Mem Inst Oswaldo Cruz, Rio de Janeiro, 113(5) May 2018
Original Article

Lower galactosylation levels of the Lipophosphoglycan from Leishmania (Leishmania) major-like strains affect interaction with Phlebotomus papatasi and Lutzomyia longipalpis

Agna Cristina Guimarães1, Paula Monalisa Nogueira2, Soraia de Oliveira Silva1, Jovana Sadlova3, Katerina Pruzinova3, Jana Hlavacova3, Maria Norma Melo1, Rodrigo Pedro Soares2,+

1Universidade Federal de Minas Gerais, Departamento de Parasitologia, Belo Horizonte, MG, Brasil
2Fundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Belo Horizonte, MG, Brasil
3Charles University, Faculty of Science, Department of Parasitology, Prague, Czech Republic

DOI: 10.1590/0074-02760170333
216 views 251 downloads
ABSTRACT

BACKGROUND Leishmania major is an Old World species causing cutaneous leishmaniasis and is transmitted by Phlebotomus papatasi and Phlebotomus duboscqi. In Brazil, two isolates from patients who never left the country were characterised as L. major-like (BH49 and BH121). Using molecular techniques, these isolates were indistinguishable from the L. major reference strain (FV1).

OBJECTIVES We evaluated the lipophosphoglycans (LPGs) of the strains and their behaviour in Old and New World sand fly vectors.

METHODS LPGs were purified, and repeat units were qualitatively evaluated by immunoblotting. Experimental in vivo infection with L. major-like strains was performed in Lutzomyia longipalpis (New World, permissive vector) and Ph. papatasi (Old World, restrictive or specific vector).

FINDINGS The LPGs of both strains were devoid of arabinosylated side chains, whereas the LPG of strain BH49 was more galactosylated than that of strain BH121. All strains with different levels of galactosylation in their LPGs were able to infect both vectors, exhibiting colonisation of the stomodeal valve and metacyclogenesis. The BH121 strain (less galactosylated) exhibited lower infection intensity compared to BH49 and FV1 in both vectors.

MAIN CONCLUSIONS Intraspecific variation in the LPG of L. major-like strains occur, and the different galactosylation levels affected interactions with the invertebrate host.

Leishmania major is one of the most important species causing cutaneous leishmaniasis (CL) in the Old World. It is widely distributed from Sub-Saharan Africa to the Indian subcontinent South-Central Asia. This species is transmitted by the bite of the sand flies, Phlebotomus papatasi and Phlebotomus duboscqi, depending on the region (Anderson et al. 2011 1 , Salam et al. 2014 23 ). In several countries of South America (Brazil, Ecuador, Paraguay, Venezuela, and Mexico), many CL isolates were biochemically and molecularly identified as L. major and were named L. major-like (Momen et al. 1985 16 , 1993, Calvopina et al. 2004 4 , Silva et al. 2009 25 , Hashiguchi et al. 2016 9 ).

In the 1970s, two isolates were recovered from CL patients from the Brazilian states, Goiás and Minas Gerais. The patients were rural workers who claimed they had never left the region. The strains remained frozen until further examination in the 1990s. Surprisingly, the isolates were shown to be identical to the World Health Organization reference strains, Friedlin (FV1) and 5-ASKH by isoenzyme, RAPD and SSR-PCR analysis (Silva et al. 2009 25 ). The L. major-like strains were named BH49 (Goiás) and BH121 (Minas Gerais). By the time they were isolated, specific epidemiological studies were not available to incriminate the vector(s) and wild host(s); however, a lot of information was available on regarding the vectors and hosts of Leishmania braziliensis (Mayrink et al. 1979 14 , Rocha et al. 1988 21 ). Although both strains were isolated from human skin lesions, a distinguishing feature exhibited by the BH49 strain was its higher virulence for the murine model compared to that of BH121 (non-virulent) (Silva et al. 2009 25 ). To ascertain the possible mechanisms underlying their virulence, two virulence genes highly expressed in the BH49 strain were recently identified; one encoded a protein homologous to α-haemolysin and another encoded a protein homologous to the β-1,3-galactosyltransferase 3 (Wu et al. 2015 32 ). The latter is a transferase responsible for galactosyl residues assembly on the LPG repeat units in L. major (Dobson et al. 2003 8 ). These residues are important for L. major/Leishmania turanica attachment to the midgut receptor, PpGalec (Kamhawi et al. 2004 10 , Volf et al. 2014 29 ). However, interactions between L. major-like strains bearing LPG polymorphisms with the invertebrate host were not examined.

