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Ecological Approaches to Studying Zoonoses

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  • Authors: Elizabeth H. Loh1, Kris A. Murray2, Carlos Zambrana-Torrelio3, Parviez R. Hosseini4, Melinda K. Rostal5, William B. Karesh6, Peter Daszak7
  • Editors: Ronald M. Atlas8, Stanley Maloy9
  • VIEW AFFILIATIONS HIDE AFFILIATIONS
    Affiliations: 1: EcoHealth Alliance, New York, NY 10001; 2: EcoHealth Alliance, New York, NY 10001; 3: EcoHealth Alliance, New York, NY 10001; 4: EcoHealth Alliance, New York, NY 10001; 5: EcoHealth Alliance, New York, NY 10001; 6: EcoHealth Alliance, New York, NY 10001; 7: EcoHealth Alliance, New York, NY 10001; 8: University of Louisville, Louisville, KY; 9: San Diego State University, San Diego, CA
    • Source: microbiolspec December 2013 vol. 1 no. 2 doi:10.1128/microbiolspec.OH-0009-2012
  • Received 09 October 2012 Accepted 08 December 2012 Published 13 December 2013
  • Elizabeth H. Loh, [email protected]
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  • Abstract:

    Concern over emerging infectious diseases (EIDs) and a better understanding of their causes has resulted in increasing recognition of the linkages among human, animal, and ecosystem health. It is now well recognized that human activities can promote the emergence of infectious diseases through the large-scale modification of natural environments and inadvertent vectoring (e.g., international trade and travel). These perturbations can alter the ecological and evolutionary relationships among humans, wildlife, and the pathogens that move between them, resulting in disease emergence. In recent years, the rise in zoonotic EIDs has not only increased our awareness of the need for cross-sectoral collaborations, but has also highlighted the disconnect between current ecological theory and biological reality. As the One Health movement continues to gain steam, further integration of ecological approaches into the One Health framework will be required. We discuss the importance of ecological methods and theory to the study of zoonotic diseases by (i) discussing key ecological concepts and approaches, (ii) reviewing methods of studying wildlife diseases and their potential applications for zoonoses, and (iii) identifying future directions in the One Health movement.

  • Citation: Loh E, Murray K, Zambrana-Torrelio C, Hosseini P, Rostal M, Karesh W, Daszak P. 2013. Ecological Approaches to Studying Zoonoses. Microbiol Spectrum 1(2):OH-0009-2012. doi:10.1128/microbiolspec.OH-0009-2012.

