Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25881258
PubMed Central
PMC4364506
DOI
10.1186/s13071-015-0765-x
PII: 10.1186/s13071-015-0765-x
Knihovny.cz E-zdroje
- MeSH
- Leishmania donovani izolace a purifikace MeSH
- leishmanióza viscerální diagnóza parazitologie přenos MeSH
- lidé MeSH
- myši inbrední BALB C MeSH
- myši MeSH
- Phlebotomus parazitologie MeSH
- xenodiagnóza metody MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
BACKGROUND: In areas endemic for visceral leishmaniasis (VL), the majority of infected hosts remain asymptomatic but potentially infectious to biting sand flies. Their infectiousness for sand fly vectors is crucial for the transmission of the disease and can be quantified only by xenodiagnosis. However, in the case of human hosts, xenodiagnosis can be problematic for ethical and logistic reasons. The BALB/c mouse model described in this paper was designed to enable xenodiagnostic studies on VL hosts circumventing the need for human volunteers, it permits xenodiagnosis using the same individual host repeatedly, over several months. METHODS: BALB/c mice were intradermally inoculated in the ear pinnae with Leishmania donovani, primarily metacyclic stages isolated from the thoracic midguts of experimentally-infected Phlebotomus orientalis females. Naïve sand flies were allowed to feed on anaesthetized mice in 1-3-weeks- interval, firstly on the site of inoculation of L. donovani (weeks 2-8 post infection, p.i.), later on the whole body of mice (weeks 9 - 15 p.i.). Infections of sand flies were evaluated microscopically or by PCR analysis. RESULTS: Although infected mice did not show any signs of disease, 19% (N = 876) of the P. orientalis females that fed at the site of inoculation, became infected. The majority of L. donovani-positive females (76%) had heavy infections with their stomodeal valves colonized by attached parasites. Inoculated mouse ears remained infective for sand flies until week 15 p.i. Females feeding on other parts of the body remained negative with exception of two groups feeding on contralateral ears by week 12 p.i. On week 15, however, these two mice returned negative at xenodiagnosis of the contralateral ears. In sacrificed mice, the highest parasite numbers were found in inoculated ears and their draining lymph nodes. Infections were detected also in the spleen, liver, blood and rarely in the contralateral ear. CONCLUSIONS: The study showed that BALB/c mice harbored parasites in sufficient numbers to promote heavy infections in P. orientalis and thus comprised a suitable laboratory model for xenodiagnoses of L. donovani. Parasites persisted in the inoculation site and were found transmissible for months to sand flies biting on the same site.
Zobrazit více v PubMed
Alvar J, Velez ID, Bern C, Herrero M, Desjeux P, Cano J, et al. Leishmaniasis worldwide and global estimates of its incidence. PLoS One. 2012;7:e35671. doi: 10.1371/journal.pone.0035671. PubMed DOI PMC
Bern C, Maguire JH, Alvar J. Complexities of assessing the disease burden attributable to leishmaniasis. PLoS Negl Trop Dis. 2008;2:e313. doi: 10.1371/journal.pntd.0000313. PubMed DOI PMC
Singh OP, Hasker E, Sacks D, Boelaert M, Sundar S. Asymptomatic Leishmania infection: a new challenge for Leishmania control. Clin Infect Dis. 2014;58:1424–9. doi: 10.1093/cid/ciu102. PubMed DOI PMC
Stauch A, Sarkar RR, Picado A, Ostyn B, Sundar S, Rijal S, et al. Visceral leishmaniasis in the Indian subcontinent: modelling epidemiology and control. PLoS Negl Trop Dis. 2011;5:e1405. doi: 10.1371/journal.pntd.0001405. PubMed DOI PMC
Miller E, Warburg A, Novikov I, Hailu A, Volf P, Seblova V, et al. Quantifying the contribution of hosts with different parasite concentrations to the transmission of visceral leishmaniasis in Ethiopia. PLoS Negl Trop Dis. 2014;8:e3288. doi: 10.1371/journal.pntd.0003288. PubMed DOI PMC
