Newcastle disease in Cyprus: A review

Summary The first Newcastle disease epidemic in Cyprus was reported in 1949 to 1950 and between 1953 and 1959 there was a second. In November 1977 another Newcastle disease outbreak occurred. Measures implemented immediately were: quarantine of all foci of infection, destruction of diseased and in-contact birds, disinfection of premises and island-wide (Government controlled) vaccination. Within a month the epidemic was brought under control. In all 47 outbreaks were recorded with the loss of about 35,000 birds. Only 2 commercial units were affected, the remaining outbreaks occurring in premises of back-yard poultry keepers. The virus was the Asiatic type.

---

La Enfermedad De Newcastle En Chipre: Revisión De La Literatura

Resumen La primera epidemia de Newcastle en Chipre se describio en 1949–50 y la segunda entre 1953 y 1959. En Noviembre de 1977 ocurrio otro brote. Las medidas tomadas fueron: cuarentena de todos los focos de infección, destrucción de todas las aves enfermas y en contacto, desinfección de los galpones y vacunación general. La epidemia se controló en un mes. En los 47 brotes diagnosticados, hubo una pérdida calculada de 35 000 aves. La enfermedad se diagnosticó en dos empresas comerciales y en unidades pequeñas familiares. El virus aislado fue el tipo Asiático.

---

La Maladie De Newcastle A Chypre—Revue

Résumé La première appartition de la maladie de Newcastle à Chypre, a eu lieu en 1949–1950, avec une seconde vague entre 1953 et 1959.La maladie est répparue en 1977. Les mesures assitôt prises ont été: la mise en quarantaine des foyers d'infection, la destruction des animaux malades et des animaux contaminés, la désinfection des locaux et une large vaccination, sous contrôle officiel, des volailles de l'Ile. En l'espace d'un mois la maladie a été enrayée. Pour les 47 foyers constatés les pertes se sont élevées à environ 35 000 têtes. Deux élevages commerciaux ont seulement été atteints, les autres foyers étant apparus dans les poulaillers des petits éleveurs.

     

A simple technique to differentiate between animals infected with Yersinia enterocolitica IX and those infected with Brucella abortus.

While both Brucella abortus and Yersinia enterocolitica IX have O antigens in common, they differ significantly with respect to motility. Thus Br abortus is always non-motile while Y enterocolitica is motile when grown at room temperature. The presence of yersinia H agglutinins in serum can be shown to be evidence of previous exposure to Y enterocolitica. These agglutinins are not generated by brucella infection. A rapid H agglutination test will serve to provide this differentiation without interference from cross-reacting O antigens.     

The susceptibility of chicken kidney and oviduct organ cultures to a vaccine strain of avian infectious bronchitis virus.

The minimal infectious dose of the H52 strain of infectious bronchitis virus for organ cultures of oviduct and kidney was compared in chickens of different ages. Organ cultures of oviduct were found to be highly susceptible to infection regardless of the age of chicken and no difference in susceptibility could be demonstrated between cultures of the magnum and uterus regions of the mature oviduct. Kidney organ cultures were less susceptible and resistance to infection increased significantly (P less than 0.001) with the age of the chicken from which cultures were prepared.     

Structure of the sheep epidermis.

The stratum corneum measured on fresh frozen sections was found to be considerably thicker than previously reported. It was uniformly permeated with sebum, which also formed an intact film over the skin surface and it could readily be divided into two zones. The living epidermis was approximately half as thick as the stratum corneum.     

The blood volumes and erythrokinetics of Ndama and Zebu cattle experimentally infected with Trypanosoma brucei.

The responses of susceptible Ndama and Zebu cattle to experimental infection with Trypanosoma brucei were compared using haematological, parasitological and radioisotopic methods. Animals of both breeds became anaemic, but this was more severe in the Zebu cattle, one of which died. Although the prepatent period was the same in animals of both breeds, the levels of the first and subsequent peaks of parasitaemia were higher in the Zebu. The anaemia was due to an accelerated rate of red cell break-down which was more marked in the Zebu cattle. Haemodilution was not a feature. There was no evidence of dyshaemopoiesis but iron reutilisation from degraded erythrocytes was impaired. The greater resistance of the Ndama to T brucei infection could not be attributed to the capacity of this breed to mount a more effective erythropoietic response than the Zebu.     

The effect of in vitro antibacterial properties of bovine milk diets on the natural colonisation of newborn piglets with coliform bacteria.

The diets suitable for the hand rearing of piglets in incubators were examined. Diet A was based on cows' milk heated to 56 degrees C and had bacteriostatic and antiadhesive properties against Escherichia coli. Diet B was based on evaporated cows' milk and did not have these properties. The numbers of coliform bacteria naturally colonising the small intestines of newborn piglets fed entirely on these diets for one week did not differ significantly, however both were significantly higher than in control piglets suckled from birth. Faecal counts of coliforms were similar in all three groups. Examination of the bacteriostatic sensitivity of the isolated strains to sows' milk indicated a predominance of milk-sensitive strains colonising the suckled piglets and a predominance of milk-resistant strains in the piglets fed diet B. This diet-dependent colonisation could not be explained by the in vitro bacteriostatic properties of the diets alone.