Although these strains were genetically similar to Old World L. major, their glycobiology and infectivity to New and Old World vectors remain unknown. Here, we qualitatively evaluated the presence of galactose/arabinose in the LPGs of L. major-like strains (BH49 and BH121). We additionally evaluated their interactions with vectors Lutzomyia longipalpis (permissive) and Ph. papatasi (restrictive).

 

MATERIALS AND METHODS

Parasites and LPG purification - World Health Reference strains of L. major (MHOM/IL/1980/Friedlin), Leishmania infantum (MCAN/BR/89/Ba-262), and L. major-like strains BH49 (MHOM/BR/1971/BH49) and BH121 (MHOM/BR/1971/BH121) were used. L. major-like strains were isolated from human CL cases in Brazil: BH49 in the State of Goiás and BH121 in the State of Minas Gerais. Frozen stocks of strains passaged in mice were characterised and typed, as previously reported (Silva et al. 2009 25 ). Promastigotes were cultured in M199 medium supplemented with 10% heat-inactivated foetal bovine serum (FBS), penicillin 100 units mL-1, streptomycin 50 mg mL-1, 12.5 mM glutamine, 0.1 M adenine, 0.0005% hemin, and 40 mM Hepes, pH 7.4 at 26ºC. LPGs from late log parasites (procyclics) were extracted in solvent E (H2O/ethanol/diethyl ether/pyridine/NH4OH, 15:15:5:1:0.017), as previously described (Soares et al. 2002 26 ). The solvent E extract was dried by N2 evaporation, resuspended in 0.1 N acetic acid/0.1 M NaCl, and applied to a column of phenyl-Sepharose (2 mL), equilibrated with the same buffer. LPG was eluted in solvent E, dried, and resuspended in sterile, LPS-free distilled water (Sanobiol, Campinas, Brazil).

Immunoblotting - Purified LPGs (10 μg) from different strains were transferred to nitrocellulose paper; the membrane was blocked in 5% milk in PBS and probed with the following antibodies (1:1,000): WIC 79.3, which recognises terminal Gal(β1,3) sequences that branch off the repeat units, and 3F12, which recognises terminal Ara(β1,2)Gal(β1,3) (Kelleher et al. 1992 11 , 1994). For dot-blots, LPGs (5 μg) were applied to the nitrocellulose membrane; the membranes were blocked as described above and probed with CA7AE (1:1000), which recognises the Gal(β1,4)Man(α1)-PO4 repeat units (Tolson et al. 1989 28 ). After three washes in PBS for 10 min, membranes were incubated with anti-mouse IgG conjugated with horseradish peroxidase (1:10,000), and the reaction was visualized using Luminol (Nogueira et al. 2016 19 ).

Sand fly colonies, experimental infections, and morphometry - Colonies of Lu. longipalpis (originating from Jacobina, Brazil) and Ph. papatasi (originating from Cukurova, Turkey) were maintained in the insectary at the Department of Parasitology, Charles University in Prague under standard conditions (Volf & Volfova 2011). Sand fly females (2-6 d old) were fed through a chick-skin membrane on heat-inactivated rabbit blood containing 106 promastigotes/mL. Reference strain of L. major (MHOM/IL/1980/Friedlin) was used as the control since it is the most used model for sand fly infections. Sand-flies were infected with the strains in two parallel sets of experiments using all sand-fly Leishmania combinations. Engorged females were separated, maintained in the same conditions as the colony, and dissected on days 1, 5, and 8 post-infection (PI). Dissected guts were divided into several parts: the abdominal midgut (AMG), thoracic midgut (TMG), stomodeal valve (SV), cardia, and endoperithrophic space. They were examined under a microscope to determine the localisation and intensity of Leishmania infections. Parasite loads were graded as light (< 100 parasites/gut), moderate (100-1000 parasites/gut), or heavy (> 1000 parasites/gut), as described by Myskova et al. (2008) 18 . To evaluate the morphological forms of Leishmania, midgut smears fixed with methanol and stained with Giemsa were examined under a light microscope with an oil-immersion objective and photographed with an Olympus D70 camera. Body length, body width, and flagellar length of 120 randomly selected promastigotes from three females/smears were measured for each sand fly species and time interval using Image-J software. The morphological forms were distinguished, according to the criteria described by Walters (1993) 31 and Cihakova and Volf (1997). Data were evaluated statistically by means of the Fisher's exact or Chi-square (χ2) tests using SPSS statistics 23 software.

