Artigo Revisado por pares

Epidemic Models: Thresholds and Population Regulation

1983; University of Chicago Press; Volume: 121; Issue: 6 Linguagem: Inglês

10.1086/284112

ISSN

1537-5323

Autores

Wayne M. Getz, John Pickering,

Tópico(s)

Evolution and Genetic Dynamics

Resumo

Previous articleNext article No AccessNotes and CommentsEpidemic Models: Thresholds and Population RegulationWayne M. Getz and John PickeringWayne M. Getz and John PickeringPDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 121, Number 6Jun., 1983 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/284112 Views: 33Total views on this site Citations: 148Citations are reported from Crossref Copyright 1983 The University of ChicagoPDF download Crossref reports the following articles citing this article:Wayne M Getz, Richard Salter, Ludovica Luisa Vissat Simulation applications to support teaching and research in epidemiological dynamics, BMC Medical Education 22, no.11 (Aug 2022).https://doi.org/10.1186/s12909-022-03674-3Natalia Tepox-Vivar, Jessica F. Stephenson, Palestina Guevara-Fiore Transmission dynamics of ectoparasitic gyrodactylids (Platyhelminthes, Monogenea): An integrative review, Parasitology 149, no.77 (Apr 2022): 865–877.https://doi.org/10.1017/S0031182022000361Christopher A. Whittier, Felicia B. Nutter, Philip L. F. Johnson, Paul Cross, James O. Lloyd‐Smith, Barrett D. Slenning, Michael K. Stoskopf Population structure, intergroup interaction, and human contact govern infectious disease impacts in mountain gorilla populations, American Journal of Primatology 84, no.4-54-5 (Dec 2021).https://doi.org/10.1002/ajp.23350Hongrui Wei, Xianping He, Yong Li Dynamical analysis of an impulsive stochastic infected predator-prey system with BD functional response and modified saturated incidence, Journal of Applied Mathematics and Computing 167 (Jan 2022).https://doi.org/10.1007/s12190-021-01678-8Shi Zhao, Salihu S Musa, Marc KC Chong, Jinjun Ran, Mohammad Javanbakht, Lefei Han, Kai Wang, Nafiu Hussaini, Abdulrazaq G Habib, Maggie H Wang, Daihai He The co-circulating transmission dynamics of SARS-CoV-2 Alpha and Eta variants in Nigeria: A retrospective modeling study of COVID-19, Journal of Global Health 11 (Dec 2021).https://doi.org/10.7189/jogh.11.05028Catherine L. Searle, Mark R. Christie Evolutionary rescue in host‐pathogen systems*, Evolution 75, no.1111 (Jun 2021): 2948–2958.https://doi.org/10.1111/evo.14269Danail Takov, Daniela Pilarska, Andreas Linde, Marek Barta Infectious and parasitic diseases of phytophagous insect pests in the context of extreme environmental conditions, Central European Forestry Journal 67, no.22 (May 2021): 72–84.https://doi.org/10.2478/forj-2020-0018Daniel A. Malagon, Luis A. Melara, Olivia F. Prosper, Suzanne Lenhart, Edward Davis Carter, J. A. Fordyce, Anna C. Peterson, Debra L. Miller, Matthew J. Gray Host density and habitat structure influence host contact rates and Batrachochytrium salamandrivorans transmission, Scientific Reports 10, no.11 (Mar 2020).https://doi.org/10.1038/s41598-020-62351-xGabriel Natalio Castillo, Juan Carlos Acosta, Cynthia Jessica Gonzalez-Rivas, Geraldine Ramallo Parasitic nematodes of reptiles (lizards and snakes) in the Monte Desert of Argentina, Acta Zoologica Academiae Scientiarum Hungaricae 66, no.44 (Nov 2020).https://doi.org/10.17109/AZH.66.4.319.2020Erica M. Goss, Amy E. Kendig, Ashish Adhikari, Brett Lane, Nicholas Kortessis, Robert D. Holt, Keith Clay, Philip F. Harmon, S. Luke Flory Disease in Invasive Plant Populations, Annual Review of Phytopathology 58, no.11 (Aug 2020): 97–117.https://doi.org/10.1146/annurev-phyto-010820-012757Carly Rozins, Michael E. Hood, Jae Hoon Cho, Janis Antonovics, David Murrell Exploring density‐ and frequency‐dependent interactions experimentally: An r program for generating hexagonal fan designs, Methods in Ecology and Evolution 11, no.55 (Apr 2020): 678–683.https://doi.org/10.1111/2041-210X.13382Chenjing Fan, Tianmin Cai, Zhenyu Gai, Yuerong Wu The Relationship between the Migrant Population's Migration Network and the Risk of COVID-19 Transmission in China—Empirical Analysis and Prediction in Prefecture-Level Cities, International Journal of Environmental Research and Public Health 17, no.88 (Apr 2020): 2630.https://doi.org/10.3390/ijerph17082630Skylar R. Hopkins, Arietta E. Fleming‐Davies, Lisa K. Belden, Jeremy M. Wojdak, Nick Golding Systematic review of modelling assumptions and empirical evidence: Does parasite transmission increase nonlinearly with host density?, Methods in Ecology and Evolution 11, no.44 (Apr 2020): 476–486.https://doi.org/10.1111/2041-210X.13361Emily Bruns