Emerging arboviruses: Why today? One Health, vol.4, pp.1-13, 2017. ,
Present and future arboviral threats, Antiviral Res, vol.85, pp.328-345, 2010. ,
Estimating the proportion of vaccine-induced hospitalized dengue cases among Dengvaxia vaccinees in the Philippines, Wellcome Open Res, 2019. ,
Vaccine-attributable severe dengue in the Philippines, Lancet, vol.394, pp.2151-2152, 2019. ,
Changing patterns of chikungunya virus: Re-emergence of a zoonotic arbovirus, J. Gen. Virol, vol.88, pp.2363-2377, 2007. ,
A single mutation in chikungunya virus affects vector specificity and epidemic potential, PLoS Pathog, 2007. ,
Two Chikungunya isolates from the outbreak of La Reunion (Indian Ocean) exhibit different patterns of infection in the mosquito, Aedes albopictus, PLoS ONE, vol.2, 1168. ,
URL : https://hal.archives-ouvertes.fr/hal-00196860
Introduction and establishment of Aedes (Stegomyia) albopictus skuse (Diptera: Culicidae) in Albania, J. Am. Mosq. Control Assoc, vol.14, pp.340-343, 1998. ,
, Euro Surveill, vol.20, 2014.
Leparc-Goffart, I.; et al. Chikungunya virus, southeastern France, Emerg. Infect. Dis, vol.17, pp.910-913, 2011. ,
An outbreak of chikungunya fever in the province of, Euro Surveill, vol.12, 2007. ,
The global distribution and burden of dengue, Nature, vol.496, pp.504-507, 2013. ,
Adaptive immune responses to primary and secondary dengue virus infections, Nat. Rev. Immunol, vol.19, pp.218-230, 2019. ,
Secondary infection as a risk factor for dengue hemorrhagic fever/dengue shock syndrome: An historical perspective and role of antibody-dependent enhancement of infection, Arch. Virol, vol.158, pp.1445-1459, 2013. ,
Antibody-dependent enhancement of dengue virus growth in human monocytes as a risk factor for dengue hemorrhagic fever, Am. J. Trop Med. Hyg, vol.40, pp.444-451, 1989. ,
Existing and potential infection risk zones of yellow fever worldwide: A modelling analysis, Lancet Glob. Health, vol.6, pp.270-278, 2018. ,
Recent sylvatic yellow fever virus transmission in Brazil: The news from an old disease, Virol. J, vol.17, issue.9, 2020. ,
, WHO Expert Committee on Biological Standardization. Forty-fifth report. World Health Organ. Tech. Rep. Ser, vol.858, pp.1-101, 1995.
Yellow Fever importation to China -a failure of pre-and post-travel control systems?, Int. J. Infect. Dis, vol.60, pp.91-92, 2017. ,
Yellow fever: Is Asia prepared for an epidemic?, Lancet Infect. Dis, vol.19, pp.241-242, 2019. ,
Yellow fever cases in Asia: Primed for an epidemic, Int. J. Infect. Dis, vol.48, pp.98-103, 2016. ,
Zika virus outbreak on Yap Island, Federated States of Micronesia, N. Engl. J. Med, vol.360, pp.2536-2543, 2009. ,
URL : https://hal.archives-ouvertes.fr/pasteur-00734543
Zika virus in French Polynesia 2013-14: Anatomy of a completed outbreak, Lancet Infect. Dis, vol.18, pp.172-182, 2018. ,
URL : https://hal.archives-ouvertes.fr/hal-01789246
, Zika virus in the Americas: Early epidemiological and genetic findings, vol.352, pp.345-349, 2016.
URL : https://hal.archives-ouvertes.fr/hal-02641629
Asymptomatic Prenatal Zika Virus Infection and Congenital Zika Syndrome. Open Forum, Infect. Dis, vol.5, p.73, 2018. ,
Asymptomatic Transmission and the Dynamics of Zika Infection, Sci. Rep, vol.7, p.5829, 2017. ,
Past and future spread of the arbovirus vectors Aedes aegypti and Aedes albopictus, Nat. Microbiol, vol.4, pp.404-414, 2019. ,
URL : https://hal.archives-ouvertes.fr/pasteur-02067318
Mayaro virus: A new human disease agent. II. Isolation from blood of patients in Trinidad, B.W.I. Am, J. Trop. Med. Hyg, vol.6, pp.1012-1016, 1957. ,
Reconstruction of the Evolutionary History and Dispersal of Usutu Virus, a Neglected Emerging Arbovirus in Europe and Africa, vol.7, 2016. ,
Mayaro: An emerging viral threat? Emerg, Microbes Infect, vol.7, p.163, 2018. ,
Usutu virus in Africa. Vector Borne Zoonotic Dis, vol.11, pp.1417-1423, 2011. ,
Usutu virus: An emerging flavivirus in Europe, vol.7, pp.219-238, 2015. ,
, The global distribution of the arbovirus vectors Aedes aegypti and Ae. albopictus. Elife, 2015.
