Structural studies of hemoglobin chains from Virginia white-tailed deer

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1. Structural and quantitative studies have been made on hemoglobins of Virginia white-tailed deer, Odocoilus virginianus, with emphasis on the α chains. Hemoglobins with ^Iα chains have been termed “major” and those with ^IIα chains “minor.” Previous studies of over 400 deer have shown that all animals produce major components, but many do not have the minor components. These observations as well as data showing that the minor component can be present in 15% or 30% proportions have been considered to indicate the presence of two nonallelic Hb_α structural loci.     

Immunologic and molecular identification of Babesia bovis and Babesia bigemina in free-ranging white-tailed deer in northern Mexico

The suitability of white-tailed deer (Odocoileus virginianus) as hosts for the cattle ticks Rhipicephalus (Boophilus) microplus and Rhipicephalus (Boophilus) annulatus, has been well documented. These ticks have a wide host range, and both transmit Babesia bovis and Babesia bigemina, the agents responsible for bovine babesiosis. Although this disease and its vectors have been eradicated from the United States and some states in northern Mexico, it still is a problem in other Mexican states. It is not known if wild cervids like white-tailed deer can act as reservoirs for bovine babesiosis. The purpose of this study was to determine if B. bovis and B. bigemina or antibodies against them occur in white-tailed deer in the states of Nuevo Leon and Tamaulipas, Mexico. Twenty blood samples from white-tailed deer from two ranches were collected and tested with a nested polymerase chain reaction (nested PCR) and indirect immunofluorescence antibody test (IFAT) for B. bovis and B. bigemina. Eleven samples were positive for B. bigemina and four for B. bovis by nested PCR; amplicon sequences were identical to those reported in GenBank for B. bovis (Rap 1) and B. bigemina. Results of the IFA test showed the presence of specific antibodies in serum samples. This is the first report of the presence of B. bovis and B. bigemina in white-tailed deer using these techniques and underscores the importance of cervids as possible reservoirs for bovine babesiosis.     

Prevalence of antibody titers to Leptospira spp. in Minnesota white-tailed deer.

Serum samples (n = 204) from 124 white-tailed deer (Odocoileus virginianus) in northeastern Minnesota (USA) were collected from 1984 through 1989 and tested for antibodies to six serovars of Leptospira interrogans (bratislava, canicola, grippotyphosa, hardjo, icterohemorrhagiae, and pomona) using a microtiter agglutination test. Eighty-eight (43%) sera were positive at greater than or equal to 1:100 for antibodies against serovars pomona and/or bratislava; none was positive for any of the other four serovars. None of the 31 sera collected in 1984-85 was positive, whereas all 54 sera collected from 1986 through 1988 had titers of greater than or equal to 1:100. During 1989, only 34 (29%) of 119 sera had titers of greater than or equal to 1:100. Based on these results, we believe there to be wide variability in exposure of Minnesota deer to Leptospira interrogans.     

E. coli O157 and Salmonella spp. in white-tailed deer and livestock

Escherichia coli O157 and Salmonella spp. are among the leading causes of food-borne illness in the United Sates and bacteria have been isolated from numerous ruminant animal sources. The objective of this study was to assess the incidence of E. coli O157 and Salmonella spp. in white-tailed deer (Odocoileus virginianus) and livestock simultaneously grazing the same rangeland. Escherichia coli O157 was found in 1.25% of cattle, 1.22% of sheep, and 5.00% of water all from samples taken in September; however, no E. coli O157 was found in other sampled months or any species. Salmonella spp. were found in the highest quantities in deer and sheep, 7.69% and 7.32%, respectively. Salmonella spp. were also found in sampled water troughs, goats, and cattle (5.00%, 3.70%, and 1.25%, respectively). Further research examining pathogen distribution is needed to determine if white-tailed deer are a natural reservoir for these bacteria.     

Prevalence of Borrelia burgdorferi and Babesia microti in mice on islands inhabited by white-tailed deer.

Borrelia burgdorferi and Babesia microti were isolated from 35 of 51 white-footed mice (Peromyscus leucopus) and meadow voles (Microtus pennsylvanicus) captured on two Narragansett Bay, R.I., islands inhabited by deer, the principal host for the adult stages of the vector tick, Ixodes dammini. Immature ticks parasitized mice from both islands. From 105 mice captured on four other islands not inhabited by deer neither pathogen was isolated, nor were I. dammini found.     