 

RESULTS

LPGs from L. major-like strains display intraspecific polymorphisms - For preliminary qualitative analysis, immunoblotting (western-blot and dot-blot) techniques were performed using standard mAbs specific for the repeat unit epitopes of Leishmania spp. By western-blot, LPGs purified from L. major-like strains were differentially recognised by antibody WIC 79.3, specific for terminal β-galactosyl residues. LPGs from FV1 and BH49 strains were strongly recognised by this antibody. However, the LPG from BH121 reacted very poorly with the antibody (Fig. 1A). In contrast, none of the LPGs from L. major-like strains were recognized by 3F12, suggesting that their repeat units were devoid of arabinose side chains (Fig. 1B). As expected, only the LPG from L. major (FV1) reacted with 3F12. Since the LPGs from L. major-like strains exhibited different levels of glycosylation in their side-chains, they were subjected to a dot-blot assay using CA7AE that recognizes unbranched repeat units. Consistent with these observations, LPGs from L. major-like strains and the positive L. infantum control (Ba262) were recognised by this antibody. Moreover, a very clear cline was observed where the lower galactosylated LPGs were more reactive for CA7AE. The pattern could be seen more clearly in the dot-blot compared to western-blot. As expected, the LPG from L. major (FV1) reacted poorly with this antibody (Fig. 1C). Together, these data indicate that the LPGs from L. major-like strains display polymorphisms in their structures. They are not arabinosylated, but have galactosylated or unbranched side-chains (Table).

Sand fly infections and morphometry of promastigotes - Since LPGs from L. major-like strains displayed intraspecific variations in galactose residues; the impact of the variations on the interaction with sand flies was evaluated. All strains successfully infected Lu. longipalpis (LL) and Ph. papatasi (PP) sand flies (Figs 2-4). The intensity of infection of the BH49 strain was very similar to FV1 in both vectors, except on day 8 in Ph. papatasi (p < 0.05) (Fig. 2A). Interestingly, the BH121 strain infection rate was always lower in both vectors on all days (p < 0.05) (Fig. 2B). Similar to the infection intensity pattern, both strains were equally able to colonise all parts of the foregut and midgut and reached the stomodeal valve (SV) in both sand fly species (Fig. 3). Colonisation of SV by the BH49 strain was not different from FV1 (p > 0.05). The ability of the BH121 strain to reach SV was lower than that of FV1 (p < 0.05) (Fig. 3B). All expected promastigote forms were observed in both vectors with variations in the nectomonad/metacyclic density, depending on the strain (Fig. 4). For example, the FV1 strain produced a greater number of nectomonads on day 5 compared to BH49/BH121 (p < 0.01) (Fig. 4A-B). Additionally, the ability of the BH49 strain to produce metacyclics on day 8 was higher than that of FV1 in Ph. papatasi (p < 0.05) (Fig. 4A). Similar to the other parameters, metacyclogenesis in the strain BH121 was lower than that in FV1 on day 8 for both vectors (p < 0.05) (Fig. 4B).

 

DISCUSSION

L. major-like strains have been isolated in several countries in Latin America, despite the fact that this species in commonly found in Old World regions. Several aspects of their epidemiology regarding vectors and reservoirs are scarce. Only two studies have addressed some biological, biochemical, and molecular parameters using L. major-like strains (Silva et al. 2009 25 , Wu et al. 2015 32 ). Here, we qualitatively evaluated LPG structures in L. major-like strains and determined their impact during in vivo interaction with sand flies. LPG is the major glycoconjugate of Leishmania; LPG is involved in a wide range of functions (Assis et al. 2012 2 ). The LPG of L. major (FV1) has β-1,3 galactosyl side-chains (McConville et al. 1992 15 ) that are important in the interaction with the midgut of Ph. papatasi (Kamhawi et al. 2004 10 ). Similar to L. major (FV1), BH49 exhibited β-galactosyl residues in their LPGs. An interesting feature of the BH121 strain was its absent or low galactosylation level, based on WIC 79.3 recognition. Although both strains did not show arabinosyl residues in their LPGs, these sugars are not important for attachment to the sand fly midgut and may be absent in other L. major strains, such as LV39 (Dobson et al. 2003 8 ). The LPGs of the strains BH49 and BH121 differed from those of FV1 strain and exhibited some repeat units devoid of side-chains when probed with mAb, CA7AE. The reactivity of the LPG of the FV1 strain to this antibody is very low or absent (Butcher et al. 1996 3 , Volf et al. 2014 29 ) while the reactivity of the LPG of BH121 is increased; the BH121 LPG is poorly galactosylated. In conclusion, the LPGs from Brazilian L. major-like strains possess intraspecific polymorphisms.

