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Temporal variation in parasite infestation of a host individual: does a parasite-free host remain uninfested permanently?

Host individuals not infested by parasites at a given time are either permanently free from parasites or could be infested at other times. We studied temporal variation in the presence or absence of fleas (Siphonaptera) on individual rodents of two species (Gerbillus dasyurus and Acomys cahirinus) and questioned if and how an individual rodent can change its infestation status temporally. Change in infestation status by fleas over time was found in 45.5% of G. dasyurus and 35.9% of A. cahirinus. In both host species, the proportion of individuals that either changed or did not change their infestation status did not differ from the null expectation of 1:1. No difference between the proportions of infested at two consecutive captures and uninfested at two consecutive captures animals was found in A. cahirinus, whereas the proportion of G. dasyurus infested by fleas at two consecutive captures was significantly greater than that of uninfested at two consecutive captures individuals. In both host species, similar proportions of individuals changed their infestation status either from being infested to being uninfested or vice versa. Among individuals of both species that were initially infested by fleas, similar proportions changed and did not change their subsequent infestation status. The same was true for the uninfested at the first capture A. cahirinus. However, among initially uninfested G. dasyurus, the proportion of individuals that remained uninfested was significantly greater than that of the individuals newly infested by fleas. In A. cahirinus, the probability to change the infestation status did not depend on the initial status of an individual. In G. dasyurus, the probability of the initially uninfested individuals to be subsequently found still uninfested was higher than to be subsequently found harboring fleas, whereas initially infested individuals could be subsequently found either still infested or flea-free with equal probability.

Animals↗

Host association, on-host longevity and egg production of Ctenocephalides felis felis.

Host association, on-host longevity and egg production of Ctenocephalides felis felis (Bouché) were evaluated using fleas from a commercial laboratory colony and first generation, laboratory-reared, native Indiana fleas. Fleas were placed on cats that were declawed, fitted with Elizabethan collars and housed in specially designed metabolic cages. An average of 85% of the female and 58% of the male fleas stayed continuously on the cats for at least 50 days, indicating that the cat flea is a permanent ectoparasite. The maximum longevity of the cat flea was not determined, but it was shown that it can survive and reproduce on the cat for at least 113 days. A female cat flea may produce up to 1745 eggs during a 50-day period.

Animals↗

Activity of a deltamethrin shampoo against Ctenocephalides felis and Rhipicephalus sanguineus in dogs.

A controlled clinical trial was undertaken to assess the efficacy of an application of a 0.07% deltamethrin shampoo against fleas and ticks in dogs. Twenty beagles, housed in separate cages, were randomly allocated into two groups of 10. The dogs were infested with 50 Ctenocephalides felis and 50 Rhipicephalus sanguineus each, and parasites were counted 24 h (fleas) and 72 h (ticks) later (Day 0). Dogs, when state, were then treated with 25 ml of a shampoo containing 0.07% deltamethrin (Group 1). Dogs in Group 2 were the controls. Fleas and ticks were counted 24 h (Day 1) and 48 h (Day 2) after the shampoo was applied, and the parasites were then removed. All the dogs were reinfested with fleas and ticks on Days 2, 7, 9, 14, 16 and 20. Parasites were counted 24 and 48 h after each reinfestation. Effectiveness against fleas was calculated 24 h after infestation, and against ticks 48 h after infestation. This study showed that the application of 25 ml of shampoo containing 0.07% deltamethrin to beagle dogs weighing between 10.2 and 12 kg was very well tolerated. It controlled the parasites present on the animals at the time of application: with an efficacy of 100% against fleas 24 h after treatment and an efficacy of 95% against ticks 48 h after treatment. The treatment protected against flea reinfestations with an efficacy of 100% during the first week, >98% in the second week and >95% in the third week. It also gave >99% protection against tick reinfestations in the first week and >96% in the second week.

Animals↗

Antifeeding effect of several insecticidal formulations against Ctenocephalides felis on cats.