Dynamics of flavivirus infection in mosquitoes, Adv. Virus Res, vol.60, pp.187-232, 2003. ,
Mosquito immunity against arboviruses, Viruses, vol.6, pp.4479-4504, 2014. ,
Mosquito RNAi is the major innate immune pathway controlling arbovirus infection and transmission, Future Microbiol, vol.6, pp.265-277, 2011. ,
Mosquito bottlenecks alter viral mutant swarm in a tissue and time-dependent manner with contraction and expansion of variant positions and diversity, Virus Evol, 2018. ,
Genetic Drift during Systemic Arbovirus Infection of Mosquito Vectors Leads to Decreased Relative Fitness during Host Switching, Cell Host Microbe, vol.19, pp.481-492, 2016. ,
Factors shaping the adaptive landscape for arboviruses: Implications for the emergence of disease, Future Microbiol, vol.8, pp.155-176, 2013. ,
Controlling vector-borne diseases by releasing modified mosquitoes, Nat. Rev. Microbiol, vol.16, pp.508-518, 2018. ,
Ecology: A world without mosquitoes, Nature, vol.466, pp.432-434, 2010. ,
Biosafety concerns involving genetically modified mosquitoes to combat malaria and dengue in developing countries, JAMA, vol.305, pp.930-931, 2011. ,
Population modification of Anopheline species to control malaria transmission, vol.111, pp.424-435, 2017. ,
Cheating evolution: Engineering gene drives to manipulate the fate of wild populations, Nat. Rev. Genet, vol.17, pp.146-159, 2016. ,
Engineering RNA interference-based resistance to dengue virus type 2 in genetically modified Aedes aegypti, Proc. Natl. Acad. Sci, vol.103, pp.4198-4203, 2006. ,
Transgene-mediated suppression of dengue viruses in the salivary glands of the yellow fever mosquito, Aedes aegypti, Insect Mol. Biol, vol.19, pp.753-763, 2010. ,
Synthetic miRNAs induce dual arboviral-resistance phenotypes in the vector mosquito Aedes aegypti, Commun. Biol, 2011. ,
URL : https://hal.archives-ouvertes.fr/pasteur-01718640
Multiple dengue virus serotypes resistant transgenic Aedes aegypti fitness evaluated under laboratory conditions, RNA Biol, vol.2020, pp.1-21 ,
Engineered resistance to Zika virus in transgenic Aedes aegypti expressing a polycistronic cluster of synthetic small RNAs, Proc. Natl. Acad. Sci, vol.116, pp.3656-3661, 2019. ,
Antiviral Hammerhead Ribozymes Are Effective for Developing Transgenic Suppression of Chikungunya Virus in Aedes aegypti Mosquitoes, Viruses, vol.8, p.163, 2016. ,
Effective suppression of dengue virus using a novel group-I intron that induces apoptotic cell death upon infection through conditional expression of the Bax C-terminal domain, Virol. J, vol.11, issue.111, 2014. ,
Wolbachia induces reactive oxygen species (ROS)-dependent activation of the Toll pathway to control dengue virus in the mosquito Aedes aegypti, Proc. Natl. Acad. Sci, vol.109, pp.23-31, 2012. ,
Broad dengue neutralization in mosquitoes expressing an engineered antibody, PLoS Pathog, vol.16, 2020. ,
URL : https://hal.archives-ouvertes.fr/pasteur-02653696
Perceptions and recommendations by scientists for a potential release of genetically modified mosquitoes in Nigeria, Malar J, vol.13, 2014. ,
Manipulating Mosquito Tolerance for Arbovirus Control, Cell Host Microbe, vol.26, pp.309-313, 2019. ,
URL : https://hal.archives-ouvertes.fr/hal-02863592
Native microbiota shape insect vector competence for human pathogens, Cell Host Microbe, vol.10, pp.307-310, 2011. ,
Valiente Moro, C. Prevalence, genomic and metabolic profiles of Acinetobacter and Asaia associated with field-caught Aedes albopictus from Madagascar, FEMS Microbiol. Ecol, vol.83, pp.63-73, 2013. ,
Harnessing mosquito-Wolbachia symbiosis for vector and disease control, Acta Trop, vol.132, pp.150-163, 2014. ,
URL : https://hal.archives-ouvertes.fr/hal-02522213
Wolbachia blocks currently circulating Zika virus isolates in Brazilian Aedes aegypti mosquitoes, Cell Host Microbe, vol.19, pp.771-774, 2016. ,
Distribution and evolution of bacteriophage WO in Wolbachia, the endosymbiont causing sexual alterations in arthropods, J. Mol. Evol, vol.51, pp.491-497, 2000. ,
Studies on Rickettsia-Like Micro-Organisms in Insects, J. Med. Res, vol.44, pp.329-374, 1924. ,
Master manipulators of invertebrate biology, Nat. Rev. Microbiol, vol.6, pp.741-751, 2008. ,
, The Wolbachia Endosymbionts. Microbiol. Spectr, vol.7, 2019.
