The suitability of laboratory-bred Anopheles cracens for the production of Plasmodium vivax sporozoites

Malaria Journal

Volumn 14, Issue 1, 2015, Pages

  Andolina, Chiara ^a   Landier, Jordi ^a   Carrara, Verena ^a   Chu, Cindy S ^a   Franetich, Jean François ^c,d,e   Roth, Alison ^f   Rénia, Laurent ^g   Roucher, Clémentine ^c,d,e   White, Nick J ^a,b   Snounou, Georges ^c,d,e   Nosten, François ^a,b  

^a MAHIDOL UNIVERSITY   (Thailand)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c SORBONNE UNIVERSITÉ   (France)

^d INSERM   (France)

^e Assistance publique Hôpitaux de Paris   (France)

^f UNIVERSITY OF SOUTH FLORIDA   (United States)

^g AGENCY FOR SCIENCE   (Singapore)

Author keywords

Anopheles cracens; Insectary; Plasmodium vivax; Sporozoites; Transmission

Indexed keywords

ADULT; ANOPHELES; ANOPHELES CRACENS; ARTICLE; BIOASSAY; BLOOD SAMPLING; DISEASE CARRIER; FEMALE; HUMAN; MAJOR CLINICAL STUDY; MYANMAR; NONHUMAN; ORGANISM COLONY; PARASITE TRANSMISSION; PARASITE VIRULENCE; PETRI DISH; PLASMODIUM VIVAX; PLASMODIUM VIVAX MALARIA; SPOROZOITE; THAILAND; ANIMAL; BREEDING; EXPERIMENTAL ANIMAL; MALE; MEDICAL RESEARCH; PARASITOLOGY; PHYSIOLOGY; PROCEDURES; STANDARDS;

ANIMALS; ANIMALS, LABORATORY; ANOPHELES; BIOMEDICAL RESEARCH; BREEDING; FEMALE; MALE; PLASMODIUM VIVAX; SPOROZOITES;

EID: 84938861478     PISSN: None     EISSN: 14752875     Source Type: Journal    
DOI: 10.1186/s12936-015-0830-0     Document Type: Article

References (33)

