Mycoplasma gallisepticum in house finches (Carpodacus mexicanus) and other wild birds associated with poultry production facilities.

Since 1994, an epidemic of conjunctivitis caused by Mycoplasma gallisepticum (MG) has spread throughout the eastern population of house finches (Carpodacus mexicanus). The adaptation of MG to a free-flying avian species presents potential problems for the control of mycoplasmosis in commercial poultry. To evaluate risks associated with this emerging problem, a field survey was conducted to assess prevalence of MG infection in house finches and other passerine birds associated with poultry farms. Between November 1997 and March 1999, 1058 birds were captured by mist net or trap at 17 farms and at 10 feeder stations in northeast Georgia. Birds were bled and screened by serum plate agglutination (SPA) for antibodies to MG. Birds with negative or weak positive SPA results were released at capture sites, and those with strong positive SPA reactions were kept for further evaluation. Necropsies were performed on selected house finches and individuals of 11 other passerine species, and samples were collected for MG testing by culture, polymerase chain reaction (PCR), hemagglutination inhibition, and histopathology. Testing revealed 19.1% of 671 birds caught at farms and 11.6% of 387 birds caught at feeder sites were SPA positive for MG. Three house finches captured on farms were positive for MG by culture and PCR, whereas three from feeder sites were positive only by PCR. No MG isolates were made from tufted titmice (Baeolophus bicolor), but 40% were positive by PCR. Individuals from 10 additional species were SPA positive only. Results suggest that MG persists at low levels in house finches in northeast Georgia and that tufted titmice may be nonclinical carriers of MG or a related mycoplasma. Positive SPA reactions in other species may be caused by nonspecific reactions or contact exposure. Current biosecurity recommendations should be sufficient to minimize risks of transmission between wild and domestic birds.

Experimental and field studies of Escherichia coli O157:H7 in white-tailed deer.

Studies were conducted to evaluate fecal shedding of Escherichia coli O157:H7 in a small group of inoculated deer, determine the prevalence of the bacterium in free-ranging white-tailed deer, and elucidate relationships between E. coli O157:H7 in wild deer and domestic cattle at the same site. Six young, white-tailed deer were orally administered 10(8) CFU of E. coli O157:H7. Inoculated deer were shedding E. coli O157:H7 by 1 day postinoculation (DPI) and continued to shed decreasing numbers of the bacteria throughout the 26-day trial. Horizontal transmission to an uninoculated deer was demonstrated. Although E. coli O157:H7 bacteria were recovered from the gastrointestinal tracts of deer necropsied from 4 to 26 DPI, attaching and effacing lesions were not apparent in any deer. Results are similar to those of inoculation studies in calves and sheep. In field studies, E. coli O157 was not detected in 310 fresh deer fecal samples collected from the ground. It was detected in feces, but not in meat, from 3 of 469 free-ranging deer in 1997. In 1998, E. coli O157 was not detected in 140 deer at the single positive site found in 1997; however, it was recovered from 13 of 305 dairy and beef cattle at the same location. Isolates of E. coli O157:H7 from deer and cattle at this site differed with respect to pulsed-field gel electrophoresis patterns and genes encoding Shiga toxins. The low overall prevalence of E. coli O157:H7 and the identification of only one site with positive deer suggest that wild deer are not a major reservoir of E. coli O157:H7 in the southeastern United States. However, there may be individual locations where deer sporadically harbor the bacterium, and venison should be handled with the same precautions recommended for beef, pork, and poultry.

A modified bait for oral delivery of biological agents to raccoons and feral swine.

A field study was conducted on Ossabaw Island (Georgia, USA) in March 1994 to evaluate four different types of bait for delivering orally effective biological agents to raccoons (Procyon lotor) and feral swine (Sus scrofa). A deep-fried corndog batter bait, which was previously shown to be ingested by both captive and free-ranging raccoons, and a polymer fishmeal bait which had been shown effective for both raccoons and feral swine were compared with a grain-based dog food meal polymer bait topically coated with corn oil and cornmeal or with fish oil and fishmeal. Tracking stations were used to determine the number of each bait type visited and removed by animals visiting stations. We found no significant differences in the numbers of different baits removed by either species. These data support the results of earlier studies which also indicated that an inexpensive grain-based matrix bait surface-coated with attractive flavors can be used to deliver oral biologics to problem species.

Spontaneous cryptosporidiosis in captive white-tailed deer (Odocoileus virginianus).

In August 1994, cryptosporidiosis was diagnosed in a diarrheic fawn from a captive white-tailed deer (Odocoileus virginianus) herd maintained for research purposes at The University of Georgia's Warnell School of Forest Resources in Athens, Georgia (USA). From June through August 1995, 11 captive female white-tailed deer were housed in individual barn stalls where they gave birth to 18 fawns. Feces collected at 2 or 3 day intervals from the 18 neonatal fawns for at least 21 days and from 11 adult females once from 1 to 30 days before fawns were born and on three to 12 occasions after their birth were examined for oocysts of Cryptosporidium spp. Feces from all animals appeared normal throughout the period of examination. Oocysts morphologically indistinguishable from those of Cryptosporidium parvum were detected intermittently in the feces of one adult female from 1 to 25 days after parturition and in the feces of her fawn from 11 to 22 days of age. Oocysts also were detected intermittently in feces from twin fawns from 9 to 20 days of age, but not from their mother. Oocysts from deer were infectious for neonatal mice as determined histologically, and for calves as determined by clinical signs and excretion of oocysts.

