Ticks (Acari:Ixodidae) of the Blue and White Nile ecosystems in the Sudan with particular reference to theRhipicephalus sanguineus group

Twenty-four adult ixodid tick species, infesting livestock and some wildlife hosts along the Blue and White Nile in the Sudan, were identified. Three species,Boophilus geigyi, Rhipicephalus camicasi andR. bergeoni, were recorded for the first time from the Sudan. Tick numbers on indigenous breeds of cattle (Bos indicus) were relatively low, ranging between 17.1 and 40.5 per animal. Young cattle grazing with the herd carried significantly fewer ticks than older animals. With the exception ofB. annulatus andR. simus, which have extended their distribution further north into Blue Nile, Gezira and Khartoum Provinces, the distribution patterns of the most important cattle ticks have been relatively unchanged over the past 30 years.TheRhicicephalus sanguineus group was represented by six species.R. camicasi was the only species present on cattle, sheep and goats in the north in Kassala and Khartoum Provinces, whereas this species occurred sympatrically withR. guilhoni andR. turanicus further south in Gezira and Blue Nile Provinces. In the Southern Region of the Sudan onlyR. turanicus andR. guilhoni were present, the latter being by far the predominant species, with peak activity towards the end of the rains in the Jonglei Canal Area.R. bergeoni was collected once, from cattle near the Ethiopian border in Blue Nile Province, whereasR. sanguineus sensu stricto was collected throughout the study area, from domestic dogs only. Finally,R. sulcatus was found once on a hare.The distributions of the common tick species are correlated with the occurrence of tick-borne diseases of domestic animals and recommendations for the control of tick-borne diseases and their vectors in the Sudan are given.     

18-Substituted steroids. Part 15. 6 beta-Hydroxylation of aldosterone by liver

6 beta-Hydroxyaldosterone and 6 beta-hydroxy-17-isoaldosterone, characterized by high-field NMR studies, are among the major polar metabolites formed from aldosterone by incubation with rat liver slices or microsomal fraction. It is uncertain at present whether the 17-iso product results from an enzymatic or a chemical inversion of configuration. Periodate degradation of the 6 beta-hydroxyaldosterone gave 6 beta-hydroxyaldosterone gamma-lactone, identical with a synthetic sample.     

A genetic linkage map of 96 loci on the short arm of human chromosome 3.

We constructed a genetic map of 96 loci on the short arm of human chromosome 3 (3p) in 59 families provided by the Centre d'Etude du Polymorphisme Humaine (CEPH). Twenty-nine continuously linked loci were placed on the map with likelihood support of at least 1000:1; one locus, D3S213, was placed on the map with likelihood support of 871:1; D3Z1, an alpha satellite centromeric repeat probe, was placed on the map with likelihood support of 159:1; 65 loci were assigned regional locations. The average heterozygosity of the uniquely ordered markers was 49%. The map extends from 3p26, the terminal band of 3p, to the centromere (from D3S211 to D3Z1). Multipoint linkage analysis indicated that the male, female, and sex-averaged maps extend for 102, 147, and 116 cM, respectively. The mean genetic distance between uniquely ordered loci on the sex-averaged map was 4.0 cM. Probe density was greatest for the region of 3p between D3F15S2e and the telomere. The sex-averaged map contained two intervals greater than 10 cM. Seventeen probes were localized by fluorescence in situ hybridization. The loci described in this report will be useful in building an integrated genetic and physical map of this chromosome.     

Studies on the agglutinating activity of pancreatic extracts and its relevance to function

Summary Agglutination of washed rabbit erythrocytes caused by pancreatic acinar cell extract was inhibited by glucose, maltose and cellobiose. Process of elimination and purification divulged that the acinar cell enzyme -amylase was responsible for attributing the agglutinin activity. Assay of enzyme and agglutinin activity data of different fractions of re-purified -amylase eluted from HPLC column showed that both the activity resides in the same fraction which suggests that the enzyme binds to the glucosyl residues of the rabbit erythrocytes via the carbohydrate binding/catalytic sites. Similar properties of other glycosidases were also noted.