Global Effect of Climate Change on Seasonal Cycles, Vector Population and Rising Challenges of Communicable Diseases: A Review
DOI:
https://doi.org/10.30564/jasr.v6i1.5165Abstract
This article explains ongoing changes in global climate and their effect on the resurgence of vector and pathogen populations in various parts of the world. Today, major prevailing changes are the elevation of global temperature and accidental torrent rains, floods, droughts, and loss of productivity and food commodities. Due to the increase in water surface area and the longer presence of flood water, the breeding of insect vectors becomes very high; it is responsible for the emergence and re-emergence of so many communicable diseases. Due to the development of resistance to chemicals in insect pests, and pathogens and lack of control measures, communicable zoonotic diseases are remerging with high infectivity and mortality. This condition is becoming more alarming as the climate is favoring pathogen-host interactions and vector populations. Rapid changes seen in meteorology are promoting an unmanageable array of vector-borne infectious diseases, such as malaria, Japanese encephalitis, filarial, dengue, and leishmaniasis. Similarly, due to unhygienic conditions, poor sanitation, and infected ground and surface water outbreak of enteric infections such as cholera, vibriosis, and rotavirus is seen on the rise. In addition, parasitic infection ascariasis, fasciolosis, schistosomiasis, and dysentery cases are increasing. Today climate change is a major issue and challenge that needs timely quick solutions. Climate change is imposing non-adaptive forced human migration territorial conflicts, decreasing ecosystem productivity, disease outbreaks, and impelling unequal resource utilization. Rapid climate changes, parasites, pathogens, and vector populations are on the rise, which is making great threats to global health and the environment. This article highlighted the necessity to develop new strategies and control measures to cut down rising vector and pathogen populations in endemic areas. For finding quick solutions educational awareness, technology up-gradation, new vaccines, and safety measures have to be adopted to break the cycle of dreadful communicable diseases shortly.Keywords:
Global climate change; Biodiversity loss; Loss of life; Habitat; Economic losses; Biomarkers; Challenges and solutionsReferences
[1] Olivier, J.G.J., Peters, J.A.H.W. (editors), 2019. Trends in global CO2 and total greenhouse gas emissions: 2019 report; 2020 May 26; PBL Netherlands Environmental Assessment Agency, The Hague. Australia: PBL Publishers. Avail-able from: https://www.pbl.nl/sites/default/files/downloads/pbl-2020-trends-in-global-co2-and-total-greenhouse-gas-emissions-2019-re-port_4068.pdf
[2] Olivier, J.G.J., Peters, J.A.H.W., 2018. Trends in global CO2 and total GHG emissions: 2018 report; 2018 May 12; PBL Netherlands Environ-mental Assessment Agency, The Hague. Avail-able from: https://www.pbl.nl/en/publications/trends-in-global-co2-and-total-greenhouse-gase-missions-2018-report
[3] IPCC, 2014. The Fifth Assessment Report (AR5) of the United Nations Intergovernmental Panel on Climate Change (IPCC) [Internet]. Available from: https://www.ipcc.ch/report/ar5/syr/
[4] Lüthi, D., Le Floch, M., Bereiter, B., et al., 2008. High-resolution carbon dioxide concen-tration record 650,000-800,000 years before present. Nature. 453(7193), 379-382.
[5] IPCC, 2018. Global Warming of 1.5°C: IPCC Spe-cial Report on impacts of global warming of 1.5°C above pre-industrial levels in context of strength-ening response to climate change, sustainable development, and efforts to eradicate poverty (1st edition). Cambridge University Press: Cambridge. DOI: https://doi.org/10.1017/9781009157940.001
[6] Schuckman, K., Cheng, L., Palmer, M.D., et al., 2020. Heat stored in the earth system: Where does the energy go? Earth System Science Data. 12(3), 2013-2041.
[7] Broeker, W.S., 1975. Climatic change: Are we on the brink of a pronounced global warming?Science. 189(4201), 460-463.
