Wikisource:WikiProject Open Access/Programmatic import from PubMed Central/Neglected Tropical Diseases in the Anthropocene The Cases of Zika Ebola and Other Infections
While we advance through a geological epoch that increasingly reflects human intervention on a massive scale, we might expect to see the continued expansion of epidemic neglected tropical diseases, as we have recently seen for Zika and Ebola virus infections.
Emerging evidence indicates that the Holocene, our most recent geological epoch that began at the end of the last ice age almost 12,000 years ago, has undergone some fundamental changes because of human activity. Since the origins of agriculture and deforestation and later accelerating with the industrial revolution, followed by rapid 20th century population growth extending into the nuclear age, our planet has undergone a fundamental and seemingly irreversible geological shift [[1]]. According to many (but not all) prominent Earth scientists, humans have profoundly altered the planet, thereby ushering in a new and so-called Anthropocene epoch (Fig 1).
In a January 2016 article in Science, Colin Waters from the British Geological Survey and his colleagues provide important geochemical evidence to support designating the end of the Holocene as the Anthropocene [[1]]. It includes data showing increasing lead levels after World War II, altered soil nitrogen and phosphorous levels because of increased fertilizer use, and the appearance of newly created radionuclides, beginning with the atomic bomb tests in the New Mexico desert at Los Alamos [[1]]. Alongside these human-induced geochemical signatures are elevated carbon dioxide and methane levels and sharp increases in average global temperatures [[1]].
Levels of concrete and plastic have also dramatically increased in recent years, while in parallel, there has been massive loss of animal and plant species [[2]]. Species extinctions have reached unprecedented levels [[1],[3]].
In this late Anthropocene epoch, we have seen significant increases in the incidence or prevalence rates of several neglected tropical diseases (NTDs), due partly or mostly to human-induced changes to our planet. This is especially true for NTDs transmitted by invertebrate vectors, including mosquitoes, kissing bugs, and snails, as well as highly lethal zoonotic virus infections from bats and other mammals. For example, in the Americas, dengue fever reemerged in the 1980s, while chikungunya and Zika virus infections have aggressively spread across the Latin American and Caribbean region. Venezuela in particular has seen dramatic increases in malaria and most of its neglected tropical diseases (NTDs), including Chagas disease, schistosomiasis, and Zika virus infection, for which unprecedented urban foci are also occurring [[4]]. Across the Atlantic Ocean, Southern Europe has of late seen the emergence or reemergence of malaria in Greece, West Nile virus infection and chikungunya in Italy and Spain, dengue in Portugal, and schistosomiasis on the French island of Corsica [[5]]. The Middle East and North Africa (MENA) region is now considered one of the worst-affected global hotspots for NTDs and other emerging infections such as leishmaniasis, schistosomiasis, and MERS coronavirus infection; measles and polio have also returned [[6]]. Ebola caused thousands of deaths and overwhelmed the health systems of Guinea, Liberia, and Sierra Leone in West Africa in 2014–2015 [[7]], while East Africa and the Sahel are considered among the most important regions for kala-azar and multiple other NTDs [[8]]. Schistosomiasis continues to increase throughout Africa, where it is now a major cofactor in its AIDS epidemic [[9]]. Southeast Asia has seen the rise of Nipah and Hendra virus from bats, in addition to drug resistant malaria, enterovirus 71, melioidosis, and foodborne trematodiases transmitted by snails [[10]].
Several human activities that characterize the Anthropocene account for the increases in NTDs. It is instructive to see how some of these factors illustrated in Fig 2 helped to facilitate the emergence of two of the most devastating NTDs in 2014 and 2015—Ebola and Zika virus infections, respectively, as well as other high-disease-burden NTDs such as the cutaneous and visceral forms of leishmaniasis and schistosomiasis.
Poverty and Blue Marble Health[edit]
As has been said very frequently in our editorials, poverty is front and center. NTDs are most common in the setting of poverty [[11],[12]], while simultaneously helping to perpetuate poverty through their long-standing negative effects on maternal and child health and human productivity and labor [[13],[14]]. Ebola has so far emerged almost exclusively in impoverished nations such as the Democratic Republic of Congo or Guinea, Liberia, and Sierra Leone, while Zika is disproportionately affecting impoverished areas such as Brazil’s poorest northeastern provinces. In the case of Zika or other vector-borne NTDs such as leishmaniasis and Chagas disease, poverty equates to poor quality housing, in addition to uncollected garbage and standing water in poor neighborhoods that allow certain insects to breed nearby. For these reasons, we might expect poor countries such as Haiti or Jamaica to suffer greatly from the advance of Zika in the Caribbean region.
