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The successful raising one young of one female Crocidura f. flavescens by another is reported. Attempts at using C. h. hirta and Myosorex varius as foster parents, and as well as at hand rearing of C. f. flavescens were unsuccessful. An attempt is made to explain the significance of this occurrence.
This work presents results of the research on the occurrence of Coxiella burnetii and Francisella tularensis in the tissues of wild-living animals and ticks collected from Drawsko County, West Pomeranian Voivodeship. The real-time PCR testing for the pathogens comprised 928 samples of animal internal organs and 1551 ticks. The presence of C. burnetii was detected in 3% of wild-living animals and in 0.45–3.45% (dependent on collection areas) of ticks. The genetic sequences of F. tularensis were present in 0.49 % of ticks (only in one location – Drawa) and were not detected in animal tissues. The results indicate respectively low proportion of animals and ticks infected with C. burnetii and F. tularensis.
The structure and morphometry of the epididymis in the greater cane rat were studied in this work. In assessing the morphology and characterising the morphometric values, a total of 15 adult male greater cane rats, bred and raised in captivity, were used. All the animals had brownish perineal staining, which was taken as index of sexual maturity in male cane rats, and they were maintained on elephant grass stems with water given ad libitum. From this work, the epididymis of the greater cane rat was observed to have a mean weight of 0.0365 ± 0.091 g, forming about 0.016% of the total body weight and an average volume of 0.36 ± 0.08 mL. There was a positive correlation between the epididymal weights, testicular weight, and the body weight in this animal. However, the gross divisions of the epididymis into head, body, and tail were not conspicuous in the cane rat; instead it had two divisions — the cranial and the caudal divisions. In addition, based on the histological and histomorphometric analyses, five zones were observed in the epididymal epithelium of this animal. This preliminary information on the epididymis will serve as a basis for further research on the epididymis of the greater cane rat and will contribute to the knowledge of the its reproductive biology, which will subsequently aid in the captive rearing and domestication of this animal. (Folia Morphol 2010; 69, 4: 246–252)
Over the last three decades, a variety of approaches have been investigated to develop new types of bluetongue virus (BTB) vaccines, ranging from baculovirus-expressed subunit vaccines to live vector vaccines. DNA vaccines against BTV consist of DNA plasmid expressing different BTV proteins after inoculation of the animals. The recombinant viral vector vaccines against BTV are based on recombinant viruses that express desired BTV antigens in the host upon inoculation. Viruses such as vaccinia, modified vaccinia Ancara (MVA), capripox, canarypox, herpes, myxoma and fowlpox viruses have been used as vectors of BTV genes. The reverse genetics (RG) systems for BTV are useful tools for BTV vaccine development. Disabled infectious single-cycle (DISC) vaccines make it possible to restore virus replication and can be used for differentiating infected from vaccinated animals (DIVA). These vaccines are based on the production of a modified virus with a deletion in one or more genes that are essential for virus replication. Another approach for BTV vaccine development using RG is the disabled infectious single-animal (DISA) vaccine, generated by deletion of NS3/NS3a expression. DISC and DISA vaccines can mimic the natural tropism of the virus and can express BTV proteins at the site of infection. Important advantages of these new generation vaccines over the conventional BTV vaccines are their high efficacy as well as the possibility of applying them for DIVA. At present, there are a number of novel laboratoryscale BTV vaccines that could meet vaccine profiles required for different field situations. However, further development and licensing of these vaccine candidates for many BTV serotypes is needed in order to prepare for future BT outbreaks. To date, all novel BTV vaccines described in this paper are still under laboratory testing. They are not available commercially, and the time of their application in the field is still indefinite.
The biology of the ascarid nematodes has been discussed in the context of their important economic role in farm animals, pet animals and zoo animals with special attention to carnivores and primates. In farm animals, infection with the most common roundworm of horses (Parascaris equorum) and swine (Ascaris suum) depend on many factors such as environmental conditions (larval development in the egg and egg survival), age of the host, breed, husbandry system, hygiene and treatment schedule. The monoxenic ascarids Toxocara canis and T. cali are the most important nematodes in carnivorous animals (dogs, cats, foxes) and carnivores in the zoo. In the period of March 2000 till March 2001, 57,1% of examined representatives of Felidae, Ursidae and Canidae in the Zoological Garden of Wroclaw were found to be infected with ascarids (T. canis, T. cati, Toxascaris leonina). The prevalence of T. canis in the Canidae was 66,7%, of T. cati in the Felidae was 14,3%, while 57,1% of the Felidae carried T. leonina infection. Ascaris lumbricoides, a typical parasite of primates, was found in some gorillas, chimpanzees and orang-utans during parasitological survey.
The aim of the study was to develop RT-PCR and Nested-PCR methods for the detection and identification of the West Nile virus in wild birds. The method was based on West Nile Virus genome non-coding region 3'NCR. All the samples were examined with NRT-PCR and also with a commercial West Nile Virus Kit Prodesse™. There was no positive case of West Nile virus infection in the examined samples. All control samples were positive in both methods. The NRT-PCR method proved to be quick and reliable for the testing of wild birds' tissue samples for WNV.
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