Genotype x environment interaction for root traits in maize,as analysed with factorial regression models

Summary The efficiency of genotopic and climatic characteristics in accounting for the interaction between genotypes and environments has been assessed in a three-year trial involving a set of genotypes presenting a range of root morphology characteristics (number and size). Climatic information on rainfall and temperature was recorded during the experiments, together with extra data on the growth and development of the genotypes. Their effects have been tested in factorial regression models.Climatic covariates were very powerful in accounting for the genotype by year interaction as well as the year main effect alone. For the number of adventitious roots on internode 7, the main effect of year could be described as a linear function of the average temperature and precipitation that occurred during the period of root initiation and growth. For internode 6, no clear conclusion was possible. For the root traits studied, 74 to 98% of the interaction could be explained by one climatic covariate. The regression coefficients can be considered as measures of genotypic stability.The genotypic covariates describing aerial development performed rather poorly, compared with environmental ones, even though the physiological and functional relationships between root and shoot are well known. Neither genotype main effect nor genotype by year interaction could be described sufficiently by factorial regression. Still, the genotypic covariates performing best clearly differed between root counts and size. Also the best genotypic covariates differed for main effect and interaction.     

Genetic basis of species differentiation between <Emphasis Type="Italic">Coffea liberica</Emphasis> Hiern and <Emphasis Type="Italic">C. canephora</Emphasis> Pierre: Analysis of an interspecific cross

The phenotypic and genetic differentiation between the two related Coffea species (C. liberica Hiern and C. canephora Pierre) was examined. These species differed markedly in terms of leaf, inflorescence, fruit and seed characters. A genetic map of the interspecific cross Coffea liberica × C. canephora was constructed on the basis of 72 BC1 hybrids. Eighty-three AFLP markers, four inter simple sequence repeats (ISSR) and five microsatellites corresponding to Coffea liberica species-specific markers were mapped into 16 linkage groups. The total length of the map was 1502.5 cM, with an average of 16.3 cM between markers and an estimated genome coverage of 81%. The two species were evaluated relative to 16 quantitative traits and found to be significantly different for 15 of them. Eight QTLs were detected, associated with variations in petiole length, leaf area, number of flowers per inflorescence, fruit shape, fruit disc diameter, seed shape and seed length. Results on segregation distortion and the under-representation of particular markers were interpreted in terms of genome differentiation. The implications for the introgression of QTLs involved in advantageous morphological traits (number of flowers per inflorescence, fruit and seed shape) are discussed.     

The principal component scoring: A new method of constituting a core collection using quantitative data

The principal aims of a core collection are: 1) to include the maximum of diversity of the base collection in a sample of minimum size; and 2) to avoid redundancies. We present here a new method (the Principal Component Scoring) which fulfills these aims. The use of P.C.S. has consequences for sampling stratification and choice of sample size. P.C.S. requires quantitative data, but with small changes can be used for qualitative data.     

Acquisition of haemoglobin-bound iron by Histophilus somni

Histophilus somni is an important pathogen of cattle and sheep. H. somni requires iron and can use ruminant transferrins as iron sources for growth. Here, we investigated the abilities of bovine (strains 649 and 2,336) and ovine (strains 9L and 3384Y) isolates of H. somni to acquire iron from haemoglobins. Using growth assays, the bovine isolates were shown to acquire iron from bovine haemoglobin, but not from ovine, porcine or human haemoglobins; the ovine isolates, however, failed to use any of these haemoglobins as iron sources for growth. In solid phase binding assays, the bovine isolates, grown under iron-restricted conditions in the presence of bovine haemoglobin, bound not only bovine but also ovine and human haemoglobins. Competition binding assays indicated that all three haemoglobins were bound by the same receptor(s) and SDS-PAGE of membrane fractions revealed that expression of haemoglobin-binding activity was associated with the production of an approximately 120-kDa outer membrane protein. PCR approaches allowed the amplification and sequencing of hgbA, and also hugX and hugZ homologues from strains 649, 9L and 3384Y. While hgbA of strain 649 was predicted to encode an HgbA precursor that is processed to yield a mature, 123.9-kDa haemoglobin-binding protein, the hgbA genes of strains 9L and 3384Y were predicted to give rise to truncated products. RT-PCR experiments revealed that in strain 649, hugX, hugZ and hgbA are co-transcribed and iron-regulated and additional sequencing suggested that in strain 2336, expression of HgbA is subject to phase variation involving a poly C tract within hgbA.     