References

1. Zinsstag J, Schelling E, Waltner-Toews D, Tanner M. 2011. From “one medicine” to “one health” and systemic approaches to health and well-being. Prev Vet Med 101:148–156. [PubMed][CrossRef]
2. Conrad PA, Mazet JA, Clifford D, Scott C, Wilkes M. 2009. Evolution of a transdisciplinary “One Medicine-One Health” approach to global health education at the University of California, Davis. Prev Vet Med 92:268–274. [PubMed][CrossRef]
3. Kahn LH, Kaplan B, Monath TP, Steele JH. 2008. Teaching “One Medicine, One Health.” Am J Med 121:169–170.
4. Daszak P, Cunningham A, Hyatt A. 2000. Emerging infectious diseases of wildlife—threats to biodiversity and human health. Science 287:443–449. [PubMed]
5. Patz JA, Daszak P, Tabor GM, Aguirre AA, Pearl M, Epstein J, Wolfe ND, Kilpatrick AM, Foufopoulos J, Molyneux D, Bradley DJ, Members of the Working Group on Land Use Change and Disease Emergence. 2004. Unhealthy landscapes: policy recommendations on land use change and infectious disease emergence. Environ Health Perspect 112:1092–1098. [PubMed]
6. Pulliam JR, Epstein JH, Dushoff J, Rahman SA, Bunning M, Jamaluddin AA, Hyatt AD, Field HE, Dobson AP, Daszak P, Henipavirus Ecology Research Group (HERG). 2012. Agricultural intensification, priming for persistence and the emergence of Nipah virus: a lethal bat-borne zoonosis. J R Soc Interface 9:89–101. [PubMed][CrossRef]
7. Dobson A, Foufopoulos J. 2001. Emerging infectious pathogens of wildlife. Philos Trans R Soc Lond B Biol Sci 356:1001–1012. [PubMed][CrossRef]
8. Jones KE, Patel NG, Levy MA, Storeygard A, Balk D, Gittleman JL, Daszak P. 2008. Global trends in emerging infectious diseases. Nature 451:990–993. [PubMed][CrossRef]
9. Harvell CD, Kim K, Burkholder JM, Colwell RR, Epstein PR, Grimes DJ, Hofmann EE, Lipp EK, Osterhaus ADME, Overstreet RM, Porter JW, Smith GW, Vasta GR. 1999. Emerging marine diseases—climate links and anthropogenic factors. Science 285:1505–1510. [PubMed]
10. Macdonald DW, Laurenson MK. 2006. Infectious disease: inextricable linkages between human and ecosystem health. Biol Conserv 131:143–150.
11. Woolhouse ME, Gowtage-Sequeria S. 2005. Host range and emerging and reemerging pathogens. Emerg Infect Dis 11:1842–1847. [PubMed][CrossRef]
12. Nunn CL, Altizer S. 2006. Infectious Diseases in Primates: Behavior, Ecology and Evolution. Oxford University Press, Oxford, United Kingdom.
13. Nizeyi JB, Innocent RB, Erume J, Kalema G, Cranfield MR, Graczyk TK. 2001. Campylobacteriosis, salmonellosis, and shigellosis in free-ranging human-habituated mountain gorillas of Uganda. J Wildl Dis 37:239–244. [PubMed][CrossRef]
14. Daszak P, Zambrana-Torrelio C, Bogich TL, Fernandez M, Epstein JH, Murray KA, Hamilton H. 2013. Interdisciplinary approaches to understanding disease emergence: the past, present, and future drivers of Nipah virus emergence. Proc Natl Acad Sci USA 110(Suppl 1) :3681–3688. [PubMed][CrossRef]
15. Dedmon R, Briggs D, Lembo T, Cleaveland S. 2010. One health: collaboration, recent research and developments in the global effort to eliminate rabies. Int J Infect Dis 14:e159. doi:10.1016/j.ijid.2010.02.1833. [CrossRef]
16. Greene M. 2010. The “One Health” initiative: using open source data for disease surveillance. Int J Infect Dis 14:e162. doi:10.1016/j.ijid.2010.02.1841. [CrossRef]
17. Kahn RE, Clouser DF, Richt JA. 2009. Emerging infections: a tribute to the One Medicine, One Health concept. Zoonoses Publ Health 56:407–428. [PubMed][CrossRef]
18. Mazet JA, Clifford DL, Coppolillo PB, Deolalikar AB, Erickson JD, Kazwala RR. 2009. A “One Health” approach to address emerging zoonoses: the HALI project in Tanzania. PLOS Med 6:e1000190. doi:10.1371/journal.pmed.1000190. [PubMed][CrossRef]
19. Mullins G, Jagne J, Stone L, Konings E, Howard-Grabman L, Hartman F, Fulton M. 2010. “One World One Health” in practice: integrating public health and veterinary curricula on emerging infectious diseases in Africa. Int J Infect Dis 14:e377–e378. doi:10.1016/j.ijid.2010.02.460. [CrossRef]
