
Photo by Courtney Celley, USFWS.

Photo by Courtney Celley, USFWS.
Every year hunters in Illinois head into the woods to continue a tradition of hunting deer passed down through generations. They prepare through education, obtain permits, and follow mandatory tagging and processing rules (Hunt Illinois). And every year they may also ask themselves: Is our herd safe from chronic wasting disease (CWD)? Managing the threat of a disease such as CWD requires a massive effort, but wildlife officials aren’t just guessing how many deer to sample. By using computer models to analyze field data, scientists determine exactly where, when, and how much we need to test to accurately understand the disease.
For a disease that affects wildlife, testing only captive animals does not provide the answers needed to understand disease occurrence and spread dynamics in wild populations. This is where computer models are handy: they let us create virtual scenarios that otherwise would be impossible to evaluate. For wildlife disease surveillance, computer models are particularly useful because wildlife populations are difficult to observe, sampling is often opportunistic, animals move across large areas, and only a subset of infected animals are detected. Therefore, computer models help researchers bypass these limitations, reduce uncertainty in decision making, and answer questions that would otherwise be impossible due to the difficulties mentioned above and the costs of testing wildlife directly. It is important to note, however, that a model is an imperfect approximation of reality that provides estimates with a certain level of error.

CWD was first detected in northern Illinois 24 years ago. Since then, diagnostic testing as part of an overall surveillance effort has been essential to understanding and managing the disease in Illinois. The Illinois Department of Natural Resources (IDNR) collects retropharyngeal lymph nodes (located between the throat and spine), which are first tested by enzyme-linked immunosorbent assay (ELISA). Lymph nodes designated as “initial reactors” (potential positives) are then tested with immunohistochemistry (IHC) to confirm a positive CWD result. IDNR then uses these data to inform disease management decisions, and researchers use them to learn more about CWD and its impact on the deer herd.
Surveillance for CWD through diagnostic testing is vital, but how many deer need to be tested? The best answer is “as many as possible.” The more data we have, the clearer the picture is, so there is no such thing as “too many” tests. However the opposite is not true: having “too few” tests weakens our ability to accurately determine what is happening on the ground (the true levels of disease), which limits the knowledge required to determine disease risk and management opportunities.
So, how do we know how many deer to test to get a sufficiently accurate picture? To find the answer to testing requirements, our study published in the journal Prion titled “Monte Carlo simulation of testing requirements for chronic wasting disease (CWD) surveillance via hunter-harvest in Illinois, USA,” used mathematical models representing herds of deer to calculate apparent prevalence for various CWD surveillance levels (Mori et al., 2026). Apparent prevalence (the percentage of animals that test positive for a disease using a particular test) is an estimate of the true prevalence calculated from a sample of the total population, with the true prevalence being the percentage of animals that are actually infected with CWD in the population. In our simulation this calculation is repeated over and over until a distribution of potential outcomes is generated for analysis. Figure 1 below visually describes the Monte Carlo simulation for Illinois’ CWD surveillance.

Our simulation of Illinois’ CWD surveillance examined true prevalences from 0.5-20 percent in increments of 0.5 percent (0.5, 1…19.5, 20 percent) and deer harvest values from 100-5,000 in increments of 100 (100, 200…4,900, 5,000) (Mori et al., 2026). The number of deer tested from those harvested ranged from 10 to 5,000 in increments of 10 (10, 20…4,990, 5,000), with the maximum number of tests in a single simulation run set equal to the size of the harvested group, with all values based on past CWD surveillance data. The size of the total population being sampled was set at four times the number of deer harvested (Nixon et al., 1991; Brinkman et al., 2004), making the results of this simulation applicable to any herd with as many as 20,000 animals.

Our computer simulations help us determine how many deer to test each year to obtain an accurate estimate of CWD in a population. In this study, we define accuracy as calculating an apparent prevalence that is within ±2 percent of the true prevalence with 95 percent confidence. We developed an easy-to-use table that wildlife managers can use to plan the testing of deer for CWD and make the most of limited resources. Table 1 shows a subset of the resulting guidelines, with the full table available at https://databank.illinois.edu/datasets/IDB-5785068.
Table 1 summarizes our simulation results in an easy-to-use format. The table can be used both to set future management goals and to evaluate past surveillance efforts. For example, to identify a true prevalence of 1 percent with accuracy within ±2 percent (between 0.01 percent and 3 percent), we should test at least 330 deer. Similarly, to identify, with the same accuracy, whether the true prevalence in an area is 20 percent, we should test at least 2,760 deer. However, if we test just 1,300 deer, this can only reveal that the true prevalence is at least 12.5 percent. The table also shows that if the true prevalence in an area is ≤ 1.5 percent and we want to accurately estimate it, we will need to test more than 170 deer.
With this in mind, IDNR can use the table to see whether the sample size collected in an area was sufficient for the calculated apparent prevalence to accurately reflect the true prevalence present in that area, or to set the target number of deer to be tested according to the desired true prevalence that they want to identify. As always, more is better, but the numbers in Table 1 provide a scientifically valid and cost-effective testing quota to aim for, generated in a way that reflects the CWD surveillance process and helps integrate management with hunter harvest testing needs. Together, we can take those numbers and develop efforts to combat CWD.
Happy hunting!
Dr. Jameson Mori is a research scientist with the Mateus & Novakofski Chronic Wasting Disease Collaborative Labs. Their research focuses on using data and modeling to determine the impact of chronic wasting disease on white-tailed deer in Illinois and the effectiveness of management efforts to control the disease. They earned their B.S. at the University of Massachusetts Dartmouth and Ph.D. from the University of Illinois Urbana-Champaign.
Dr. Nelda Rivera's research focuses on the ecology and evolution of new and re-emerging infectious diseases and the epidemiology of infectious diseases, disease surveillance, and reservoir hosts’ determination. She is a member of the Wildlife Veterinary Epidemiology Laboratory and the Novakofski & Mateus Chronic Wasting Disease Collaborative Labs. She earned her M.S. at the University of Illinois at Urbana-Champaign and D.V.M at the University of Panamá, Republic of Panamá.
Dr. Jan Novakofski studies prion diseases or infectious agents composed entirely of protein in animals such as “mad cow disease” and scrapie. His efforts are contributing to better understanding the genetics and transmission of these types of diseases to protect the health of animals and humans. He earned his B.S., M.S. and PhD from the University of Wisconsin, Madison.
Dr. Nohra Mateus-Pinilla is a veterinary Epidemiologist working in wildlife diseases, conservation, and zoonoses. She studies Chronic Wasting Disease (CWD) transmission and control strategies to protect the free-ranging deer herd’s health. Dr. Mateus works at the Illinois Natural History Survey- University of Illinois. She earned her M.S. and Ph.D. from the University of Illinois Urbana-Champaign.
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