In order to determine whether such variations could have an impact during development within the invertebrate host, sand flies were infected with the strains in vivo. Although we used recently frozen stocks isolated from mouse (Silva et al. 2009 25 ), it is already known that long term in vitro passaging has a negligible effect on Leishmania infectivity in sand flies (Cihakova & Volf 1997, Sádlová et al. 1999 22 ). Since no vector species were incriminated at the time that L. major-like strains were isolated, we chose one vector that was present in the area (Lu. longipalpis) (Mayrink et al. 1979 14 ) and the Old World vector for L. major (Ph. papatasi). In permissive vectors such as Lu. longipalpis and Lu. migonei, intraspecies variations in the LPGs of L. infantum and L. amazonensis did not affect interaction (Coelho-Finamore et al. 2011 7 , Nogueira et al. 2016 19 , 2017). We also evaluated the interaction with a restrictive vector (Ph. papatasi). This vector is only susceptible to Old World L. major and L. turanica (Chajbullinova et al. 2012 5 ). In contrast with previous studies, L. major-like strains bearing variations in their LPG galactosylation levels differently infected both vectors. Previous reports have shown that Lu. longipalpis is a permissive vector able to sustain infection with different Leishmania species including L. major (reviewed by Soares & Turco 2003). Consistent with those observations, both strains and the control (FV1) successfully colonized the foregut and midgut of Lu. longipalpis and Ph. papatasi. Although both strains were able to infect both vectors and accomplish metacyclogenesis, the intensity of this infection was significantly lower in the BH121 strain. This is the first evidence that Leishmania strains bearing intraspecies polymorphisms in their LPG exhibited variations during the interaction with restrictive and permissive sand-flies. One of the hypotheses is that the presence of a smaller number of galactose residues in the LPG could adversely affect parasite attachment to the midgut. Since both L. major-like strains were able to survive and sustain infection in Ph. papatasi, a restrictive vector, this is a strong indication that galactosylation may be one of the factors involved. Besides, since Ph. papatasi is not found in Brazil, those strains may have used an alternative vector in the New World. Although Lu. longipalpis has urbanized in many cities in Latin America (revised by Salomon et al. 2015 24 ) and its occurrence in rural areas is rare, it could be one of the suspected vectors for transmitting L. major-like strains. Although Lu. longipalpis is a proven vector for L. infantum, the transmission of L. major-like strains by this vector and other vectors has not been observed yet. More importantly, other CL vectors in those geographical regions such as Lu. whitmani, Lu. migonei and Lu. intermedia should also be investigated. This work highlights the importance of returning to the field to address these questions.

In conclusion, L. major-like strains were able to successfully infect Lu. longipalpis and Ph. papatasi. The observed differences, among other factors, seemed to be controlled by variations in the galactose residues in the LPG. However, there are still many uncertainties regarding the origin and introduction of L. major-like strains in the Americas. Like L. infantum, this could have occurred after the introduction of infected dogs (reviewed by Mauricio et al. 2000 13 ), but the reservoir(s) of L. major-like strains in the Americas remain unknown. After more than 40 years, the regions from where these strains were isolated were modified by anthropic action, and the eco epidemiology of leishmaniasis may have changed completely. This reinforces the need for novel epidemiological studies in those areas; we must also search for new L. major-like strains, vectors, and hosts.

 

ACKNOWLEDGEMENTS

To Dr Petr Volf from Charles University, for providing all conditions for the sand fly experiments.