Evaluation of insecticidal activity of flea products is generally based on counting live fleas in the animal's coat 24 and 48 hours following artificial infestation. This approach, however, does not allow to specify whether the fleas have had the opportunity to bite and take a bloodmeal prior to their death. To address this question, 30 cats were alloted to six groups of five animals. Each cat was housed in a separate cage. At Day 0, each group of cats received a single treatment as follows: Group 1: spot-on application of imidacloprid: cats < 4 kg: 40 mg/cat, cats > or = 4 kg: 80 mg/cat (Advantage). Group 2: spot-on application of fipronil: 50 mg/cat (Frontline spot-on). Group 3: spray application of fipronil: 7.5 mg/kg b.w. (Frontline spray). Group 4: foam application of permethrin 40/60: 50 mg/kg b.w. (Defencat). Group 5: aerosol spray application of dichlorvos + fenitrothion: one second/kg b.w. (NuvanTop). Group 6: control group: cats were left untreated. One hour after treatment, each cat was infested with 50 unengorged young adult fleas, Ctenocephalides felis, deposited along the dorsal midline. One hour later, each cat was carefully combed using a fine-toothed comb (13 teeth/cm). Collected fleas were swatted to deteci blood in their abdomen. To the manufacturers respective product use instructions and efficacy claims, reeinfestations were made at Days 3, 7, 14 in all groups; at Days 21 and 30 in Groups 1, 2, 4, 6; at Days 35 and 42 in Groups 3 and 6. The cats were combed one hour after each reinfestation. The results indicate that the topical application of imidacloprid or fipronil does not prevent fleas from biting and feeding within the first hour after infestation prior to being killed while the topical application of dichlorvos/fenitrothion and permethrin let to a better than 80% decrease of the number of engorged fleas for three and seven days post treatment, respectively.

Administration, Topical↗

Arthropod-borne diseases in homeless.

Homeless people are particularly exposed to ectoparasite. The living conditions and the crowded shelters provide ideal conditions for the spread of lice, fleas, ticks, and mites. Body lice have long been recognized as human parasites and although typically prevalent in rural communities in upland areas of countries close to the equator, it is now increasingly encountered in developed countries especially in homeless people or inner city economically deprived population. Fleas are widespread but are not adapted to a specific host and may occasionally bite humans. Most common fleas that parasite humans are the cat, the rat, and the human fleas, Ctenocephalides felis, Xenopsylla cheopis, and Pulex irritans, respectively. Ticks belonging to the family Ixodidae, in particular, the genera Dermacentor, Rhipicephalus, and Ixodes, are frequent parasites in humans. Sarcoptes scabiei var. hominis is a mite (Arachnida class) responsible for scabies. It is an obligate parasite of human skin. The hematophagic-biting mite, Liponyssoides sanguineus, is a mite of the rat, mouse, and other domestic rodents but can also bite humans. Finally, the incidence of skin disease secondary to infestation with the human bedbug, Cimex lectularius, has increased recently. Bacteria, such as Wolbacchia spp. have been detected in bedbug. The threat posed by the ectoparasite in homeless is not the ectoparasite themselves but the associated infectious diseases that they may transmit to humans. Except for scabies all these ectoparasites are potential vectors for infectious agents. Three louse-borne diseases are known at this time. Trench fever caused by Bartonella quintana (B. quintana), epidemic typhus caused by Rickettsia prowazekii, and relapsing fever caused by the spirochete Borrelia recurrentis. Fleas transmit plague (Xenopsylla cheopis and Pulex irritans), murine typhus (Xenopsylla cheopis), flea-borne spotted rickettsiosis on account of the recently described species Rickettsia felis (C. felis), and occasionally cat scratch disease on account of Bartonella henselae (C. felis). The role of fleas as potential vector of B. quintana has recently been suggested. Among the hematophagic-biting mites, L. sanguineus, is responsible for the transmission of Rickettsia akari, the etiologic agent of rickettsialpox. Virtually, no data are available on tick-borne disease in this population. This article will deal with epidemiology, diagnosis, prevention, and treatment of these ectoparasite and the infectious diseases they transmit to the homeless people.

Animals↗

Attempted transmission of Candidatus Mycoplasma haemominutum and Mycoplasma haemofelis by feeding cats infected Ctenocephalides felis.

