RESUMEN
Annual antigen testing is a mainstay for diagnosing infection with Dirofiliaria immitis in dogs; yet, it has been documented that some heartworm-infected dogs and cats test false-negative for antigen due to the presence of antigen-antibody complexes. Several studies have reported the use of heat as a reliable means of immune-complex dissociation (ICD) in recent years; however, the data regarding the use of acid as a reliable method of ICD for D. immitis detection are limited. The objective of this study was to compare an acid-based form of ICD to the more established and evaluated method of heat-based ICD in experimentally infected and non-infected dogs. Plasma from class A dogs experimentally infected â¼4 months prior with D. immitis (infected; nâ¯=â¯24) and dogs reared indoors with no history of exposure to mosquitoes (non-infected; nâ¯=â¯75) were evaluated for presence of D. immitis antigen (DiroCHEK® Heartworm antigen test kit). Each sample was divided into three aliquots for testing: [1] Control plasma (no acid- or heat-treatment), [2] acid-treated plasma (trichloroacetic acid (TCA), incubation, centrifugation for 5â¯min at 16,000 X g, buffer), and [3] heat-treated plasma (104⯰C followed by centrifugation at 16,000 X g). Treatments for each aliquot were performed and tested in triplicate; results were determined both visually (color change) and by spectrophotometric analysis (optical density [OD] value). Of the 24 infected dogs, 0/24 tested positive for antigen in the absence of acid- or heat-treatment. Those same plasma samples following processing by either acid- or heat-treatment yielded 18/24 (75.0%) and 19/24 (79.2%) antigen-positive results, respectively. Of the 75 plasma samples from non-infected dogs, neither acid- nor heat-treatment of plasma caused any false-positive color changes or spectrophotometric values. These results indicate that acid as a means of ICD reliably allowed for the detection of D. immitis antigen in infected plasma while not inducing false-positive results in non-infected plasma samples.
Asunto(s)
Ácidos , Complejo Antígeno-Anticuerpo/análisis , Antígenos Helmínticos/sangre , Pruebas Diagnósticas de Rutina/veterinaria , Dirofilaria immitis/aislamiento & purificación , Calor , Animales , Pruebas Diagnósticas de Rutina/métodos , Dirofilariasis/diagnóstico , Enfermedades de los Perros/diagnóstico , Perros , Plasma/químicaRESUMEN
An international team of scientists and veterinarians was assembled in 1999 to develop a monitoring program to determine the susceptibility of cat fleas, Ctenocephalides felis felis (Bouché) (Siphonaptera: Pulicidae), to imidacloprid. Cat flea eggs were collected, shipped to laboratories, and tested for their susceptibility to imidacloprid. Over 3,000 C. felis populations were collected from 2002 to 2017 from 10 different countries. Of these, 66.3% were collected from cats and 33.7% from dogs. C. f. felis populations (n = 2,200) were bioassayed by exposing cat flea eggs and the emerging larvae to a Diagnostic Dose (DD) of 3 ppm imidacloprid in larval rearing medium. Flea eggs hatched and developed in the untreated controls in 1,837 of the isolates (83.5%) bioassayed. Flea isolates (n = 61) that had ≥5% survival at the DD of 3 ppm were retested with a second DD of 3 ppm. None of them had ≥5% survival to the second dose of 3 ppm. Of the 1,837 valid C. felis isolates tested, there has been no evidence of a decreased susceptibility to imidacloprid over the past 17 yr. The methods outlined in this article should provide an acceptable protocol for testing many of the new active ingredients that have been registered for cat flea control.
