Particle and Fibre Toxicology | |
Effects of Aedes aegypti salivary components on dendritic cell and lymphocyte biology | |
Anderson Sá-Nunes1  Margareth L Capurro1  Eric Calvo2  Gustavo P Amarante-Mendes6  Michalis Kotsyfakis5  Júlia Campopiano4  Ciro N Lino3  Daniele I Gueroni3  Ceres Maciel3  Michele S Barros3  Bruna Bizzarro3  | |
[1] Instituto Nacional de Ciência e Tecnologia em Entomologia Molecular, Conselho Nacional de Desenvolvimento Científico e Tecnológico (INCT-EM/CNPq), Rio de Janeiro, Brazil;Section of Vector Biology, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852, USA;Laboratório de Imunologia Experimental, Departamento de Imunologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, 05508-900, SP, Brazil;Laboratório de Biologia Celular e Molecular, Departamento de Imunologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, SP 05508-900, Brazil;Laboratory of Genomics and Proteomics of Disease Vectors, Institute of Parasitology, Biology Centre of the Academy of Sciences of Czech Republic, Ceske Budejovice 37005, Czech Republic;Instituto de Investigação em Imunologia, Instituto Nacional de Ciência e Tecnologia, INCT, São Paulo, Brazil | |
关键词: Apoptosis; Saliva; Aedes aegypti; T cells; Dendritic cells; | |
Others : 823847 DOI : 10.1186/1756-3305-6-329 |
|
received in 2013-09-28, accepted in 2013-11-05, 发布年份 2013 | |
【 摘 要 】
Background
Saliva is a key element of interaction between hematophagous mosquitoes and their vertebrate hosts. In addition to allowing a successful blood meal by neutralizing or delaying hemostatic responses, the salivary cocktail is also able to modulate the effector mechanisms of host immune responses facilitating, in turn, the transmission of several types of microorganisms. Understanding how the mosquito uses its salivary components to circumvent host immunity might help to clarify the mechanisms of transmission of such pathogens and disease establishment.
Methods
Flow cytometry was used to evaluate if increasing concentrations of A. aegypti salivary gland extract (SGE) affects bone marrow-derived DC differentiation and maturation. Lymphocyte proliferation in the presence of SGE was estimated by a colorimetric assay. Western blot and Annexin V staining assays were used to assess apoptosis in these cells. Naïve and memory cells from mosquito-bite exposed mice or OVA-immunized mice and their respective controls were analyzed by flow cytometry.
Results
Concentration-response curves were employed to evaluate A. aegypti SGE effects on DC and lymphocyte biology. DCs differentiation from bone marrow precursors, their maturation and function were not directly affected by A. aegypti SGE (concentrations ranging from 2.5 to 40 μg/mL). On the other hand, lymphocytes were very sensitive to the salivary components and died in the presence of A. aegypti SGE, even at concentrations as low as 0.1 μg/mL. In addition, A. aegypti SGE was shown to induce apoptosis in all lymphocyte populations evaluated (CD4+ and CD8+ T cells, and B cells) through a mechanism involving caspase-3 and caspase-8, but not Bim. By using different approaches to generate memory cells, we were able to verify that these cells are resistant to SGE effects.
Conclusion
Our results show that lymphocytes, and not DCs, are the primary target of A. aegypti salivary components. In the presence of A. aegypti SGE, naïve lymphocyte populations die by apoptosis in a caspase-3- and caspase-8-dependent pathway, while memory cells are selectively more resistant to its effects. The present work contributes to elucidate the activities of A. aegypti salivary molecules on the antigen presenting cell-lymphocyte axis and in the biology of these cells.
【 授权许可】
2013 Bizzarro et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
20140713014601415.pdf | 1690KB | download | |
Figure 5. | 86KB | Image | download |
Figure 4. | 46KB | Image | download |
Figure 3. | 51KB | Image | download |
Figure 2. | 94KB | Image | download |
Figure 1. | 74KB | Image | download |
【 图 表 】
Figure 1.
Figure 2.
Figure 3.
Figure 4.
Figure 5.
【 参考文献 】
- [1]Morens DM, Folkers GK, Fauci AS: The challenge of emerging and re-emerging infectious diseases. Nature 2004, 430(6996):242-249.