[8] NASA, 2019. The Causes of Climate Change[Internet]. Climate Change: Vital signs of the planet. [retrieved 2019 May 8]. Available from: https://climate.nasa.gov/
[9] Wu, Sh.P., Kroeker, A., Wong, G., et al., 2016. An adenovirus vaccine expressing ebola virus variant makona glycoprotein is efficacious in guinea pigs and nonhuman primates. The Jour-nal of Infectious Diseases. 215(1), 165. DOI: https://doi.org/10.1093/infdis/jiw554
[10] Burroughs, W.J., 2005. Climate change in pre-history. Cambridge University Press: New York. DOI: https://doi.org/10.1017/CBO9780511535826.
[11] Patz, J.A., Frumkin, H., Holloway, T., et al., 2014. Climate change: Challenges and opportu-nities for global health. Journal of the American Medical Association. 312(15), 1565-1580.
[12] Clancy, K.M., Wagner, M.R., Reich, P.B., 1995. Ecophysiology and insect herbivory. Ecophysi-ology of Coniferous Forests. 125-180. DOI: https://doi.org/10.1016/B978-0-08-092593-6.50011-6.
[13] Broghton, W., 2012. Assessing the moisture resistance of adhesives for marine environments. Adhesives in Marine Engineering. Woodhead Publishing: Sawton. pp. 155-186.
[14] Arnold, B.F., Colford, J.M., 2007. Treating water with chlorine at point-of-use to improve water quality and reduce child diarrhea in de-veloping countries: a systematic review and meta-analysis. The American Journal of Trop-ical Medicine and Hygiene. 76, 354-364. DOI: https://doi.org/10.4269/ajtmh.2007.76.354.
[15] Zoysa, I., Feachem, R.G., 1985. Interventions for the control of diarrhoeal diseases among young children: Rotavirus and cholera immuni-zation. Bulletin of the World Health Organiza-tion. 63(3), 569-583.
[16] Click, R., Dahl-Smith, J., Fowler, L., et al., 2013. An osteopathic approach to reduction of readmissions for neonatal jaundice. Osteopathic Family Physician. 5(1), 17.
[17] Collier, J., Longore, M., Turmezei, T., et al., 2010. Neonatal jaundice. Oxford Handbook of Clinical Specialties. Oxford University Press: New York.
[18] Hashizume, M., Armstrong, B., Hajat, S., et al., 2007. Association between climate variability and hospital visits for non-cholera diarrhoea in Bangladesh: Effects and vulnerable groups. International Journal of Epidemiology. 36(5), 1030-1037.
[19] Rossati, A., 2017. Global warming and its health impact. The International Journal of Occupa-tional and Environmental Medicine. 8(1), 7-20.
[20] Fung, I.C., 2014. Cholera transmission dynamic models for public health practitioners. Emerging Themes in Epidemiology. 11(1), 1.
[21] Pascual, J., Macian, M.C., Arahal, D.R., et al., 2009. Description of Enterovibrio nigricans sp. nov., reclassification of Vibrio calviensis as En-terovibrio calviensis comb. nov. and emended description of the genus Enterovibrio Thompson et al. 2002. International Journal of Systematic and Evolutionary Microbiology. 59(Pt 4), 698-704.
[22] Jesudason, M.V., Balaji, V., Mukundan, U., et al., 2000. Ecological study of Vibrio cholerae in Vellore. Epidemiology & Infection. 124(2), 201-206.
[23] Sheikh, N.M., Philen, R.M., Love, L.A., 1997. Chaparral-associated hepatotoxicity. Archives of Internal Medicine. 157(8), 913-919.
[24] Glass, R.I., Backer, S., Huq, M.I., et al., 1982. Endemic cholera in rural Bangladesh, 1966-1980. American Journal of Epidemiology. 116, 959-970.
[25] Lipp, E.K., Huq, A., Colwell, R.R., 2002. Ef-fects of global climate on infectious disease: The cholera model. Clinical Microbiology Reviews. 15(4), 757-770.