Asunto(s)
Ctenocephalides , Control de Insectos/organización & administración , Insecticidas , Neonicotinoides , Nitrocompuestos , Animales , Gatos , Femenino , Resistencia a los Insecticidas , Cooperación Internacional , MasculinoRESUMEN
The monitoring of the susceptibility offleas to insecticides has typically been conducted by exposing adults on treated surfaces. Other methods such as topical applications of insecticides to adults and larval bioassays on treated rearing media have been developed. Unfortunately, baseline responses of susceptible strains of cat flea, Ctenocephalides felis (Bouchè), except for imidacloprid, have not been determined for all on-animal therapies and new classes of chemistry now being used. However, the relationship between adult and larval bioassays of fleas has not been previously investigated. The adult and larval bioassays of fipronil and imidacloprid were compared for both field-collected isolates and laboratory strains. Adult topical bioassays of fipronil and imidacloprid to laboratory strains and field-collected isolates demonstrated that LD50s of fipronil and imidacloprid ranged from 0.11 to 0.40 nanograms per flea and 0.02 to 0.18 nanograms per flea, respectively. Resistance ratios for fipronil and imidacloprid ranged from 0.11 to 2.21. Based on the larval bioassay published for imidacloprid, a larval bioassay was established for fipronil and reported in this article. The ranges of the LC50s of fipronil and imidacloprid in the larval rearing media were 0.07-0.16 and 0.11-0.21 ppm, respectively. Resistance ratios for adult and larval bioassays ranged from 0.11 to 2.2 and 0.58 to 1.75, respectively. Both adult and larval bioassays provided similar patterns for fipronil and imidacloprid. Although the adult bioassays permitted a more precise dosage applied, the larval bioassays allowed for testing isolates without the need to maintain on synthetic or natural hosts.
Asunto(s)
Ctenocephalides/efectos de los fármacos , Imidazoles/farmacología , Resistencia a los Insecticidas , Insecticidas/farmacología , Nitrocompuestos/farmacología , Pirazoles/farmacología , Animales , Ctenocephalides/genética , Ctenocephalides/crecimiento & desarrollo , Ctenocephalides/fisiología , Femenino , Larva/efectos de los fármacos , Larva/genética , Larva/fisiología , Dosificación Letal Mediana , Masculino , NeonicotinoidesRESUMEN
A controlled laboratory study was conducted to evaluate the efficacy of four commercial products administered as a single treatment for the prevention of heartworm disease caused by Dirofilaria immitis in dogs. Forty-four commercially sourced Beagle dogs, 6-7 months of age, were received at the test site (Auburn University, Department of Pathobiology) on Study Day (SD) -72 to begin acclimation. On SD -30, each dog was inoculated subcutaneously with 100 infective, third-stage D. immitis larvae (MP3 strain, TRS Laboratories, Inc., Athens, GA). On SD -1, 40 dogs weighing 18.2-25.3 lbs were ranked by decreasing body weight and randomized to five groups of eight dogs each. On SD 0, the dogs assigned to Group 1 were treated orally with ivermectin/pyrantel pamoate chewable tablets, Group 2 dogs were treated orally with milbemycin oxime flavored tablets, Group 3 dogs were treated with selamectin topical solution, and Group 4 dogs were treated with imidacloprid/moxidectin topical solution. Group 5 dogs remained nontreated. Dosages for dogs in Groups 1-4 were based on the individual body weight of each dog and current labeled dose banding for each commercial product. All dogs were fasted overnight prior to treatment. Food was returned four hours after treatment. Animals were observed for abnormal clinical signs involving eyes, feces, respiration, behavioral attitude, locomotion/musculature, or skin conditions at prescribed intervals immediately after treatment and at twice daily intervals thereafter. On SD 90, whole blood was collected and tested for adult heartworm antigen. On SDs 119/120, the dogs were euthanized and subjected to necropsy examination for recovery of adult D. immitis and/or worm fragments. At necropsy, all 8 dogs in the nontreated group were infected with adult D. immitis (34-70 worms/dog, geometric mean (GM)=51.6 worms/dog). One or more adult D. immitis and/or worm fragments were recovered from 7 of 8 of the dogs each in Groups 1-3 (87.5% were heartworm positive). The respective GM worm burdens/dog for Groups 1-3 was 2.3, 2.4, and 2.3 which resulted in 95.6, 95.4 and 95.5% efficacy, respectively. No worms were recovered from any of the 8 dogs in Group 4 resulting in 100% efficacy.