OBJECTIVE: To determine whether Mycoplasma haemofelis (Mhf) and Candidatus Mycoplasma haemominutum (Mhm) can be transmitted by ingestion of Mycoplasma-infected Ctenocephalides felis and by-products (feces, larvae, and eggs). ANIMALS: 10 cats. PROCEDURE: 3 cats were carriers of Mhf, and 1 was a carrier of Mhm. Six cats had negative results of PCR assay for Mhf and Mhm DNA. A chamber containing 100 C felis was bandaged to 2 Mhf carrier cats. Five days later, fleas and by-products were analyzed for Mycoplasma spp DNA. The remaining fleas and a sample of by-products were fed to 2 Mycoplasma-naïve cats. A chamber containing 200 C felis was bandaged to the Mhm carrier cat. Five days later, fleas and by-products were analyzed for Mycoplasma spp DNA. The remaining fleas and a sample of by-products were fed to 2 Mycoplasma-naïve cats. A chamber containing 200 C felis was bandaged to an Mhf carrier cat and Mhm-carrier cat. Three days later, fleas and by-products were analyzed for Mycoplasma spp DNA. The remaining fleas and a random sample of by products were fed to 4 Mycoplasma-naïve cats. All cats were monitored for infection for >or=7 weeks. RESULTS: Uptake of Mhf and Mhm DNA into fleas and by-products was detected. None of the naïve cats became infected. CONCLUSIONS AND CLINICAL RELEVANCE: Results suggested that ingestion of Mycoplasma-infected C felis or by-products is not an important means of transmission for Mhf or Mhm.

Animals↗

[Siphonaptera/fleas (author's transl)].

Fleas are small, reddish-brown, wingless insects with a laterally compressed body and a pronounced third pair of legs adapted to leaping. Of the 100 species found in Middle Europe, hardly a dozen are of medical importance, they concern mainly people in contact with domestic animals. The cat flea, Ctenocephalides felis felis, and the bird flea. Ceratophyllus gallinae, are the most important human-pathogenic species in our region. A flea bite shows first as a haemorrhagic punctum, accompanied by itching, and leads to an erythema with or without central wheal. After 12--24 hours a papule appears which persists up to 2 weeks. Linimentum zinci with 10% Neocid alleviates the itching and prevents further infestation. The fleas are destroyed in their hiding places and on their animal host by applying Toxical-, Neocid- or Noflo-powder. The tropical sand flea, Tunga penetrans, is a permanent ectoparasite of man. It is seen in people returning from the tropics. Fleas may, even in our region, be vectors of bacteria, viruses, rickettsiae and intestinal parasites.

Adult↗

Ectoparasite fauna of the eastern woodrat, Neotoma floridana: composition, origin, and comparison with ectoparasite faunas of western woodrat species.

We collected ectoparasites from eastern woodrats, Neotoma floridana, from 3 sites in the southeastern United States: coastal South Carolina, southeast Georgia, and south-central Georgia. Twelve ectoparasite species were recovered from 47 woodrats in South Carolina (5 ticks, 5 mites, 2 fleas), 13 from 35 woodrats in south-central Georgia (1 tick, 10 mites, 2 fleas), and 4 from a small host sample (7) in southeast Georgia (2 ticks, 1 mite, 1 flea). New state records are established for the listrophorid mite Listrophorus neotomae from both Georgia and South Carolina, the myocoptid mite Myocoptes neotomae from Georgia, and the ceratophyllid flea Orchopeas sexdentatus pennsylvanicus from South Carolina. Different ectoparasites predominated on woodrats at each site with the tick Ixodes minor being the most commonly collected species in South Carolina, the American dog tick Dermacentor variabilis in southeast Georgia, and the chigger Euschoengastia peromysci in south-central Georgia. Most of the 17 species recovered are known to parasitize several species of mammals, especially rodents, and none of them are host specific to N. floridana. However, the fleas Epitedia cavernicola and Epitedia neotomae are host-specific ectoparasites of eastern woodrats in other parts of their range. Also, 1 species of tick, 2 mites, and 3 fleas parasitize eastern woodrats in addition to western woodrats. A similar lack of host specificity is apparent for the few previously documented collections of ectoparasites from eastern woodrats, including 1 detailed survey in Indiana. Conversely, Neotoma spp. woodrats inhabiting western North America are parasitized by a plethora of host-specific ectoparasites including 2 tick species, 5 mites (other than chiggers), 20 chiggers, 2 sucking lice, and 42 fleas. Recognizing that western biotas are typically more speciose than corresponding eastern biotas in North America, we further propose that because eastern woodrats are the most recent and eastern descendants of the ancestral Neotoma stock, (1) some ectoparasite species failed to accompany the eastern woodrat lineage in its eastward dispersals, and (2) there has been insufficient time for a diverse assemblage of ectoparasites to co-evolve with eastern woodrats.

