Identifying Potential Super-Spreaders and Disease Transmission Hotspots Using White-Tailed Deer Scraping Networks.

White-tailed deer (Odocoileus virginianus, WTD) spread communicable diseases such the zoonotic coronavirus SARS-CoV-2, which is a major public health concern, and chronic wasting disease (CWD), a fatal, highly contagious prion disease occurring in cervids. Currently, it is not well understood how WTD are spreading these diseases. In this paper, we speculate that "super-spreaders" mediate disease transmission via direct social interactions and indirectly via body fluids exchanged at scrape sites. Super-spreaders are infected individuals that infect more contacts than other infectious individuals within a population. In this study, we used network analysis from scrape visitation data to identify potential super-spreaders among multiple communities of a rural WTD herd. We combined local network communities to form a large region-wide social network consisting of 96 male WTD. Analysis of WTD bachelor groups and random network modeling demonstrated that scraping networks depict real social networks, allowing detection of direct and indirect contacts, which could spread diseases. Using this regional network, we model three major types of potential super-spreaders of communicable disease: in-degree, out-degree, and betweenness potential super-spreaders. We found out-degree and betweenness potential super-spreaders to be critical for disease transmission across multiple communities. Analysis of age structure revealed that potential super-spreaders were mostly young males, less than 2.5 years of age. We also used social network analysis to measure the outbreak potential across the landscape using a new technique to locate disease transmission hotspots. To model indirect transmission risk, we developed the first scrape-to-scrape network model demonstrating connectivity of scrape sites. Comparing scrape betweenness scores allowed us to locate high-risk transmission crossroads between communities. We also monitored predator activity, hunting activity, and hunter harvests to better understand how predation influences social networks and potential disease transmission. We found that predator activity significantly influenced the age structure of scraping communities. We assessed disease-management strategies by social-network modeling using hunter harvests or removal of potential super-spreaders, which fragmented WTD social networks reducing the potential spread of disease. Overall, this study demonstrates a model capable of predicting potential super-spreaders of diseases, outlines methods to locate transmission hotspots and community crossroads, and provides new insight for disease management and outbreak prevention strategies.

Location of mechanically-evoked referred sensations within the trigeminal region are not altered following a heterotopic painful stimulus.

To investigate whether the location, area and frequency of referred sensations occurring during palpation of the masseter muscle can be influenced by application of a conditioning painful stimulus to the temporalis muscle. Thirty healthy participants were included in this cross-over study, performed in two sessions with > 48 h in between. At each session, palpation of the masseter muscle was performed before and after 0.2 ml of glutamate (1 mol/L) or isotonic saline (control) were injected into the anterior portion of the temporalis muscle. Palpation of the masseter muscle was done using four different forces (0.5 kg, 1 kg, 2 kg and 4 kg). Participants rated the perceived intensity of the palpation and any referred sensations on a 0-50-100 numeric rating scale, the perceived pain intensity following the injections on an electronic visual analogue scale and drew any referred sensations they experienced. No difference in referred sensations location, area and frequency was shown r during palpation either before or after injections (P > 0.05). A moderate correlation was found between perceived sensation scores and referred sensations intensity for the temporalis muscle following glutamate injection (r = 0.407, P < 0.05). Moreover, significantly more participants reported referred sensations for glutamate injections into the temporalis muscle when compared to isotonic saline (P < 0.05). Finally, a significant decrease in the perceived intensity of palpation of the masseter muscle was seen after glutamate injection in the temporalis muscle (P < 0.05). In the current study, location, area and frequency of referred sensations following mechanical stimulation of the masseter muscle were not altered by the application of a painful stimulus to the temporalis muscle. In addition, there seems to be a positive relationship between painful stimuli and referred sensations frequency and intensity elicited from the temporalis muscle.

Analysis of supplemental wildlife feeding in Mississippi and environmental gastrointestinal parasite load.

