The effects of cowpox virus on survival in natural rodent populations: increases and decreases

Summary 1 The effect of cowpox virus on survival in two rodent hosts was investigated using nearly 4 years of longitudinal data from two sites. 2 We investigated whether an individual's probability of infection influenced the probability of surviving the next month. We also investigated the effect at the population level, examining whether, in addition to seasonal effects, changes in cowpox prevalence explained further temporal variation in survival rates. 3 In bank voles, but not wood mice, individuals with high probabilities of infection survived better than uninfected animals. 4 At the level of the population, the effect of infection on survival varied through the year in both species. Survival rates in late summer increased with cowpox prevalence, whilst survival rates in winter decreased with cowpox prevalence. 5 We discuss why parasites such as cowpox virus may increase or decrease host survival and why the effect may depend on the time of year.

[1]  D. Baxby,et al.  COWPOX VIRUS (POXVIRIDAE) , 1999 .

[2]  N. Stenseth,et al.  Survival-variation within and between functional categories of the African multimammate rat , 1999 .

[3]  A. Osterhaus,et al.  Morbillivirus infections of aquatic mammals: newly identified members of the genus. , 1995, Veterinary microbiology.

[4]  R. Chandra,et al.  Nutrition and the immune system: an introduction. , 1997, The American journal of clinical nutrition.

[5]  C. Krebs Demographic Changes in Fluctuating Populations of Microtus californicus , 1966 .

[6]  M. Begon,et al.  Cowpox in British voles and mice. , 1997, Journal of comparative pathology.

[7]  P. Schmid-Hempel,et al.  Condition-dependent expression of virulence in a trypanosome infecting bumblebees , 2000 .

[8]  M. Scott The Impact of Infection and Disease on Animal Populations: Implications for Conservation Biology , 1988 .

[9]  G. L. Pearson,et al.  POPULATION AND MOVEMENT CHARACTERISTICS OF RADIO-COLLARED STRIPED SKUNKS IN NORTH DAKOTA DURING AN EPIZOOTIC OF RABIES , 1997, Journal of wildlife diseases.

[10]  R. Poulin "Adaptive" changes in the behaviour of parasitized animals: a critical review. , 1995, International journal for parasitology.

[11]  J. Jaenike,et al.  Parasite‐Induced Mortality in Mycophagous Drosophila , 1995 .

[12]  A. Dobson,et al.  Prevention of population cycles by parasite removal. , 1998, Science.

[13]  M. Begon,et al.  Transmission dynamics of a zoonotic pathogen within and between wildlife host species , 1999, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[14]  R. Gaskell,et al.  Serological evidence for the reservoir hosts of cowpox virus in British wildlife , 1995, Epidemiology and Infection.

[15]  R. May,et al.  Population biology of infectious diseases: Part I , 1979, Nature.

[16]  E. Warr,et al.  A parasite that increases host lifespan , 2001, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[17]  N. Yoccoz,et al.  Adaptive precocial reproduction in voles: reproductive costs and multivoltine life‐history strategies in seasonal environments , 2001 .

[18]  M. Begon,et al.  Cowpox: reservoir hosts and geographic range , 1999, Epidemiology and Infection.

[19]  A. Dobson,et al.  Ecology of Infectious Diseases in Natural Populations , 1996 .

[20]  S. Obrebski Parasite reproductive strategy and evolution of castration of hosts by parasites. , 1975, Science.

[21]  H. McCallum,et al.  Population Parameters: Estimation for Ecological Models , 2000 .

[22]  M. Begon,et al.  Population and transmission dynamics of cowpox in bank voles: testing fundamental assumptions , 1998 .

[23]  R. Anderson,et al.  Evolutionary pressures in the spread and persistence of infectious agents in vertebrate populations , 1995, Parasitology.

[24]  M. Massot,et al.  Maternal Parasite Load Increases Sprint Speed and Philopatry in Female Offspring of the Common Lizard , 1994, The American Naturalist.

[25]  C. M. Lessells,et al.  The Evolution of Life Histories , 1994 .

[26]  R. May,et al.  Population biology of infectious diseases: Part II , 1979, Nature.

[27]  K. Burnham,et al.  Program MARK: survival estimation from populations of marked animals , 1999 .

[28]  Peter J. Hudson,et al.  system: Trichostrongylus tenuis in red grouse. II. Population models , 1992 .

[29]  C. Krebs,et al.  Natal dispersal of juvenile arctic ground squirrels in the boreal forest , 1999 .

[30]  F. Gulland,et al.  Ecology of Infectious Diseases in Natural Populations: Impact of Infectious Diseases on Wild Animal Populations: a Review , 1995 .

[31]  C. Combes Fitness of parasites: pathology and selection. , 1997, International journal for parasitology.

[32]  M. Scott,et al.  Parasitism: A cryptic determinant of animal community structure. , 1991, Trends in ecology & evolution.

[33]  David R. Anderson,et al.  AIC MODEL SELECTION IN OVERDISPERSED CAPTURE-RECAPTURE DATA' , 1994 .

[34]  A. Dobson,et al.  Regulation and stability of a free-living host-parasite system : Trichostrongylus tenuis in red grouse. I. Monitoring and parasite reduction experiments , 1992 .

[35]  M. Begon,et al.  The effect of cowpox virus infection on fecundity in bank voles and wood mice , 1997, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[36]  David R. Anderson,et al.  Data-Based Selection of an Appropriate Biological Model: The Key to Modern Data Analysis , 1992 .

[37]  David R. Anderson,et al.  General strategies for the analysis of ringing data , 1999 .

[38]  S. Bensch,et al.  Good genes, oxidative stress and condition–dependent sexual signals , 1999, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[39]  David R. Anderson,et al.  Modeling Survival and Testing Biological Hypotheses Using Marked Animals: A Unified Approach with Case Studies , 1992 .

[40]  J. Gliwicz Seasonal Dispersal in Non-Cyclic Populations of Clethrionomys glareolus and Apodemus flavicollis , 1988 .

[41]  B. Jędrzejewska,et al.  Rodent population dynamics in a primeval deciduous forest (Białowieża National Park) in relation to weather, seed crop, and predation , 1993 .

[42]  M. Begon,et al.  A longitudinal study of an endemic disease in its wildlife reservoir: cowpox and wild rodents , 2000, Epidemiology and Infection.

[43]  R. May,et al.  Population Biology of Infectious Diseases , 1982, Dahlem Workshop Reports.