Aedes aegypti saliva impairs M1-associated proinflammatory phenotype without promoting or affecting M2 polarization of murine macrophages, Parasites Vectors, vol.12, p.239, 2019. ,
Extracts of mosquito salivary gland inhibit tumour necrosis factor alpha release from mast cells, Parasite Immunol, vol.15, pp.27-33, 1993. ,
Effects of Aedes aegypti salivary components on dendritic cell and lymphocyte biology, Parasites Vectors, vol.6, p.329, 2013. ,
Complex modulation of the Aedes aegypti transcriptome in response to dengue virus infection, PLoS ONE, vol.7, p.50512, 2012. ,
SAAG-4 is a novel mosquito salivary protein that programmes host CD4 T cells to express IL-4, Parasite Immunol, vol.31, pp.287-295, 2009. ,
Role of skin immune cells on the host susceptibility to mosquito-borne viruses, Virology, vol.464, pp.26-32, 2014. ,
URL : https://hal.archives-ouvertes.fr/pasteur-01054562
Interleukin-10 determines viral clearance or persistence in vivo, Nat. Med, vol.12, pp.1301-1309, 2006. ,
Interferon lambda protects the female reproductive tract against zika virus infection, Nat. Commun, vol.10, p.280, 2019. ,
Anti-complement activity in the saliva of phlebotomine sand flies and other haematophagous insects, Parasitology, vol.127, pp.87-93, 2003. ,
Different clinical and laboratory manifestations between dengue haemorrhagic fever and dengue fever with bleeding tendency, Trans. R. Soc. Trop. Med. Hyg, vol.101, pp.1106-1113, 2007. ,
Role of autophagy in zika virus infection and pathogenesis, Virus Res, vol.254, pp.34-40, 2018. ,
Effect of dengue-2 virus infection on protein expression in the salivary glands of Aedes aegypti mosquitoes, Am. J. Trop. Med. Hyg, vol.90, pp.431-437, 2014. ,
Mosquito saliva serine protease enhances dissemination of dengue virus into the mammalian host, J. Virol, vol.88, pp.164-175, 2014. ,
Mosquito bite delivery of dengue virus enhances immunogenicity and pathogenesis in humanized mice, J. Virol, vol.86, pp.7637-7649, 2012. ,
Differential modulation of murine cellular immune responses by salivary gland extract of Aedes aegypti, Am. J. Trop. Med. Hyg, vol.51, pp.690-696, 1994. ,
Mosquito-borne diseases and omics: salivary gland proteome of the female Aedes aegypti mosquito, OMICS J. Integr. Biol, vol.21, pp.45-54, 2017. ,
A new mouse model reveals a critical role for host innate immunity in resistance to rift valley fever, J. Immunol, vol.185, pp.6146-6156, 2010. ,
URL : https://hal.archives-ouvertes.fr/pasteur-01325858
Immunization with AgTRIO, a protein in anopheles saliva, contributes to protection against plasmodium infection in mice, Cell Host Microbe, vol.23, pp.523-535, 2018. ,
Infection via mosquito bite alters zika virus tissue tropism and replication kinetics in rhesus macaques, Nat. Commun, vol.8, p.2096, 2017. ,
Phenotyping of peripheral blood mononuclear cells during acute dengue illness demonstrates infection and increased activation of monocytes in severe cases compared to classic dengue fever, Virology, vol.376, pp.429-435, 2008. ,
Inflammasome signaling pathways exert antiviral effect against chikungunya virus in human dermal fibroblasts, Infect. Genet. Evol, vol.32, pp.401-408, 2015. ,
URL : https://hal.archives-ouvertes.fr/hal-01148961
Innate immune response of primary human keratinocytes to west nile virus infection and its modulation by mosquito saliva, Front. Cell. Infect. Microbiol, vol.8, p.387, 2018. ,
Different subsets of T cells, memory, effector functions, and CAR-T immunotherapy, Cancers, vol.8, p.36, 2016. ,
