42, 928–938 (2005).
Sadlova, J., Homola, M., Myskova, J., Jancarova, M. & Volf, P. Refractoriness of Sergentomyia schwetzi to Leishmania spp. is mediated through the peritrophic matrix. PLoS Negl. Trop. Dis. 12, e0006382 (2018).
Wilson, R. et al. Level-specific adhesion of Leishmania promastigotes to sand fly midguts assessed the usage of an advanced comparative binding assay. PLoS Negl. Trop. Dis. https://doi.org/10.1371/magazine.pntd.0000816 (2010).
Sadlova, J. et al. Sergentomyia schwetzi isn’t a reliable vector for Leishmania donovani and different Leishmania species pathogenic to people. Parasit. Vectors 6, 186 (2013).
Gossage, S. M., Rogers, M. E. & Bates, P. A. Two separate expansion levels right through the advance of Leishmania in sand flies: Implications for working out the existence cycle. Int. J. Parasitol. 33, 1027–1034 (2003).
Rogers, M. E., Probability, M. L. & Bates, P. A. The function of promastigote secretory gel within the beginning and transmission of the infective degree of Leishmania mexicana through the sandfly Lutzomyia longipalpis. Parasitology 124, 495–507 (2002).
Serafim, T. D. et al. Leishmania metacyclogenesis is promoted within the absence of purines. PLoS Negl. Trop. Dis. 6, e1833 (2012).
Sunter, J. & Gull, Ok. Form, shape, serve as and Leishmania pathogenicity: from textbook descriptions to organic working out. Open Biol. https://doi.org/10.1098/rsob.170165 (2017).
Rogers, M. E. et al. Leishmania chitinase facilitates colonization of sand fly vectors and complements transmission to mice. Cellular Microbiol. 10, 1363–1372 (2008).
Schlein, Y., Jacobson, R. L. & Messer, G. Leishmania infections harm the feeding mechanism of the sandfly vector and put in force parasite transmission through chunk. Proc. Natl Acad. Sci. USA 89, 9944–9948 (1992).
Volf, P., Hajmova, M., Sadlova, J. & Votypka, J. Blocked stomodeal valve of the insect vector: identical mechanism of transmission in two trypanosomatid fashions. Int. J. Parasitol. 34, 1221–1227 (2004).
Coutinho-Abreu, I. V. et al. Distinct gene expression patterns in vector-residing Leishmania infantum determine parasite stage-enriched markers. PLoS Negl. Trop. Dis. 14, e0008014 (2020).
In a position, P. D. Biology of phlebotomine sand flies as vectors of illness brokers. Annu. Rev. Entomol. 58, 227–250 (2013).
Serafim, T. D. et al. Sequential blood foods advertise Leishmania replication and opposite metacyclogenesis augmenting vector infectivity. Nat. Microbiol. 3, 548–555 (2018).
Loeuillet, C., Banuls, A. L. & Cover, M. Find out about of Leishmania pathogenesis in mice: Experimental concerns. Parasit. Vectors 9, 144 (2016).
Rogers, M. E. & Bates, P. A. Leishmania manipulation of sand fly feeding habits leads to enhanced transmission. PLoS Pathog. 3, e91 (2007).
Giraud, E. et al. Leishmania proteophosphoglycans regurgitated from inflamed sand flies boost up dermal wound restore and exacerbate Leishmaniasis by means of insulin-like expansion issue 1-dependent signalling. PLoS Pathog. 14, e1006794 (2018).
Abdoli, A., Maspi, N. & Ghaffarifar, F. Wound therapeutic in cutaneous Leishmaniasis: A double edged sword of IL-10 and TGF-beta. Comp. Immunol. Microbiol. Infect. Dis. 51, 15–26 (2017).
1st Earl Baldwin of Bewdley, T. et al. Wound therapeutic reaction is a significant contributor to the severity of cutaneous Leishmaniasis within the ear type of an infection. Parasite Immunol. 29, 501–513 (2007).
Atayde, V. D. et al. Exosome secretion through the parasitic protozoan Leishmania throughout the sand fly midgut. Cellular Rep. 13, 957–967 (2015).