[26] Faruque, S.M., Islam, M.J., Ahmad, Q.S., et al., 2005. Self-limiting nature of seasonal cholera epidemics: Role of host-mediated amplification of phage. Proceedings of the National Academy of Sciences. 102(17), 6119-6124.
[27] Faruque, S.M., Naser, I.B., Islam, M.J., et al., 2005. Seasonal epidemics of cholera inversely correlate with the prevalence of environmental cholera phages. Proceedings of the National Academy of Sciences. 102(5), 1702-1707.
[28] Ogden, N.H., 2017. Climate change and vec-tor-borne diseases of public health significance. FEMS Microbiology Letters. 364(19).
[29] Caminade, C., McIntyre, K.M., Jones, A.E., 2019. Impact of recent and future climate change on vector-borne diseases. Annals of the New York Academy of Sciences. 1436(1), 157-173.
[30] Hall, N.L., Barnes, S., Canuto, C., et al., 2021. Climate change and infectious diseases in Aus-tralia’s Torres Strait Islands. Australian and New Zealand Journal of Public Health. 45(2), 122-128.
[31] McMichael, C., 2015. Climate change-related migration and infectious disease. Virulence. 6(6), 548-553.
[32] Steen, C.J., Carbonaro, P.A., Schwartz, R.A., 2004. Arthropods in dermatology. Journal of the American Academy of Dermatology. 50(6), 819-842.
[33] Prieto, A., Díaz-Cao, J.M., Fernández-Antonio, R., et al., 2018. Lesser housefly (Fannia canicu-laris) as possible mechanical vector for Aleutian mink disease virus. Veterinary Microbiology. 221, 90-93.
[34] Souza Barbosa, T., Salvitti Sá Rocha, R.A., Guirado, C.G., et al., 2008. Oral infection by Diptera larvae in children: A case report. Inter-national Journal of Dermatology. 47(7), 696-699.
[35] Hassona, Y., Scully, C., Aguida, M., et al., 2014. Flies and the mouth. Journal of Investigative and Clinical Dentistry. 5(2), 98-103.
[36] Pearce, J.C., Learoyd, T.P., Langendorf, B.J., et al., 2018. Japanese encephalitis: The vectors, ecology and potential for expansion. Journal of Travel Medicine. 25(Suppl_1), S16-S26.
[37] Meneghim, R.L.F.S., Madeira, N.G., Ribolla, P.E.M., et al., 2021. Flies as possible vectors of inflammatory trachoma transmission in a Brazilian municipality. Revista do Instituto de Medicina Tropical de São Paulo. 63. DOI: https://doi.org/10.1590/S1678-9946202163066
[38] Hassan, M.U., Khan, M.N., Abubakar, M., et al., 2010. Bovine hypodermosis—a global aspect. Tropical Animal Health and Production. 42(8), 1615-1625.
[39] Yadav, S., Thakur, R., Georgiev, P., et al., 2018. RDGBα localization and function at mem-brane contact sites is regulated by FFAT-VAP interactions. Journal of Cell Science. 131(1), jcs207985.
[40] Asbakk, K., Kumpula, J., Oksanen, A., et al., 2014. Infestation by Hypoderma tarandi in rein-deer calves from northern Finland—prevalence and risk factors. Veterinary Parasitology. 200(1-2), 172-178.
[41] Hou, W., Armstrong, N., Obwolo, L.A., et al., 2017. Determination of the cell permissive-ness spectrum, mode of RNA replication, and RNA-Protein interaction of Zika virus. BMC Infectious Diseases. 17(1), 239.
[42] Deng, S.Q., Yang, X., Wei, Y., et al., 2020. A re-view on dengue vaccine development. Vaccines. 8(1), 63.
[43] Nigrovic, L.E., Malley, R., Macias, C.G., et al., 2008. Effect of antibiotic pretreatment on cere-brospinal fluid profiles of children with bacterial meningitis. Pediatrics. 122(4), 726-730.
[44] Malvy, D., Chappuis, F., 2011. Sleeping sick-ness. Clinical Microbiology and Infection. 17(7), 986-995.