Effects of host lifespan on the evolution of age-specific resistance: a case study of anther-smut disease on wild carnations, (Nov 2019): 161–186.https://doi.org/10.1017/9781316479964.006Ben Ashby, Jordan E. Jones, Robert J. Knell, Gregory D.D. Hurst Sexually transmitted infections in natural populations: what have we learnt from beetles and beyond?, (Nov 2019): 187–222.https://doi.org/10.1017/9781316479964.007Ania A. Majewska, Stuart Sims, Anna Schneider, Sonia Altizer, Richard J. Hall Multiple transmission routes sustain high prevalence of a virulent parasite in a butterfly host, Proceedings of the Royal Society B: Biological Sciences 286, no.19101910 (Sep 2019): 20191630.https://doi.org/10.1098/rspb.2019.1630Iulia Martina Bulai, Frank M. Hilker Eco-epidemiological interactions with predator interference and infection, Theoretical Population Biology (Aug 2019).https://doi.org/10.1016/j.tpb.2019.07.016Wayne M. Getz, Richard Salter, Whitney Mgbara Adequacy of SEIR models when epidemics have spatial structure: Ebola in Sierra Leone, Philosophical Transactions of the Royal Society B: Biological Sciences 374, no.17751775 (May 2019): 20180282.https://doi.org/10.1098/rstb.2018.0282David V. McLeod, Troy Day Why is sterility virulence most common in sexually transmitted infections? Examining the role of epidemiology, Evolution 73, no.55 (Mar 2019): 872–882.https://doi.org/10.1111/evo.13718Wayne M Getz, Colin Carlson, Eric Dougherty, Travis C Porco, Richard Salter An agent-based model of school closing in under-vaccinated communities during measles outbreaks, SIMULATION 95, no.55 (Jul 2017): 385–393.https://doi.org/10.1177/0037549717721754Alejandro Feged-Rivadeneira, Carlos Del Cairo, William Vargas Demographic and epidemic transitions in peri-urban areas of Colombia: a multilevel study of malaria in the Amazonian city of San José del Guaviare, Environment and Urbanization 31, no.11 (Oct 2018): 325–348.https://doi.org/10.1177/0956247818808207Mudasir Gani, Taskeena Hassan, Pawan Saini, Rakesh Kumar Gupta, Kamlesh Bali Molecular Phylogeny of Entomopathogens, (Sep 2019): 43–113.https://doi.org/10.1007/978-3-030-23045-6_3Emily L. Bruns, Janis Antonovics, Michael Hood, Brian Silliman Is there a disease‐free halo at species range limits? The codistribution of anther‐smut disease and its host species, Journal of Ecology 107, no.11 (Jun 2018): 1–11.https://doi.org/10.1111/1365-2745.13009Alex P. Farrell, James P. Collins, Amy L. Greer, Horst R. Thieme Do fatal infectious diseases eradicate host species?, Journal of Mathematical Biology 77, no.6-76-7 (May 2018): 2103–2164.https://doi.org/10.1007/s00285-018-1249-3Wayne M. Getz, Richard Salter, Oliver Muellerklein, Hyun S. Yoon, Krti Tallam Modeling epidemics: A primer and Numerus Model Builder implementation, Epidemics 25 (Dec 2018): 9–19.https://doi.org/10.1016/j.epidem.2018.06.001Michal Theuer, Luděk Berec Impacts of infection avoidance for populations affected by sexually transmitted infections, Journal of Theoretical Biology 455 (Oct 2018): 64–74.https://doi.org/10.1016/j.jtbi.2018.06.030Alexandra L. DeCandia, Andrew P. Dobson, Bridgett M. vonHoldt Toward an integrative molecular approach to wildlife disease, Conservation Biology 32, no.44 (Mar 2018): 798–807.https://doi.org/10.1111/cobi.13083Ben Ashby, Emily Bruns The evolution of juvenile susceptibility to infectious disease, Proceedings of the Royal Society B: Biological Sciences 285, no.18811881 (Jun 2018): 20180844.https://doi.org/10.1098/rspb.2018.0844Olivia Tardy, Ariane Massé, Fanie Pelletier, Daniel Fortin Interplay between contact risk, conspecific density, and landscape connectivity: An individual-based modeling framework, Ecological Modelling 373 (Apr 2018): 25–38.https://doi.org/10.1016/j.ecolmodel.2018.02.003Kathleen A. Alexander, Colin J. Carlson, Bryan L. Lewis, Wayne M. Getz, Madhav V. Marathe, Stephen G. Eubank, Claire E. Sanderson, Jason K. Blackburn The Ecology of Pathogen Spillover and Disease Emergence at the Human-Wildlife-Environment Interface, (Aug 2018): 267–298.https://doi.org/10.1007/978-3-319-92373-4_8Wayne M. Getz, Eric R. Dougherty Discrete stochastic analogs of Erlang epidemic models, Journal of Biological Dynamics 12, no.11 (Nov 2017): 16–38.https://doi.org/10.1080/17513758.2017.1401677Benny Borremans, Jonas Reijniers, Niel Hens, Herwig Leirs The shape of the contact–density function matters when modelling parasite transmission in fluctuating populations, Royal Society Open Science 4, no.1111 (Nov 2017): 171308.https://doi.org/10.1098/rsos.171308Frédéric M. Hamelin, Frank M. Hilker, T. Anthony Sun, Michael J. Jeger, M. Reza Hajimorad, Linda J.S. Allen, Holly