The mtDNA legacy of the Levantine early Upper Palaeolithic in Africa

Sequencing of 81 entire human mitochondrial DNAs (mtDNAs) belonging to haplogroups M1 and U6 reveals that these predominantly North African clades arose in southwestern Asia and moved together to Africa about 40,000 to 45,000 years ago. Their arrival temporally overlaps with the event(s) that led to the peopling of Europe by modern humans and was most likely the result of the same change in climate conditions that allowed humans to enter the Levant, opening the way to the colonization of both Europe and North Africa. Thus, the early Upper Palaeolithic population(s) carrying M1 and U6 did not return to Africa along the southern coastal route of the "out of Africa" exit, but from the Mediterranean area; and the North African Dabban and European Aurignacian industries derived from a common Levantine source.     

Variation in competitive abilities of plants and microbes for specific amino acids

 Microbes are assumed to possess strong competitive advantages over plants for uptake of nutrients from the soil. The finding that non-mycorrhizal plants can obtain a significant fraction of their N requirement from soil amino acids contradicts this assumption. The amino acid glycine (Gly) has been used as a model amino acid in many recent studies. Our preliminary studies showed that Gly was a poor substrate for microbial growth compared to other amino acids. We tested the hypothesis that the alpine sedge Kobresia myosuroides competes better for Gly than for other amino acids because of decreased microbial demand for this compound. Soil microbial populations that could grow using Gly as a sole carbon source were about 5 times lower than those that could grow on glutamate (Glu). Gly supported a significantly lower population than any of the ten other amino acids tested except serine. In contrast, K. myosuroides took up Gly from hydroponic solution at faster rates than Glu. In plant-soil microcosms, plants competed with soil microbes 3.25 times better for Gly than for Glu. We conclude that the low microbial demand and the rapid plant uptake of Gly relative to other amino acids allow Gly to be an especially important nitrogen source for K. myosuroides. Received: 9 February 1998     

Pseudomonas fluorescens contamination of a feline packed red blood cell unit and studies of canine units

Background: While screening programs have reduced the risk of infectious disease transmission by donors in human and veterinary blood banking, bacterial contamination of blood products has emerged as a major complication in human medicine. Objectives: To describe a Pseudomonas fluorescens (Pf)‐contaminated feline packed RBC (pRBC) unit and experimentally investigate Pf‐contaminated canine pRBCs. Methods: Canine pRBCs were inoculated with Pf‐rich pRBCs from the sentinel feline unit and stored at 4°C or 20°C for 72 hours. Aliquots from the pRBCs were serially evaluated by microscopy, culture, and a eubacterial 16S rRNA real‐time PCR assay. Results: One Pf‐contaminated feline unit turned black after 22 days of storage and was removed from the blood bank; a source was not found, and no other contaminated units were identified. Canine pRBCs spiked with 5 or 25 μL of the sentinel unit became culture‐ and/or 16S PCR‐positive at ≥8 hours at 20°C and 48 hours at 4°C and developed a color change at ≥24 hours. Sensitivity studies indicated that without incubation, inoculation of ≥100 μL Pf‐rich pRBCs was necessary for a positive 16S PCR test result. Conclusions: P. fluorescens grows in stored pRBCs slowly at 4°C and rapidly at 20°C. Screening of blood products for color change, estimating bacterial concentration with microscopy, and 16S PCR testing are simple and fast ways to detect bacteria in stored blood. Aseptic collection, temperature‐controlled storage, and regular visual monitoring of stored units is recommended. Discolored units should not be transfused, but examined for bacterial contamination or other blood product quality problems.     

Performance of ‘Coscia’ pear (Pyrus communis) on seven rootstocks in a warm climate

Summary

The vegetative and reproductive performance of ‘Coscia’ pear (Pyrus communis L.) growing on seven rootstocks [OHF 69, OHF 97, OHF 513 and BP 1 (P. communis), clonal seedling (Davis AxB) of P. betulifolia, and quince BA 29 and EMA (Cydonia oblonga)] were compared over an 8-year period. The trial was conducted at the Experimental Orchard Farm Station in northern Israel, on a well-drained soil with pH 7.5. Trees were planted in December 1998 at a distance of 4.0 m 2.0 m, and trained with a central axis. The most vigorous trees were on P. betulifolia seedling, followed by BP 1 and the three OHF rootstocks (69, 97, 513). All the above rootstocks demonstrated greater vigour than quince BA 29 or EMA. The reason for this effect, at least in part, appeared to be the excellent water status (high midday stem water potential values) of trees on P. betulifolia in comparison with the other rootstocks. The highest cumulative yields per tree were harvested from trees on P. betulifolia and BP 1, followed by the three OHF rootstocks (69, 97, 513). However, the highest cumulative yield of large fruit (> 60 mm) was obtained from trees on P. betulifolia, followed by the OHF series and BP 1. The two quince rootstocks had the lowest cumulative yield, and the lowest yield of large fruit. A positive correlation was found between the vigour of the tree, as affected by the rootstock, and both total yield and fruit size. We conclude that, in a warm climate, yield efficiency is not the only parameter that should be taken into account, and building a strong tree for the weak scion cultivar is the first requirement for establishing an orchard. Fruit quality at harvest and during cold storage were examined for fruit from three rootstocks only. The highest soluble solids content values at harvest were obtained in fruit grown on quince EMA, compared to values for BP 1 and P. betulifolia fruit.     