 

AUTHORS' CONTRIBUTION

ACG, PMN and SOS - LPG purification, western-blots, sand fly experiments and writing of the manuscript; JS, KP and JH - sand fly experiments, analysis and writing of the manuscript; MNM and RPS - coordinators of the project, analysis and writing of the manuscript.

 

REFERENCES
01. Anderson JM, Samake S, Jaramillo-Gutierrez G, Sissoko I, Coulibaly A, Traoré B, et al. Seasonality and prevalence of Leishmania major infection in Phlebotomus duboscqi Neveu-Lemaire from two neighboring villages in central Mali. PLoS Negl Trop Dis. 2011; 5(5): e1139.

02. Assis RR, Ibraim IC, Nogueira PM, Soares RP, Turco SJ. Glycoconjugates in New World species of Leishmania: polymorphisms in lipophosphoglycan and glycoinositolphospholipids and interaction with hosts. Biochim Biophys Acta. 2012; 1820(9): 1354-65.
03. Butcher BA, Turco SJ, Hilty BA, Pimenta PF, Panunzio M, Sacks DL. Deficiency in beta1,3-galactosyltransferase of a Leishmania major lipophosphoglycan mutant adversely influences the Leishmania- sand fly interaction. J Biol Chem. 1996; 271(34): 20573-9.
04. Calvopina M, Armijos RX, Hashiguchi Y. Epidemiology of Leishmaniasis in Ecuador: current status of knowledge - A Review. Mem Inst Oswaldo Cruz. 2004; 99(7): 663-72.
05. Chajbullinova A, Votypka J, Sadlova J, Kvapilova K, Seblova V, Kreisinger J, et al. The development of Leishmania turanica in sand flies and competition with L. major. Parasit Vectors. 2012; 5: 219.
06. Cihakova J, Volf P. Development of different Leishmania major strains in the vector sandflies Phlebotomus papatasi and P. duboscqi. Ann Trop Med Parasitol. 1997; 91(3): 267-79.
07. Coelho-Finamore JM, Freitas VC, Assis RR, Melo MN, Novozhilova N, Secundino NF, et al. Leishmania infantum: lipophosphoglycan intraspecific variation and interaction with vertebrate and invertebrate hosts. Int J Parasitol. 2011; 41(3-4): 333-42.
08. Dobson DE, Scholtes LD, Valdez KE, Sullivan DR, Mengeling BJ, Cilmi S, et al. Functional identification of galactosyltransferases (SCGs) required species-specific modifications of the lipophosphoglycan adhesin controlling Leishmania major-sand fly interactions. J Biol Chem. 2003; 278(18): 15523-31.
09. Hashiguchi Y, Velez LN, Villegas NV, Mimori T, Gomez EA, Kato H. Leishmaniases in Ecuador: comprehensive review and current status. Acta Trop. 2016; 166: 299-315.
10. Kamhawi S, Ramalho-Ortigao M, Pham VM, Kumar S, Lawyer PG, Turco SJ, et al. A role for insect galectins in parasite survival. Cell. 2004; 119(3): 329-41.
11. Kelleher M, Bacic A, Handman E. Identification of a macrophage-binding determinant on lipophosphoglycan from Leishmania major promastigotes. Proc Natl Acad Sci USA. 1992; 89(1): 6-10.
12. Kelleher M, Curtis JM, Sacks DL, Handman E, Bacic A. Epitope mapping of monoclonal antibodies directed against lipophosphoglycan of Leishmania major promastigotes. Mol Biochem Parasitol. 1994; 66(2): 187-200.
13. Mauricio IL, Stothard JR, Miles MA. The strange case of Leishmania chagasi. Parasitol Today. 2000; 16(5): 188-9.
14. Mayrink W, Williams P, Coelho MV, Dias M, Martins AV, Magalhães PA, et al. Epidemiology of dermal leishmaniasis in the Rio Doce Valley, State of Minas Gerais, Brazil. Ann Trop Med Parasitol. 1979; 73(2): 123-37.
15. McConville MJ, Turco SJ, Ferguson MAJ, Sacks DL. Developmental modification of lipophosphoglycan during the differentiation of Leishmania major promastigotes to an infectious stage. EMBO J. 1992; 11(10): 3593-600.