Asunto(s)
Antihelmínticos/uso terapéutico , Dirofilaria immitis/clasificación , Dirofilariasis/tratamiento farmacológico , Enfermedades de los Perros/tratamiento farmacológico , Animales , Dirofilariasis/parasitología , Enfermedades de los Perros/parasitología , Perros , Femenino , MasculinoRESUMEN
Although on-animal topical treatment with compounds such as imidacloprid has revolutionized the control of the cat flea, Ctenocephalides felis (Bouché) (Siphonaptera: Pulicidae), the development of insecticide resistance is a continuing threat. As part of a highly co-ordinated and unprecedented resistance monitoring programme for C. felis, 1437 flea isolates were collected by veterinary clinics in Australia, Germany, France, the U.K. and 29 states in the U.S.A. from 2002 to 2009. About 65% of the collections were made from June to October each year and 71% of the collections were from cats. Collections of flea eggs were sent to one of five different laboratories, where they were tested with a diagnostic dose of imidacloprid (3 p.p.m.) applied to larval flea-rearing medium. Of the 1437 collections received, 1064 contained adequate numbers of eggs for testing. Of these isolates, untreated eggs failed to hatch in 22.7% and were not considered valid bioassays. Survival rates >5% and development of adult fleas (a threshold for further testing) occurred in only 22 isolates. They were re-tested with the same diagnostic dose and none produced >5% adult emergence. Complete dose-response bioassays were performed on three of the isolates that had triggered a second test and produced slopes, intercepts and LC(50) values similar to those for existing susceptible laboratory strains. Results confirmed sustained susceptibility of C. felis to imidacloprid, despite its widespread use for over a decade.
Asunto(s)
Enfermedades de los Gatos/prevención & control , Ctenocephalides/efectos de los fármacos , Infestaciones Ectoparasitarias/veterinaria , Imidazoles/uso terapéutico , Insecticidas/uso terapéutico , Nitrocompuestos/uso terapéutico , Óvulo/efectos de los fármacos , Animales , Enfermedades de los Gatos/tratamiento farmacológico , Gatos , Relación Dosis-Respuesta a Droga , Infestaciones Ectoparasitarias/tratamiento farmacológico , Infestaciones Ectoparasitarias/prevención & control , Imidazoles/toxicidad , Control de Insectos/métodos , Resistencia a los Insecticidas , Insecticidas/toxicidad , Neonicotinoides , Nitrocompuestos/toxicidadRESUMEN
This study was undertaken to determine whether resistance to moxidectin had developed in a large herd of draught horses, maintained on a small acreage, which had been routinely treated with moxidectin for five years. Faeces were collected for egg counts immediately before moxidectin gel was administered orally, and seven, 30, 60 and 90 days later. The faecal egg counts were significantly reduced at seven and 30 days after treatment, but were not significantly different from pretreatment counts at 60 and 90 days after treatment. There was no evidence of resistance having developed.
Asunto(s)
Antinematodos/farmacología , Enfermedades de los Caballos/tratamiento farmacológico , Infecciones por Strongylida/veterinaria , Strongyloidea/efectos de los fármacos , Alabama , Análisis de Varianza , Crianza de Animales Domésticos , Animales , Antinematodos/normas , Resistencia a Medicamentos , Quimioterapia Combinada , Heces/parasitología , Geles , Enfermedades de los Caballos/parasitología , Caballos , Macrólidos/farmacología , Macrólidos/normas , Recuento de Huevos de Parásitos/veterinaria , Praziquantel/farmacología , Praziquantel/normas , Infecciones por Strongylida/tratamiento farmacológico , Infecciones por Strongylida/parasitología , Factores de Tiempo , Resultado del TratamientoRESUMEN
These guidelines are intended to assist the planning and conduct of laboratory and clinical studies to assess the efficacy of ectoparasiticides applied to dogs or cats for the purpose of treating, preventing and controlling flea and tick infestations. The term ectoparasiticide includes insecticidal and acaricidal compounds, as well as insect growth regulators. The range of biological activities accruing from animal treatment that are considered include: repellency and anti-feeding effects, knockdown, speed of kill, immediate and persistent lethal effects, and interference with egg fertility and subsequent development of off-host life cycle stages. Information is provided on the selection of animals, dose determination, dose confirmation and field studies, record keeping, interpretation of results and animal welfare. These guidelines are also intended to assist registration authorities involved in the approval and registration of new parasiticides, and to facilitate the worldwide adoption of harmonized procedures.