Effect of triflumuron on two species of nitidulid beetles,Carpophilus hemipterus andUrophorus humeralis

Egg hatch of two nitidulids,Carpophilus hemipterus L. andUrophorus humeralis F., was affected by the chitin synthesis inhibitor triflumuron (Alsystin; BAY SIR 8514)via the adult stage of the beetle. This occurred by exposure to treated diets, by a brief dip of the adults in aqueous dilutions of the toxicant, or by contact with a treated plastic netting cage. Exposure of adults ofC. hemipterus for 24 h to 0.0125%, 0.00125%, 0.00025% or 0.000125% and ofU. humeralis to 0.0125% a.i.-treated diets completely prevented hatch of eggs laid during the subsequent 48 h on an untreated diet. Although at first sterile eggs were obtained with adults of either nitidulid species transferred to an untreated diet after 24 h exposure to the 0.0125%-treated diet, egg viability gradually recovered. The speed of recovery and the course of mortality of larvae that hatched from eggs laid by treated adults, indicated thatC. hemipterus was more susceptible thanU. humeralis to triflumuron. DippingC. hemipterus adults — males or females — in 0.0125% a.i. triflumuron also resulted in complete prevention of egg hatch. Similar results were obtained by a 1-h contact of adults with treated cages. Triflumuron had no direct ovicidal activity against the two species at the concentrations used but was very effective against larvae of both species. At 0.0125% a.i., 3-5-mm-long larvae ofU. humeralis were more tolerant than newly hatched larvae and than 3-5-mm-long larvae ofC. hemipterus. Application of 0.0125% a.i. triflumuron in a date palm grove did not prevent fruit infestation by nitidulid adults but, due to prevention of egg hatch, almost no larval development was observed.     

The alarmin interleukin-33 drives protective antiviral CD8⁺ T cell responses

Pathogen-associated molecular patterns decisively influence antiviral immune responses, whereas the contribution of endogenous signals of tissue damage, also known as damage-associated molecular patterns or alarmins, remains ill defined. We show that interleukin-33 (IL-33), an alarmin released from necrotic cells, is necessary for potent CD8(+) T cell (CTL) responses to replicating, prototypic RNA and DNA viruses in mice. IL-33 signaled through its receptor on activated CTLs, enhanced clonal expansion in a CTL-intrinsic fashion, determined plurifunctional effector cell differentiation, and was necessary for virus control. Moreover, recombinant IL-33 augmented vaccine-induced CTL responses. Radio-resistant cells of the splenic T cell zone produced IL-33, and efficient CTL responses required IL-33 from radio-resistant cells but not from hematopoietic cells. Thus, alarmin release by radio-resistant cells orchestrates protective antiviral CTL responses.     

Developmental and varietal differences in volatile ester formation and acetyl-CoA: alcohol acetyl transferase activities in apple (Malus domestica Borkh.) fruit

Apple (Malus domestica Borkh.) cultivars differ in their aroma and composition of volatile acetates in their fruit flesh and peel. Cv. Fuji flesh contains substantial levels of 2-methyl butyl acetate (fruity banana-like odor), while the flesh of cv. Granny Smith apples lacks this compound. Granny Smith apples accumulate mainly hexyl acetate (apple-pear odor) in their peel. Feeding experiments indicated that Fuji apples were able to convert hexanol and 2-methyl butanol to their respective acetate derivatives in vivo, while Granny Smith apples could only convert exogenous hexanol to hexyl acetate. Differential substrate specificities of the in vitro acetyl-CoA:alcohol acetyl transferase (AAT) activities were also detected among cultivars. In Granny Smith apples, the AAT activity was detected only in the peel, and its specificity was almost exclusively restricted to hexanol and cis-3-hexenol. In Fuji apples, the AAT activity was detected in both peel and flesh and apparently accepted a broader range of alcohols as substrates than the Granny Smith enzyme activity. Our data strongly suggest that different AAT activities are operational in apple tissues and cultivars and that these differences contribute to the variation observed in the accumulation of volatile acetates.