[45] Barrett, M.P., Burchmore, R.J., Stich, A., et al., 2003. The trypanosomiases. The Lancet. 362(9394), 1469-1480.
[46] Gherbi, R., Bounechada, M., Latrofa, M.S., et al., 2020. Phlebotomine sand flies and Leishma-nia species in a focus of cutaneous leishmaniasis in Algeria. PLoS Neglected Tropical Diseases. 14(2), e0008024.
[47] Jongejan, F., Uilenberg, G., 1994. Ticks and control methods. Revue Scientifique et Tech-nique (International Office of Epizootics). 13(4), 1201-1226.
[48] Tsuji, N., Fujisaki, K., 2007. Longicin plays a crucial role in inhibiting the transmission of Ba-besia parasites in the vector tick Haemaphysalis longicornis. Future Microbiology. 2(6), 575-578.
[49] Walker, A.R., 2001. Age structure of a popu-lation of Ixodes ricinus (Acari: Ixodidae) in relation to its seasonal questing. Bulletin of En-tomological Research. 91(1), 69-78.
[50] Randolph, S., 2002. Predicting the risk of tick-borne diseases. International Journal of Medical Microbiology. 291(33), 6-10.
[51] Roth, T., Lane, R.S., Foley, J., 2017. A molecu-lar survey for francisella tularensis and rickettsia spp. in haemaphysalis leporispalustris (Acari: Ixodidae) in Northern California. Journal of Medical Entomology. 54(2), 492-495.
[52] Guizzo, M.G., Parizi, L.F., Nunes, R.D., et al., 2017. A Coxiella mutualist symbiont is essential to the development of Rhipicephalus microplus. Scientific Reports. 7(1), 17554.
[53] Ben-Yosef, M., Rot, A., Mahagna, M., et al., 2020. Coxiella-like endosymbiont of rhipiceph-alus sanguineus is required for physiological processes during ontogeny. Frontiers in Micro-biology. 11, 493.
[54] Couper, L.I., Yang, Y., Yang, X.F., et al., 2020. Comparative vector competence of North Amer-ican lyme disease vectors. Parasites & Vectors. 13(1), 29.
[55] Rossati, A., Bargiacchi, O., Kroumova, V., et al., 2016. Climate, environment and transmission of malaria. Infezioni in Medicina. 24(2), 93-104.
[56] Abbasi, E., Vahedi, M., Bagheri, M., et al., 2022. Monitoring of synthetic insecticides resistance and mechanisms among malaria vector mosqui-toes in Iran: A systematic review. Heliyon. 8(1), e08830.
[57] Pimenta, P.F., Orfano, A.S., Bahia, A.C., et al., 2015. An overview of malaria transmission from the perspective of Amazon Anopheles vectors. Memórias do Instituto Oswaldo Cruz. 110(1), 23-47.
[58] Pocquet, N., Darriet, F., Zumbo, B., et al., 2014. Insecticide resistance in disease vectors from Mayotte: An opportunity for integrated vector management. Parasites & Vectors. 7, 299.
[59] Chira, S., Jackson, C.S., Oprea, I., et al., 2015. Progresses towards safe and efficient gene ther-apy vectors. Oncotarget. 6(31), 30675-30703.
[60] Ibraheim, R., Tai, P.W.L., Mir, A., et al., 2021. Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-di-rected repair in vivo. Nature Communications. 12(1), 62-67.
[61] Kasala, D., Yoon, A.R., Hong, J., et al., 2016. Evolving lessons on nanomaterial-coated viral vectors for local and systemic gene therapy. Nanomedicine (Lond). 11(13), 1689-1713.
[62] Weklak, D., Pembaur, D., Koukou, G., et al., 2021. Genetic and chemical capsid modifica-tions of adenovirus vectors to modulate vec-tor-host interactions. Viruses. 13(7), 1300.
[63] Coutinho-Abreu, I.V., Sharma, N.K., Ro-bles-Murguia, M., et al., 2010. Targeting the midgut secreted PpChit1 reduces Leishmania major development in its natural vector, the sand fly Phlebotomus papatasi. PLoS Neglected Tropical Diseases. 4(11), e901.