Degradation of cyclins D in pseudorabies virus (PRV) infected proliferating cells

The pseudorabies virus code for an ICP0 protein which is half the size of the HSV1 ICP0 protein. In this work, we made the assumption that some function might have been lost in the ICP0 from PRV. One function attributed to the ICP0 from HSV1 was the stabilization of cyclins D. We then looked at the stability of these cyclins during the lytic infection with the PRV. Our results show that cyclins D are not stabilized during infection with the PRV. These results are in accord with recent data from the literature.     

Identification of apolipoprotein A‐I in the α‐globulin fraction of avian plasma

Background: Plasma protein electrophoresis is frequently used in birds as a tool for the diagnosis and monitoring of disease. Identification of proteins in individual peaks can help improve our understanding of changes in protein concentration in physiologic and pathologic conditions. Objective: The aim of this study was to verify the presence and identity the protein(s) in the prominent α‐globulin peak of orange‐winged parrots (Amazona amazonica), black kites (Milvus migrans), and rock pigeons (Columba livia). Methods: Heparinized plasma samples were obtained from 12 birds of each species. Agarose gel electrophoresis and total protein concentration were determined using standard techniques. One plasma sample from each species was then electrophoresed using high‐resolution agarose gels to isolate the α‐globulin band. Gel strips were digested in trypsin and peptides were extracted and analyzed using liquid chromatography with tandem mass spectrometry. De novo sequencing was used to identify the protein based on homology scoring against a protein database. Results: Electrophoresis verified the presence of a single prominent α‐globulin peak, usually in the α₁‐region, that had a median concentration of 9.4 g/L (range, 2.1–11.7 g/L, 21.6% of total protein) in parrots, 12.2 g/L (10.4–13.2 g/L, 35.9%) in kites, and 10.7 g/L (9.0–11.5 g/L, 40.0%) in pigeons. Mass spectrometry and sequencing analysis unequivocally identified the protein as a mature circulating form of apolipoprotein A‐I (apo A‐I) in all 3 species. Conclusions: Apo A‐I accounts for the prominent α‐globulin peak and comprises a major proportion of total protein concentration in diverse avian species. As a high‐density lipoprotein and negative acute phase protein with a pivotal role in cholesterol homeostasis, further study is warranted to determine the significance of changes in apo A‐I concentration in avian electrophoretograms.     

Atypical pneumonia associated with a Mycoplasma isolate in a kitten

An atypical case of Mycoplasma pneumonia with an unusual radiographic and computed tomographic pattern was diagnosed in a Siamese kitten. The cat showed no response to broad-spectrum antibiotic therapy including enrofloxacin. The administration of doxycycline led to a dramatic clinical and radiographic improvement.     

Use of a new and rapid milk progesterone assay to monitor reproductive activity in the cow

A new and rapid enzyme-amplified immunoassay (AELIA) has been developed for the measurement of progesterone in milk. The AELIA system is a non-isotopic method that gives results within 35 minutes. Milk progesterone concentrations measured in 10 cows sampled daily at various stages of the reproductive cycle were very similar to those recorded by a validated radioimmunoassay. The results show that the speed and sensitivity of the AELIA system would make it possible to diagnose pregnancy rapidly at about 24 days after insemination, to predict the onset of behavioural oestrus from decreasing progesterone values during the third week after a preceding oestrus, and to obtain a daily record of milk progesterone levels in animals treated for infertility of ovarian origin.