20. Zinsstag J, Mackenzie JS, Jeggo M, Heymann DL, Patz JA, Daszak P. 2012. Mainstreaming One Health. EcoHealth 9:107–110. [PubMed][CrossRef]
21. Murray KA, Skerratt LF, Speare R, McCallum H. 2009. Impact and dynamics of disease in species threatened by the amphibian chytrid fungus, Batrachochytrium dendrobatidis. Conserv Biol 23:1242–1252. [PubMed]
22. Roche B, Dobson AP, Guégan JF, Rohani P. 2012. Linking community and disease ecology: the impact of biodiversity on pathogen transmission. Philos Trans R Soc Lond B Biol Sci 367:2807–2813. [PubMed][CrossRef]
23. Grenfell BT, Bjørnstad ON, Kappey J. 2001. Travelling waves and spatial hierarchies in measles epidemics. Nature 414:716–723. [PubMed][CrossRef]
24. Anderson RM, May RM. 1991. Infectious Diseases of Humans: Dynamics and Control. Oxford University Press, Oxford, United Kingdom.
25. Hudson P, Rizzoli A, Grenfell B, Heesterbeek H, Dobson A. 2002. Ecology of wildlife diseases, p 1–5. In Hudson P, Rizzoli A, Grenfell B, Heesterbeek H, Dobson A (ed), The Ecology of Wildlife Diseases. Oxford University Press, Oxford, United Kingdom.
26. Anderson RM, May RM. 1978. Regulation and stability of host-parasite population interactions. I. Regulatory processes. J Anim Ecol 47:219–247.
27. May RM, Anderson RM. 1978. Regulation and stability of host-parasite population interactions. II. Destabilizing processes. J Anim Ecol 47:249–267.
28. Altizer S, Dobson A, Hosseini P, Hudson P, Pascual M, Rohani P. 2006. Seasonality and the dynamics of infectious diseases. Ecol Lett 9:467–484. [PubMed][CrossRef]
29. Crowl TA, Crist TO, Parmenter RR, Belovsky G, Lugo AE. 2008. The spread of invasive species and infectious disease as drivers of ecosystem change. Front Ecol Environ 6:238–246.
30. Haydon DT, Laurenson MK, Sillero-Zubiri C. 2002. Integrating epidemiology into population viability analysis: managing the risk posed by rabies and canine distemper to the Ethiopian wolf. Conserv Biol 16:1372–1385.
31. Caley P, Hone J. 2005. Assessing the host disease status of wildlife and the implications for disease control: Mycobacterium bovis infection in feral ferrets. J Appl Ecol 42:708–719.
32. Smith KF, Saxdov F, Lafferty KD. 2006. Evidence for the role of infectious disease in species extinction and endangerment. Conserv Biol 20:1349–1357. [PubMed][CrossRef]
33. Altizer S, Harvell D, Friedle E. 2003. Rapid evolutionary dynamics and disease threats to biodiversity. Trends Ecol Evol 18:589–596.
34. Mackenzie JS, Chua KB, Daniels PW, Eaton BT, Field HE, Hall RA, Halpin K, Johansen CA, Kirkland PD, Lam SK, McMinn P, Nisbet DJ, Paru R, Pyke AT, Ritchie SA, Siba P, Smith DW, Smith GA, van den Hurk AF, Wang LF, Williams DT. 2001. Emerging viral diseases of Southeast Asia and the Western Pacific. Emerg Infect Dis 7:497–504. [PubMed][CrossRef]
35. O’Brien SJ, Troyer JL, Roelke M, Marker L, Pecon-Slattery J. 2006. Plagues and adaptation: lessons from the Felidae models for SARS and AIDS. Biol Conserv 131:255–267.
36. Smith KF, Acevedo-Whitehouse K, Pedersen AB. 2009. The role of infectious diseases in biological conservation. Anim Conserv 12:1–12.
37. Reference deleted.
38. Ebert D, Hamilton WD. 1996. Sex against virulence: the coevolution of parasitic diseases. Trends Ecol Evol 11:A79–A82. [PubMed]
39. Anderson RM. 1979. Parasite pathogenicity and the depression of host population equilibria. Nature 279:150–152.
40. McCallum H. 1994. Quantifying the impact of disease on threatened species. Pac Conserv Biol 1:107–117.
41. Briggs C, Knapp RA, Vredenburg VT. 2010. Enzootic and epizootic dynamics of the chytrid fungal pathogen of amphibians. Proc Natl Acad Sci USA 107:9695–9700. [PubMed][CrossRef]
42. McCallum H, Barlow N, Hone J. 2001. How should pathogen transmission be modelled? Trends Ecol Evol 16:295–300. [PubMed]