Perez-Cabezas, B. et al. Extra than simply exosomes: Distinct Leishmania infantum extracellular merchandise potentiate the status quo of an infection. J. Extracell. Vesicles 8, 1541708 (2019).
Andrade, B. B., de Oliveira, C. I., Brodskyn, C. I., Barral, A. & Barral-Netto, M. Position of sand fly saliva in human and experimental Leishmaniasis: Present insights. Scand. J. Immunol. 66, 122–127 (2007).
Lestinova, T., Rohousova, I., Sima, M., de Oliveira, C. I. & Volf, P. Insights into the sand fly saliva: Blood-feeding and immune interactions between sand flies, hosts, and Leishmania. PLoS Negl. Trop. Dis. 11, e0005600 (2017).
Telleria, E. L., Martins-da-Silva, A., Tempone, A. J. & Traub-Cseko, Y. M. Leishmania, microbiota, and sand fly immunity. Parasitology 145, 1336–1353 (2018).
Kelly, P. H. et al. The Intestine microbiome of the vector lutzomyia longipalpis is very important for survival of Leishmania infantum. mBio https://doi.org/10.1128/mBio.01121-16 (2017).
Dey, R. et al. Intestine microbes egested right through bites of inflamed sand flies increase severity of Leishmaniasis by means of inflammasome-derived IL-1beta. Cellular Host Microbe 23, 134–143 e136 (2018).
Peters, N. C. et al. In vivo imaging finds an very important function for neutrophils in Leishmaniasis transmitted through sand flies. Science 321, 970–974 (2008).
Carlsen, E. D. et al. Permissive and protecting roles for neutrophils in Leishmaniasis. Clin. Exp. Immunol. 182, 109–118 (2015).
Gomes, R. & Oliveira, F. The immune reaction to sand fly salivary proteins and its affect on Leishmania immunity. Entrance. Immunol. 3, 110 (2012).
Belkaid, Y. et al. Construction of a herbal type of cutaneous Leishmaniasis: tough results of vector saliva and saliva preexposure at the long-term consequence of Leishmania primary an infection within the mouse ear epidermis. J. Exp. Med. 188, 1941–1953 (1998).
Titus, R. G. & Ribeiro, J. M. Salivary gland lysates from the sand fly Lutzomyia longipalpis reinforce Leishmania infectivity. Science 239, 1306–1308 (1988).
Vojtkova, B. et al. Repeated sand fly bites of inflamed BALB/c mice reinforce the advance of Leishmania lesions. Entrance. Trop. Dis. https://doi.org/10.3389/fitd.2021.745104 (2021).
Guimaraes-Costa, A. B. et al. A sand fly salivary protein acts as a neutrophil chemoattractant. Nat. Commun. 12, 3213 (2021).
Courtenay, O., Peters, N. C., Rogers, M. E. & Bern, C. Combining epidemiology with elementary biology of sand flies, parasites, and hosts to tell Leishmaniasis transmission dynamics and regulate. PLoS Pathog. 13, e1006571 (2017).
Valverde, J. G. et al. Greater transmissibility of Leishmania donovani from the mammalian host to vector sand flies after a couple of exposures to sand fly bites. J. Infect. Dis. 215, 1285–1293 (2017).
Wilson, A. L. et al. The significance of vector regulate for the regulate and removing of vector-borne illnesses. PLoS Negl. Trop. Dis. 14, e0007831 (2020).
Alten, B. et al. Seasonal dynamics of phlebotomine sand fly species confirmed vectors of mediterranean Leishmaniasis brought about through Leishmania infantum. PLoS Negl. Trop. Dis. 10, e0004458 (2016).
Chalghaf, B. et al. Ecological area of interest modeling predicting the possible distribution of Leishmania vectors within the Mediterranean basin: Affect of weather trade. Parasit. Vectors 11, 461 (2018).
Louradour, I. et al. The midgut microbiota performs an very important function in sand fly vector competence for Leishmania primary. Cellular Microbiol. https://doi.org/10.1111/cmi.12755 (2017).
Sant’Anna, M. R. et al. Colonisation resistance within the sand fly intestine: Leishmania protects Lutzomyia longipalpis from bacterial an infection. Parasit. Vectors 7, 329 (2014).