Yet another feature of Zika, leishmaniasis, Chagas disease, and other NTDs are their propensity to strike the poorest people who live in the wealthier group of 20 countries, such as Brazil or Mexico. The concept of “blue marble health” has been invoked to describe the surprising disease burden of NTDs among the poor living in these countries [[15]]. Today, most of the world’s NTDs paradoxically occur in the world’s largest economies, but mostly among the disenfranchised poor in those nations [[15]].
Political Destabilization, Conflict, and Post-conflict[edit]
Next to poverty, these forces may account for the largest risk factor for NTDs [[6],[16],[17]]. The long-standing atrocities and civil and international conflicts decimated the health systems of Guinea, Liberia, and Sierra Leone, thereby allowing Ebola and Lassa fever to flourish [[7],[17]], while these same forces facilitated the rapid spread and lethality of human African trypanosomiasis and kala-azar in Africa [[8],[18]]. Conflict and post-conflict settings are central to the massive epidemic of cutaneous leishmaniasis in the Middle East [[6]]. While Zika has so far not been linked to these factors, the political destabilization in Venezuela could become a contributory factor.
Deforestation[edit]
In Asia, deforestation may have increased human and bat contact to promote Nipah and Hendra viruses and SARS [[10]]. Deforestation is also an important factor promoting the expansion of vector borne NTDs, including leishmaniasis [[19]]. Deforestation has been noted to have some possible links with the emergence of Ebola [[20]]. For instance, the Guinea forest region where Ebola emerged in 2014 has been severely and adversely affected by clear-cut logging [[7]].
Dams[edit]
Bodies of fresh water arising from large-scale hydroelectric projects can help aquatic snails to proliferate, including those that transmit schistosomiasis in Africa and foodborne trematodiases in Asia. Dams and newly formed reservoirs of fresh water also create mosquito breeding sites for arbovirus infections and malaria and also facilitate waterborne intestinal infections [[21]]. In China, on the other hand, the Three Gorges Dam on the Yangtze River has assisted flood control and so far has not been shown to promote the emergence of Schistosoma japonicum infection [[22]].
Urbanization and Human Migrations[edit]
The large-scale movement of human populations into cities can create crowded conditions, which together with destruction of the environment favor arthropod vectors [[23]], including the Aedes aegypti mosquito that transmits Zika, dengue, chikungunya, and yellow fever. Accelerated urbanization that outpaces sanitation and sewage control infrastructures is also a key factor in the endemicity of leptospirosis and enteric NTDs [[24],[25]]. Overall, human migrations of immunologically naïve populations to endemic regions have accounted for rapid spread of infections, as well as the converse—infected populations introducing new diseases. The 2014 Brazilian FIFA World Cup soccer games may have been a factor in bringing Asian populations with Zika into areas where Aedes aegypti is found, although this hypothesis has since been dismissed [[26]]. However, the annual Hajj, the Muslim pilgrimage to Mecca that brings millions of people to Saudi Arabia, has also been postulated as having helped introduce dengue [[27],[28]], as it could Zika virus infection in 2016 or 2017. The Hajj has also had a role in the emergence of meningococcal disease and other acute respiratory infections [[29],[30]].
Climate Change and El Niño Events[edit]
Major climate change events in the Anthropocene include increased temperatures and altered rainfall patterns that expand arthropod vector habitats and ranges. Such factors could be responsible for accelerating the geographic expansions of arbovirus infections [[31],[32]], leishmaniasis [[33]], and Chagas disease [[34]], but this concept requires further exploration. In addition, we are just beginning to understand the role of El Niño events in promoting these and other NTDs [[35],[36]]. The fact that Zika virus expanded dramatically in an El Niño year is also of interest, but as yet, there are no proven links.
Many of the factors highlighted above were either manufactured or shaped by human activity. The dramatic expansions in the number of cases of arbovirus infections caused by dengue, chikungunya, and now Zika in recent years, together with a recent explosive Ebola outbreak in 2014–2015, give us pause to evaluate human influence on the biosphere and to recognize that beyond globalization, the Anthropocene could become a dominant theme for spreading NTDs or creating catastrophic human epidemics in the years to come.