[64] Furuya-Kanamori, L., Liang, S., Milinovich, G., et al., 2016. Co-distribution and co-infection of chikungunya and dengue viruses. BMC Infec-tious Diseases. 16, 84.
[65] Van Looveren, D., Giacomazzi, G., Thiry, I., et al., 2021. Improved functionality and potency of next generation BinMLV viral vectors toward safer gene therapy. Molecular Therapy-Methods & Clinical Development. 23, 51-67.
[66] Nambiar, B., Cornell-Sookdeo, C., Berthelette, P., et al., 2017. Characteristics of minimally oversized adeno-associated virus vectors encod-ing human factor VIII generated using producer cell lines and triple transfection. Human Gene Therapy Methods. 28(1), 23-38.
[67] Zhou, Q., Uhlig, K.M., Muth, A., et al., 2015. Exclusive transduction of human CD4+ T Cells upon systemic delivery of CD4-Targeted Len-tiviral vectors. The Journal of Immunology. 195(5), 2493-2501.
[68] Qiu, Z.W., Zhang, X.L., 2006. Innate immune defense in anopheline mosquitoes against plas-modium infection. Chinese Journal of Parasitol-ogy & Parasitic Diseases. 24(5), 370-374.
[69] Dimopoulos, G., Müller, H.M., Kafatos, F.C., 1999. How does Anopheles gambiae kill malaria parasites? Parassitologia. 41(1-3), 169-175.
[70] Meister, S., Koutsos, A.C., Christophides, G.K., 2004. The Plasmodium parasite—a ‘new’ chal-lenge for insect innate immunity. International Journal for Parasitology. 34(13-14), 1473-1482.
[71] Chaves, L.F., Koenraadt, C.J., 2010. Climate change and highland malaria: Fresh air for a hot debate. The Quarterly Review of Biology. 85(1), 27-55.
[72] Omer, S.B., Benjamin, R.M., Brewer, N.T., et al., 2021. Promoting COVID-19 vaccine ac-ceptance: Recommendations from the Lancet Commission on vaccine refusal, acceptance, and demand in the USA. The Lancet. 398(10317), 2186-2192.
[73] Poland, G., Barrett, A., 2009. The old and the new: Successful vaccines of the 20th century and approaches to making vaccines for the im-portant diseases of the 21st century. Current Opinion in Immunology. 21(3), 305-307.
[74] Hussain, A., Ali, S., Ahmed, M., et al., 2018. The anti-vaccination movement: A regression in modern medicine. Cureus. 10(7), e2919.
[75] Drolet, M., Bénard, É., Boily, M.C., et al., 2015. Population-level impact and herd effects fol-lowing human papillomavirus vaccination pro-grammes: A systematic review and meta-analy-sis. The Lancet Infectious Diseases. 15(5), 565-580.
[76] Schiller, J.T., Müller, M., 2015. Next generation prophylactic human papillomavirus vaccines. The Lancet Oncology. 16(5), e217-e225.
[77] Wimmers, F., Pulendran, B., 2020. Emerg-ing technologies for systems vaccinology—multi-omics integration and single-cell (epi)genomic profiling. Current Opinion in Immunol-ogy. 65, 57-64.
[78] Randolph, H.E., Barreiro, L.B., 2020. Herd im-munity: Understanding COVID-19. Immunity. 52(5), 737-741.
[79] Berry, M.P.R., Blankley, S., Graham, C.M., et al., 2013. Systems approaches to studying the immune response in tuberculosis. Current Opin-ion in Immunology. 25(5), 579-587.
[80] Andersen, J., Woodworth, S., 2014. Tuberculo-sis vaccine—rethinking the current paradigm. Trends in Immunology. 35(8), 387-395.
[81] Grassly, N.C., Fraser, C., 2008. Mathematical models of infectious disease transmission. Na-ture Reviews Microbiology. 6(6), 477-487.
