The effects of three release strategies on Wolbachia infection frequency in mosquito populations

References

• F. Baldacchino, B. Caputo, F. Chandre, A. Drago, A. della Torre, F. Montarsi, and A. Rizzoli, Control methods against invasive Aedes mosquitoes in Europe: a review, Pest Manang. Sci. 71 (2015), pp. 1471–1485.
   PubMed Web of Science ®Google Scholar
• S. Bhatt, P.W. Gething, O.J. Brady, J.P. Messina, A.W. Farlow, C.L. Moyes, J.M. Drake, J.S. Brownstein, A.G. Hoen, O. Sankoh, M.F. Myers, D.B. George, T. Jaenisch, G.R. William Wint, C.P. Simmons, T.W. Scott, J.J. Farrar, and S.I. Ha, The global distribution and burden of dengue fever, Nature 496 (2013), pp. 504–507.
   PubMed Web of Science ®Google Scholar
• G. Bian, D. Joshi, Y. Dong, P. Lu, G. Zhou, X. Pan, Y. Xu, G. Dimopoulos, and Z. Xi, Wolbachia invades Anopheles stephensi populations and induces refractoriness to plasmodium infection, Science 340 (2013), pp. 748–751.
   PubMed Web of Science ®Google Scholar
• E. Caspari and G.S. Watson, On the evolutionary importance of cytoplasmic sterility in mosquitoes, Evolution 13 (1959), pp. 568–570.
   Web of Science ®Google Scholar
• J. Cohen, Dengue may bring out the worst in Zika, Science 355(6332) (2017), Article ID 1362.
   Web of Science ®Google Scholar
• P.E.M. Fine, On the dynamics of symbiote-dependent cytoplasmic incompatibility in Culicine mosquitoes, J. Invertebr. Pathol. 31(1) (1978), pp. 10–18.
   PubMed Web of Science ®Google Scholar
• A.A. Hoffmann, B.L. Montgomery, J. Popovici, I. Iturbe-Ormaetxe, P.H. Johnson, F. Muzzi, M. Greenfield, M. Durkan, Y.S. Leong, Y. Dong, H. Cook, J. Axford, A.G. Callahan, N. Kenny, C. Omodei, E.A. McGraw, P.A. Ryan, S.A. Ritchie, M. Turelli, and S.L. O'Neill, Successful establishment of Wolbachia in Aedes populations to suppress dengue transmission, Nature 476 (2011), pp. 454–457.
   PubMed Web of Science ®Google Scholar
• A.A. Hoffmann, M. Turelli, and L.G. Harshman, Factors affecting the distribution of cytoplasmic incompatibility in Drosophila simulans, Genetics 126(4) (1990), pp. 933–948.
   PubMed Web of Science ®Google Scholar
• L. Hu, M. Tang, Z. Wu, Z. Xi, and J. Yu, The threshold infection level for Wolbachia invasion in random environments, J. Differ. Equ. 266(7) (2019), pp. 4377–4393.
   Web of Science ®Google Scholar
• M.J. Keeling, F.M. Jiggins, and J.M. Read, The invasion and coexistence of competing Wolbachia strains, Heredity 91(4) (2003), pp. 382–388.
   PubMed Web of Science ®Google Scholar
• C.J. Mcmeniman, R.V. Lane, B.N. Cass, A.W.C. Fong, M. Sidhu, Y. Wang, and S.L. O'Neill, Stable introduction of a life-shortening Wolbachia infection into the mosquito Aedes aegypi, Science 323(5910) (2009), pp. 141–144.
   PubMed Web of Science ®Google Scholar
• L.M. Schwartz, M.E. Halloran, A.P. Durbin, and I.M. Longini, The dengue vaccine pipeline: implications for the future of dengue control, Vaccine 33(29) (2015), pp. 3293–3298.
   PubMed Web of Science ®Google Scholar
• Y. Shi and J. Yu, Wolbachia infection enhancing and decaying domains in mosquito population based on discrete models, J. Biol. Dyn. 14(1) (2020), pp. 679–695.
   PubMed Web of Science ®Google Scholar
• Y. Shi and B. Zheng, Discrete dynamical models on Wolbachia infection frequency in mosquito populations with biased release ratios, J. Biol. Dyn. 16(1) (2022), pp. 320–339.