Parasites, diseases, and health status of sympatric populations of sika deer and white-tailed deer in Maryland and Virginia

In July 1981, investigations on parasites, diseases, and herd health status were conducted on sympatric populations of sika deer (Cervus nippon) and white-tailed deer (Odocoileus virginianus) from Blackwater National Wildlife Refuge (Maryland) and Chincoteague National Wildlife Refuge (Virginia) on the Delmarva Peninsula. Five adult deer of each species were collected from each location and subjected to thorough necropsy examinations and laboratory tests. White-tailed deer at both locations harbored protozoan, helminth, and arthropod parasites typically associated with this species throughout the southeastern United States. In contrast, sika deer at both locations harbored only light burdens of ticks, chiggers, and sarcocysts. Serologic tests for antibodies to seven infectious disease agents revealed evidence of exposure to bovine virus diarrhea (BVD) virus, infectious bovine rhinotracheitis virus, and parainfluenza3 virus in white-tailed deer, but only BVD virus in sika deer. At both locations the general health status of sika deer was superior to that of white-tailed deer.     

Prevalence and distribution of Sarcocystis spp. among white-tailed deer of the southeastern United States

Sarcocysts were found by light microscopic examination of muscle in 199 (51%) of 390 white-tailed deer (Odocoileus virginianus) from the southeastern United States. Sarcocystis infections were detected more frequently in histologic sections of tongue (45%) than of heart (9%). Sarcocysts were significantly more prevalent in adult deer (54%) than fawns (26%) (P less than .01). Statistically significant differences in prevalence were not found in deer from different physiographic provinces or between sexes. Artificial digestion was more sensitive in detecting Sarcocystis infections than examination of histologic sections when both techniques were used to examine tongues of 35 deer. Three different size sporocysts, possibly representing at least two species of Sarcocystis, were recovered during feeding trials. Seven dogs (Canis familiaris) shed sporocysts 9 to 12 days after eating infected venison. Sporocysts measured 13.4-16.8 x 9.0-12.3 micrometers with an average measurement of 15.2 x 10.9 micrometers (N = 195). One of three cats (Felis catus) and one of two red foxes (Vulpes vulpes) first shed sporocysts of Sarcocystis 10 days after eating infected venison. Sporocysts from the cat measured 11.2-13.4 x 6.72-8.96 micrometers (avg 12.0 x 8.7 micrometers, N = 18), and those from the fox measured 11.2-15.7 x 9.0-11.2 micrometers (avg 13.6 x 10.2 micrometers, N = 7).     

Antibody prevalence and molecular identification of Babesia spp. In roe deer in France

In a region-wide serologic study carried out in 2004 on free-ranging hunted roe deer in various landscapes, we found that 58% of the animals (237 out of 406) were antibody positive for Babesia divergens antigen. Serologic and infection status was also analyzed for 327 roe deer live-trapped in two fenced forest areas over 5 yr (2004-08). For two consecutive years during this period, 92 and 94% of the deer in these closed populations were antibody-positive for B. divergens. Babesia spp. were isolated in autologous red blood cell culture for 131 of the trapped animals (40%). Molecular typing was done on 76 isolates with polymerase chain reaction (PCR)-restriction fragment length polymorphism methods targeted at the 18S ribosomal subunit gene (18 isolates) and the Bd37 gene coding for a merozo?te surface antigen implicated in a protective response (60 isolates). Results indicated continuous cocirculation of B. capreoli and B. venatorum in both forests and possible coinfection of animals with both species. No infection with B. divergens was detected. Fifteen isolates were confirmed to be B. capreoli by sequencing part of the 18S rRNA gene. Using PCR detection of the Bd37 gene, all nine isolates of B. venatorum in this study were negative, whereas the 15 confirmed and 50 putative B. capreoli isolates showed very variable restriction profiles, distinct from those known for Bd37 in B. divergens. Two isolates showed conflicting results, suggestive of mixed infection.     

Prevalence of Borrelia burgdorferi and Babesia microti in mice on islands inhabited by white-tailed deer

Borrelia burgdorferi and Babesia microti were isolated from 35 of 51 white-footed mice (Peromyscus leucopus) and meadow voles (Microtus pennsylvanicus) captured on two Narragansett Bay, R.I., islands inhabited by deer, the principal host for the adult stages of the vector tick, Ixodes dammini. Immature ticks parasitized mice from both islands. From 105 mice captured on four other islands not inhabited by deer neither pathogen was isolated, nor were I. dammini found.     