1. Mendis K, Sina BJ, Marchesini P, Carter R (2001) The neglected burden of Plasmodium vivax malaria. Am J Trop Med Hyg 64:97-106
2. Baird JK, Hoffman SL (2004) Primaquine therapy for malaria. Clin Infect Dis 39:1336-1345
3. Howes RE, Piel FB, Patil AP, Nyangiri OA, Gething PW, Dewi M et al (2012) G6PD deficiency prevalence and estimates of affected populations in malaria endemic countries: a geostatistical model-based map. PloS Med 9:e1001339
4. Rochford R, Ohrt CK, Baresel PC, Campo B, Sampath A, Magill AJ et al (2013) Humanized mouse model of glucose 6-phosphate dehydrogenase deficiency for in vivo assessment of hemolytic toxicity. Proc Natl Acad Sci USA 110:17486-17491
5. Schmidt LH, Fradkin R, Genther CS, Rossan RN, Squires WL (1982) Plasmodium cynomolgi infections in the rhesus monkey. II. Responses of sporozoite-induced and trophozoite-induced infections to standard antimalarial drugs. Am J Trop Med Hyg 31:646-665
6. Dembélé L, Gego A, Zeeman A-M, Franetich J-F, Silvie O, Rametti A et al (2011) Towards an in vitro model of Plasmodium hypnozoites suitable for drug discovery. PLoS One 6:e18162
7. Dembélé L, Franetich J-F, Lorthiois A, Gego A, Zeeman A-M, Kocken CHM et al (2014) Persistence and activation of malaria hypnozoites in long-term primary hepatocyte cultures. Nat Med 20:307-312
8. Sallum MAM (2005) Revision of the Leucosphyrus group of Anopheles (Cellia) (Diptera, Culicidae). Rev Bras Entomol 49:1-152
9. Saeung A (2012) Anopheles (Diptera: Culicidae) species complex in Thailand: identification, distribution, bionomics and malaria-vector importance. Int J Parasitol Res 4:75-82
10. Junkum A, Jitpakdi A, Jariyapan N, Komalamisra N, Somboon P, Suwonkerd W et al (2005) Susceptibility of two karyotypic forms of Anopheles aconitus (Diptera: Culicidae) to Plasmodium falciparum and P. vivax. Rev Inst Med Trop Sao Paulo 47:333-338
11. Joshi D, Choochote W, Park M-H, Kim J-Y, Kim T-S, Suwonkerd W et al (2009) The susceptibility of Anopheles lesteri to infection with Korean strain of Plasmodium vivax. Malar J 8:42
12. Thongsahuan S, Baimai V, Junkum A, Saeung A, Min G-S, Joshi D et al (2011) Susceptibility of Anopheles campestris-like and Anopheles barbirostris species complexes to Plasmodium falciparum and Plasmodium vivax in Thailand. Mem Inst Oswaldo Cruz 106:105-112
13. Parr M, Dabu CP, Wai NS, Say PS, Ner M, Tun NW et al (2014) Clinical audit to enhance safe practice of skilled birth attendants for the fetus with nuchal cord: evidence from a refugee and migrant cohort. BMC Pregnancy Childbirth 14:76
14. Robert V, Tchuinkam T, Carnevale PJ (1993) Successful eradication of a microsporidian, Nosema sp., in a mosquito colony. Ann Soc Belg Med Trop 73:71-72
15. WHO (2010) Basic malaria microscopy. World Health Organization, Geneva
16. Garnham PCC (1956) Microsporidia in laboratory colonies of Anopheles. Bull World Health Organ 15:845-847
17. Bargielowski I, Koella JC (2009) A possible mechanism for the suppression of Plasmodium berghei development in the mosquito Anopheles gambiae by the microsporidian Vavraia culicis. PLoS One 4:e4676
18. Becnel JJ, White SE, Shapiro AM (2005) Review of microsporidia-mosquito relationships: from the simple to the complex. Folia Parasitol 52:41-50
19. Sucharit S, Choochote W (1983) Comparative studies on the morphometry of male genitalia and frequency of clasper movements during induced copulation of Anopheles balabacensis (Perlis Form) and Anopheles dirus (Bangkok Colony Strain). Mosq News 15:90-95
20. Sattabongkot J, Maneechai N, Phunkitchar V, Eikarat N, Khuntirat B, Sirichaisinthop J et al (2003) Comparison of artificial membrane feeding with direct skin feeding to estimate the infectiousness of Plasmodium vivax gametocyte carriers to mosquitoes. Am J Trop Med Hyg 69:529-535
21. Solarte Y, Manzano MR, Rocha L, Hurtado H, James MA, Arévalo-Herrera M et al (2011) Plasmodium vivax sporozoite production in Anopheles albimanus mosquitoes for vaccine clinical trials. Am J Trop Med Hyg 84:28-34
22. Rios-Velásquez CM, Martins-Campos KM, Simões RC, Izzo T, Dos Santos EV, Pessoa FAC et al (2013) Experimental Plasmodium vivax infection of key Anopheles species from the Brazilian Amazon. Malar J 12:460
23. Bharti AR, Chuquiyauri R, Brouwer KC, Stancil J, Lin J, Llanos-Cuentas A et al (2006) Experimental infection of the neotropical malaria vector Anopheles darlingi by human patient-derived Plasmodium vivax in the Peruvian Amazon. Am J Trop Med Hyg 75:610-616
24. Moreno M, Tong C, Guzman M, Chuquiyauri R, Llanos-Cuentas A, Rodriguez H et al (2014) Infection of laboratory-colonized Anopheles darlingi mosquitoes by Plasmodium vivax. Am J Trop Med Hyg 90:612-616
25. Collins WE, Warren M, Huong AY, Skinner JC, Sutton BB, Stanfill PS (1986) Studies of comparative infectivity of fifteen strains of Plasmodium vivax to laboratory-reared anopheline mosquitoes, with special reference to Anopheles culicifacies. J Parasitol 72:521-524
26. Boyd MF, Stratman-Thomas WK, Muench H (1936) The occurence of gametocytes of Plasmodium vivax during the primary attack. Am J Trop Med 16:133-138
27. James SP, Nicol WD, Shute PG (1936) Clinical and parasitological observations on induced malaria. Proc R Soc Med 29:879-894
28. Boyd MF, Kitchen SF (1938) Demonstrable maturity of gametocytes as a factor in the infection of anophelines with Plasmodium vivax and Plasmodium falciparum. Am J Trop Med 18:515-520
29. Shute PG, Maryon ME (1957) A study on the infectivity of patients to mosquitoes in the early stages of primary Plasmodium vivax malaria (Madagascar strain). Trans R Soc Trop Med Hyg 51:403-410
30. Shute PG, Maryon ME (1961) A note on the infectivity to mosquitos of patients in the asymptomatic, symptomatic and post-symptomatic phases of parasitic relapses of induced infections with Plasmodium vivax (Madagascar strain). Bull World Health Organ 24:654-657
31. Jeffery GM (1960) Infectivity to mosquitoes of Plasmodium vivax and Plasmodium falciparum under various conditions. Am J Trop Med Hyg 9:315-320
32. Sattabongkot J, Maneechai N, Rosenberg R (1991) Plasmodium vivax: gametocyte infectivity of naturally infected Thai adults. Parasitology 102:27-31
33. Chansamut N, Buates S, Takhampunya R, Udomsangpetch R, Bantuchai S, Sattabongkot J (2012) Correlation of Pfg377 ortholog gene expression of Plasmodium vivax and mosquito infection. Trop Med Int Health 17:414-422