R. Prendeville The evolution of parasitic and mutualistic plant–virus symbioses through transmission-virulence trade-offs, Virus Research 241 (Sep 2017): 77–87.https://doi.org/10.1016/j.virusres.2017.04.011Janis Antonovics, Anthony J. Wilson, Mark R. Forbes, Heidi C. Hauffe, Eva R. Kallio, Helen C. Leggett, Ben Longdon, Beth Okamura, Steven M. Sait, Joanne P. Webster The evolution of transmission mode, Philosophical Transactions of the Royal Society B: Biological Sciences 372, no.17191719 (Mar 2017): 20160083.https://doi.org/10.1098/rstb.2016.0083Janis Antonovics Transmission dynamics: critical questions and challenges, Philosophical Transactions of the Royal Society B: Biological Sciences 372, no.17191719 (Mar 2017): 20160087.https://doi.org/10.1098/rstb.2016.0087Min Su, Mike Boots The impact of resource quality on the evolution of virulence in spatially heterogeneous environments, Journal of Theoretical Biology 416 (Mar 2017): 1–7.https://doi.org/10.1016/j.jtbi.2016.12.017Marie I. Tosa, Eric M. Schauber, Clayton K. Nielsen Localized removal affects white-tailed deer space use and contacts, The Journal of Wildlife Management 81, no.11 (Sep 2016): 26–37.https://doi.org/10.1002/jwmg.21176Laith Yakob How do biting disease vectors behaviourally respond to host availability?, Parasites & Vectors 9, no.11 (Aug 2016).https://doi.org/10.1186/s13071-016-1762-4Frédéric M. Hamelin, Linda J.S. Allen, Holly R. Prendeville, M. Reza Hajimorad, Michael J. Jeger The evolution of plant virus transmission pathways, Journal of Theoretical Biology 396 (May 2016): 75–89.https://doi.org/10.1016/j.jtbi.2016.02.017Barbara Boldin, Éva Kisdi Evolutionary suicide through a non-catastrophic bifurcation: adaptive dynamics of pathogens with frequency-dependent transmission, Journal of Mathematical Biology 72, no.44 (Nov 2015): 1101–1124.https://doi.org/10.1007/s00285-015-0945-5Tavis K. Anderson, Michael V. K. Sukhdeo The worm's eye view of community ecology, (Feb 2016): 110–130.https://doi.org/10.1002/9781118884799.ch8Suzanne M. O'Regan, John E. Vinson, and Andrew W. Park Interspecific Contact and Competition May Affect the Strength and Direction of Disease-Diversity Relationships for Directly Transmitted Microparasites, The American Naturalist 186, no.44 (Nov 2015): 480–494.https://doi.org/10.1086/682721Barbara A. Han, Andrew W. Park, Anna E. Jolles, Sonia Altizer, Andrew Fenton Infectious disease transmission and behavioural allometry in wild mammals, Journal of Animal Ecology 84, no.33 (Feb 2015): 637–646.https://doi.org/10.1111/1365-2656.12336E A O'Grady, S C Culloty, T C Kelly, M J A O'Callaghan, D Rachinskii A preliminary threshold model of parasitism in the Cockle Cerastoderma edule using delayed exchange of stability, Journal of Physics: Conference Series 585 (Feb 2015): 012013.https://doi.org/10.1088/1742-6596/585/1/012013Eric M. Schauber, Clayton K. Nielsen, Lene J. Kjær, Charles W. Anderson, Daniel J. Storm Social affiliation and contact patterns among white-tailed deer in disparate landscapes: implications for disease transmission, Journal of Mammalogy 96, no.11 (Mar 2015): 16–28.https://doi.org/10.1093/jmammal/gyu027Emily Bruns, Michael E. Hood, Janis Antonovics Rate of resistance evolution and polymorphism in long- and short-lived hosts, Evolution 69, no.22 (Jan 2015): 551–560.https://doi.org/10.1111/evo.12577J. Haapkyl�, J. Melbourne-Thomas, M. Flavell The association between coral communities and disease assemblages in the Wakatobi Marine National Park, south-eastern Sulawesi, Indonesia, Marine and Freshwater Research 66, no.1010 (Jan 2015): 948.https://doi.org/10.1071/MF14192Ana Montiel-Arteaga, Daniel Atilano, Alejandra Ayanegui, Gerardo Ceballos, Gerardo Suzán RISK FACTORS ASSOCIATED WITH PREVALENCE OF ANTIBODIES TO LEPTOSPIRA INTERROGANS IN A METAPOPULATION OF BLACK-TAILED PRAIRIE DOGS IN MEXICO, Journal of Wildlife Diseases 51, no.11 (Jan 2015): 28–35.https://doi.org/10.7589/2013-10-259Kezia R. Manlove, E. Frances Cassirer, Paul C. Cross, Raina K. Plowright, Peter J. Hudson Costs and benefits of group living with disease: a case study of pneumonia in bighorn lambs ( Ovis canadensis ), Proceedings of the Royal Society B: Biological Sciences 281, no.17971797 (Dec 2014): 20142331.https://doi.org/10.1098/rspb.2014.2331David V. McLeod, Troy Day Sexually transmitted infection and the evolution of serial monogamy, Proceedings of the Royal Society B: Biological Sciences 281, no.17961796 (Dec 2014): 20141726.https://doi.org/10.1098/rspb.2014.1726Angela Brennan, Paul C. Cross, Megan D. Higgs, W. Henry Edwards, Brandon M. Scurlock, Scott Creel A multi-scale assessment of animal aggregation