References[edit]
- ↑ 1.0 1.1 1.2 1.3 1.4 Waters, CN; Zalasiewicz, J; Summerhayes, C; Barnofsky, AD & Poirier, C (2016), The Anthropocene is functionally and stratigraphically distinct from the Holocene, vol. 351, p. 137 WatersCNZalasiewiczJSummerhayesCBarnofskyADPoirierCet al
- ↑ Vaughan, A (2016), [http://www.theguardian.com/environment/2016/jan/07/human-impact-has-pushed-earth-into-the-anthropocene-scientists-say VaughanA7 Human impact has pushed earth into the Anthropocene, scientists say], <http://www.theguardian.com/environment/2016/jan/07/human-impact-has-pushed-earth-into-the-anthropocene-scientists-say VaughanA7>
- ↑
- ↑ Hotez, PJ & Herricks, J (2014), Venezuela: an emerging tropical disease and humanitarian emergency?
- ↑ Hotez, PJ (2016), Southern Europe’s coming plagues: vector-borne neglected tropical diseases, vol. 10 HotezPJ
- ↑ 6.0 6.1 6.2 Hotez, PJ (2015), Vaccine Science Diplomacy: Expanding Capacity to Prevent Emerging and Neglected Tropical Diseases Arising from Islamic State (IS)–Held Territories, vol. 9, p. e0003852, 26402466 HotezPJdoi: 10.1371/journal.pntd.0003852, pmid:26402466
- ↑ 7.0 7.1 7.2 Bausch, DG & Schwarz, L (2014), Outbreak of Ebola Virus Disease in Guinea: Where Ecology Meets Economy, vol. 8, p. e3056, 25079231 BauschDGSchwarzLdoi: 10.1371/journal.pntd.0003056, pmid:25079231
- ↑ 8.0 8.1 Diro, E; Lynen, L; Ritmeijer, K; Boelaert, M; Hailu, A & van Griensven, J (2014), Visceral Leishmaniasis and HIV Coinfection in East Africa, vol. 8, p. e2869, 24968313 DiroELynenLRitmeijerKBoelaertMHailuAvan GriensvenJdoi: 10.1371/journal.pntd.0002869, pmid:24968313
- ↑ Mbabazi, PS; Andan, O; Fitzgerald, DW; Chitsulo, L; Engels, D & Downs, JA (2011), Examining the Relationship between Urogenital Schistosomiasis and HIV Infection, vol. 5, p. e1396, 22163056 MbabaziPSAndanOFitzgeraldDWChitsuloLEngelsDDownsJAdoi: 10.1371/journal.pntd.0001396, pmid:22163056
- ↑ 10.0 10.1 Hotez, PJ; Bottazzi, ME; Strych, U; Chang, L-Y; Lim, YAL & Goodenow, MM (2015), Neglected Tropical Diseases among the Association of Southeast Asian Nations (ASEAN): Overview and Update, vol. 9, p. e0003575, 25880767 HotezPJBottazziMEStrychUChangL-YLimYALGoodenowMMet aldoi: 10.1371/journal.pntd.0003575, pmid:25880767
- ↑ Fallah, MP; Skrip, LA; Gertler, S; Yamin, D & Galvani, AP (2015), Quantifying Poverty as a Driver of Ebola Transmission, vol. 9, p. e0004260, 26720278 FallahMPSkripLAGertlerSYaminDGalvaniAPdoi: 10.1371/journal.pntd.0004260, pmid:26720278
- ↑ Habtamu, E; Wondie, T; Aweke, S; Tadesse, Z; Zerihun, M & Zewdie, Z (2015), Trachoma and Relative Poverty: A Case-Control Study, vol. 9, p. e0004228, 26600211 HabtamuEWondieTAwekeSTadesseZZerihunMZewdieZet aldoi: 10.1371/journal.pntd.0004228, pmid:26600211
- ↑ Hotez, PJ & Ferris, MT (2006), The antipoverty vaccines, vol. 24, pp. 5787–99, 16759763 HotezPJFerrisMT26, pmid:16759763
- ↑ Hotez, PJ; Fenwick, A; Savioli, L & Molyneux, DH (2009), Rescuing the bottom billion through control of neglected tropical diseases, vol. 373, pp. 1570–5, 19410718 HotezPJFenwickASavioliLMolyneuxDH2doi: 10.1016/S0140-6736(09)60233-6, pmid:19410718