Morphology of typanosomes from white-tailed deer and wapiti in Michigan.

Trypanosomes were isolated from a wapiti (Cervus canadensis) and 72 white-tailed deer (Odocoileus virginianus) from several locations in Michigan. Although significantly fewer fawns were infected, there were no significant differences in rate of infection between sexes or among geographic areas. From appearance of the trypomastigote, the trypanosome from white-tailed deer belongs in the genus Trypanosoma and the subgenus Megatrypanum. It was morphometrically similar to the common trypanosome of cattle, Trypanosoma theileri.     

Elaeophorosis in sika deer in Texas.

Elaeophora schneideri was found in sika deer (Cervus nippon) from several areas in Texas. The parasite produced unilateral tumorous masses on the head and/or feet. This is the first report of E. schneideri in Texas.     

Blood characteristics of white-tailed deer from northeastern Kansas

Blood samples were collected from 118 white-tailed deer (Odocoileus virginianus) shot on the Fort Riley Military Installation in northeastern Kansas. Values for these deer for hematocrit, glucose, alkaline phosphatase, uric acid, total protein, albumin, and calcium were within the ranges reported in previous studies for undrugged white-tailed deer. Abnormally high concentrations of serum glutamic oxaloacetate transaminase (SGOT) and lactic dehydrogenase (LDH) were attributed to general trauma and tissue damage caused by shooting the deer. Fawns had higher concentrations of alkaline phosphatase than adults and had lower concentrations in winter than at other times of the year. Serum urea nitrogen (SUN) concentrations fluctuated seasonally. Elevated concentrations of SUN in adult males killed in December were attributed to an increased catabolism of muscle protein caused by low dietary intake and high energy requirements during the rut. Cholesterol concentrations varied seasonally without regard to age or sex.     

Monthly incidence of Theileria cervi and seroconversion to Babesia odocoilei in white-tailed deer (Odocoileus virginianus) in Texas.

Monthly monitoring of fawns collected from an area in Texas endemic for Theileria cervi and Babesia odocoilei showed that transmission of T. cervi occurred during July and August, a time period consistent with the occurrence of Amblyomma americanum. Seroconversion to B. odocoilei occurred during October to December and possibly continued through January and February. The time of seroconversion was more suggestive of transmission of B. odocoilei by Ixodes scapularis than by Amblyomma americanum.     

Borrelia sp. in ticks recovered from white-tailed deer in Alabama.

Six hundred sixty-five hunter-killed white-tailed deer (Odocoileus virginianus) from 18 counties in Alabama (USA) were examined for ticks. Most of the collections were made at state-operated wildlife management areas. Four species of ticks (n = 4,527) were recovered: the lone star tick Amblyomma americanum (n = 482); the Gulf Coast tick A. maculatum (n = 11); the winter tick Dermacentor albipictus (n = 1,242); and the black-legged tick Ixodes scapularis (n = 2,792). Fifty-six percent of the ticks (n = 2,555) were examined for Borrelia sp. spirochetes using an immunofluorescent, polyclonal antibody assay. Spirochetes were detected in I. scapularis (five females, seven males) from Barbour, Butler, Coosa, and Lee counties and A. americanum (four males, four nymphs) from Hale, Lee, and Wilcox counties. Area-specific prevalences in ticks were as high as 3.3% for I. scapularis and 3.8% for A. americanum.     

A search for Parelaphostrongylus andersoni in white-tailed deer from Maine.

Longissimus dorsi muscles from 42 white-tailed deer (Odocoileus virginianus) from Maine (USA) were examined for the Parelaphostrongylus andersoni. No adult nematodes were found. Prevalence based on the Poisson approximation of a binomial distribution could have been between 0 and 9% (95% C.I.). However, based on prevalence documented elsewhere (10 to 18%), it is unlikely that P. andersoni occurs in white-tailed deer in central Maine.     

Leukoencephalomalacia in a white-tailed deer from North Carolina

Leukoencephalomalacia similar to equine leukoencephalomalacia occurred in a white-tailed deer (Odocoileus virginianus) from North Carolina. The deer was recumbent and stuporous when presented for examination. It was believed that the disease resulted from ingestion of moldy field corn, infected with Fusarium moniliforme.