patterns to understand increasing pathogen seroprevalence, Ecosphere 5, no.1010 (Oct 2014): art138.https://doi.org/10.1890/ES14-00181.1Kasia A. Pawelek, Patrick Niehaus, Cristian Salmeron, Elizabeth J. Hager, Gregg J. Hunt, Tian Wang Modeling Dynamics of Culex pipiens Complex Populations and Assessing Abatement Strategies for West Nile Virus, PLoS ONE 9, no.99 (Sep 2014): e108452.https://doi.org/10.1371/journal.pone.0108452Lien T. Luong, Daniel A. Grear, Peter J. Hudson Manipulation of host-resource dynamics impacts transmission of trophic parasites, International Journal for Parasitology 44, no.1010 (Sep 2014): 737–742.https://doi.org/10.1016/j.ijpara.2014.05.004Christopher S. Jennelle, Viviane Henaux, Gideon Wasserberg, Bala Thiagarajan, Robert E. Rolley, Michael D. Samuel, Roy Martin Roop Transmission of Chronic Wasting Disease in Wisconsin White-Tailed Deer: Implications for Disease Spread and Management, PLoS ONE 9, no.33 (Mar 2014): e91043.https://doi.org/10.1371/journal.pone.0091043Souvik Bhattacharya, Maia Martcheva, Xue-Zhi Li A predator–prey–disease model with immune response in infected prey, Journal of Mathematical Analysis and Applications 411, no.11 (Mar 2014): 297–313.https://doi.org/10.1016/j.jmaa.2013.09.031Sadie J. Ryan, James H. Jones, Andrew P. Dobson, Gerardo Chowell Interactions between Social Structure, Demography, and Transmission Determine Disease Persistence in Primates, PLoS ONE 8, no.1010 (Oct 2013): e76863.https://doi.org/10.1371/journal.pone.0076863P. C. Cross, T. G. Creech, M. R. Ebinger, K. Manlove, K. Irvine, J. Henningsen, J. Rogerson, B. M. Scurlock, S. Creel Female elk contacts are neither frequency nor density dependent, Ecology 94, no.99 (Sep 2013): 2076–2086.https://doi.org/10.1890/12-2086.1R. A. RAY, J. L. BARTHOLOMEW Estimation of transmission dynamics of the Ceratomyxa shasta actinospore to the salmonid host, Parasitology 140, no.77 (Mar 2013): 907–916.https://doi.org/10.1017/S0031182013000127Maxwell B. Joseph, Joseph R. Mihaljevic, Ana Lisette Arellano, Jordan G. Kueneman, Daniel L. Preston, Paul C. Cross, Pieter T. J. Johnson, Eric Morgan Taming wildlife disease: bridging the gap between science and management, Journal of Applied Ecology 50, no.33 (Apr 2013): 702–712.https://doi.org/10.1111/1365-2664.12084Paul C. Cross, Damien Caillaud, Dennis M. Heisey Underestimating the effects of spatial heterogeneity due to individual movement and spatial scale: infectious disease as an example, Landscape Ecology 28, no.22 (Nov 2012): 247–257.https://doi.org/10.1007/s10980-012-9830-4Luděk Berec, Daniel Maxin Fatal or Harmless: Extreme Bistability Induced by Sterilizing, Sexually Transmitted Pathogens, Bulletin of Mathematical Biology 75, no.22 (Jan 2013): 258–273.https://doi.org/10.1007/s11538-012-9802-5Daniel J. Storm, Michael D. Samuel, Robert E. Rolley, Paul Shelton, Nicholas S. Keuler, Bryan J. Richards, Timothy R. Van Deelen Deer density and disease prevalence influence transmission of chronic wasting disease in white-tailed deer, Ecosphere 4, no.11 (Jan 2013): art10.https://doi.org/10.1890/ES12-00141.1S J Hoggard, P D Wilson, A J Beattie, A J Stow The Effectiveness of Antimicrobial Defenses Declines with Increasing Group Size and Genetic Similarity, Annals of the Entomological Society of America 106, no.11 (Jan 2013): 53–58.https://doi.org/10.1603/AN11187Helen R. Curran, Léanne L. Dreyer, Francois Roets Impact of disease frequency and host density on pollination and transmission of an African anther-smut fungus, Planta 236, no.66 (Aug 2012): 1677–1685.https://doi.org/10.1007/s00425-012-1727-6Kate E. Langwig, Winifred F. Frick, Jason T. Bried, Alan C. Hicks, Thomas H. Kunz, A. Marm Kilpatrick, Kevin Lafferty Sociality, density-dependence and microclimates determine the persistence of populations suffering from a novel fungal disease, white-nose syndrome, Ecology Letters 15, no.99 (Jul 2012): 1050–1057.https://doi.org/10.1111/j.1461-0248.2012.01829.xAlex Best, Steve Webb, Janis Antonovics, Mike Boots Local transmission processes and disease-driven host extinctions, Theoretical Ecology 5, no.22 (Jan 2011): 211–217.https://doi.org/10.1007/s12080-011-0111-7Viggo Andreasen The Final Size of an Epidemic and Its Relation to the Basic Reproduction Number, Bulletin of Mathematical Biology 73, no.1010 (Jan 2011): 2305–2321.https://doi.org/10.1007/s11538-010-9623-3Mirelle B. Johnson, Kevin D. Lafferty, Cock van Oosterhout, Joanne Cable, Wayne M. Getz Parasite Transmission in Social Interacting Hosts: Monogenean Epidemics in Guppies, PLoS ONE 6, no.88 (Aug 2011): e22634.https://doi.org/10.1371/journal.pone.0022634Janis Antonovics, Mike Boots, Jessie