- [2]Tolle MA: Mosquito-borne diseases. Curr Probl Pediatr Adolesc Health Care 2009, 39(4):97-140.
- [3]Scott TW, Takken W: Feeding strategies of anthropophilic mosquitoes result in increased risk of pathogen transmission. Trends Parasitol 2012, 28(3):114-121.
- [4]Fontaine A, Diouf I, Bakkali N, Misse D, Pages F, Fusai T, Rogier C, Almeras L: Implication of haematophagous arthropod salivary proteins in host-vector interactions. Parasit Vectors 2011, 4:187. BioMed Central Full Text
- [5]Francischetti IM, Sa-Nunes A, Mans BJ, Santos IM, Ribeiro JM: The role of saliva in tick feeding. Front Biosci 2009, 14:2051-2088.
- [6]Ribeiro JM, Francischetti IM: Role of arthropod saliva in blood feeding: sialome and post-sialome perspectives. Annu Rev Entomol 2003, 48:73-88.
- [7]Edwards JF, Higgs S, Beaty BJ: Mosquito feeding-induced enhancement of Cache Valley Virus (Bunyaviridae) infection in mice. J Med Entomol 1998, 35(3):261-265.
- [8]Limesand KH, Higgs S, Pearson LD, Beaty BJ: Effect of mosquito salivary gland treatment on vesicular stomatitis New Jersey virus replication and interferon alpha/beta expression in vitro. J Med Entomol 2003, 40(2):199-205.
- [9]Schneider BS, Soong L, Coffey LL, Stevenson HL, McGee CE, Higgs S: Aedes aegypti saliva alters leukocyte recruitment and cytokine signaling by antigen-presenting cells during West Nile virus infection. PLoS One 2010, 5(7):e11704.
- [10]Styer LM, Bernard KA, Kramer LD: Enhanced early West Nile virus infection in young chickens infected by mosquito bite: effect of viral dose. Am J Trop Med Hyg 2006, 75(2):337-345.
- [11]Styer LM, Lim PY, Louie KL, Albright RG, Kramer LD, Bernard KA: Mosquito saliva causes enhancement of West Nile virus infection in mice. J Virol 2011, 85(4):1517-1527.
- [12]Surasombatpattana P, Patramool S, Luplertlop N, Yssel H, Misse D: Aedes aegypti Saliva Enhances Dengue Virus Infection of Human Keratinocytes by Suppressing Innate Immune Responses. J Invest Dermatol 2012, 132(8):2103-2105.
- [13]Machain-Williams C, Mammen MP Jr, Zeidner NS, Beaty BJ, Prenni JE, Nisalak A, Blair CD: Association of human immune response to Aedes aegypti salivary proteins with dengue disease severity. Parasite Immunol 2012, 34(1):15-22.
- [14]Schneider BS, Higgs S: The enhancement of arbovirus transmission and disease by mosquito saliva is associated with modulation of the host immune response. Trans R Soc Trop Med Hyg 2008, 102(5):400-408.
- [15]Banchereau J, Steinman RM: Dendritic cells and the control of immunity. Nature 1998, 392(6673):245-252.
- [16]Wasserman HA, Singh S, Champagne DE: Saliva of the Yellow Fever mosquito, Aedes aegypti, modulates murine lymphocyte function. Parasite Immunol 2004, 26(6–7):295-306.
- [17]Cross ML, Cupp EW, Enriquez FJ: Differential modulation of murine cellular immune responses by salivary gland extract of Aedes aegypti. Am J Trop Med Hyg 1994, 51(5):690-696.
- [18]Wanasen N, Nussenzveig RH, Champagne DE, Soong L, Higgs S: Differential modulation of murine host immune response by salivary gland extracts from the mosquitoes Aedes aegypti and Culex quinquefasciatus. Med Vet Entomol 2004, 18(2):191-199.
- [19]Boppana VD, Thangamani S, Adler AJ, Wikel SK: SAAG-4 is a novel mosquito salivary protein that programmes host CD4 T cells to express IL-4. Parasite Immunol 2009, 31(6):287-295.
- [20]Zeidner NS, Higgs S, Happ CM, Beaty BJ, Miller BR: Mosquito feeding modulates Th1 and Th2 cytokines in flavivirus susceptible mice: an effect mimicked by injection of sialokinins, but not demonstrated in flavivirus resistant mice. Parasite Immunol 1999, 21(1):35-44.