43. Godfrey SS, Bull CM, Murray K, Gardner MG. 2006. Transmission mode and distribution of parasites among groups of the social lizard Egernia stokesii. Parasitol Res 99:223–230. [PubMed][CrossRef]
44. Grenfell BT, Bolker BM. 1998. Cities and villages: infection hierarchies in a measles metapopulation. Ecol Lett 1:63–70.
45. Begon M, Hazel SM, Telfer S, Bown K, Carslake D, Cavanagh R, Chantrey J, Jones T, Bennett M. 2003. Rodents, cowpox virus and islands: densities, numbers and thresholds. J Anim Ecol 72:343–355.
46. Fenton A, Fairbairn JP, Norman R, Hudson PJ. 2002. Parasite transmission: reconciling theory and reality. J Anim Ecol 71:893–905.
47. de Castro F, Bolker B. 2005. Mechanisms of disease-induced extinction. Ecol Lett 8:117–126.
48. Lloyd-Smith JO, Cross PC, Briggs CJ, Daugherty M, Getz WM, Latto J, Sanchez MS, Smith AB, Swei A. 2005. Should we expect population thresholds for wildlife disease? Trends Ecol Evol 20:511–519. [PubMed][CrossRef]
49. Hochachka WM, Dhondt AA. 2000. Density-dependent decline of host abundance resulting from a new infectious disease. Proc Natl Acad Sci USA 97:5303–5306. [PubMed][CrossRef]
50. Davis S, Calvet E, Leirs H. 2005. Fluctuating rodent populations and risk to humans from rodent-borne zoonoses. Vector Borne Zoonotic Dis 5:305–314. [PubMed][CrossRef]
51. Heisey DM, Joly DO, Messier F. 2006. The fitting of general force-of-infection models to wildlife disease prevalence data. Ecology 88:2356–2365. [PubMed]
52. Woolhouse ME, Taylor LH, Haydon DT. 2001. Population biology of multihost pathogens. Science 292:1109–1112. [PubMed]
53. Craft ME, Hawthorne PL, Packer C, Dobson AP. 2008. Dynamics of a multihost pathogen in a carnivore community. J Anim Ecol 77:1257–1264. [PubMed][CrossRef]
54. Dietz K. 1993. The estimation of the basic reproduction number for infectious diseases. Stat Methods Med Res 2:23–41. [PubMed]
55. Hasibeder G, Dye C, Carpenter J. 1992. Mathematical-modeling and theory for estimating the basic reproduction number of canine leishmaniasis. Parasitology 105:43–53. [PubMed]
56. Diekmann O, Heesterbeek H, Metz J. 2000. Mathematical Epidemiology of Infectious Diseases: Model Building, Analysis and Interpretation. John Wiley and Sons, Chichester, United Kingdom.
57. Hampson K, Dushoff J, Cleaveland S, Haydon DT, Kaare M, Packer C, Dobson A. 2009. Transmission dynamics and prospects for the elimination of canine rabies. PLoS Biol 7:462–471. [PubMed][CrossRef]
58. Altizer S, Bartel R, Han BA. 2011. Animal migration and infectious disease risk. Science 331:296–302. [PubMed][CrossRef]
59. Koelle K, Kamradt M, Pascual M. 2009. Understanding the dynamics of rapidly evolving pathogens through modeling the tempo of antigenic change: influenza as a case study. Epidemics 1:129–137. [PubMed][CrossRef]
60. Real LA, Biek R. 2007. Spatial dynamics and genetics of infectious diseases on heterogeneous landscapes. J R Soc Interface 4:935–948. [PubMed][CrossRef]
61. Pascual M, Rodo X, Ellner SP, Colwell R, Bouma MJ. 2000. Cholera dynamics and El Nino-Southern Oscillation. Science 289:1766–1769. [PubMed]
62. Colwell RR. 1996. Global climate and infectious disease: the cholera paradigm. Science 274:2025–2031. [PubMed]
63. Tompkins DM, Dunn AM, Smith MJ, Telfer S. 2011. Wildlife diseases: from individuals to ecosystems. J Anim Ecol 80:19–38. [PubMed][CrossRef]
64. Weiss RA, McMichael AJ. 2004. Social and environmental risk factors in the emergence of infectious diseases. Nat Med 10:S70–S76. [PubMed][CrossRef]
65. Smolinski MS, Hamburg MA, Lederberg J (ed). 2003. Microbial Threats to Health: Emergence, Detection, and Response. National Academies Press, Washington, DC.
66. LoGiudice K, Ostfeld RS, Schmidt KA, Keesing F. 2003. The ecology of infectious disease: effects of host diversity and community composition on Lyme disease risk. Proc Natl Acad Sci USA 100:567–571. [PubMed][CrossRef]