Abbate, Christi Baker, Quinn McFrederick, Vijay Panjeti Biology and evolution of sexual transmission, Annals of the New York Academy of Sciences 1230, no.11 (Aug 2011): 12–24.https://doi.org/10.1111/j.1749-6632.2011.06127.xGlen A. Sargeant, Duane C. Weber, Daniel E. Roddy Implications of chronic wasting disease, cougar predation, and reduced recruitment for elk management, The Journal of Wildlife Management 75, no.11 (Jan 2011): 171–177.https://doi.org/10.1002/jwmg.27 10.1007/BF00349593, CrossRef Listing of Deleted DOIs 280 (Jan 2011).https://doi.org/10.1007/BF00349593Matthew J. Ferrari, Sarah E. Perkins, Laura W. Pomeroy, Ottar N. Bjørnstad Pathogens, Social Networks, and the Paradox of Transmission Scaling, Interdisciplinary Perspectives on Infectious Diseases 2011 (Jan 2011): 1–10.https://doi.org/10.1155/2011/267049J. Haapkylä, J. Melbourne-Thomas, M. Flavell, B. L. Willis Spatiotemporal patterns of coral disease prevalence on Heron Island, Great Barrier Reef, Australia, Coral Reefs 29, no.44 (Jul 2010): 1035–1045.https://doi.org/10.1007/s00338-010-0660-zSean M. Moore, Elizabeth T. Borer, Parviez R. Hosseini Predators indirectly control vector-borne disease: linking predator–prey and host–pathogen models, Journal of The Royal Society Interface 7, no.4242 (May 2009): 161–176.https://doi.org/10.1098/rsif.2009.0131T. Dhirasakdanon, H. R. Thieme Stability of the Endemic Coexistence Equilibrium for One Host and Two Parasites, Mathematical Modelling of Natural Phenomena 5, no.66 (Apr 2010): 109–138.https://doi.org/10.1051/mmnp/20105606Frank M. Hilker Population collapse to extinction: the catastrophic combination of parasitism and Allee effect, Journal of Biological Dynamics 4, no.11 (Jan 2010): 86–101.https://doi.org/10.1080/17513750903026429Michael B. Bonsall, Robert D. Holt Apparent Competition and Vector-Host Interactions, Israel Journal of Ecology & Evolution 56, no.3-43-4 (Mar 2013): 393–416.https://doi.org/10.1560/IJEE.56.3-4.393Alex Best, Andy White, and Mike Boots The Implications of Coevolutionary Dynamics to Host‐Parasite Interactions. A. Best et al., The American Naturalist 173, no.66 (Jul 2015): 779–791.https://doi.org/10.1086/598494Vincent Laperrière, Dominique Badariotti, Arnaud Banos, Jean-Pierre Müller Structural validation of an individual-based model for plague epidemics simulation, Ecological Complexity 6, no.22 (Jun 2009): 102–112.https://doi.org/10.1016/j.ecocom.2008.08.001Pierre Auger, Rachid Mchich, Tanmay Chowdhury, Gauthier Sallet, Maurice Tchuente, Joydev Chattopadhyay Effects of a disease affecting a predator on the dynamics of a predator–prey system, Journal of Theoretical Biology 258, no.33 (Jun 2009): 344–351.https://doi.org/10.1016/j.jtbi.2008.10.030Horst R. Thieme, Thanate Dhirasakdanon, Zhun Han, Roy Trevino Species decline and extinction: synergy of infectious disease and Allee effect?, Journal of Biological Dynamics 3, no.2-32-3 (May 2009): 305–323.https://doi.org/10.1080/17513750802376313Janis Antonovics The effect of sterilizing diseases on host abundance and distribution along environmental gradients, Proceedings of the Royal Society B: Biological Sciences 276, no.16611661 (Feb 2009): 1443–1448.https://doi.org/10.1098/rspb.2008.1256Daniel Coombs, Michael A. Gilchrist, Colleen L. Ball Evaluating the importance of within- and between-host selection pressures on the evolution of chronic pathogens, Theoretical Population Biology 72, no.44 (Dec 2007): 576–591.https://doi.org/10.1016/j.tpb.2007.08.005Jonathan J. Ryder, Martin R. Miller, Andy White, Robert J. Knell, Michael Boots Host-parasite population dynamics under combined frequency- and density-dependent transmission, Oikos 116, no.1212 (Sep 2007): 2017–2026.https://doi.org/10.1111/j.2007.0030-1299.15863.xAMY B. PEDERSEN, KATE E. JONES, CHARLES L. NUNN, SONIA ALTIZER Infectious Diseases and Extinction Risk in Wild Mammals, Conservation Biology 21, no.55 (Oct 2007): 1269–1279.https://doi.org/10.1111/j.1523-1739.2007.00776.xLARA J. RACHOWICZ, CHERYL J. BRIGGS Quantifying the disease transmission function: effects of density on Batrachochytrium dendrobatidis transmission in the mountain yellow-legged frog Rana muscosa, Journal of Animal Ecology 76, no.44 (Jul 2007): 711–721.https://doi.org/10.1111/j.1365-2656.2007.01256.xPaul C Cross, Philip L.F Johnson, James O Lloyd-Smith, Wayne M Getz Utility of R0 as a predictor of disease invasion in structured populations, Journal of The Royal Society Interface 4, no.1313 (Nov 2006): 315–324.https://doi.org/10.1098/rsif.2006.0185Jonathan J. Ryder, Jenna Hathway, Robert J. Knell Constraints on parasite fecundity and transmission in an insect-STD