- [21]Opal SM, Esmon CT: Bench-to-bedside review: functional relationships between coagulation and the innate immune response and their respective roles in the pathogenesis of sepsis. Crit Care 2003, 7(1):23-38.
- [22]Niessen F, Schaffner F, Furlan-Freguia C, Pawlinski R, Bhattacharjee G, Chun J, Derian CK, Andrade-Gordon P, Rosen H, Ruf W: Dendritic cell PAR1-S1P3 signalling couples coagulation and inflammation. Nature 2008, 452(7187):654-658.
- [23]Ruf W, Furlan-Freguia C, Niessen F: Vascular and dendritic cell coagulation signaling in sepsis progression. J Thromb Haemost 2009, 7(Suppl 1):118-121.
- [24]Sa-Nunes A, Bafica A, Lucas DA, Conrads TP, Veenstra TD, Andersen JF, Mather TN, Ribeiro JM, Francischetti IM: Prostaglandin E2 is a major inhibitor of dendritic cell maturation and function in Ixodes scapularis saliva. J Immunol 2007, 179(3):1497-1505.
- [25]Carregaro V, Sa-Nunes A, Cunha TM, Grespan R, Oliveira CJ, Lima-Junior DS, Costa DL, Verri WA Jr, Milanezi CM, Pham VM, et al.: Nucleosides from Phlebotomus papatasi salivary gland ameliorate murine collagen-induced arthritis by impairing dendritic cell functions. J Immunol 2011, 187(8):4347-4359.
- [26]Collin N, Assumpcao TC, Mizurini DM, Gilmore DC, Dutra-Oliveira A, Kotsyfakis M, Sa-Nunes A, Teixeira C, Ribeiro JM, Monteiro RQ, et al.: Lufaxin, a novel factor Xa inhibitor from the salivary gland of the sand fly Lutzomyia longipalpis blocks protease-activated receptor 2 activation and inhibits inflammation and thrombosis in vivo. Arterioscler Thromb Vasc Biol 2012, 32(9):2185-2198.
- [27]Sa-Nunes A, Bafica A, Antonelli LR, Choi EY, Francischetti IM, Andersen JF, Shi GP, Chavakis T, Ribeiro JM, Kotsyfakis M: The immunomodulatory action of sialostatin L on dendritic cells reveals its potential to interfere with autoimmunity. J Immunol 2009, 182(12):7422-7429.
- [28]Ahmed SA, Gogal RM Jr, Walsh JE: A new rapid and simple non-radioactive assay to monitor and determine the proliferation of lymphocytes: an alternative to [3H]thymidine incorporation assay. J Immunol Methods 1994, 170(2):211-224.
- [29]Wojciechowski S, Tripathi P, Bourdeau T, Acero L, Grimes HL, Katz JD, Finkelman FD, Hildeman DA: Bim/Bcl-2 balance is critical for maintaining naive and memory T cell homeostasis. J Exp Med 2007, 204(7):1665-1675.
- [30]Kurtulus S, Tripathi P, Hildeman DA: Protecting and rescuing the effectors: roles of differentiation and survival in the control of memory T cell development. Front Immunol 2012, 3:404.
- [31]Dutton RW, Bradley LM, Swain SL: T cell memory. Annu Rev Immunol 1998, 16:201-223.
- [32]Reinhardt RL, Khoruts A, Merica R, Zell T, Jenkins MK: Visualizing the generation of memory CD4 T cells in the whole body. Nature 2001, 410(6824):101-105.
- [33]Masopust D, Vezys V, Marzo AL, Lefrancois L: Preferential localization of effector memory cells in nonlymphoid tissue. Science 2001, 291(5512):2413-2417.
- [34]Sallusto F, Lenig D, Forster R, Lipp M, Lanzavecchia A: Two subsets of memory T lymphocytes with distinct homing potentials and effector functions. Nature 1999, 401(6754):708-712.
- [35]Medeiros AI, Sa-Nunes A, Turato WM, Secatto A, Frantz FG, Sorgi CA, Serezani CH, Deepe GS Jr, Faccioli LH: Leukotrienes are potent adjuvant during fungal infection: effects on memory T cells. J Immunol 2008, 181(12):8544-8551.