Seblova V, Volfova V, Dvorak V, Pruzinova K, Votypka J, Kassahun A, et al. Phlebotomus orientalis sand flies from two geographically distant Ethiopian localities: biology, genetic analyses and susceptibility to Leishmania donovani. PLoS Negl Trop Dis. 2013;7:e2187. doi: 10.1371/journal.pntd.0002187. PubMed DOI PMC
Quinnell RJ, Courtenay O. Transmission, reservoir hosts and control of zoonotic visceral leishmaniasis. Parasitology. 2009;136:1915–34. doi: 10.1017/S0031182009991156. PubMed DOI
Costa CHN, Gomes RBB, Silva MRB, Garcez LM, Ramos PKS, Santos RS, et al. Competence of the human host as a reservoir for Leishmania chagasi. J Infect Dis. 2000;182:997–1000. doi: 10.1086/315795. PubMed DOI
Gidwani K, Rai M, Chakravarty J, Boelaert M, Sundar S. Evaluation of leishmanin skin test in Indian visceral leishmaniasis. Am J Trop Med Hyg. 2009;80:566–7. PubMed
Molina R, Lohse JM, Pulido F, Laguna R, Lopez-Velez R, Alvar J. Infection of sand flies by humans coinfected with Leishmania infantum and human immunodeficiency virus. Am J Trop Med Hyg. 1999;60:51–3. PubMed
Kamhawi S. The biological and immunomodulatory properties of sand fly saliva and its role in the establishment of Leishmania infections. Microbes Infect. 2000;2:1765–73. doi: 10.1016/S1286-4579(00)01331-9. PubMed DOI
Ribeiro JMC. Blood-feeding arthropods: live syringes or invertebrate pharmacologists? Infect Agent Dis. 1995;4:143–52. PubMed
Sacks D, Kamhawi S. Molecular aspects of parasite-vector and vector-host interactions in Leishmaniasis. Ann Rev Microbiol. 2001;55:453–83. doi: 10.1146/annurev.micro.55.1.453. PubMed DOI
Ready PD. Biology of phlebotomine sand flies as vectors of disease agents. Annu Rev Entomol. 2013;58:227–50. doi: 10.1146/annurev-ento-120811-153557. PubMed DOI
Volf P, Volfova V. Establishment and maintenance of sand fly colonies. J Vector Ecol. 2011;36(Suppl 1):S1–9. doi: 10.1111/j.1948-7134.2011.00106.x. PubMed DOI
Sadlova J, Dvorak V, Seblova V, Warburg A, Votypka J, Volf P. Sergentomyia schwetzi is not a competent vector for Leishmania donovani and other Leishmania species pathogenic to humans. Parasit Vectors. 2013;6:186. doi: 10.1186/1756-3305-6-186. PubMed DOI PMC
Sadlova J, Price HP, Smith BA, Votypka J, Volf P, Smith DF. The stage-regulated HASPB and SHERP proteins are essential for differentiation of the protozoan parasite Leishmania major in its sand fly vector, Phlebotomus papatasi. Cell Microbiol. 2010;12:1765–79. doi: 10.1111/j.1462-5822.2010.01507.x. PubMed DOI PMC
Myskova J, Votypka J, Volf P. Leishmania in sand flies: comparison of quantitative polymerase chain reaction with other techniques to determine the intensity of infection. J Med Entomol. 2008;45:133–8. doi: 10.1093/jmedent/45.1.133. PubMed DOI
Volf P, Hajmova M, Sadlova J, Votypka J. Blocked stomodeal valve of the insect vector: similar mechanism of transmission in two trypanosomatid models. Int J Parasitol. 2004;34:1221–7. doi: 10.1016/j.ijpara.2004.07.010. PubMed DOI
Wilson ME, Jeronimo SM, Pearson RD. Immunopathogenesis of infection with the visceralizing Leishmania species. Microb Pathog. 2005;38:147–60. doi: 10.1016/j.micpath.2004.11.002. PubMed DOI
Garg VK, Agrawal S, Rani S, Joshi A, Agarwalla A, Das ML, et al. Post-kala-azar dermal leishmaniasis in Nepal. Int J Dermatol. 2001;40:179–84. doi: 10.1046/j.1365-4362.2001.01198.x. PubMed DOI
Lima LVR, Carneiro LA, Campos MB, Chagas EJ, Laurenti MD, Corbett CEP, et al. Canine visceral Leishmaniasis Due to Leishmania (L.) Infantum chagasi in Amazonian brazil: comparison of the parasite density from the skin, lymph node and visceral tissues between symptomatic and asymptomatic, seropositive dogs. Rev Inst Med Trop Sao Paulo. 2010;52:259–65. doi: 10.1590/S0036-46652010000100002. PubMed DOI
Michalsky EM, Rocha MF, da Rocha Lima AC, Franca-Silva JC, Pires MQ, Oliveira FS, et al. Infectivity of seropositive dogs, showing different clinical forms of leishmaniasis, to Lutzomyia longipalpis phlebotomine sand flies. Vet Parasitol. 2007;147:67–76. doi: 10.1016/j.vetpar.2007.03.004. PubMed DOI