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Cloning, partial purification and in vivo developmental profile of expression of the juvenile hormone epoxide hydrolase of Ctenocephalides felis.

cDNAs encoding two different epoxide hydrolases (nCfEH1 and nCfEH2) were cloned from a cDNA library prepared from the wandering larval stage of the cat flea, Ctenocephalides felis. Predicted translations of the open reading frames indicated the clones encoded proteins of 464 (CfEH1) and 465 (CfEH2) amino acids. These proteins have a predicted molecular weight of 53 kDa and a putative 22 amino acid N-terminal hydrophobic membrane anchor. The amino acid sequences are 77% identical, and both are homologous to previously isolated epoxide hydrolases from Manduca sexta, Trichoplusia ni, and Rattus norvegicus. Purification of native juvenile hormone epoxide hydrolase (JHEH) from unfed adult cat fleas generated a partially pure protein that hydrolyzed juvenile hormone III to juvenile hormone III-diol. The amino terminal sequence of this;50-kDa protein is identical to the deduced amino terminus of the protein encoded by the nCfEH1 clone. Affinity-purified rabbit polyclonal antibodies raised against Escherichia coli-expressed HisCfEH1 recognized a approximately 50-kDa protein present in the partially purified fraction containing JHEH activity. Immunohistochemistry experiments using the same affinity-purified rabbit polyclonal antibodies localized the epoxide hydrolase in developing oocytes, fat body, and midgut epithelium of the adult flea. The presence of JHEH in various flea life stages and tissues was assessed by Northern blot and enzymatic activity assays. JHEH mRNA expression remained relatively constant throughout the different flea larval stages and was slightly elevated in the unfed adult flea. JHEH enzymatic activity was highest in the late larval, pupal, and adult stages. In all stages and tissues examined, JHEH activity was significantly lower than juvenile hormone esterase (JHE) activity, the other enzyme responsible for JH catalysis.

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A further comparison of the thumb-counting and comb-counting techniques used to determine Ctenocephalides felis infestation levels on dogs.

A comparison was made to determine whether thumb-counting or comb-counting was more accurate for determining flea infestation levels on dogs when performed for equal periods of time. To accomplish this, ten beagle dogs were each infested with 100 adult fleas, Ctenocephalides felis. After the fleas were allowed to disperse for 1 h the dogs were examined using the thumb-counting method. The time required to cover each dog and the number of fleas counted were recorded. Thumb-counting times ranged from 3.0 to 4.8 min. Each of the dogs was then examined by the comb-counting method for the same amount of time it had been thumb-counted. The thumb-counting method detected a geometric mean of five (range, 0-13) fleas per dog, while comb-counting recovered a mean of 73.5 (range, 57-87) fleas per dog. These results were significantly different (P < 0.01), indicating that the differences in accuracy previously recorded for the two methods are independent of time. The standard deviations for both methods were also statistically significantly different, suggesting that comb-counting is also more precise than the thumb-counting method.

Animals↗

The ACVD task force on canine atopic dermatitis (XI): the relationship between arthropod hypersensitivity and atopic dermatitis in the dog.

The relationship between arthropod allergen hypersensitivity and the development of canine atopic dermatitis (AD) is unclear. It has been shown that dogs with AD are more likely to exhibit positive intradermal reactivity to flea allergens than non-pruritic dogs from the same flea-endemic geographic region. Also, dogs in a flea endemic region are four times more likely to suffer from flea allergy dermatitis (FAD) and AD than from FAD alone. These results provide indirect evidence to support the hypothesis that, in the canine species, atopy predisposes to the development of hypersensitivity to flea allergens and eventually to FAD. A causal relationship between insects other than fleas and canine AD has not been identified with certainty.

Animals↗

Contrasting dynamics of Bartonella spp. in cyclic field vole populations: the impact of vector and host dynamics.

