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USGS2024

Prairie dog responses to vector control and vaccination during an initial Yersinia pestis invasion

We evaluated the invasion of plague bacteria Yersinia pestis into a population of black-tailed prairie dogs (Cynomys ludovicianus; BTPDs) in South Dakota. We aimed to ascertain if Y. pestis invaded slowly or rapidly, and to determine if vector (flea) control or vaccination of BTPDs assisted in increasing survival rates. We sampled BTPDs in 2007 (before Y. pestis documentation), 2008 (year of confirmed invasion), and 2009 (after invasion). We estimated annual BTPD re-encounter rates on three 9-ha plots treated annually with deltamethrin dust for flea control and three 9-ha plots lacking dust. In 2007 and 2008, approximately half the adult BTPDs live-trapped were injected subcutaneously with either an experimental plague vaccine (F1–V fusion protein) or placebo formulation; the remaining individuals were not inoculated. From 2007 to 2009, we sampled 1559 BTPDs on 2542 occasions. During 2007–2008, the prevalence and intensity of fleas on BTPDs were 69–97% lower on the dusted vs. no dust plots. From 2007 to 2008, the annual re-encounter rate of non-inoculated BTPDs was 150% higher on the dusted vs. no dust plots. During the same interval on the dusted plots, the re-encounter rate was 55% higher for vaccinated adult female BTPDs vs. nonvaccinated adult females, but the annual re-encounter rate was 19% lower for vaccinated adult males. By late August 2008, BTPDs were nearly extirpated from the no dust plots. During 2007–2008 and 2008–2009 on the dusted plots, which persisted, the BTPD re-encounter rate was 41% higher for vaccinated vs. non-vaccinated adult females but 35% lower for vaccinated adult males. Yersinia pestis erupted with vigor as it invaded. Flea control enhanced BTPD survival but did not offer full protection. Flea control and F1–V vaccination seemed to have additive, positive effects on adult females. Annual re-encounter rates were reduced for vaccinated adult males; additional experimentation is needed to further evaluate this trend.

International Journal of Parasitology: Parasites a↗

USGS2026

Contrasting haemosporidian infections in two ecologically distinct wading birds from breeding colonies in the southeastern United States

Wading birds may serve as ideal hosts for avian hemoparasites, as they are long-lived, undertake extensive movements, form dense breeding colonies, and inhabit water-associated environments that support vectors. Although previous studies have reported parasite species and prevalence in various wading bird species, little is known about their associations with bird behavior and life stage. To address this gap, we examined haemosporidian infections in two ecologically distinct species, white ibis ( Eudocimus albus ) and tricolored heron ( Egretta tricolor ), to explore differences in life stage and movement that may explain prevalence differences. We combined blood screening for hemoparasites with satellite tracking data describing birds’ movement patterns. We screened 95 white ibis (67 juveniles and 28 adults or subadults) and 69 tricolored herons (45 juveniles and 24 adults). We detected a single Haemoproteus plataleae lineage in both species, with higher infection prevalence in white ibis (42.1 %) than in tricolored herons (14.5 %). Among white ibis, adults showed a higher prevalence (67.9 %) than juveniles (31.3 %), whereas in tricolored herons, adults had a prevalence of 8.3 % and juveniles 17.8 %. Non-breeding season movement data showed that white ibis used both freshwater and saline habitats across the southeastern United States, which may also serve as habitats for vectors. In contrast, tricolored herons remained mainly along coastal areas, using saline habitats in the southeastern United States and wintering sites in Central America, which may be less favorable for vectors. Overall, white ibis may serve as major reservoirs and sources of reinfection for H. plataleae , whereas tricolored herons may facilitate parasite dispersal between breeding colonies along the coasts of the southeastern United States and wintering areas in Central America. This study presents the first direct comparison of hemoparasite infections in two ecologically distinct wading birds and highlights movement data as key to explaining infection differences, providing a baseline for future studies.

Alabama↗

USGS2004

Transmission of Neospora caninum between wild and domestic animals

To determine whether deer can transmit Neospora caninum , brains of naturally infected white-tailed deer ( Odocoileus virginianus ) were fed to 4 dogs; 2 of these dogs shed oocysts. Oocysts from 1 of the dogs were tested by polymerase chain reaction and found to be positive for N. caninum and negative for Hammondia heydorni . The internal transcribed spacer 1 sequence of the new strain (designated NC-deer1) was identical to N. caninum from domestic animals, indicating that N. caninum is transmitted between wild and domestic animals, often enough to prevent divergent evolution of isolated populations of the parasite. NC-deer1 oocysts were administered to a calf that developed a high antibody titer, providing evidence that N. caninum from wildlife can infect cattle. In addition, N. caninum antibody seroprevalence was detected in 64/164 (39%) free-ranging gray wolves ( Canis lupus ), 12/113 (11%) coyotes ( Canis latrans ), 50/193 (26%) white-tailed deer, and 8/61 (13%) moose ( Alces alces ). These data are consistent with a sylvatic transmission cycle of N. caninum between cervids and canids. We speculate that hunting by humans favors the transmission of N. caninum from deer to canids, because deer carcasses are usually eviscerated in the field. Infection of canids in turn increases the risk of transmitting the parasite to domestic livestock.

Illinois, Wisconsin↗

USGS2011

Genetic characterisation of Toxoplasma gondii in wildlife from North America revealed widespread and high prevalence of the fourth clonal type

Little is known of the genetic diversity of Toxoplasma gondii circulating in wildlife. In the present study wild animals, from the USA were examined for T. gondii infection. Tissues of naturally exposed animals were bioassayed in mice for isolation of viable parasites. Viable T. gondii was isolated from 31 animals including, to our knowledge for the first time, from a bald eagle ( Haliaeetus leucocephalus ), five gray wolves ( Canis lupus ), a woodrat ( Neotoma micropus) , and five Arctic foxes (Alopex lagopus) . Additionally, 66 T. gondii isolates obtained previously, but not genetically characterised, were revived in mice. Toxoplasma gondii DNA isolated from these 97 samples (31 + 66) was characterised using 11 PCR-restriction fragment length polymorphism (RFLP) markers (SAG1, 5′- and 3′-SAG2, alt.SAG2, SAG3, BTUB, GRA6, c22–8, c29–2, L358, PK1 and Apico). A total of 95 isolates were successfully genotyped. In addition to clonal Types II, and III, 12 different genotypes were found. These genotype data were combined with 74 T. gondii isolates previously characterised from wildlife from North America and a composite data set of 169 isolates comprised 22 genotypes, including clonal Types II, III and 20 atypical genotypes. Phylogenetic network analysis showed limited diversity with dominance of a recently designated fourth clonal type (Type 12) in North America, followed by the Type II and III lineages. These three major lineages together accounted for 85% of strains in North America. The Type 12 lineage includes previously identified Type A and X strains from sea otters. This study revealed that the Type 12 lineage accounts for 46.7% (79/169) of isolates and is dominant in wildlife of North America. No clonal Type I strain was identified among these wildlife isolates. These results suggest that T. gondii strains in wildlife from North America have limited diversity, with the occurrence of only a few major clonal types.

International Journal for Parasitology↗