How many species are infected with Wolbachia?-A statistical analysis of current data, FEMS Microbiol. Lett, vol.281, pp.215-220, 2008. ,
The cellular phenotype of cytoplasmic incompatibility in Culex pipiens in the light of cidB diversity, PLoS Pathog, vol.14, 2018. ,
URL : https://hal.archives-ouvertes.fr/hal-01938013
A Wolbachia deubiquitylating enzyme induces cytoplasmic incompatibility, Nat. Microbiol, 2017. ,
The rich somatic life of Wolbachia, vol.5, pp.923-936, 2016. ,
Variation in antiviral protection mediated by different Wolbachia strains in Drosophila simulans, PLoS Pathog, vol.5, 2009. ,
The bacterial symbiont Wolbachia induces resistance to RNA viral infections in Drosophila melanogaster, PLoS Biol, vol.6, 2008. ,
A Wolbachia symbiont in Aedes aegypti limits infection with dengue, vol.139, pp.1268-1278, 2009. ,
Wolbachia and virus protection in insects, Science, vol.322, 2008. ,
Aedes aegypti vector competence studies: A review, Infect. Genet. Evol, vol.67, pp.191-209, 2019. ,
Successful establishment of Wolbachia in Aedes populations to suppress dengue transmission, Nature, vol.476, pp.454-457, 2011. ,
Persistent Wolbachia and cultivable bacteria infection in the reproductive and somatic tissues of the mosquito vector Aedes albopictus, PLoS ONE, 2009. ,
URL : https://hal.archives-ouvertes.fr/pasteur-01681435
Wolbachia induces density-dependent inhibition to dengue virus in mosquito cells, PLoS Negl. Trop. Dis, vol.6, 1754. ,
Should Symbionts Be Nice or Selfish? Antiviral Effects of Wolbachia Are Costly but Reproductive Parasitism Is Not, PLoS Pathog, vol.11, 2015. ,
Virus evolution in Wolbachia-infected Drosophila, Proc. Biol. Sci, vol.286, 2019. ,
Immune activation by life-shortening Wolbachia and reduced filarial competence in mosquitoes, Science, vol.326, pp.134-136, 2009. ,
Wolbachia stimulates immune gene expression and inhibits plasmodium development in Anopheles gambiae, PLoS Pathog, vol.6, 2010. ,
Wolbachia and dengue virus infection in the mosquito Aedes fluviatilis (Diptera: Culicidae), PLoS ONE, vol.12, 2017. ,
Wolbachia uses a host microRNA to regulate transcripts of a methyltransferase, contributing to dengue virus inhibition in Aedes aegypti, Proc. Natl. Acad. Sci, vol.110, pp.10276-10281, 2013. ,
Wolbachia infection modifies the profile, shuttling and structure of microRNAs in a mosquito cell line, PLoS ONE, vol.9, p.96107, 2014. ,
Expression of mosquito microRNA Aae-miR-2940-5p is downregulated in response to West Nile virus infection to restrict viral replication, J. Virol, vol.88, pp.8457-8467, 2014. ,
Wolbachia Blocks Viral Genome Replication Early in Infection without a Transcriptional Response by the Endosymbiont or Host Small RNA Pathways, PLoS Pathog, vol.12, 2016. ,
Perturbed cholesterol and vesicular trafficking associated with dengue blocking in Wolbachia-infected Aedes aegypti cells, Nat. Commun, vol.8, p.526, 2017. ,
Sustained Wolbachia-mediated blocking of dengue virus isolates following serial passage in Aedes aegypti cell culture, Virus Evol, vol.5, p.12, 2019. ,
Infection of Aedes albopictus Mosquito C6/36 Cells with the wMelpop Strain of Wolbachia Modulates Dengue Virus-Induced Host Cellular Transcripts and Induces Critical Sequence Alterations in the Dengue Viral Genome, J. Virol, vol.93, 2019. ,
A Wolbachia wMel transinfection in Aedes albopictus is not detrimental to host fitness and inhibits Chikungunya virus, PLoS Negl. Trop. Dis, 2013. ,
URL : https://hal.archives-ouvertes.fr/pasteur-01680359
Detection of Wolbachia in Aedes albopictus and Their Effects on Chikungunya Virus, Am. J. Trop. Med. Hyg, vol.96, pp.148-156, 2017. ,
The native Wolbachia symbionts limit transmission of dengue virus in Aedes albopictus, PLoS Negl. Trop. Dis, vol.6, 1989. ,
URL : https://hal.archives-ouvertes.fr/pasteur-01680937
Wolbachia modulates Chikungunya replication in Aedes albopictus, Mol. Ecol, vol.19, pp.404-417, 1953. ,
URL : https://hal.archives-ouvertes.fr/pasteur-00467675
The endosymbiotic bacterium Wolbachia induces resistance to dengue virus in Aedes aegypti, PLoS Pathog, vol.6, 2010. ,
, Wolbachia invades Anopheles stephensi populations and induces refractoriness to Plasmodium infection, vol.340, pp.748-751, 2013.