Asunto(s)
Enfermedades de los Gatos/prevención & control , Ensayos Clínicos como Asunto/veterinaria , Enfermedades de los Perros/prevención & control , Infestaciones Ectoparasitarias/veterinaria , Insecticidas/farmacología , Investigación/normas , Animales , Enfermedades de los Gatos/parasitología , Gatos , Ensayos Clínicos como Asunto/normas , Enfermedades de los Perros/parasitología , Perros , Infestaciones Ectoparasitarias/prevención & control , Salud Global , Parasitología/organización & administración , Medicina Veterinaria/organización & administraciónRESUMEN
The susceptibility of four laboratory strains of cat fleas, Ctenocephalides felis (Bouche), to imidacloprid was determined by three different laboratories, by using a standardized bioassay protocol. The probit lines generated by the different laboratories were very similar, with LC50 values ranging from 0.32 to 0.81 ppm. Based on these data, a diagnostic dose (DD) of 3 ppm imidacloprid in larval rearing media was provisionally identified for detecting shifts in tolerance, possibly as a consequence of incipient imidacloprid resistance. None of the larvae from the susceptible laboratory strains survived the DD. Eighteen field-collected isolates were evaluated for their susceptibility to imidacloprid and to validate a DD of 3 ppm. Probit lines from 18 field-collected isolates were very similar, with LC50 values ranging from 0.14 to 1.52 ppm. When exposed to the DD, between 3 and 10% of the exposed larvae emerged as adults from only three of the 18 isolates. All other field isolates gave 100% mortality at the DD. Under the criteria established (>5% survivorship at 3 ppm), two isolates would be established on mammalian hosts and more extensive tests conducted to exclude or confirm the presence of resistance. The DD of 3 ppm is robust enough to eliminate most of the susceptible isolates collected until today, yet low enough to identify possible isolates for further testing.
Asunto(s)
Imidazoles/administración & dosificación , Insecticidas/administración & dosificación , Siphonaptera , Animales , Gatos , Relación Dosis-Respuesta a Droga , Resistencia a los Insecticidas , Larva , Neonicotinoides , NitrocompuestosRESUMEN
We evaluated a 15% paste formulation of ponazuril in outbred Swiss mice that were experimentally infected with Eimeria vermiformis. Thirty, 8-week-old female mice (approximately 20 g) were placed in one group of 10 mice and one group of 20 mice. Mice in both groups were gavaged with approximately 5,000 sporulated oocysts of E. vermiformis on day 0. Mice in group 2 (n=10) were treated orally on days 3 and 4 with ponazuril (suspended in 30% propylene glycol) at the rate of 20 mg/kg. Mice in group 1 (n=20) were gavaged with a similar volume of 30% propylene glycol. Rates of oocyst passage (oocysts/g feces) were determined on day 10 (peak patency) for treated and nontreated mice using a fecal aliquot oocyst counting technique. Oocysts were not observed in the feces of treated mice using the aliquot technique. Control mice passaged oocysts at a geometric mean rate of >104,000 oocysts/g feces. Control mice also produced significantly less feces on day 10. These results indicate that ponazuril is effective against E. vermiformis under the conditions utilized in this study, and that the E. vermiformis mouse model could be useful in predicting the efficacy of new anticoccidial drugs.
Asunto(s)
Coccidiosis/tratamiento farmacológico , Coccidiostáticos/uso terapéutico , Eimeria/efectos de los fármacos , Eimeria/crecimiento & desarrollo , Triazinas/uso terapéutico , Animales , Coccidiosis/parasitología , Coccidiostáticos/administración & dosificación , Coccidiostáticos/farmacología , Modelos Animales de Enfermedad , Heces/parasitología , Femenino , Ratones , Recuento de Huevos de Parásitos , Triazinas/administración & dosificación , Triazinas/farmacologíaRESUMEN
A 3-yr-old secundiparous female ring-tailed lemur presented to the Auburn University Small Animal Clinic with signs of dyspnea, lethargy, and anorexia. The animal died before she could be examined, and a full necropsy was immediately performed. Provisional necropsy findings included moderate pneumonia and hepatopathy. Acute interstitial pneumonia and focal hepatocellular necrosis were confirmed histologically. Lung impression smears, histopathology, electron microscopy, immunohistochemistry, and tissue culture isolation resulted in a diagnosis of acute disseminated Toxoplasma gondii infection, which was confirmed by polymerase chain reaction. The isolate of T. gondii was avirulent for mice and was named AU Tgl and genetically is type II. The source of the infection remains unclear, but speculation suggests contaminated fruit or blackbirds (Passeriformes: Icteridae) acting as transport hosts for oocysts from nondomestic felids and feral cats on the property.