- ↑ 15.0 15.1 Hotez, PJ (2013), NTDs V.2.0: “Blue Marble Health”—Neglected Tropical Disease Control and Elimination in a Shifting Health Policy Landscape, vol. 7, p. e2570, 24278496 HotezPJdoi: 10.1371/journal.pntd.0002570, pmid:24278496
- ↑ Fürst, T; Raso, G; Acka, CA; Tschannen, AB; N'Goran, EK & Utzinger, J (2009), Dynamics of Socioeconomic Risk Factors for Neglected Tropical Diseases and Malaria in an Armed Conflict, vol. 3, p. e513, 19907632 FürstTRasoGAckaCATschannenABN'GoranEKUtzingerJdoi: 10.1371/journal.pntd.0000513, pmid:19907632
- ↑ 17.0 17.1 Shaffer, JG; Grant, DS; Schieffelin, JS; Boisen, ML; Goba, A & Hartnett, JN (2014), Lassa Fever in Post-Conflict Sierra Leone, vol. 8, p. e2748, 24651047 ShafferJGGrantDSSchieffelinJSBoisenMLGobaAHartnettJNet aldoi: 10.1371/journal.pntd.0002748, pmid:24651047
- ↑ Hotez, PJ (2015), Combating the next lethal epidemic, vol. 348, pp. 296–7, 25883348 HotezPJ, pmid:25883348
- ↑ Chaves, LF; Cohen, JM; Pascual, M & Wilson, ML (2008), Social Exclusion Modifies Climate and Deforestation Impacts on a Vector-Borne Disease, vol. 2, p. e176, 18265876 ChavesLFCohenJMPascualMWilsonML, pmid:18265876
- ↑ Agoramoorthy, G & Chakraborty, C (2014), Ebola eradication may need wider partnership, vol. 186, p. 1170, 25332426 AgoramoorthyGChakrabortyC, pmid:25332426
- ↑ Ziegler, AD; Petney, TN; Grundy-Warr, C; Andrews, RH; Baird, IG & Wasson, RJ (2013), Dams and Disease Triggers on the Lower Mekong River, vol. 7, p. e2166, 23853695 ZieglerADPetneyTNGrundy-WarrCAndrewsRHBairdIGWassonRJet aldoi: 10.1371/journal.pntd.0002166, pmid:23853695
- ↑ Gray, DJ; Thrift, AP; Williams, GM; Zheng, F; Li Y-, S & Guo, J (2012), Five-Year Longitudinal Assessment of the Downstream Impact on Schistosomiasis Transmission following Closure of the Three Gorges Dam, vol. 6, p. e1588, 22506083 GrayDJThriftAPWilliamsGMZhengFLi Y-SGuoJet aldoi: 10.1371/journal.pntd.0001588, pmid:22506083
- ↑ Stoddard, ST; Morrison, AC; Vazquez-Prokopec, GM; Paz Soldan, V; Kochel, TJ & Kitron, U (2009), The Role of Human Movement in the Transmission of Vector-Borne Pathogens, vol. 3, p. e481, 19621090 StoddardSTMorrisonACVazquez-ProkopecGMPaz SoldanVKochelTJKitronUet aldoi: 10.1371/journal.pntd.0000481, pmid:19621090
- ↑ Maciel, EAP; de Carvalho, ALF; Nascimento, SF; de Matos, RB; Gouveia, EL & Reis, MG (2008), Household Transmission of Leptospira Infection in Urban Slum Communities, vol. 2, p. e154, 18357340 MacielEAPde CarvalhoALFNascimentoSFde MatosRBGouveiaELReisMGet aldoi: 10.1371/journal.pntd.0000154, pmid:18357340
- ↑ Akullian, A; Ng’eno, E; Matheson, AI; Cosmas, L; Macharia, D & Fields, B (2015), Environmental Transmission of Typhoid Fever in an Urban Slum, vol. 9, p. e0004212, 26633656 AkullianANg’enoEMathesonAICosmasLMachariaDFieldsBet aldoi: 10.1371/journal.pntd.0004212, pmid:26633656