   PubMed Web of Science ®Google Scholar
• P. Somwang, J. Yanola, W. Suwan, C. Walton, N. Lumjuan, L.A. Prapanthadara, and P. Somboon, Enzymes-based resistant mechanism in pyrethroid resistant and susceptible Aedes aegypti strains from northern Thailand, Parasitol. Res. 109(3) (2011), pp. 531–537.
   PubMed Web of Science ®Google Scholar
• J.D. Stanaway, D.S. Shepard, E.A. Undurraga, Y.A. Halasa, L.E. Coffeng, O.J. Brady, S.I. Hay, N. Bedi, I.M. Bensenor, C.A. Castaneda-Orjuela, T. Chuang, K.B. Gibney, Z.A. Memish, A. Rafay, K.N. Ukwaja, N. Yonemoto, and C.J.L. Murray, The global burden of dengue: an analysis from the global burden of disease study 2013, Lancet Infect. Dis. 16(6) (2016), pp. 712–723.
   PubMed Web of Science ®Google Scholar
• S.J. Thomas and I.K. Yoon, A review of Dengvaxia: development to deployment, Hum. Vaccin. Immunother. 15(10) (2019), pp. 2295–2314.
   PubMed Web of Science ®Google Scholar
• M. Turelli, Evolution of incompatibility-inducing microbes and their hosts, Evolution 48(5) (1994), pp. 1500–1513.
   PubMed Web of Science ®Google Scholar
• M. Turelli, Cytoplasmic incompatibility in populations with overlapping generations, Evolution 64(1) (2010), pp. 232–241.
   PubMed Web of Science ®Google Scholar
• M. Turelli and A.A. Hoffmann, Rapid spread of an inherited incompatibility factor in California Drosophila, Nature 353(6343) (1991), pp. 440–442.
   PubMed Web of Science ®Google Scholar
• M. Turelli and A.A. Hoffmann, Cytoplasmic incompatibility in Drosophila simulans: dynamics and parameter estimates from natural populations, Genetics 140(4) (1995), pp. 1319–1338.
   PubMed Web of Science ®Google Scholar
• M. Turelli and A.A. Hoffmann, Microbe-induced cytoplasmic incompatibility as a mechanism for introducing transgenes into arthropod populations, Insect. Mol. Biol. 8(2) (1999), pp. 243–255.
   PubMed Web of Science ®Google Scholar
• Z. Xi and S.L. Dobson, Characterization of Wolbachia transfection efficiency by using microinjection of embryonic cytoplasm and embryo homogenate, Appl. Environ. Microbiol. 71(6) (2005), pp. 3199–3204.
   PubMed Web of Science ®Google Scholar
• Z. Xi, C.C. Khoo, and S.L. Dobson, Wolbachia establishment and invasion in an Aedes aegypti laboratory population, Science 310(5746) (2005), pp. 326–328.
   PubMed Web of Science ®Google Scholar
• J.H. Yen and A.R. Barr, New hypothesis of the cause of cytoplasmic incompatibility in Culex pipiens L., Nature 232(5313) (1971), pp. 657–658.
   PubMed Web of Science ®Google Scholar
• J. Yu and J. Li, Discrete-time models for interactive wild and sterile mosquitoes with general time steps, Math. Biosci. 346 (2022), Article ID 108797.
   PubMed Web of Science ®Google Scholar
• J. Yu and B. Zheng, Modeling Wolbachia infection in mosquito population via discrete dynamical models, J. Differ. Equ. Appl. 25(11) (2019), pp. 1549–1567.
   Web of Science ®Google Scholar
• B. Zheng and J. Yu, Existence and uniqueness of periodic orbits in a discrete model on Wolbachia infection frequency, Adv. Nonlinear Anal. 11(1) (2022), pp. 212–224.
   Web of Science ®Google Scholar
• B. Zheng, J. Li, and J. Yu, One discrete dynamical model on Wolbachia infection frequency in mosquito populations, Sci. China Math. 65(8) (2022), pp. 1749–1764.
   Web of Science ®Google Scholar
• B. Zheng, M. Tang, and J. Yu, Modeling Wolbachia spread in mosquitoes through delay differential equations, SIAM J. Appl. Math. 74(3) (2014), pp. 743–770.
   Web of Science ®Google Scholar
• B. Zheng, J. Yu, Z. Xi, and M. Tang, The annual abundance of dengue and Zika vector Aedes albopictus and its stubbornness to suppression, Ecol. Model. 387 (2018), pp. 38–48.
   Web of Science ®Google Scholar