Asunto(s)
Lemur/parasitología , Pulmón/parasitología , Enfermedades de los Primates/patología , Toxoplasma/aislamiento & purificación , Toxoplasmosis Animal/patología , Alabama , Animales , Animales de Zoológico , Encéfalo/parasitología , ADN Protozoario/análisis , Resultado Fatal , Femenino , Inmunohistoquímica/veterinaria , Intestinos/parasitología , Hígado/parasitología , Pulmón/patología , Pulmón/ultraestructura , Ratones , Microscopía Electrónica/veterinaria , Reacción en Cadena de la Polimerasa/veterinaria , Enfermedades de los Primates/parasitología , Toxoplasma/genética , Toxoplasma/inmunología , Toxoplasma/ultraestructura , Toxoplasmosis Animal/parasitologíaRESUMEN
The phylogenetic relationships among 31 different flea isolates representing seven different species were studied by nucleotide sequence comparison of the internal transcribed spacer 1 (ITS1), internal transcribed spacer 2 (ITS2) and/or mitochondrial 16S ribosomal RNA gene (mt16S-rDNA) to examine the patterns of variation. Results show that all regions are useful in discriminating among flea species. In Ctenocephalides felis and Tunga penetrans, some differences in these gene regions occurred among different isolates within the same species. In the latter case, the differences are in the mt16S-rDNA region, with one isolate showing 48% divergence in nucleotide sequence. The taxonomic implications of this result are unclear at present. The gene regions revealed differences between C. felis isolates only after DNA sequencing the PCR products. Further differentiation among C. felis isolates was obtained using four different random binding primers (decamers) and primers for mammalian aldolase to amplify narrow differences in the genome. Using these primers we were able to discriminate between different C. felis isolates and determine that some of the genetic variation coincided with minor differences in response to the control agent imidacloprid. However, overall findings do not support the existence of subspecies of C. felis.
Asunto(s)
Siphonaptera/clasificación , Siphonaptera/genética , Animales , Secuencia de Bases , Gatos , Cartilla de ADN/genética , ADN Mitocondrial/genética , ADN Espaciador Ribosómico/genética , Perros , Evolución Molecular , Variación Genética , Filogenia , Reacción en Cadena de la Polimerasa , ARN Ribosómico 16S/genética , Especificidad de la EspecieAsunto(s)
Enfermedades de los Perros/prevención & control , Imidazoles/administración & dosificación , Insecticidas/administración & dosificación , Ixodes/efectos de los fármacos , Enfermedad de Lyme/veterinaria , Permetrina/administración & dosificación , Infestaciones por Garrapatas/veterinaria , Animales , Anticuerpos Antibacterianos/sangre , Borrelia burgdorferi/inmunología , Enfermedades de los Perros/microbiología , Enfermedades de los Perros/parasitología , Perros , Quimioterapia Combinada , Ixodes/microbiología , Enfermedad de Lyme/prevención & control , Enfermedad de Lyme/transmisión , Neonicotinoides , Nitrocompuestos , Infestaciones por Garrapatas/parasitología , Infestaciones por Garrapatas/prevención & control , Resultado del TratamientoAsunto(s)
Imidazoles/farmacología , Insecticidas/farmacología , Plantas , Siphonaptera/efectos de los fármacos , Animales , Bioensayo , Resistencia a Medicamentos/genética , Larva/efectos de los fármacos , Neonicotinoides , Nitrocompuestos , Pruebas de Sensibilidad Parasitaria/métodos , Siphonaptera/genética , Siphonaptera/crecimiento & desarrolloRESUMEN
Strategies for controlling cat fleas, Ctenocephalidesfelisfelis (Bouché), have undergone dramatic changes in the past 5 yr. With the advent of on-animal treatments with residual activity the potential for the development of insecticide resistance increases. A larval bioassay was developed to determine the baseline susceptibility of field-collected strains of cat fleas to imidacloprid. All four laboratory strains tested showed a similar level of susceptibility to imidacloprid. Advantages of this bioassay are that smaller numbers of fleas are required because flea eggs are collected for the test. Insect growth regulators and other novel insecticides can also be evaluated. Using a discriminating dose, the detection of reduced susceptibility in field strains can be determined with as few as 40 eggs.