Wildlife species are host to a variety of gastrointestinal parasites (GIPs). Artificially concentrating animals may increase the risk of disease spread due to increased GIP load and associated environmental load. Supplemental feeding of deer is common among hunters and known to concentrate animals, but there is limited knowledge of how it affects GIP environmental load. GIP load was compared between ecologically-equivalent pairs of sites in Mississippi with and without year-round supplemental feeding (average distance between pairs = 147 m). During May-August in 2019 and 2020, feces from white-tailed deer and raccoons were collected and examined for the presence of nematodes, coccidia, Giardia spp., Cryptosporidium spp., and Baylisascaris procyonis. On average, fed sites had 8 more deer (241% increase) and 2 more raccoon fecal piles (540% increase) than unfed sites. Average parasite loads for individual fecal samples did not differ between fed and unfed sites, but the greater number of deer and raccoon fecal piles at fed sites (p < 0.0001) produced 231% and 308% greater environmental loads of nematodes and coccidia, respectively. Spin feeders, the only feeder type that distributed feed on the ground, had 326% more coccidia in feces on average compared to other feeder types (p < 0.03). These results show that supplemental feeding of white-tailed deer, especially with spin feeders, increases environmental loads of GIP and the potential for transmission of parasitic diseases.

Identifying Aflatoxin Exposure Risk from Supplemental Feeding of Deer.

Aflatoxins, common contaminants of crops and feed, are a health risk to wild and domestic animals. Past research found aflatoxins in feed and feeders provided for wild herbivores valued for recreational hunting (hereafter: game) species but are consumed by various species. We determined the current extent of aflatoxin contamination in wildlife feed and white-tailed deer (Odocoileus virginianus) feeders, examined aflatoxin production in corn piles over time, and quantified nontarget wildlife visitation to deer feeders. We sampled feeders (n=107) in Mississippi, US, bagged/bulk feed sources (n=64) in the southeastern US, as well as corn piles exposed to environmental contamination over 10 d (n=20) during May-January of 2019 and 2020. We found aflatoxins (≥5 parts per billion [ppb]) in feeders during summer (4% prevalence, 58±71 ppb mean±SD) and hunting season (October-January, 6%, 60±1 ppb) and in bagged/bulk feed during hunting season (11%, 13±8 ppb). After 8 d, aflatoxins were detected in all summer corn piles at toxic levels (483-3,475 ppb), although none were detected in hunting season piles after day one. Nontarget wildlife identified at feeders included 16 mammalian and 18 avian species. Numerous wildlife species are at risk for aflatoxin exposure due to supplemental feeding of deer, with the primary risk factor in the southeastern US being summertime environmental exposure of feed to aflatoxin-producing fungi.

Managing plague on prairie dog colonies: insecticides as ectoparasiticides.

Human health practitioners and wildlife biologists use insecticides to manage plague by suppressing fleas (Siphonaptera), but insecticides can also kill other ectoparasites. We investigated effects of deltamethrin and fipronil on ectoparasites from black-tailed prairie dogs (Cynomys ludovicianus, BTPDs). In late July, 2018, we treated three sites with 0.05% deltamethrin dust and 5 sites with host-fed 0.005% fipronil grain. Three non-treated sites functioned as experimental baselines. We collected ectoparasites before treatments (June-July, 2018) and after treatments (August-October, 2018, June-July, 2019). Both deltamethrin and fipronil suppressed fleas for at least 12 months. Deltamethrin had no detectable effect on mites (Arachnida). Fipronil suppressed mites for at least 12 months. Lice (Phthiraptera) were scarce on non-treated sites throughout the study, complicating interpretation. Concentrating on eight sites where all three ectoparasites where found in June-July, 2018 (before treatments), flea intensity was greatest on BTPDs carrying many lice and mites. These three ectoparasites co-occurred at high numbers, which might facilitate plague transmission in some cases. Lethal effects of insecticides on ectoparasite communities are potentially advantageous in the context of plague management.