Faucher, B. et al. Presence of sandflies inflamed with Leishmania infantum and Massilia virus within the Marseille city space. Clin. Microbiol Infect. 20, O340–O343 (2014).
Crompton, P. D. et al. Malaria immunity in guy and mosquito: Insights into unsolved mysteries of a perilous infectious illness. Annu. Rev. Immunol. 32, 157–187 (2014).
Vargas, V., Cime-Castillo, J. & Lanz-Mendoza, H. Immune priming with inactive dengue virus right through the larval degree of Aedes aegypti protects in opposition to the an infection in grownup mosquitoes. Sci. Rep. 10, 6723 (2020).
Cecilio, P., Oliveira, F. & Cordeiro-da-Silva, A. Vaccines for Human Leishmaniasis: The place Do We Stand and What Is Nonetheless Lacking? Leishmaniases as Re-emerging Illnesses (ed. Afrin, F.) (IntechOpen, 2018).
Cecilio, P. et al. Engineering a vector-based pan-Leishmania vaccine for people: evidence of concept. Sci. Rep. 10, 18653 (2020).
Cecilio, P. et al. Pre-clinical antigenicity research of an cutting edge multivalent vaccine for human visceral Leishmaniasis. PLoS Negl. Trop. Dis. 11, e0005951 (2017).
Fernandez, L. et al. Protecting efficacy in a Hamster type of a multivalent vaccine for human visceral Leishmaniasis (MuLeVaClin) consisting of the KMP11, LEISH-F3+, and LJL143 antigens in virosomes, plus GLA-SE adjuvant. Microorganisms https://doi.org/10.3390/microorganisms9112253 (2021).
Chagas, A. C. et al. Lundep, a sand fly salivary endonuclease will increase Leishmania parasite survival in neutrophils and inhibits XIIa touch activation in human plasma. PLoS Pathog. 10, e1003923 (2014).
Martin-Martin, I. et al. Immunity to LuloHya and Lundep, the salivary spreading elements from Lutzomyia longipalpis, protects in opposition to Leishmania primary an infection. PLoS Pathog. 14, e1007006 (2018).
Peters, N. C. et al. Vector transmission of Leishmania abrogates vaccine-induced protecting immunity. PLoS Pathog. 5, e1000484 (2009).
Cotton, J. A. The increasing global of human Leishmaniasis. Developments Parasitol. 33, 341–344 (2017).
Desbois, N., Pratlong, F., Quist, D. & Dedet, J. P. Leishmania (Leishmania) martiniquensis n. sp. (Kinetoplastida: Trypanosomatidae), description of the parasite chargeable for cutaneous Leishmaniasis in Martinique Island (French West Indies). Parasite 21, 12 (2014).
Jariyapan, N. et al. Leishmania (Mundinia) orientalis n. sp. (Trypanosomatidae), a parasite from Thailand chargeable for localised cutaneous Leishmaniasis. Parasit. Vectors 11, 351 (2018).
Olivo Freites, C. et al. First case of diffuse Leishmaniasis related to leishmania panamensis. Open Discussion board Infect. Dis. 5, ofy281 (2018).
Pothirat, T. et al. First isolation of Leishmania from Northern Thailand: Case document, id as Leishmania martiniquensis and phylogenetic place throughout the Leishmania enriettii advanced. PLoS Negl. Trop. Dis. 8, e3339 (2014).
Roque, A. L. & Jansen, A. M. Wild and synanthropic reservoirs of Leishmania species within the Americas. Int. J. Parasitol. Parasites Wildl. 3, 251–262 (2014).
Espinosa, O. A., Serrano, M. G., Camargo, E. P., Teixeira, M. M. G. & Shaw, J. J. An appraisal of the taxonomy and nomenclature of trypanosomatids at this time categorised as Leishmania and Endotrypanum. Parasitology 145, 430–442 (2018).
Dillon, R. Creation to sand flies: existence cycle, http://pcwww.liv.ac.united kingdom/leishmania/life_cycle__habitats.htm (2008).
Martin-Martin, I., Aryan, A., Meneses, C., Adelman, Z. N. & Calvo, E. Optimization of sand fly embryo microinjection for gene modifying through CRISPR/Cas9. PLoS Negl. Trop. Dis. 12, e0006769 (2018).