Population dynamics of Lutzomyia shannoni (Diptera: Psychodidae) in relation to the epizootiology of vesicular stomatitis virus on Ossabaw Island, Georgia.

Population dynamics of Lutzomyia shannoni Dyar were studied on Ossabaw Island, GA, to define further the role of this species in the epizootiology of the New Jersey serotype of vesicular stomatitis (VSNJ) virus. Bimonthly collections of sand flies egressing from hollow trees from April to November 1991 indicated that there were three generations of sand flies. Data from light trap collections from 1986 through 1989 indicated that similar seasonal cycles occurred during previous years. At this site, we hypothesize that L. shannoni undergoes facultative diapause. Two isolates of VSNJ virus were obtained from female sand flies collected in May and June of 1991. We believe that the virus overwinters in immature L. shannoni and that transovarially infected sand flies emerging each spring initiate a summer amplification cycle in swine on Ossabaw Island.

Hosts of Lutzomyia shannoni (Diptera: Psychodidae) in relation to vesicular stomatitis virus on Ossabaw Island, Georgia, U.S.A.

Hosts of Lutzomyia shannoni Dyar, a suspected biological vector of the New Jersey serotype of vesicular stomatitis (VSNJ) virus, were determined using an indirect enzyme-linked immunosorbent assay (ELISA) of 333 blood-fed female sandflies collected from their diurnal resting shelters on Ossabaw Island, Georgia, U.S.A. Sandflies had fed primarily on white-tailed deer (Odocoileus virginianus) (81%) and to a lesser extent on feral swine (Sus scrofa) (16%), two species of host infected annually with VSNJ. Other hosts were raccoons (Procyon lotor) and horses (Equus caballus) or donkeys (E. asinus), with only two (< 1%) mixed bloodmeals from deer/raccoon and deer/swine. A larger proportion of feedings on feral swine was detected in maritime live oak forests than in mixed hardwood forests. These findings are consistent with the hypothesis that L.shannoni is a primary vector of VSNJ virus on Ossabaw Island.

Wildlife as hosts for ticks (Acari) in Antigua, West Indies.

A survey was conducted to determine the status of wild mammals and birds as hosts for Amblyomma variegatum (F.) and other tick species in Antigua. Surveys of wild mammals and birds were conducted periodically from September 1988 through May 1991. Wild mammals surveyed included the small Indian mongoose (Herpestes auropunctatus Hodgson), Norway rat (Rattus norvegicus Berkenhout), and house mouse (Mus musculus L.), but only mongooses were surveyed intensively. Larvae and nymphs of A. variegatum, larvae of Boophilus microplus (Canestrini), and larvae of Ornithodoros puertoricensis (Fox) were recovered. The mean prevalences of infestation of mongooses by A. variegatum larvae and nymphs were 4.7 and 1.3%, respectively; maximums were 16.1 and 5.0%, respectively. The mean prevalence of infestation of mongooses by B. microplus was 3.2%. O. puertoricensis is reported from Antigua for the first time. The mean prevalence of infestation of mongooses by O. puertoricensis larvae was 41.2%, but seasonal prevalences ranged from 27.8 to 55.0%. Of 610 birds representing 16 species, three Carib grackles (Quiscalus lugubris Swainson) were each infested with one larva of A. variegatum.

Feral swine as a potential amplifying host for vesicular stomatitis virus New Jersey serotype on Ossabaw Island, Georgia.

Sentinel feral swine (Sus scrofa) on Ossabaw Island, Georgia (USA), were serologically monitored for antibodies to vesicular stomatitis New Jersey serotype (VSNJ) virus from 17 April to 27 August 1990. Seroconversions to VSNJ virus were detected in 24% of swine island-wide. Differences in the incidence of seroconversion were detected between swine sampled in the Pleistocene and Holocene formations of the island suggesting that the presence of virus is forest type dependent. Based on the consistency in onset and spatial distribution of seroconversions with data from 1981 to 1985, this is a very stable host-parasite system. Sequential virus isolation attempts from nasal swabs, tonsil swabs, and blood were made on a subsample of 54 sentinel swine from 9 May to 4 July 1990. The VSNJ virus was isolated from five swine from 16 May to 20 June. Vesicular lesions were detected on only two of these animals. Although infections in these feral swine were short-lived (< 7 days) and were followed by a strong neutralizing antibody response, VSNJ virus was detected in a single group of swine for a period exceeding 1 month. From these data, it appears that feral swine could provide a source of virus to feeding arthropods for extended periods of time. The failure to detect a viremia in these animals, however, indicates that a source other than blood may be required for transmission to occur.

Effect of forest type on the distribution of Lutzomyia shannoni (Diptera: Psychodidae) and vesicular stomatitis virus on Ossabaw Island, Georgia.

We studied the effects of three forest types on multiple factors that are believed to influence the transmission of the New Jersey serotype of vesicular stomatitis (VSNJ) virus on Ossabaw Island, GA. These factors included availability of tree hole diurnal resting habitat for the presumed sand fly vector, Lutzomyia shannoni Dyar; relative abundance of L. shannoni; prevalence of VSNJ virus infection in sand flies; and prevalence of VSNJ virus antibodies in wild swine. Tree hole availability, sand fly abundance, and antibody prevalence in swine were significantly greater in maritime live oak forest than in other forest types. A single isolate of VSNJ virus was obtained from sand flies collected in maritime live oak forest. These data indicate that the relative abundance of adult L. shannoni is influenced significantly by the availability of tree holes and that VSNJ virus infection in wild swine is linked to forest type and is greatest in areas capable of supporting abundant populations of L. shannoni.