- ↑ Faria, NR; Azevedo, RSS; Kraemer, MUG; Souza, R & Cunha, MS (2016), Zika virus in the Americas: Early epidemiological and genetic findings
- ↑ Azhar, EI; Hashem, AM; El-Kafrawy, SA; Abol-Ela, S; Abd-Alla, AM; Sohrab, SS; Farraj, SA; Othman, NA; et al. (2015), Complete genome sequencing and phylogenetic analysis of dengue type 1 virus isolated from Jeddah, Saudi Arabia, vol. 12, p. 1, 25591713 AzharEIHashemAMEl-KafrawySAAbol-ElaSAbd-AllaAMSohrabSSFarrajSAOthmanNABen-HelabyHGAshshiAMadaniTAJamjoomG16doi: 10.1186/s12985-014-0235-7, pmid:25591713
- ↑ Aziz, AT; Al-Shami, SA; Mahyoub, JA; Hatabbi, M; Ahmad, AH & Rawi, CS (2014), An update on the incidence of dengue gaining strength in Saudi Arabia and current control approaches for its vector mosquito, vol. 7, p. 258, 24890567 AzizATAl-ShamiSAMahyoubJAHatabbiMAhmadAHRawiCSdoi: 10.1186/1756-3305-7-258, pmid:24890567
- ↑ Lingappa, JR; Al-Rabeah, AM; Haijeh, R; Mustafa, T & Fatani, A (2003), Serogroup W-135 meningococcal disease during the Hajj, 2000, vol. 9, pp. 665–71, 12781005 LingappaJRAl-RabeahAMHaijehRMustafaTFataniAet al, pmid:12781005
- ↑ Gautret, P; Soula, G; Parola, P & Brouqui, P (2009), Hajj pilgrims’ knowledge about acute respiratory infections, vol. 15, pp. 1861–2, 19891890 GautretPSoulaGParolaPBrouquiPdoi: 10.3201/eid1511.090201, pmid:19891890
- ↑ Colón-González, FJ; Fezzi, C; Lake, IR & Hunter, PR (2013), The Effects of Weather and Climate Change on Dengue, vol. 7, p. e2503, 24244765 Colón-GonzálezFJFezziCLakeIRHunterPRdoi: 10.1371/journal.pntd.0002503, pmid:24244765
- ↑ Beebe, NW; Cooper, RD; Mottram, P & Sweeney, AW (2009), Australia's Dengue Risk Driven by Human Adaptation to Climate Change, vol. 3, p. e429, 19415109 BeebeNWCooperRDMottramPSweeneyAWdoi: 10.1371/journal.pntd.0000429, pmid:19415109
- ↑ Fischer, D; Moeller, P; Thomas, SM; Naucke, TJ & Beierkuhnlein, C (2011), Combining Climatic Projections and Dispersal Ability: A Method for Estimating the Responses of Sandfly Vector Species to Climate Change, vol. 5, p. e1407, 22140590 FischerDMoellerPThomasSMNauckeTJBeierkuhnleinCdoi: 10.1371/journal.pntd.0001407, pmid:22140590
- ↑ Garza, M; Feria, Arroyo TP; Casillas, EA; Sanchez-Cordero, V; Rivaldi, C-L & Sarkar, S (2014), Projected Future Distributions of Vectors of Trypanosoma cruzi in North America under Climate Change Scenarios, vol. 8, p. e2818, 24831117 GarzaMFeriaArroyo TPCasillasEASanchez-CorderoVRivaldiC-LSarkarSdoi: 10.1371/journal.pntd.0002818, pmid:24831117
- ↑ Chaves, LF; Calzada, JE; Valderrama, A & Saldaña, A (2014), Cutaneous Leishmaniasis and Sand Fly Fluctuations Are Associated with El Niño in Panamá, vol. 8, p. e3210, 25275503 ChavesLFCalzadaJEValderramaASaldañaAdoi: 10.1371/journal.pntd.0003210, pmid:25275503
- ↑ Weinberger, D; Baroux, N; Grangeon, J-P; Ko, AI & Goarant, C (2014), El Niño Southern Oscillation and Leptospirosis Outbreaks in New Caledonia, vol. 8, p. e2798, 24743322 WeinbergerDBarouxNGrangeonJ-PKoAIGoarantCdoi: 10.1371/journal.pntd.0002798, pmid:24743322
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