Many zoonotic disease agents are transmitted between hosts by arthropod vectors, including fleas, but few empirical studies of host-vector-microparasite dynamics have investigated the relative importance of hosts and vectors. This study investigates the dynamics of 4 closely related Bartonella species and their flea vectors in cyclic populations of field voles (Microtus agrestis) over 3 years. The probability of flea infestation was positively related to field vole density 12 months previously in autumn, but negatively related to more recent host densities, suggesting a dilution effect. The 4 Bartonella species exhibited contrasting dynamics. Only B. grahamii, showed a distinct seasonal pattern. Infection probability increased with field vole density for B. doshiae, B. taylorii and BGA (a previously unidentified species) and with density of coexisting wood mice for B. doshiae and B. grahamii. However, only the infection probability of BGA in spring was related to flea prevalence. B. doshiae and BGA were most common in older animals, but the other 2 were most common in non-reproductive hosts. Generally, host density rather than vector abundance appears most important for the dynamics of flea-transmitted Bartonella spp., possibly reflecting the importance of flea exchange between hosts. However, even closely related species showed quite different dynamics, emphasising that other factors such as population age structure can impact on zoonotic risk.

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Techniques for estimating on-animal populations of Ctenocephalides felis (Siphonaptera: Pulicidae).

Effectiveness of two sampling techniques to estimate cat flea populations were compared on beagles (short-haired dogs). Overall, 23.5 and 81.6% of known flea populations on the beagles were detected using area and comb counting techniques, respectively. Using comb counts, we were able to differentiate among beagles that were infested experimentally to produce densities of 21.6 (low), 42.2 (medium), and 82.5 (high) fleas per dog. Using the area counting technique, we were able to differentiate between the medium and high flea population groups, but not the low- and medium-density groups. A weighted regression analysis gave prediction intervals for flea densities that provided satisfactory estimates of the actual numbers of fleas on the dogs.

Animals↗

First bloodmeal of Ctenocephalides felis felis (Siphonaptera: Pulicidae) on cats: time to initiation and duration of feeding.

Three experiments were conducted on cats to evaluate precocity and duration of the first blood meal of Ctenocephalides felis felis (Bouché). Percentage of engorged fleas was calculated for fleas held on cats for 5, 15, 30, and 60 min. Duration of first blood meal was also measured for individual fleas confined on cats. When fleas are free in the hair coat, 24.9% are engorged after 5 min and 97.2% are engorged after 1 h. Fleas confined to a vial on the cats fed significantly sooner; 60% of females were engorged within 5 min. The mean delay between deposition and biting for fleas, which began feeding within 15 min, was 24 s +/- 31 s for females and 23 s +/- 44 s for males. The mean duration of meals was 25 +/- 18 min for females and 11 +/- 8 min for males.

Animals↗

Seasonal occurrence of Ctenocephalides felis felis and Ctenocephalides canis (Siphonaptera: Pulicidae) infesting dogs and cats in an urban area in Cuernavaca, Mexico.

The seasonal occurrence of Ctenocephalides felis felis (Bouché and Ctenocephalides canis (Curtis) infestation on dogs and cats in Cuernavaca City in Mexico, was determined by examining 1,803 dogs and 517 cats at two veterinary clinics during 1995-1997. The overall flea infestation was 30.3 and 30.1% for dogs and cats, respectively. There were no significant differences (P > 0.05) in percentage of infestation among years for both hosts. The infestation was somewhat higher in spring, summer, and autumn than in winter, but no statistical differences was found among seasons (P > 0.05) for both pets. No relationship existed between percentage of flea infestation and temperature or rainfall among seasons. On dogs, 81.1% were infested with only C. felis felis, 16.8% with C. canis, and 2% had both flea species; whereas 92.3% of the cats were infested with C. felis felis and 7.7% with C. felis felis and C. canis. The cat flea was the most prevalent flea species found other than C. canis; no other species were found on the dogs and cats. It appeared that flea life cycle development continued throughout the year.

Animals↗

Laboratory evaluation of fipronil and imidacloprid topical insecticides for control of the plague vector Oropsylla montana (Siphonaptera: Ceratophyllidae) on california ground squirrels (Rodentia: Sciuridae).