Cross-Generational Effects of Heat Stress on Fitness and Wolbachia Density in Aedes aegypti Mosquitoes, Trop. Med. Infect. Dis, 2019. ,
Loss of cytoplasmic incompatibility in Wolbachia-infected Aedes aegypti under field conditions, PLoS Negl. Trop. Dis, vol.13, p.7357, 2019. ,
Heat Sensitivity of wMel Wolbachia during Aedes aegypti Development, PLoS Negl. Trop. Dis, vol.10, 2016. ,
The Effect of Temperature on Wolbachia-Mediated Dengue Virus Blocking in Aedes aegypti, Am. J. Trop. Med. Hyg, vol.94, pp.812-819, 2016. ,
A Survey of the bacteriophage WO in the endosymbiotic bacteria Wolbachia, Mol. Biol. Evol, vol.24, pp.427-435, 2007. ,
URL : https://hal.archives-ouvertes.fr/hal-00434685
Diversity, distribution and specificity of WO phage infection in Wolbachia of four insect species, Insect Mol. Biol, vol.13, pp.147-153, 2004. ,
URL : https://hal.archives-ouvertes.fr/hal-00427580
Bacteriophage WO-B and Wolbachia in natural mosquito hosts: Infection incidence, transmission mode and relative density, Mol. Ecol, vol.15, pp.2451-2461, 2006. ,
Temperature affects the tripartite interactions between bacteriophage WO, Wolbachia, and cytoplasmic incompatibility, PLoS ONE, vol.6, 2011. ,
The impact of temperature and Wolbachia infection on vector competence of potential dengue vectors Aedes aegypti and Aedes albopictus in the transmission of dengue virus serotype 1 in southern Taiwan, Parasit Vectors, vol.10, p.551, 2017. ,
Fluctuations at a low mean temperature accelerate dengue virus transmission by Aedes aegypti, PLoS Negl. Trop. Dis, 2013. ,
URL : https://hal.archives-ouvertes.fr/pasteur-02011018
Effect of environmental temperature on the ability of Culex pipiens (Diptera: Culicidae) to transmit West Nile virus, J. Med. Entomol, vol.39, pp.221-225, 2002. ,
Effect of temperature stress on immature stages and susceptibility of Aedes aegypti mosquitoes to chikungunya virus, Am. J. Trop. Med. Hyg, vol.70, pp.346-350, 2004. ,
The impact of host diet on Wolbachia titer in Drosophila, PLoS Pathog, vol.11, 2015. ,
The wMel Wolbachia strain blocks dengue and invades caged Aedes aegypti populations, Nature, vol.476, pp.450-453, 2011. ,
Evidence for the natural occurrence of Wolbachia in Aedes aegypti mosquitoes, FEMS Microbiol. Lett, p.366, 2019. ,
Detection of dengue viruses and Wolbachia in Aedes aegypti and Aedes albopictus larvae from four urban localities in Kuala Lumpur, vol.34, p.14, 2017. ,
Dynamics and diversity of bacteria associated with the disease vectors Aedes aegypti and Aedes albopictus, Sci. Rep, vol.9, 2019. ,
Mosquito vector-associated microbiota: Metabarcoding bacteria and eukaryotic symbionts across habitat types in Thailand endemic for dengue and other arthropod-borne diseases, Ecol. Evol, vol.8, pp.1352-1368, 2018. ,
Detection of Wolbachia in field-collected Aedes aegypti mosquitoes in metropolitan Manila, Philippines. Parasit Vectors, vol.12, p.361, 2019. ,
, Wolbachia pipientis occurs in Aedes aegypti populations in New Mexico and Florida, vol.9, pp.6148-6156, 2019.
Mosquitoes host communities of bacteria that are essential for development but vary greatly between local habitats, Mol. Ecol, vol.25, pp.5806-5826, 2016. ,
Microbiome Interaction Networks and Community Structure From Laboratory-Reared and Field-Collected Aedes aegypti, Aedes albopictus, and Culex quinquefasciatus Mosquito Vectors, Front. Microbiol, vol.9, 2018. ,
Wolbachia re-replacement without incompatibility: Potential for intended and unintended consequences, J. Med. Entomol, vol.50, pp.1152-1158, 2013. ,
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