67. Barbour AG, Fish D. 1993. The biological and social phenomenon of Lyme disease. Science 260:1610–1616. [PubMed]
68. Levi T, Kilpatrick AM, Mangel M, Wilmers CC. 2012. Deer, predators, and the emergence of Lyme disease. Proc Natl Acad Sci USA 109:10942–10947. [PubMed][CrossRef]
69. Walsh JF, Molyneux DH, Birley MH. 1993. Deforestation: effects on vector-borne disease. Parasitology 106:S55–S75. [PubMed]
70. Wilcox BA, Ellis B. 2006. Forests and emerging infectious diseases of humans. Unasylva 224:11–18.
71. Orta-Martinez M, Finer M. 2010. Oil frontiers and indigenous resistance in the Peruvian Amazon. Ecol Econ 70:207–218.
72. Vittor AY, Pan W, Gilman RH, Tielsch J, Glass G, Shields T, Sánchez-Lozano W, Pinedo VV, Salas-Cobos E, Flores S, Patz JA. 2009. Linking deforestation to malaria in the Amazon: characterization of the breeding habitat of the principal malaria vector, Anopheles darlingi. Am J Trop Med Hyg 81:5–12. [PubMed]
73. Dhondt AA, Altizer S, Cooch EG, Davis AK, Dobson A, Driscoll MJ, Hartup BK, Hawley DM, Hochachka WM, Hosseini PR, Jennelle CS, Kollias GV, Ley DH, Swarthout EC, Sydenstricker KV. 2005. Dynamics of a novel pathogen in an avian host: mycoplasmal conjunctivitis in house finches. Acta Tropica 94:77–93. [PubMed][CrossRef]
74. Lachish S, Gopalaswamy AM, Knowles SC, Sheldon BC. 2012. Site-occupancy modelling as a novel framework for assessing test sensitivity and estimating wildlife disease prevalence from imperfect diagnostic tests. Methods Ecol Evol 3:339–348.
75. Jennelle CS, Cooch EG, Conroy MJ, Senar JC. 2007. State-specific detection probabilities and disease prevalence. Ecol Appl 17:154–167. [PubMed]
76. Senar JC, Conroy MJ. 2004. Multi-state analysis of the impacts of avian pox on a population of Serins ( Serinus serinus): the importance of estimating recapture rates. Anim Biodivers Conserv 27:133–146.
77. Cooch EG, Conn PB, Ellner SP, Dobson AP, Pollock KH. 2012. Disease dynamics in wild populations: modeling and estimation: a review. J Ornithol 152:485–509.
78. McClintock BT, Nichols JD, Bailey LL, MacKenzie DI, Kendall WL, Franklin AB. 2010. Seeking a second opinion: uncertainty in disease ecology. Ecol Lett 13:659–674. [PubMed][CrossRef]
79. Faustino CR, Jennelle CS, Connolly V, Davis AK, Swarthout EC, Dhondt AA, Cooch EG. 2004. Mycoplasma gallisepticum infection dynamics in a house finch population: seasonal variation in survival, encounter and transmission rate. J Anim Ecol 73:651–669.
80. Lomolino MV, Riddle BR, Whittaker RJ, Brown JH. 2010. Biogeography, 4th ed. Sinauer Associates, Inc., Sunderland, MA.
81. Cox CB, Moore PD. 2010. Biogeography: an Ecological and Evolutionary Approach, 8th ed. John Wiley & Sons, Hoboken, NJ.
82. Morand S, Krasnov BR (ed). 2010. The Biogeography of Host-Parasite Interactions. Oxford University Press, New York, NY.
83. MacArthur RH, Wilson EO. 1967. The Theory of Island Biogeography. Princeton University Press, Princeton, NJ.
84. Kuris AM, Blaustein AR, Alio JJ. 1980. Hosts as islands. Am Nat 116:570–586.
85. Reperant L. 2010. Applying the theory of island biogeography to emerging pathogens: toward predicting the sources of future emerging zoonotic and vector-borne diseases. Vector Borne Zoonotic Dis 10:105–110. [PubMed][CrossRef]
86. Poulin R. 2004. Macroecological patterns of species richness in parasite assemblages. Basic Appl Ecol 5:423–434.
87. May RM, Gupta S, McLean AR. 2001. Infectious disease dynamics: what characterizes a successful invader? Philos Trans R Soc Lond B Biol Sci 356:901–910. [PubMed][CrossRef]
88. Murray KA, Skerratt LF, Speare R, Ritchie S, Smout F, Hedlefs R, Lee J. 2012. Cooling off health security hot spots: getting on top of it down under. Environ Int 48:56–64. [PubMed][CrossRef]
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2013-12-13
2019-11-22