Asunto(s)
Gatos/parasitología , Imidazoles/farmacología , Insecticidas/farmacología , Plantas , Siphonaptera/efectos de los fármacos , Acetona , Animales , Bioensayo/métodos , Hexanos , Larva/efectos de los fármacos , Cloruro de Metileno , Neonicotinoides , Nitrocompuestos , Óvulo , Solventes , AguaRESUMEN
Neospora caninum is a protozoan parasite of animals, which before 1984 was misidentified as Toxoplasma gondii. Infection by this parasite is a major cause of abortion in cattle and causes paralysis in dogs. Since the original description of N. caninum in 1988, considerable progress has been made in the understanding of its life cycle, biology, genetics and diagnosis. In this article, the authors redescribe the parasite, distinguish it from related coccidia, and provide accession numbers to its type specimens deposited in museums.
Asunto(s)
Coccidios/clasificación , Neospora/clasificación , Neospora/citología , Animales , Bancos de Muestras Biológicas , Coccidios/citología , Coccidios/fisiología , Coccidiosis/parasitología , Coccidiosis/patología , Perros/parasitología , Zorros/parasitología , Microscopía , Museos , Neospora/genética , Neospora/fisiología , Filogenia , Especificidad de la EspecieRESUMEN
Toxoplasma gondii oocysts are excreted nonsporulated in the feces of the cats into the environment. These oocysts must undergo sporulation to become infectious. Little is known about the factors that influence sporulation of T. gondii oocysts. The present study examined the survival of nonsporulated oocysts under refrigerated conditions over 11-week observation period. Microscopic examination of oocysts indicated that no visible development occurred under refrigerator conditions. The nonsporulated oocysts retained their ability to sporulate when placed at room temperature. The numbers of visually viable appearing oocysts decreased over time. Some oocysts in all samples were infectious for mice despite being refrigerated for up to an 11 weeks before undergoing sporulation. Results indicate that nonsporulated oocysts can survive in the environment for at least 3 months and retain their ability to become infectious when placed under appropriate conditions.
Asunto(s)
Enfermedades de los Gatos/parasitología , Toxoplasma/crecimiento & desarrollo , Toxoplasmosis Animal/parasitología , Animales , Enfermedades de los Gatos/transmisión , Gatos , Frío , Femenino , Ratones , Ratones Endogámicos ICR , Refrigeración , Esporas , Factores de Tiempo , Toxoplasma/patogenicidad , Toxoplasmosis Animal/transmisión , Zoonosis/parasitologíaRESUMEN
Neospora caninum is an apicomplexan parasite that causes neonatal neuromuscular disease in dogs and abortions in cattle. Dogs are the only proven definitive host. Little is known about the prevalence of antibodies to this parasite in wildlife. Sera from 99 raccoons (Procyon lotor) were examined for agglutinating antibodies to N. caninum using the modified agglutination test employing formalin-fixed tachyzoites as antigen. Raccoons originated in Florida (n = 24, collected in 1996), New Jersey (n = 25, collected in 1993), Pennsylvania (n = 25, collected in 1999), and Massachusetts (n = 25, collected in 1993 and 1994). Ten (10%) had antibodies to N. caninum; 9 had titers of 1:50, and 1 (1%) had a titer of 1:100. The present study indicates that raccoons have minimal exposure to N. caninum. The sera were also tested for agglutinating antibodies to Toxoplasma gondii and 46 (46%) were positive; 16 had titers of 1:50, 8 had titers of 1:100, and 22 had titers of > or = 1:500.