system, Oikos 116, no.44 (Apr 2007): 578–584.https://doi.org/10.1111/j.0030-1299.2007.15574.xA Tellier, L M M A Villaréal, T Giraud Antagonistic pleiotropy may help population-level selection in maintaining genetic polymorphism for transmission rate in a model phytopathogenic fungus, Heredity 98, no.11 (Oct 2006): 45–52.https://doi.org/10.1038/sj.hdy.6800902N. J. OUBORG, P. VERGEER, C. MIX The rough edges of the conservation genetics paradigm for plants, Journal of Ecology 94, no.66 (Nov 2006): 1233–1248.https://doi.org/10.1111/j.1365-2745.2006.01167.xA. Fenton, S. A. Rands THE IMPACT OF PARASITE MANIPULATION AND PREDATOR FORAGING BEHAVIOR ON PREDATOR–PREY COMMUNITIES, Ecology 87, no.1111 (Nov 2006): 2832–2841.https://doi.org/10.1890/0012-9658(2006)87[2832:TIOPMA]2.0.CO;2Henry K. Ngugi, Harald Scherm Biology of Flower-Infecting Fungi, Annual Review of Phytopathology 44, no.11 (Sep 2006): 261–282.https://doi.org/10.1146/annurev.phyto.44.070505.143405Marjorie J. Wonham, Mark A. Lewis, Joanna Renclawowicz, P. van den Driessche Transmission assumptions generate conflicting predictions in host-vector disease models: a case study in West Nile virus, Ecology Letters 9, no.66 (Jun 2006): 706–725.https://doi.org/10.1111/j.1461-0248.2006.00912.xF. Keesing, R. D. Holt, R. S. Ostfeld Effects of species diversity on disease risk, Ecology Letters 9, no.44 (Mar 2006): 485–498.https://doi.org/10.1111/j.1461-0248.2006.00885.xAnne Deredec, Franck Courchamp Combined impacts of Allee effects and parasitism, Oikos 112, no.33 (Mar 2006): 667–679.https://doi.org/10.1111/j.0030-1299.2006.14243.xK. MARY WEBBERLEY, JAROSLAW BUSZKO, VALERIE ISHAM, GREGORY D. D. HURST Sexually transmitted disease epidemics in a natural insect population, Journal of Animal Ecology 75, no.11 (Jan 2006): 33–43.https://doi.org/10.1111/j.1365-2656.2005.01020.xJonathan J. Ryder, K. Mary Webberley, Michael Boots, Robert J. Knell Measuring the transmission dynamics of a sexually transmitted disease, Proceedings of the National Academy of Sciences 102, no.4242 (Oct 2005): 15140–15143.https://doi.org/10.1073/pnas.0505139102James O. Lloyd-Smith, Paul C. Cross, Cheryl J. Briggs, Matt Daugherty, Wayne M. Getz, John Latto, Maria S. Sanchez, Adam B. Smith, Andrea Swei Should we expect population thresholds for wildlife disease?, Trends in Ecology & Evolution 20, no.99 (Sep 2005): 511–519.https://doi.org/10.1016/j.tree.2005.07.004 Volker H. W. Rudolf and Janis Antonovics Species Coexistence and Pathogens with Frequency‐Dependent Transmission. V. H. W. Rudolf and J. Antonovics, The American Naturalist 166, no.11 (Jul 2015): 112–118.https://doi.org/10.1086/430674Paul C. Cross, James O. Lloyd-Smith, Philip L. F. Johnson, Wayne M. Getz Duelling timescales of host movement and disease recovery determine invasion of disease in structured populations, Ecology Letters 8, no.66 (Jun 2005): 587–595.https://doi.org/10.1111/j.1461-0248.2005.00760.x Aurélien Tellier , Lorys M. M. A. Villaréal , and Tatiana Giraud Maintenance of Sex‐Linked Deleterious Alleles by Selfing and Group Selection in Metapopulations of the Phytopathogenic Fungus Microbotryum violaceum. A. Tellier et al., The American Naturalist 165, no.55 (Jul 2015): 577–589.https://doi.org/10.1086/428680Kara J. O'Keefe The evolution of virulence in pathogens with frequency-dependent transmission, Journal of Theoretical Biology 233, no.11 (Mar 2005): 55–64.https://doi.org/10.1016/j.jtbi.2004.09.005Francisco De Castro, Benjamin Bolker Mechanisms of disease-induced extinction, Ecology Letters 8, no.11 (Dec 2004): 117–126.https://doi.org/10.1111/j.1461-0248.2004.00693.xJanis Antonovics Plant venereal diseases: insights from a messy metaphor, New Phytologist 165, no.11 (Oct 2004): 71–80.https://doi.org/10.1111/j.1469-8137.2004.01215.xCharles L. Nunn, Sonia M. Altizer Sexual selection, behaviour and sexually transmitted diseases, (May 2004): 117–130.https://doi.org/10.1017/CBO9780511542459.009James O. Lloyd-Smith, Wayne M. Getz, Hans V. Westerhoff Frequency–dependent incidence in models of sexually transmitted diseases: portrayal of pair–based transmission and effects of illness on contact behaviour, Proceedings of the Royal Society of London. Series B: Biological Sciences 271, no.15391539 (Mar 2004): 625–634.https://doi.org/10.1098/rspb.2003.2632Linda J.S. Allen, Michel Langlais, Carleton J. Phillips The dynamics of two viral infections in a single host population with applications to hantavirus, Mathematical Biosciences 186, no.22 (Dec 2003): 191–217.https://doi.org/10.1016/j.mbs.2003.08.002Thomas Alerstam, Anders Hedenström, Susanne Åkesson Long-distance migration: evolution and determinants, Oikos 