[82] McLeman, R.A., Smit, B., 2006. Migration as an adaptation to climate change. Climatic Change. 76, 31-53.
[83] Hunter, L.M., 2005. Migration and environmen-tal hazards. Population and Environment. 26, 273-302.
[84] Adger, W.N., 2006. Vulnerability. Global Envi-ronmental Change. 16(3), 268-281.
[85] Smit, B., Wandel, J., 2006. Adaptation, adaptive capacity and vulnerability. Global Environmen-tal Change. 16, 282-292.
[86] Glantz, M., 1991. The use of analogies in fore-casting ecological and societal responses to global warming. Environment. 33, 10-33.
[87] Gutmann, M., Field, V., 2010. Katrina in histor-ical context: Environment and migration in the US. Population and Environment. 31(1), 3-19.
[88] Rosenzweig, C., Hillel, D., 1993. The Dust Bowl of the 1930s: Analog of greenhouse effect in the Great Plains? American Society of Agron-omy, Crop Science Society of America, and Soil Science Society of America. 22, 9-22.
[89] Perch-Nielsen, S., Bättig, M., Imboden, D., 2008. Exploring the link between climate change and migration. Climatic Change. 91, 375-393.
[90] Tacoli, C., 2009. Crisis or adaptation? Migration and climate change in a context of high mobili-ty. Environment and Urbanization. 21, 513-525.
[91] Adam, R.D., 2001. Biology of Giardia lamblia. Clinical Microbiology Reviews. 14(3), 447-475.
[92] Sabbatani, S., Manfredi, R., Fiorino, S., 2010. Malaria infection and human evolution. Infezi-oni in Medicina. 18(1), 56-74.
[93] Hicks, D.J., Fooks, A.R., Johnson, N., 2012. Developments in rabies vaccines. Clinical & Experimental Immunology. 169(3), 199-204.
[94] Ma, P.Y., Tan, J.E., Hee, E.W., et al., 2021. Hu-man genetic variation influences enteric fever progression. Cells. 10, 345.
[95] Asadgol, Z., et al., 2019. The effect of climate change on cholera disease: The road ahead us-ing artificial neural network. PLoS One. 14(11), e0224813.
[96] Nahid, P., Dorman, S.E., Alipanah, N., et al., 2016. Official American thoracic society/centers for disease control and prevention/infectious diseases society of America clinical practice guidelines: Treatment of drug-susceptible tu-berculosis. Clinical Infectious Diseases. 63(7), e147-e195.
[97] Richardson, M., 2009. The ecology of the Zygo-mycetes and its impact on environmental expo-sure. Clinical Infectious Diseases. 15(5), 2-9.
[98] Roden, M.M., Zaoutis, T.E., Buchanan, W.L., et al., 2005. Epidemiology and outcome of zygo-mycosis: A review of 929 reported cases. Clini-cal Infectious Diseases. 41(5), 634-653.
[99] Wucherpfenning, K.W., 2001. Mechanism of induction of autoimmunity by infectious agents. Journal of Clinical Investigation. 108, 1097.
[100] Carlson, C.J., Albery, G.F., Merow, C., et al., 2022. Climate change increases cross-species viral transmission risk. Nature. 607, 555-562. Available from: https://www.nature.com/arti-cles/s41586-022-04788-w
[101] Shope, R., 1991. Global climate change and infectious diseases. Environmental Health Per-spectives. 96, 171-174.
[102] O’Neill, L.A.J., Netea, M.G., 2020. BCG-in-duced trained immunity: Can it offer protection against COVID-19? Nature Reviews Immunol-ogy. 20(6), 335-337.
[103] Woolhouse, M.E., Webster, J.P., Domingo, E., et al., 2002. Biological and biomedical impli-cations of the co-evolution of pathogens and their hosts. Nature Genetics. 32(4), 569-577.
[104] Rinker, D.C., Pitts, R.J., Zwiebel, L.J., 2016. Disease vectors in the era of next generation sequencing. Genome Biology. 17(1), 95.
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