Influence of sugary-Brawn2 or dent corn at two forage levels on intake, digestion, and milk production by dairy cows.

Sugary-Brawn2 (su-Bn2) corn endosperm contains higher concentrations of watersoluble polysaccharides than dent corn. Eight multiparous Holstein cows averaging 48 d in milk and 667 kg BW at trial initiation were in a replicated 4 x 4 Latin square design with 28-d periods. Only cows in one square were ruminally cannulated. Treatments were su-Bn2 or dent corn and 45 or 60% of ration DM as alfalfa silage arranged as a 2 x 2 factorial within each square. Diets, formulated to contain 19% CP, were fed as total mixed rations twice daily. Intake of DM and milk yield averaged 26.8 and 39.9 kg/d, respectively, and were not affected by treatment (P > .10). Sugary-Brawn2 corn decreased milkfat percentage (3.27 vs 3.45%), particularly for the low-forage diet (3.15 vs 3.40%). Milk protein percentage was higher (3.15 vs 3.10%) for low-forage diets but was not affected (P > .10) by corn type. Ruminal pH was lower for low-forage diets. Feeding su-Bn2 corn decreased ruminal pH only at 4 h after feeding. Total VFA in ruminal fluid (millimolar) 6 h after feeding were higher, whereas acetate molar percentage and acetate:propionate ratio were lower for su-Bn2 corn. Ruminal in situ evaluation of su-Bn2 and dent corn revealed a larger soluble fraction, a faster rate of degradation, and higher availabilities of both DM and starch for su-Bn2 corn. Ruminal in situ rate of degradation and availability of alfalfa hay DM were reduced by su-Bn2 corn. Total tract apparent digestibilities of DM, CP, and starch were greater for su-Bn2 diets.(ABSTRACT TRUNCATED AT 250 WORDS)

Abnormal haemoglobins among pregnant women from Mozambique.

In a survey of 601 pregnant women in Mozambique, 34 (5.6%) were sickle cell trait carriers. Beta thalassaemia trait did not appear to be common. There was a slight rise in Hb F values in 49 women of the type reported previously in early pregnancy.

The effect of persistent malarial infections on haemoglobin A2 levels in Liberian children.

Children two to nine years old from an area of holoendemic malaria in northern Liberia had mean HbA2 and haematocrit values significantly (P less than 0.001) lower than others from a neighbouring town where malaria is hypoendemic. After regular administration of chloroquine over two years to 38 children living in a holoendemic village, their mean HbA2 rose from 2.1%, SE +/- 0.04, to 2.6%, SE +/- 0.08 (P less than 0.001) and their mean haematocrit from 0.348, SEM +/- 0.004, to 0.382, SE +/- 0.004 (P less than 0.001), values similar to those of children from the neighbouring town. In another village where chloroquine was not given regularly, mean HbA2, haematocrit and malariometric indices were little changed at the end of the two-year period. We conclude that persistent malarial parasitaemia was the main factor in the relatively low values of the village children. Although it is not clear how malaria depresses HbA, the findings were consistent with the hypothesis that chronic malaria induces iron-deficiency.

Haemoglobin variants, beta-thalassaemia and G-6-PD types in Liberia.

Haemoglobin variants, beta-thalassaemia and glucose-6-phosphate dehydrogenase (G-6-PD) types were studied in 702 individuals from Buchanan, Liberia. In this population haemoglobins S and C, beta-thalassaemia and G-6-PD deficiency were found together. There was a considerable tribal variation. In the tribes of eastern Liberia the S- and C-genes were uncommon and the beta-thalassaemia gene was rather frequent, while in western Liberia the S- and C-genes were more frequent and beta-thalassaemia uncommon. In the central and northern parts the S- and beta-thalassaemia genes were found together in relatively high frequencies. The rate of malaria infection was found to be lower in individuals with the sickle cell and beta-thalassaemia traits than in individuals with haemoglobin AA, but the difference was not statistically significant. The frequency of the delta-chain gene B2 was 1.4% in the total material and there was no significant tribal variation for this gene. The frequency of G-6-PD deficiency estimated in males was 16%.

Heterotypic antibodies in Liberian sera causing anomalous reactions when using a commercial haemagglutination test for hepatitis-B surface antigen.

Agglutinins reacting with normal and tanned sheep erythrocytes were the probable cause of false positive reactions given by 51 of 214 Liberian sera when using a commercial passive-haemagglutination test for hepatitis-B surface antigen. Absorption showed these agglutinins to be identical to those described earlier in Nigerian sera. Rheumatoid factor and anti-sheep-serum antibodies although present in 12 and five per cent respectively of all sera were not responsible for any false positive reactions. The practical conclusion is that such tests, based on sheep erythrocytes are unsuitable for screening this population.

Homozygous beta thalassaemia in Liberia.

The clinical and haematological findings in 19 Liberians probably homozygous for beta thalassaemia are described. The haemoglobin patterns were similar with Hb F levels in the 30-50% range and a raised level of Hb A2 and, although the clinical severity varied widely, over half the cases were symptomless and even the more severely affected ones showed a milder picture than that found in Mediterranean races. Haemoglobin-synthesis studies carried out on three homozygotes and two heterozygotes indicated a variable degree of globin-chain imbalance. The reasons for the mild course of the disease in Liberians and other African races are discussed; it is likely that the beta-thalassaemia genes in these populations are different from those in other racial groups. It is noted that all persons in this study belong to tribes which have a low incidence of the sickle-cell gene.

Thalassaemia in northern Liberia. A survey in the Mount Nimba area.

A population survey in northern Liberia showed an average incidence of 9 percent of beta-thalassaemia trait. There was considerable tribal variation, the highest rates being mainly found in tribes having a low incidence of Hb S. A single example of deltabeta-thalassaemia trait was also found; the incidence of delta-chain variants was 1.8 percent. The effect of malaria on Hb A2 levels was investigated but appeared to be negligible. The problems of beta-thalassaemia and Hb S occurring in the same population are discussed. It is considered that, although made on a local sample, the results of this survey indicate a high incidence of beta-thalassaemia trait elsewhere in Liberia and that this is a suitable are for investigations of linkage at beta- and delta-chain loci. No conclusion is at present possible from the data on the presence of alpha-thalassaemia although 10 percent of neonates were found to have increased levels of Hb Barts.