Immunity to a salivary protein of a sand fly vector protects against the fatal outcome of visceral leishmaniasis in a hamster model, Proc. Natl. Acad. Sci. U.S.A, vol.105, pp.7845-7850, 2008. ,
The lymphotoxin network: orchestrating a type I interferon response to optimize adaptive immunity, Cytokine Growth Factor Rev, vol.25, pp.139-145, 2014. ,
Emerging arboviruses: why today? One Health, vol.4, pp.1-13, 2017. ,
Lessons from mosquitoes' painless piercing, J. Mech. Behav. Biomed. Mater, vol.84, pp.178-187, 2018. ,
Biology of zika virus infection in human skin cells, J. Virol, vol.89, pp.8880-8896, 2015. ,
URL : https://hal.archives-ouvertes.fr/hal-01228435
CD4 T cells, CD8 T cells, and monocytes coordinate to prevent rift valley fever virus encephalitis, J. Virol, vol.92, pp.1270-1288, 2018. ,
Rift valley fever, Clin. Lab. Med, vol.37, pp.285-301, 2017. ,
Aedes aegypti NeSt1 protein enhances zika virus pathogenesis by activating neutrophils, J. Virol, vol.93, pp.395-414, 2019. ,
Neutrophil extracellular traps effectively control acute chikungunya virus infection, Front. Immunol, vol.10, p.3108, 2020. ,
The role of interferon antagonist, non-structural proteins in the pathogenesis and emergence of arboviruses, Viruses, vol.3, pp.629-658, 2011. ,
Arbovirusmosquito vector-host interactions and the impact on transmission and disease pathogenesis of arboviruses, Front. Microbiol, vol.10, p.22, 2019. ,
CD8 T cells protect adult naive mice from JEV-induced morbidity via lytic function, PLoS Neglected Trop. Dis, vol.11, p.5329, 2017. ,
Identification of five interferon-induced cellular proteins that inhibit west nile virus and dengue virus infections, J. Virol, vol.84, pp.8332-8341, 2010. ,
Salivary factor LTRIN from Aedes aegypti facilitates the transmission of zika virus by interfering with the lymphotoxin-? receptor, Nat. Immunol, vol.19, pp.342-353, 2018. ,
Signaling to NF-?B by toll-like receptors, Trends Mol. Med, vol.13, pp.460-469, 2007. ,
Drivers, dynamics, and control of emerging vector-borne zoonotic diseases, Lancet, vol.380, pp.61151-61160, 2012. ,
Measuring the burden of arboviral diseases: the spectrum of morbidity and mortality from four prevalent infections, Popul. Health Metrics, vol.9, p.1, 2011. ,
Flavivirus receptors: diversity, identity, and cell entry, Front. Immunol, vol.9, p.2180, 2018. ,
Aedes mosquito saliva modulates rift valley fever virus pathogenicity, PLoS Neglected Trop. Dis, vol.7, p.2237, 2013. ,
URL : https://hal.archives-ouvertes.fr/pasteur-01054567
Dengue virus inoculation to human skin explants: an effective approach to assess in situ the early infection and the effects on cutaneous dendritic cells: cutaneous infection with dengue virus, Int. J. Exp. Pathol, vol.86, pp.505-512, 2005. ,
Protective and pathogenic responses to chikungunya virus infection, Curr. Trop. Med. Rep, vol.2, pp.13-21, 2015. ,
Critical role of CD4+ T cells and IFN? signaling in antibody-mediated resistance to zika virus infection, Nat. Commun, vol.9, p.3136, 2018. ,
Discovery of mosquito saliva microRNAs during CHIKV Infection, PLoS Neglected Trop. Dis, vol.9, p.3386, 2015. ,
Time to micromanage the pathogenhost-vector interface: considerations for vaccine development, vol.7, p.10, 2019. ,
Mosquito saliva: the hope for a universal arbovirus vaccine?, J. Infect. Dis, vol.218, pp.7-15, 2018. ,
Safety and immunogenicity of a mosquito saliva peptide-based vaccine: a randomised, placebo-controlled, double-blind, phase 1 trial, Lancet, vol.395, 1998. ,
Skin immunity, Arch. Immunol. Ther. Exp, vol.66, pp.45-54, 2018. ,