16. Momen H, Grimaldi JR, Pacheco RS, Jaffe CL, Pratt DM, Marzochi MCA. Brazilian Leishmania stocks phenotypically similar to Leishmania major. Am J Trop Med Hyg. 1985; 34(6): 1076-84.
17. Momen H, Pacheco RS, Cupolillo E, Grimaldi Jr G. Molecular evidence for the importation of Old World Leishmania into the Americas. Biol Res. 1993; 26(1-2): 249-55.
18. 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(1): 133-8.
19. Nogueira PM, Assis RR, Torrecilhas AC, Saraiva EM, Pessoa NL, Campos MAS, et al. Lipophosphoglycans from Leishmania amazonensis strains display immunomodulatory properties via TLR4 and do not affect sand fly infection. PLoS Negl Trop Dis. 2016; 10(8): e0004848.
20. Nogueira PM, Guimarães AC, Assis RR, Sadlova J, Myskova J, Pruzinova K, et al. Lipophosphoglycan polymorphisms do not affect Leishmania amazonensis development in permissive vectors Lutzomyia migonei and Lutzomyia longipalpis. Parasit Vectors. 2017; 10: 608.
21. Rocha NM, Melo MN, Babá EH, Dias M, Michalick MS, da Costa CA, et al. Leishmania braziliensis braziliensis isolated from Akodon arviculoides captured in Caratinga, Minas Gerais, Brazil. Trans R Soc Trop Med Hyg. 1988; 82(1): 68.
22. Sádlová J, Svobodová M, Volf P. Leishmania major: effect of repeated passages through sandfly vectors or murine hosts. Ann Trop Med Parasitol. 1999; 93(6): 599-611.
23. Salam N, Al-Shaqha WM, Azzi A. Leishmaniasis in the Middle East: incidence and epidemiology. PLoS Negl Trop Dis. 2014; 8(10): e3208.
24. Salomón OD, Feliciangeli MD, Quintana MG, Afonso MMS, Rangel EF. Lutzomyia longipalpis urbanisation and control. Mem Inst Oswaldo Cruz. 2015; 110(7): 831-46.
25. Silva SO, Wu AA, Evans DA, Vieira LQ, Melo MN. Leishmania sp. isolated from human cases of cutaneous leishmaniasis in Brazil characterized as Leishmania major-like. Acta Trop. 2009; 112(3): 239-48.
26. Soares RPP, Macedo ME, Ropert C, Gontijo NF, Almeida IC, Gazzinelli RT, et al. Leishmania chagasi: lipophosphoglycan characterization and binding to the midgut of sand fly vector Lutzomyia longipalpis. Mol Biochem Parasitol. 2002; 121: 213-24.
27. Soares RP, Turco SJ. Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae): a review. An Acad Bras Cienc. 2003; 75(3): 301-30.
28. Tolson DL, Turco SJ, Beecroft RP, Pearson TW. The immunochemical structure and surface arrangement of Leishmania donovani lipophosphoglycan determined using monoclonal antibodies. Mol Biochem Parasitol. 1989; 35(2): 109-18.
29. Volf P, Nogueira PM, Myskova J, Turco SJ, Soares RP. Structural comparison of lipophosphoglycan from Leishmania turanica and L. major, two species transmitted by Phlebotomus papatasi. Parasitol Int. 2014; 63(5): 683-6.
30. Volf P, Volfova V. Establishment and maintenance of sand fly colonies. J Vector Ecol. 2011; 36(Suppl. 1): S1-9.
31. Walters LL. Leishmania differentiation in natural and unnatural sand fly hosts. J Eukaryot Microbiol. 1993; 40(2): 196-206.
32. Wu ÂC, Freitas MA, Silva SO, Nogueira PM, Soares RP, Pesquero JB, et al. Genetic differences between two Leishmania major-like strains revealed by suppression subtractive hybridization. Mol Biochem Parasitol. 2015; 203(1-2): 34-8.

Financial support: CNPq, FAPEMIG.
+ Corresponding author: rsoares@minas.fiocruz.br
Received 16 August 2017
Accepted 17 January 2018

Our Location

Memórias do Instituto Oswaldo Cruz

Av. Brasil 4365, Castelo Mourisco 
sala 201, Manguinhos, 21040-900 
Rio de Janeiro, RJ, Brazil

Tel.: +55-21-2562-1222

This email address is being protected from spambots. You need JavaScript enabled to view it.

Support Program

logo fiocruz logo governo
logo faperj logo cnpq marca capes