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1.
J S Afr Vet Assoc ; 82(4): 232-8, 2011 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-22616438

RESUMEN

The treatment rationale for dogs poisoned by aldicarb is reviewed from a pharmacological perspective. The illegal use of aldicarb to maliciously poison dogs is a major problem in some parts of the world. In South Africa, it is probably the most common canine poisoning treated by companion animal veterinarians. Aldicarb poisoning is an emergency and veterinarians need to be able to diagnose it and start with effective treatment immediately to ensure a reasonable prognosis. Successful treatment depends on the timely use of an anti-muscarinic drug (e.g. atropine). Additional supportive treatment options, including fluid therapy, diphenhydramine, benzodiazepines and the prevention of further absorption (activated charcoal) should also be considered. Possible complications after treatment are also briefly discussed.


Asunto(s)
Aldicarb/envenenamiento , Enfermedades de los Perros/terapia , Insecticidas/envenenamiento , Intoxicación/veterinaria , Animales , Atropina/uso terapéutico , Enfermedades de los Perros/diagnóstico , Perros , Fluidoterapia/veterinaria , Antagonistas Muscarínicos/uso terapéutico , Intoxicación/diagnóstico , Intoxicación/terapia
2.
Med Vet Entomol ; 23(4): 399-409, 2009 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19941606

RESUMEN

African swine fever virus (ASFV) infection in adult Ornithodoros porcinus (Murry 1877, sensuWalton 1979) ticks collected from warthog burrows in southern and East Africa was assessed using a duplex genomic amplification approach that is informative with respect to the invertebrate host species and infecting sylvatic cycle virus. DNA extracted from individual ticks was used as template for the simultaneous amplification of a C-terminal 478-bp ASFV p72 gene region and a approximately 313-bp fragment of the tick mitochondrial 16S rRNA gene, under optimized reaction conditions. Within-warthog burrow infection rates ranged from 0% to 43% using this approach, and phylogenetic analysis of 16S gene sequences revealed the presence of three geographically discrete O. porcinus lineages, but no support for subspecies recognition. False negatives are precluded by the inclusion of host species-informative primers that ensure the DNA integrity of cytoplasmically located genome extracts. In addition, infection rate estimates are further improved as false positives arising from carry-over contamination when performing a two-step nested polymerase chain reaction are negated by the one-step approach. Phylogenetic comparison of full-length virus gene sequences with the partial C-terminal p72 gene target confirmed the epidemiological utility of the latter in a sylvatic setting. The method is therefore of particular value in studies assessing the prevalence and diversity of ASFV in relation to the African sylvatic tick vector and holds potential for investigating the role of alternative tick species in virus maintenance and transmission.


Asunto(s)
Virus de la Fiebre Porcina Africana/aislamiento & purificación , Fiebre Porcina Africana/virología , Reservorios de Enfermedades/veterinaria , Ornithodoros/virología , Porcinos/parasitología , África Oriental/epidemiología , Fiebre Porcina Africana/epidemiología , Fiebre Porcina Africana/genética , Virus de la Fiebre Porcina Africana/genética , Animales , Secuencia de Bases , ADN Mitocondrial/química , ADN Mitocondrial/genética , ADN Viral/química , ADN Viral/genética , Reservorios de Enfermedades/virología , Variación Genética , Genotipo , Datos de Secuencia Molecular , Filogenia , Reacción en Cadena de la Polimerasa , ARN Ribosómico 16S/química , ARN Ribosómico 16S/genética , Alineación de Secuencia , Árboles
3.
Onderstepoort J Vet Res ; 76(4): 385-92, 2009 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21344788

RESUMEN

The Mkuze Game Reserve (MGR), in north-eastern KwaZulu-Natal Province, South Africa is an African swine fever virus (ASF) controlled area. In a survey conducted in 1978, ASF prevalence in warthogs and Ornithodoros ticks in MGR was determined to be 2% and 0.06%, respectively. These values, acknowledged as being unusually low compared to other East and southern African ASF-positive sylvatic-cycle host populations, have not been assessed since. The availability of a sensitive PCR-based virus detection method, developed specifically for the sylvatic tampan host, prompted a re-evaluation of ASF virus (ASFV) prevalence in MGR ticks. Of the 98 warthog burrows inspected for Ornithodoros presence, 59 (60.2%) were found to contain tampans and tick sampling was significantly male-biased. Whilst gender sampling-bias is not unusual, the 27% increase in infestation rate of warthog burrows since the 1978 survey is noteworthy as it anticipates a concomitant increase in ASFV prevalence, particularly in light of the high proportion (75%) of adult ticks sampled. However, despite DNA integrity being confirmed by internal control amplification of the host 16S gene, PCR screening failed to detect ASFV. These results suggest that ASFV has either disappeared from MGR or if present, is localized, occurring at exceptionally low levels. Further extensive surveys are required to establish the ASFV status of sylvatic hosts in this controlled area.


Asunto(s)
Virus de la Fiebre Porcina Africana/aislamiento & purificación , Fiebre Porcina Africana/epidemiología , Vectores Arácnidos/virología , Ornithodoros/virología , Infestaciones por Garrapatas/veterinaria , Fiebre Porcina Africana/virología , Virus de la Fiebre Porcina Africana/clasificación , Virus de la Fiebre Porcina Africana/genética , Animales , ADN Viral/análisis , Femenino , Genotipo , Masculino , Filogenia , Reacción en Cadena de la Polimerasa/veterinaria , Factores Sexuales , Sudáfrica/epidemiología , Porcinos , Infestaciones por Garrapatas/epidemiología
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