Route of inoculation and mosquito vector exposure modulate dengue virus replication kinetics and immune responses in rhesus macaques, PLoS Neglected Trop. Dis, vol.14, p.8191, 2020. ,
Protective immune responses against west nile virus are primed by distinct complement activation pathways, J. Exp. Med, vol.203, pp.1371-1381, 2006. ,
Complement activation is required for induction of a protective antibody response against west nile virus infection, J. Virol, vol.79, pp.7466-7477, 2005. ,
An inhibitor of the alternative pathway of complement in saliva of new world anopheline mosquitoes, J. Immunol, vol.197, pp.599-610, 2016. ,
Inhibition of the complement system by saliva of Anopheles (Nyssorhynchus) aquasalis, Insect Biochem. Mol. Biol, vol.92, pp.12-20, 2018. ,
Toll-like receptors in skin, Adv. Dermatol, vol.24, pp.71-87, 2008. ,
Prevention of rift valley fever in rhesus monkeys with interferon-?, Clin. Infect. Dis, vol.11, 1989. ,
Interplay between janus kinase/signal transducer and activator of transcription signaling activated by type I interferons and viral antagonism, Front. Immunol, vol.8, p.1758, 2017. ,
Neutrophil Activation and early features of NET formation are associated with dengue virus infection in human, Front. Immunol, vol.9, p.3007, 2019. ,
URL : https://hal.archives-ouvertes.fr/pasteur-02048214
Emerging arboviruses of medical importance in the mediterranean region, J. Clin. Virol, vol.115, pp.5-10, 2019. ,
The gut anticomplement activity of Aedes aegypti: investigating new ways to control the major human arboviruses vector in the Americas, Insect Biochem. Mol. Biol, vol.120, p.103338, 2020. ,
Emergence of zoonotic arboviruses by animal trade and migration, Parasites Vectors, vol.3, p.35, 2010. ,
Host inflammatory response to mosquito bites enhances the severity of arbovirus infection, Immunity, vol.44, pp.1455-1469, 2016. ,
Mosquito biting modulates skin response to virus infection, Trends Parasitol, vol.33, pp.645-657, 2017. ,
Characterization of chikungunya virus infection of a human keratinocyte cell line: role of mosquito salivary gland protein in suppressing the host immune response, Infect. Genet. Evol, vol.17, pp.210-215, 2013. ,
An annotated catalogue of salivary gland transcripts in the adult female mosquito, AEdes aegypti * . BMC Genomics, vol.8, p.6, 2007. ,
The risk of rift valley fever virus introduction and establishment in the United States and European Union, Emerg. Microbes Infect, vol.2, pp.1-8, 2013. ,
Neutrophil: a cell with many roles in inflammation or several cell types?, Front. Physiol, vol.9, p.113, 2018. ,
Interferon response factors 3 and 7 protect against chikungunya virus hemorrhagic fever and shock, J. Virol, vol.86, pp.9888-9898, 2012. ,
URL : https://hal.archives-ouvertes.fr/hal-01191139
Cutting edge: independent roles for IRF-3 and IRF-7 in hematopoietic and nonhematopoietic cells during host response to chikungunya infection, J. Immunol, vol.188, pp.2967-2971, 2012. ,
URL : https://hal.archives-ouvertes.fr/pasteur-01372485
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, vol.102, pp.400-408, 2008. ,
Aedes aegypti saliva alters leukocyte recruitment and cytokine signaling by antigen-presenting cells during west nile virus infection, PLoS ONE, vol.5, p.11704, 2010. ,
Aedes aegypti salivary gland extracts modulate anti-viral and TH1/TH2 cytokine responses to sindbis virus infection, Viral. Immunol, vol.17, pp.565-573, 2004. ,