Asunto(s)
Coccidiosis/veterinaria , Neospora/aislamiento & purificación , Mapaches/parasitología , Pruebas de Aglutinación/veterinaria , Animales , Anticuerpos Antiprotozoarios/sangre , Coccidiosis/epidemiología , Coccidiosis/parasitología , Florida/epidemiología , Massachusetts/epidemiología , New Jersey/epidemiología , Pennsylvania/epidemiología , Estudios SeroepidemiológicosRESUMEN
Equine protozoal myeloencephalitis (EPM) is the most important protozoal disease of horses in North America and it is caused by Sarcocystis neurona. Natural cases of encephalitis due to S. neurona have been reported in raccoons, Procyon lotor. We examined 99 raccoons for agglutinating antibodies to S. neurona using the S. neurona agglutination test (SAT) employing formalin-fixed merozoites as antigen. Raccoons originated in Florida (N=24, collected in 1996), New Jersey (N=25, collected in 1993), Pennsylvania (N=25, collected in 1999), and Massachusetts (N=25, collected in 1993 and 1994). We found that 58 (58.6%) of the 99 raccoons were positive for antibodies to S. neurona using the SAT; 44 of 99 raccoons (44%) had titers of > or =1:500. This prevalence is similar to the reported seroprevalence of 33-60% for S. neurona antibodies in horses from the United States using the Western blot test.
Asunto(s)
Anticuerpos Antiprotozoarios/sangre , Mapaches/parasitología , Sarcocystis/inmunología , Sarcocistosis/veterinaria , Pruebas de Aglutinación/veterinaria , Animales , Prevalencia , Mapaches/sangre , Sarcocistosis/epidemiología , Sarcocistosis/inmunología , Estudios Seroepidemiológicos , Estados Unidos/epidemiologíaRESUMEN
Avian isolates of Cryptosporidium species from different geographic locations were sequenced at two loci, the 18S rRNA gene and the heat shock gene (HSP-70). Phylogenetic analysis of the sequence data provided support for the existence of a new avian species of Cryptosporidium infecting finches and a second species infecting a black duck. The identity of Cryptosporidium baileyi and Cryptosporidium meleagridis as valid species was confirmed. Also, C. baileyi was identified in a number of isolates from the brown quail extending the host range of this species.
Asunto(s)
Enfermedades de las Aves/parasitología , Criptosporidiosis/veterinaria , Cryptosporidium/clasificación , Cryptosporidium/genética , Filogenia , Animales , Aves , Criptosporidiosis/parasitología , ADN Protozoario/análisis , ADN Protozoario/genética , ADN Ribosómico/análisis , ADN Ribosómico/genética , Patos , Genes de ARNr , Proteínas HSP70 de Choque Térmico/genética , Datos de Secuencia Molecular , ARN Ribosómico 18S/genética , Análisis de Secuencia de ADN , Pájaros CantoresRESUMEN
OBJECTIVE: To determine clinical and pathologic findings before and after short-term (group 1) and long-term (group 2) treatment in dogs with Hepatozoon americanum infection. DESIGN: Retrospective study. ANIMALS: 53 dogs with H. americanum infection. PROCEDURE: Medical records of dogs that were treated for hepatozoonosis diagnosed on the basis of meront or merozoite stages in skeletal muscle were reviewed. RESULTS: Circulating gametocytes of H. americanum were identified in 12 of 53 dogs. Dogs were treated with various drugs, including toltrazuril, trimethoprim-sulfadiazine, clindamycin, pyrimethamine, and decoquinate. Mean WBC counts prior to treatment were 85,700 and 75,200 cells/microl in groups 1 and 2, respectively, and 1 month after initiation of treatment were 12,600 and 14,600 cells/microl, respectively. Initial response to treatment was excellent in all dogs. Twenty-three of 26 dogs in group 1 relapsed at least once and died within 2 years; mean (+/- SD) survival time was 12.6+/-2.2 months. Twenty-two of 27 group-2 dogs survived; 11 dogs had no clinical signs and were still receiving decoquinate (mean duration of treatment, 21 months), 11 dogs had no clinical signs after treatment for 14 months (range, 3 to 33 months; mean survival time, 39 months [range, 26 to 53 months]), 2 dogs were lost to follow-up, and 3 dogs were euthanatized because of severe disease. CONCLUSIONS AND CLINICAL RELEVANCE: Although no treatment effectively eliminated the tissue stages of H. americanum, treatment with trimethoprim-sulfadiazine, clindamycin, and pyrimethamine followed by long-term administration of decoquinate resulted in extended survival times and excellent quality of life.