103, no.22 (Oct 2003): 247–260.https://doi.org/10.1034/j.1600-0706.2003.12559.xSonia Altizer, Charles L. Nunn, Peter H. Thrall, John L. Gittleman, Janis Antonovics, Andrew A. Cunningham, Andrew P. Dobson, Vanessa Ezenwa, Kate E. Jones, Amy B. Pedersen, Mary Poss, Juliet R.C. Pulliam Social Organization and Parasite Risk in Mammals: Integrating Theory and Empirical Studies, Annual Review of Ecology, Evolution, and Systematics 34, no.11 (Nov 2003): 517–547.https://doi.org/10.1146/annurev.ecolsys.34.030102.151725Jenny S. Cory, Judith H. Myers The Ecology and Evolution of Insect Baculoviruses, Annual Review of Ecology, Evolution, and Systematics 34, no.11 (Nov 2003): 239–272.https://doi.org/10.1146/annurev.ecolsys.34.011802.132402Eran Karmon, Malcolm Potts, Wayne M. Getz Microbicides and HIV: Help or Hindrance?, JAIDS Journal of Acquired Immune Deficiency Syndromes 34, no.11 (Sep 2003): 71–75.https://doi.org/10.1097/00126334-200309010-00011 Anne Thomas , Jacqui Shykoff , Odile Jonot , and Tatiana Giraud Sex‐Ratio Bias in Populations of the Phytopathogenic Fungus Microbotryum violaceum from Several Host Species Thomas et al., International Journal of Plant Sciences 164, no.44 (Jul 2015): 641–647.https://doi.org/10.1086/375374Michael Boots, Akira Sasaki Parasite evolution and extinctions, Ecology Letters 6, no.33 (Mar 2003): 176–182.https://doi.org/10.1046/j.1461-0248.2003.00426.xN. J. Ouborg, A. Biere The Relationship Between Plant-Pathogen and Plant-Herbivore Interactions and Plant Population Persistence in a Fragmented Landscape, (Jan 2003): 99–116.https://doi.org/10.1007/978-3-662-09389-4_4Victoria L. Welch, John J. Sloggett, K. Mary Webberley, Gregory D. D. Hurst Short-range clinal variation in the prevalence of a sexually transmitted fungus associated with urbanisation, Ecological Entomology 26, no.55 (Jul 2008): 547–550.https://doi.org/10.1046/j.1365-2311.2001.00352.xSonia Altizer, Johannes Foufopoulos, Andrea Gager Diseases, Conservation and, (Jan 2001): 109–126.https://doi.org/10.1016/B0-12-226865-2/00072-9Peter H. Thrall, Janis Antonovics, Andrew P. Dobson Sexually transmitted diseases in polygynous mating systems: prevalence and impact on reproductive success, Proceedings of the Royal Society of London. Series B: Biological Sciences 267, no.14521452 (Aug 2000): 1555–1563.https://doi.org/10.1098/rspb.2000.1178Sonia M. Altizer, Karen S. Oberhauser, Lincoln P. Brower Associations between host migration and the prevalence of a protozoan parasite in natural populations of adult monarch butterflies, Ecological Entomology 25, no.22 (Dec 2001): 125–139.https://doi.org/10.1046/j.1365-2311.2000.00246.xRobert J. Knell SEXUALLY TRANSMITTED DISEASE AND PARASITE-MEDIATED SEXUAL SELECTION, Evolution 53, no.33 (May 2017): 957–961.https://doi.org/10.1111/j.1558-5646.1999.tb05389.x Oppliger, Clobert, Lecomte, Lorenzon, Boudjemadi, John-Alder Environmental stress increases the prevalence and intensity of blood parasite infection in the common lizard Lacerta vivipara, Ecology Letters 1, no.22 (Sep 1998): 129–138.https://doi.org/10.1046/j.1461-0248.1998.00028.xEmmanuelle Fromont, Dominique Pontier, Michel Langlais Dynamics of a feline retrovirus (FeLV) in host populations with variable spatial structure, Proceedings of the Royal Society of London. Series B: Biological Sciences 265, no.14011401 (Jun 1998): 1097–1104.https://doi.org/10.1098/rspb.1998.0404 Peter H. Thrall , Janis Antonovics , and William G. Wilson Allocation to Sexual versus Nonsexual Disease Transmission Thrall, Antonovics, Wilson, The American Naturalist 151, no.11 (Jul 2015): 29–45.https://doi.org/10.1086/286100 John Jaenike On the Capacity of Macroparasites to Control Insect Populations Jaenike, The American Naturalist 151, no.11 (Jul 2015): 84–96.https://doi.org/10.1086/286104Sonia M. Altizer, Peter H. Thrall, Janis Antonovics Vector Behavior and the Transmission of Anther-smut Infection in Silene alba, The American Midland Naturalist 139, no.11 (Jan 1998): 147–163.https://doi.org/10.1674/0003-0031(1998)139[0147:VBATTO]2.0.CO;2Sonia M. Altizer, David J. Augustine Interactions between frequency–dependent and vertical transmission in host–parasite systems, Proceedings of the Royal Society of London. Series B: Biological Sciences 264, no.13831383 (Jun 1997): 807–814.https://doi.org/10.1098/rspb.1997.0113Peter H. Thrall, Janis Antonovics Polymorphism in sexual versus non-sexual disease transmission, Proceedings of the Royal Society of London. Series B: Biological Sciences 264, no.13811381 (Apr 1997): 581–587.https://doi.org/10.1098/rspb.1997.0083Ben C. Sheldon, Andrew F. Read Comparative biology and disease