A diverse range of gene products are effectors of the type I interferon antiviral response, Nature, vol.472, pp.481-485, 2011. ,
Viruses and interferons, Annu. Rev. Microbiol, vol.55, pp.255-281, 2001. ,
Triggering the interferon antiviral response through an IKKrelated pathway, Science, vol.300, pp.1148-1151, 2003. ,
Human T lymphocytes are permissive for dengue virus replication, J. Virol, vol.92, pp.2181-02117, 2018. ,
Complement and viral pathogenesis, Virology, vol.411, pp.362-373, 2011. ,
Increasing dengue incidence in Singapore over the past 40 years: population growth, climate and mobility, PLoS ONE, vol.10, p.136286, 2015. ,
Mosquito saliva causes enhancement of west nile virus infection in mice, J. Virol, vol.85, pp.1517-1527, 2011. ,
A mosquito salivary protein promotes flavivirus transmission by activation of autophagy, Nat. Commun, vol.11, p.260, 2020. ,
Aedes aegypti saliva contains a prominent 34-kDa protein that strongly enhances dengue virus replication in human keratinocytes, J. Invest. Dermatol, vol.134, pp.281-284, 2014. ,
URL : https://hal.archives-ouvertes.fr/hal-02513214
Aedes aegypti saliva enhances dengue virus infection of human keratinocytes by suppressing innate immune responses, J. Invest. Dermatol, vol.132, pp.2103-2105, 2012. ,
URL : https://hal.archives-ouvertes.fr/hal-02959112
Host immune response to mosquito-transmitted chikungunya virus differs from that elicited by needle inoculated virus, PLoS ONE, vol.5, p.12137, 2010. ,
Differential expression of Aedes aegypti salivary transcriptome upon blood feeding. Parasites Vectors 2:34, 2009. ,
Development, nutrition and reproduction, Bull. Entomol. Res, vol.1, pp.307-308, 1992. ,
Impaired antibody-independent immune response of B cells in patients with acute dengue infection, Front. Immunol, vol.10, p.2500, 2019. ,
Aedes aegypti AgBR1 antibodies modulate early zika virus infection of mice, Nat. Microbiol, vol.4, pp.948-955, 2019. ,
Mosquito saliva alone has profound effects on the human immune system, PLoS Neglected Trop. Dis, vol.12, p.6439, 2018. ,
Chikungunya virus, Clin. Lab. Med, vol.37, pp.371-382, 2017. ,
Differential modulation of murine host immune response by salivary gland extracts from the mosquitoes Aedes aegypti and Culex quinquefasciatus, Med. Vet. Entomol, vol.18, pp.191-199, 2004. ,
NETWORK COMMUNICATIONS: lymphotoxins, LIGHT, and TNF, Annu. Rev. Immunol, vol.23, pp.787-819, 2005. ,
Saliva of the yellow fever mosquito, Aedes aegypti, modulates murine lymphocyte function, Parasite Immunol, vol.26, pp.295-306, 2004. ,
Present and future arboviral threats, Antiviral Res, vol.85, pp.328-345, 2010. ,
, A Global Brief on Vector-Borne Diseases. WHO. Available online at: www.who.int, WHO, 2020.
, , 2017.
, Aedes Aegypti saliva enhances chikungunya virus replication in human skin fibroblasts via inhibition of the type I interferon signaling pathway, Infect. Genet. Evol, vol.55, pp.68-70
Epidemic arboviral diseases: priorities for research and public health, Lancet Infect. Dis, vol.17, issue.16, pp.30518-30525, 2017. ,
Human skin langerhans cells are targets of dengue virus infection, Nat. Med, vol.6, pp.816-820, 2000. ,
Cutting edge: a novel Toll/IL-1 receptor domain-containing adapter that preferentially activates the IFN-? promoter in the toll-like receptor signaling, J. Immunol, vol.169, pp.6668-6672, 2002. ,
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, vol.21, pp.35-44, 1999. ,
Differential proteomics of Aedes albopictus salivary gland, midgut and C6/36 cell induced by dengue virus infection, Virology, vol.444, pp.109-118, 2013. ,