- [36]Lehane M: The Biology of Blood-Sucking in Insects. 2nd edition. Cambridge: Cambridge University Press; 2005.
- [37]Cavassani KA, Aliberti JC, Dias AR, Silva JS, Ferreira BR: Tick saliva inhibits differentiation, maturation and function of murine bone-marrow-derived dendritic cells. Immunology 2005, 114(2):235-245.
- [38]Poole NM, Mamidanna G, Smith RA, Coons LB, Cole JA: Prostaglandin E2 in tick saliva regulates macrophage cell migration and cytokine profile. Parasit Vectors 2013, 6(1):261. BioMed Central Full Text
- [39]Oliveira CJ, Sa-Nunes A, Francischetti IM, Carregaro V, Anatriello E, Silva JS, de Miranda Santos IK, Ribeiro JM, Ferreira BR: Deconstructing tick saliva: non-protein molecules with potent immunomodulatory properties. J Biol Chem 2011, 286(13):10960-10969.
- [40]Chen G, Severo MS, Sohail M, Sakhon OS, Wikel SK, Kotsyfakis M, Pedra JH: Ixodes scapularis saliva mitigates inflammatory cytokine secretion during Anaplasma phagocytophilum stimulation of immune cells. Parasit Vectors 2012, 5:229. BioMed Central Full Text
- [41]Brake DK, Perez de Leon AA: Immunoregulation of bovine macrophages by factors in the salivary glands of Rhipicephalus microplus. Parasit Vectors 2012, 5:38. BioMed Central Full Text
- [42]Hovius JW, de Jong MA, den Dunnen J, Litjens M, Fikrig E, van der Poll T, Gringhuis SI, Geijtenbeek TB: Salp15 binding to DC-SIGN inhibits cytokine expression by impairing both nucleosome remodeling and mRNA stabilization. PLoS Pathog 2008, 4(2):e31.
- [43]Costa DJ, Favali C, Clarencio J, Afonso L, Conceicao V, Miranda JC, Titus RG, Valenzuela J, Barral-Netto M, Barral A, et al.: Lutzomyia longipalpis salivary gland homogenate impairs cytokine production and costimulatory molecule expression on human monocytes and dendritic cells. Infect Immun 2004, 72(3):1298-1305.
- [44]Carregaro V, Valenzuela JG, Cunha TM, Verri WA Jr, Grespan R, Matsumura G, Ribeiro JM, Elnaiem DE, Silva JS, Cunha FQ: Phlebotomine salivas inhibit immune inflammation-induced neutrophil migration via an autocrine DC-derived PGE2/IL-10 sequential pathway. J Leukoc Biol 2008, 84(1):104-114.
- [45]Merad M, Sathe P, Helft J, Miller J, Mortha A: The dendritic cell lineage: ontogeny and function of dendritic cells and their subsets in the steady state and the inflamed setting. Annu Rev Immunol 2013, 31:563-604.
- [46]Merad M, Ginhoux F, Collin M: Origin, homeostasis and function of Langerhans cells and other langerin-expressing dendritic cells. Nat Rev Immunol 2008, 8(12):935-947.
- [47]Oliveira CJ, Sa-Nunes A, Francischetti IM, Carregaro V, Anatriello E, Silva JS, Santos IK, Ribeiro JM, Ferreira BR: Deconstructing tick saliva: non-protein molecules with potent immunomodulatory properties. J Biol Chem 2011, 286(13):10960-10969.
- [48]Tsujimoto H, Gray EW, Champagne DE: Black fly salivary gland extract inhibits proliferation and induces apoptosis in murine splenocytes. Parasite Immunol 2010, 32(4):275-284.
- [49]Sutherland GB, Ewen AB: Fecundity decrease in mosquitoes ingesting blood from specifically sensitized mammals. J Insect Physiol 1974, 20(4):655-660.
- [50]Garg R, Juncadella IJ, Ramamoorthi Ashish N, Ananthanarayanan SK, Thomas V, Rincon M, Krueger JK, Fikrig E, Yengo CM: Cutting edge: CD4 is the receptor for the tick saliva immunosuppressor, Salp15. J Immunol 2006, 177(10):6579-6583.