Two insecticides, fipronil and imidacloprid, were evaluated for efficacy and longevity against Oropsylla montana (Baker), the most important vector of plague in California. Wild-caught California ground squirrels, Spermophilus beecheyi (Richardson), were individually housed in the laboratory to serve as natural hosts to O. montana and for on-animal insecticide trials. Several concentrations oftechnical grade fipronil and imidacloprid in acetone were applied to samples of clean rodent bedding to determine residual activity and longevity against fleas. Immature and adult cat fleas, Ctenocephalides felis (Bouche), were used as representative fleas for periodic assays in place of less fecund O. montana. Toxicity of treated bedding did not decrease significantly for 1 yr at all applied concentrations. Fipronil provided 100% kill for at least 1 yr at > or = 100 ppm, whereas imidacloprid required 10,000 ppm for similar performance. Laboratory squirrels were treated with topical formulations of fipronil (Frontline Top Spot) and imidacloprid (Advantage Flea Adulticide) at a dosage rate of 15 mg/kg and evaluated for residual activity every 2 wk against adult O. montana. Residual activity was determined by percent recovery of O. montana adults released on treated and untreated animals after 48 h. Frontline provided 100% kill of adult fleas for at least 10 wk, and up to 26 wk on one animal. Advantage failed to provide 100% kill of adult fleas at 2 wk, with complete loss of efficacy by week 6. Concurrent assays with bedding samples from squirrel nest boxes showed negligible toxicity transfer from treated animals to nest bedding.

Animals↗

Therapy and prevention of parasitic insects in veterinary medicine using imidacloprid.

Ectoparasitic insects play a major role in veterinary medicine. The flea, especially the cat flea (Ctenocephalides felis felis Bouch 1835) is the most important ectoparasite worldwide. The cat flea parasitizes not only on dogs and cats but also on other warm-blooded animals including humans. The veterinary importance of flea infestation are dermatological conditions due to allergic reactions to antigens in the flea saliva and the transmission of infectious agents like bacteria, viruses and helminths. Insecticides used in veterinary medicine today have to fulfil criteria of elimination of a existing flea infestation (therapy) and prevention (prophylaxis) of new infestation for weeks. Imidacloprid is a compound of the chemical class of CNI (chloronicotinyl insecticides syn. neonicotinoids) that fits these criteria. The high selectivity towards the site of action within insects together with the high safety margin on mammals allowed to develop imidacloprid as an insecticide for agricultural use and finally for the application as a veterinary medicine. The major features of imidacloprid chemistry, toxicology and the development and use as a veterinary medicinal remedy are described.

Animals↗

Dynamics of plague in a Gunnison's prairie dog colony complex from New Mexico.

A plague (Yersinia pestis) epizootic spread through Gunnison's prairie dogs (Cynomys gunnisoni), and possibly other rodent species, in the Moreno Valley in north-central New Mexico between winter 1984-1985 and autumn 1987. We observed the progress of the epizootic and subsequent population recovery at four prairie dog towns within the valley during this period. At two towns (Midlake and Val Verde) the prairie dogs were marked prior to the epizootic. At two additional towns (Vega and South Entrance) prairie dogs were marked following the epizootic. In 1988, a second epizootic occurred at Vega. One hundred thirty-nine serum samples were collected from prairie dogs and other rodents and 1,750 fleas were collected from animals and burrows. Fleas infected with Y. pestis were collected from prairie dogs, deer mice (Peromyscus maniculatus), and thirteen-lined ground squirrels (Spermophilus tridecemlineatus). Prairie dog fleas included Oropsylla hirsuta, O. labis and O. tuberculata, deermouse associated fleas were Aetheca wagneri and Rhadinopsylla sectilis, and Oropsylla bacchi was associated with thirteen-lined ground squirrels. All of the above flea species were collected from prairie dog burrows. All rodent species shared some flea species. Thirteen-lined ground squirrels disappeared shortly before plague was identified in prairie dogs at Midlake. Meadow voles were rare following the epizootic at Vega in 1986, became abundant in 1987, and disappeared at the time of the second prairie dog epizootic in summer 1988. Although we collected serum from Gunnison's prairie dogs, thirteen-lined ground squirrels, deer mice, and meadow voles (Microtus pennsylvanicus), we identified elevated serum titers against Y. pestis only in Gunnison's prairie dogs. Prairie dog mortality at all towns affected by plague was in excess of 99%. Serum antibody titers indicate that more than 40% of the few prairie dogs left to establish colonies following epizootics survived plague infection.

Animals↗