ecology, Trends in Ecology & Evolution 12, no.22 (Feb 1997): 43–44.https://doi.org/10.1016/S0169-5347(96)30062-1Jenny S. Cory, Rosemary S. Hails, Steven M. Sait Baculovirus Ecology, (Jan 1997): 301–339.https://doi.org/10.1007/978-1-4899-1834-5_12I. Saloniemi Mathematical Models of Plant/Fungus Interactions, (Jan 1997): 239–256.https://doi.org/10.1007/978-3-642-60647-2_15ANN B. LOCKHART, PETER H. THRALL, JANIS ANTONOVICS SEXUALLY TRANSMITTED DISEASES IN ANIMALS: ECOLOGICAL AND EVOLUTIONARY IMPLICATIONS, Biological Reviews 71, no.33 (Aug 1996): 415–471.https://doi.org/10.1111/j.1469-185X.1996.tb01281.xPeter H. Thrall, Janis Antonovics Theoretical and empirical studies of metapopulations: population and genetic dynamics of the Silene ? Ustilago system, Canadian Journal of Botany 73, no.S1S1 (Dec 1995): 1249–1258.https://doi.org/10.1139/b95-385Marc Lipsitch, Martin A. Nowak The evolution of virulence in sexually transmitted HIV/AIDS, Journal of Theoretical Biology 174, no.44 (Jun 1995): 427–440.https://doi.org/10.1006/jtbi.1995.0109Oliver Kaltz Plant venereal disease: a model for integrating genetics, ecology and epidemiology, Trends in Ecology & Evolution 10, no.66 (Jun 1995): 221–222.https://doi.org/10.1016/S0169-5347(00)89067-9 The cost of resistance and the maintenance of genetic polymorphism in host—pathogen systems, Proceedings of the Royal Society of London. Series B: Biological Sciences 257, no.13491349 (Jan 1997): 105–110.https://doi.org/10.1098/rspb.1994.0101 Epidemiology of anther-smut infection of Silene alba (= S. latifolia ) caused by Ustilago violacea : patterns of spore deposition in experimental populations, Proceedings of the Royal Society of London. Series B: Biological Sciences 250, no.13281328 (Jan 1997): 157–163.https://doi.org/10.1098/rspb.1992.0144David W. Onstad Temporal and spatial scales in epidemiological concepts, Journal of Theoretical Biology 158, no.44 (Oct 1992): 495–515.https://doi.org/10.1016/S0022-5193(05)80712-XUlla Carlsson, Thomas Elmqvist Epidemiology of anther-smut disease (Microbotryum violaceum) and numeric regulation of populations ofSilene dioica, Oecologia 90, no.44 (Jul 1992): 509–517.https://doi.org/10.1007/BF01875444J. Pickering, A.P. Gutierrez DIFFERENTIAL IMPACT OF THE PATHOGEN PANDORA NEOAPHIDIS (R.&H.) HUMBER (ZYGOMYCETES: ENTOMOPHTHORALES) ON THE SPECIES COMPOSITION OF ACYRTHOSIPHON APHIDS IN ALFALFA, The Canadian Entomologist 123, no.22 (May 2012): 315–320.https://doi.org/10.4039/Ent123315-2Barbara Sohm Ekbom, John Pickering Pathogenic fungal dynamics in a fall population of the blackmargined aphid (Monellia caryella), Entomologia Experimentalis et Applicata 57, no.11 (Apr 2011): 29–37.https://doi.org/10.1111/j.1570-7458.1990.tb01413.xDavid W. Onstad, Joseph V. Maddox, Donna J. Cox, Edward A. Kornkven Spatial and temporal dynamics of animals and the host-density threshold in epizootiology, Journal of Invertebrate Pathology 55, no.11 (Jan 1990): 76–84.https://doi.org/10.1016/0022-2011(90)90035-5Viggo Andreasen Disease regulation of age-structured host populations, Theoretical Population Biology 36, no.22 (Oct 1989): 214–239.https://doi.org/10.1016/0040-5809(89)90031-2A.D. Cliff, P. Haggett Spatial aspects of epidemic control, Progress in Human Geography 13, no.33 (Sep 1989): 315–347.https://doi.org/10.1177/030913258901300301Robert M. May, Roy M. Anderson, Angela R. McLean Possible Demographic Consequences of HIV/AIDS Epidemics: II, Assuming HIV Infection does not Necessarily Lead to AIDS, (Jan 1989): 220–248.https://doi.org/10.1007/978-3-642-46693-9_16Robert M. May, Roy M. Anderson, Angela R. McLean Possible demographic consequences of HIV/AIDS epidemics. I. assuming HIV infection always leads to AIDS, Mathematical Biosciences 90, no.1-21-2 (Jul 1988): 475–505.https://doi.org/10.1016/0025-5564(88)90079-XJudith H. Myers Can a General Hypothesis Explain Population Cycles of Forest Lepidoptera?, (Jan 1988): 179–242.https://doi.org/10.1016/S0065-2504(08)60181-6John Pickering, James A. Wiley, Nancy S. Padian, Loren E. Lieb, Dean F. Echenberg, Juliette Walker Modeling the incidence of Acquired Immunodeficiency Syndrome (AIDS) in San Francisco, Los Angeles, and New York, Mathematical Modelling 7, no.5-85-8 (Jan 1986): 661–688.https://doi.org/10.1016/0270-0255(86)90127-2 Robert D. Holt , and John Pickering Infectious Disease and Species Coexistence: A Model of Lotka-Volterra Form, The American Naturalist 126, no.22 (Oct 2015): 196–211.https://doi.org/10.1086/284409John Impagliazzo Extensions of Stable Population Theory, (Jan 1985): 133–153.https://doi.org/10.1007/978-3-642-82319-0_7

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