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Whole-genome sequencing has provided fundamental insights into infectious disease epidemiology, but has rarely been used for examining transmission dynamics of a bacterial pathogen in wildlife. In the Greater Yellowstone Ecosystem (GYE), outbreaks of brucellosis have increased in cattle along with rising seroprevalence in elk. Here we use a genomic approach to examine Brucella abortus evolution, cross-species transmission and spatial spread in the GYE. We find that brucellosis was introduced into wildlife in this region at least five times. The diffusion rate varies among Brucella lineages (∼3 to 8 km per year) and over time. We also estimate 12 host transitions from bison to elk, and 5 from elk to bison. Our results support the notion that free-ranging elk are currently a self-sustaining brucellosis reservoir and the source of livestock infections, and that control measures in bison are unlikely to affect the dynamics of unrelated strains circulating in nearby elk populations.

The seasonal availability of food resources is an important factor shaping the life-history strategies of organisms. During times of nutritional restriction, physiological trade-offs can induce periods of immune suppression, thereby increasing susceptibility to infectious disease. Our goal was to provide a conceptual framework describing how the endemic level bovine brucellosis ( Brucella abortus) may be maintained in Yellowstone bison based on the seasonality of food resources and the life-history strategies of the host and pathogen. Our analysis was based on active B. abortus infection (measured via bacterial culture), nutritional indicators (measured as metabolites and hormones in plasma), and carcass measurements of 402 slaughtered bison. Data from Yellowstone bison were used to investigate (1) whether seasonal changes in diet quality affect nutritional condition and coincide with the reproductive needs of female bison; (2) whether active B. abortus infection and infection intensities vary with host nutrition and nutritional condition; and (3) the evidence for seasonal changes in immune responses, which may offer protection against B. abortus, in relation to nutritional condition. Female bison experienced a decline in nutritional condition during winter as reproductive demands of late gestation increased while forage quality and availability declined. Active B. abortus infection was negatively associated with bison age and nutritional condition, with the intensity of infection negatively associated with indicators of nutrition (e.g., dietary protein and energy) and body weight. Data suggest that protective cell-mediated immune responses may be reduced during the B. abortus transmission period, which coincides with nutritional insufficiencies and elevated reproductive demands during spring. Our results illustrate how seasonal food restriction can drive physiological trade-offs that suppress immune function and create infection and transmission opportunities for pathogens. [ABSTRACT FROM AUTHOR]

Yellowstone bison Bison bison are chronically infected with brucellosis (caused by the bacterium Brucella abortus), which raises concerns about possible transmission to cattle when they migrate to winter ranges outside the Yellowstone National Park. We monitored bison from April to mid-June during 2004-2007 to estimate the timing and location of parturition events that may shed tissues infected by B. abortus. Observed abortions (N¼29) occurred from January through 19 May, while peak calving (80% of births) occurred from 25 April to 26 May, and calving was finished by 5 June. Observed parturition events (N¼115) occurred in the Park and on the Horse Butte peninsula in Montana, USA, where cattle were not present at any time of the year. Allowing bison to occupy public lands outside the Park where cattle are never present (e.g. Horse Butte peninsula) until most bison calving is completed (late May or early June) is not expected to significantly increase the risk of brucellosis transmission from bison to cattle because: 1) bison parturition is essentially completed weeks before cattle occupy nearby ranges, 2) female bison meticulously consume birthing tissues, 3) ultraviolet light and heat degrade B. abortus on tissues, vegetation and soil, 4) scavengers remove fetuses and remaining birth tissues and 5) management maintains separation between bison and cattle on nearby ranges. Allowing bison to occupy public lands outside the Park through their calving season will help conserve bison migratory behaviour and reduce stress on pregnant females and their newborn calves, while still minimizing the risk of brucellosis transmission to cattle. [ABSTRACT FROM AUTHOR]