Amorim IF, Silva SM, Figueiredo MM, Moura EP, Castro RS, Lima TK, et al. Toll receptors type-2 and CR3 expression of canine monocytes and its correlation with immunohistochemistry and xenodiagnosis in visceral leishmaniasis. PLoS One. 2011;6:e27679. doi: 10.1371/journal.pone.0027679. PubMed DOI PMC
Zhang WW, Matlashewski G. Screening Leishmania donovani-specific genes required for visceral infection. Mol Microbiol. 2010;77:505–17. doi: 10.1111/j.1365-2958.2010.07230.x. PubMed DOI
Aslan H, Dey R, Meneses C, Castrovinci P, Jeronimo SM, Oliva G, et al. A new model of progressive visceral leishmaniasis in hamsters by natural transmission via bites of vector sand flies. J Infect Dis. 2013;207:1328–38. doi: 10.1093/infdis/jis932. PubMed DOI PMC
McCall LI, Zhang WW, Matlashewski G. Determinants for the development of visceral leishmaniasis disease. PLoS Pathog. 2013;9:e1003053. doi: 10.1371/journal.ppat.1003053. PubMed DOI PMC
Ahmed S, Colmenares M, Soong L, Goldsmith-Pestana K, Munstermann L, Molina R, et al. Intradermal infection model for pathogenesis and vaccine studies of murine visceral leishmaniasis. Infec Immun. 2003;71:401–10. doi: 10.1128/IAI.71.1.401-410.2003. PubMed DOI PMC
Courtenay O, Quinnell RJ, Garcez LM, Shaw JJ, Dye C. Infectiousness in a cohort of brazilian dogs: why culling fails to control visceral leishmaniasis in areas of high transmission. J Infect Dis. 2002;186:1314–20. doi: 10.1086/344312. PubMed DOI
Soares MR, de Mendonca IL, do Bonfim JM, Rodrigues JA, Werneck GL, Costa CH. Canine visceral leishmaniasis in Teresina, Brazil: Relationship between clinical features and infectivity for sand flies. Acta Trop. 2011;117:6–9. doi: 10.1016/j.actatropica.2010.08.015. PubMed DOI
Laurenti MD, Rossi CN, Matta VL, Tomokane TY, Corbett CE, Secundino NF, et al. Asymptomatic dogs are highly competent to transmit Leishmania (Leishmania) infantum chagasi to the natural vector. Vet Parasitol. 2013;196:296–300. doi: 10.1016/j.vetpar.2013.03.017. PubMed DOI
Travi BL, Tabares CJ, Cadena H, Ferro C, Osorio Y. Canine visceral leishmaniasis in Colombia: relationship between clinical and parasitologic status and infectivity for sand flies. Am J Trop Med Hyg. 2001;64:119–24. PubMed
Kimblin N, Peters N, Debrabant A, Secundino N, Egen J, Lawyer P, et al. Quantification of the infectious dose of Leishmania major transmitted to the skin by single sand flies. Proc Natl Acad Sci U S A. 2008;105:10125–30. doi: 10.1073/pnas.0802331105. PubMed DOI PMC
Maia C, Seblova V, Sadlova J, Votypka J, Volf P. Experimental transmission of Leishmania infantum by two major vectors: a comparison between a viscerotropic and a dermotropic strain. PLoS Negl Trop Dis. 2011;5:e1181. doi: 10.1371/journal.pntd.0001181. PubMed DOI PMC
Secundino NFC, de Freitas VC, Monteiro CC, Pires ACAM, David BA, Pimenta PFP. The transmission of Leishmania infantum chagasi by the bite of the Lutzomyia longipalpis to two different vertebrates. Parasit Vectors. 2012;5:20. doi: 10.1186/1756-3305-5-20. PubMed DOI PMC
Garg R, Dube A. Animal models for vaccine studies for visceral leishmaniasis. Indian J Med Res. 2006;123:439–54. PubMed
Bern C, Courtenay O, Alvar J. Of cattle, sand flies and men: a systematic review of risk factor analyses for South Asian visceral leishmaniasis and implications for elimination. PLoS Negl Trop Dis. 2010;4:e599. doi: 10.1371/journal.pntd.0000599. PubMed DOI PMC
Dereure J, El-Safi SH, Bucheton B, Boni M, Kheir MM, Davoust B, et al. Visceral leishmaniasis in eastern Sudan: parasite identification in humans and dogs; host-parasite relationships. Microbes Infect. 2003;5:1103–8. doi: 10.1016/j.micinf.2003.07.003. PubMed DOI
Singh N, Mishra J, Singh R, Singh S. Animal reservoirs of visceral leishmaniasis in India. J Parasitol. 2013;99:64–7. doi: 10.1645/GE-3085.1. PubMed DOI
Infectiousness of Asymptomatic Meriones shawi, Reservoir Host of Leishmania major
Central Asian Rodents as Model Animals for Leishmania major and Leishmania donovani Research
CRISPR/Cas9 in Leishmania mexicana: A case study of LmxBTN1