Abstract:

Concern over emerging infectious diseases (EIDs) and a better understanding of their causes has resulted in increasing recognition of the linkages among human, animal, and ecosystem health. It is now well recognized that human activities can promote the emergence of infectious diseases through the large-scale modification of natural environments and inadvertent vectoring (e.g., international trade and travel). These perturbations can alter the ecological and evolutionary relationships among humans, wildlife, and the pathogens that move between them, resulting in disease emergence. In recent years, the rise in zoonotic EIDs has not only increased our awareness of the need for cross-sectoral collaborations, but has also highlighted the disconnect between current ecological theory and biological reality. As the One Health movement continues to gain steam, further integration of ecological approaches into the One Health framework will be required. We discuss the importance of ecological methods and theory to the study of zoonotic diseases by (i) discussing key ecological concepts and approaches, (ii) reviewing methods of studying wildlife diseases and their potential applications for zoonoses, and (iii) identifying future directions in the One Health movement.

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Ecological Approaches to Studying Zoonoses
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Citation: Loh E, Murray K, Zambrana-Torrelio C, Hosseini P, Rostal M, Karesh W, Daszak P. 2013. Ecological approaches to studying zoonoses. microbiolspec 1(2): doi:10.1128/microbiolspec.OH-0009-2012
/content/microbiolspec/10.1128/microbiolspec.OH-0009-2012.fig1
FIGURE 1

The One Health approach recognizes the inherent relationships among human, environmental, and animal health. doi:10.1128/microbiolspec.OH-0009-2012.f1

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microbiolspec/1/2/OH-0009-2012-fig1.gif
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FIGURE 1

The One Health approach recognizes the inherent relationships among human, environmental, and animal health. doi:10.1128/microbiolspec.OH-0009-2012.f1

Source: microbiolspec December 2013 vol. 1 no. 2 doi:10.1128/microbiolspec.OH-0009-2012
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FIGURE 2

Dynamic equilibrium model of island biogeography. The effects of island size (small [S] and large [L]) and island isolation (near [N] and far [F]) on the number of species (S) and the rate of species turnover (T) are represented. From reference 83 . doi:10.1128/microbiolspec.OH-0009-2012.f2

microbiolspec/1/2/OH-0009-2012-fig2_thmb.gif
microbiolspec/1/2/OH-0009-2012-fig2.gif
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FIGURE 2

Dynamic equilibrium model of island biogeography. The effects of island size (small [S] and large [L]) and island isolation (near [N] and far [F]) on the number of species (S) and the rate of species turnover (T) are represented. From reference 83 . doi:10.1128/microbiolspec.OH-0009-2012.f2

Source: microbiolspec December 2013 vol. 1 no. 2 doi:10.1128/microbiolspec.OH-0009-2012
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