Isolation in east Senegal of a yellow fever virus strain from a pool of Aedes belonging to the subgenus Diceromyia]

During an epidemiological survey of yellow fever in Eastern Senegal, one strain of yellow fever virus was isolated in December 1976 from wild Mosquitoes. This first isolate obtained in nature from Aedes subgenus Diceromyia shows the primordial part these vectors may have in the area studied. It corroborates the existence of a selvatic focus of yellow fever in this region. It also gives information on the transmission cycle in a dry area.     

A strain of amaril virus isolated from Aedes africanus in the Ivory Coast]

The yellow fever virus has been isolated from a pool of Aedes africanus caught on men in a region situated between forest and savannah near Touba, in the Ivory Coast. This isolation, occurring at an interepidemic period, proves for the first time in West Africa, the part played by this mosquito in the transmission of the yellow fever virus.     

Kristalloide Strukturen im Zytoplasma von lymphatischen Zellen verschiedener Affen

Summary In the endoplasmic reticulum of cells of spleen and lymphnodes of different monkeys, crystalloid inclusions were often found. These inclusions show a pattern of small balls with a diameter of 250 Å, which are connected by 100 Å long bridges. It is supposed that these crystalloid inclusions are produced by the lymphatic cells as a reaction to virus infection, which remains clinically non-apparent, because the same pattern was observed in cells, which were experimentally infected with yellow fever virus, West Nile virus, and rubella virus.     

Biological and biochemical characterization of a new isolate of baboon Papio papio endogenous type C virus]

A new strain of Baboon Papio papio endogeneous type C virus was isolated from the testis of an animal of this species. The strain was characterized biochemically and biologically. It presents a host-range different from that of the prototype strain of the same virus.     

Some metabolic disorders affecting the carotenoid-linked haemolymph proteins inRhynchosciara americana (Diptera,Sciaridae)

Summary Disorders in the carotenoid metabolism are proposed to explain the absence of the yellow and violet or only the violet carotenoid-linked proteins from the haemolymph of someR. americana larvae. The lack of only the yellow chromoprotein is considered to be due to a failure in the biosynthesis of its apoprotein.Supported by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) and Conselho Nacional de Pesquisas (CNP_q). W.R.T. and A.G. de B. are indebted to Prof.F. J. S. Lara for advice, encouragement and for laboratory facilities. We thank Mr.A. Malavasi for collecting larvae in nature, Mrs.R. M. Zanelato for larvae culture and MissI. L. Jorge for typing.     

Isoenzymes of glutamate-oxalacetate transaminase in the larvae of silkwormsBombyx mori infected with nuclear polyhedrosis virus

Summary Nuclear polyhedrosis virus infection induced changes in the activity and isoenzyme pattern of glutamate-oxalacetate transaminase in the larvae of silkworm,Bombyx mori.The author wish to thank the director of CSRTI, Mysore for providing the virus preparation and the silkworm larvae.     

Die Pterine in der Haut und in den Augen vonSalamandra salamandra nach Aufzucht auf verschiedenfarbigem Untergrund

Summary Concomitantly with the morphological colour-change, larvae of Salamandra salamandra show a quantitative change in their pteridines. After being reared on a yellow background, all pteridines of the skin (isoxanthopterin and its derivatives, yellow pteridine, photosensitive pteridine) increase by about 1/3 as compared with the animals on a black background. In the retinal pigmentlayer especially, the photosensitive pteridine is augmented.     

Orientation ofPapilio demoleus larvae to coloured solutions

Summary The present work compares the taxis ofPapilio demoleus larvae to different coloured solutions. The larval positive taxis, i.e., attraction, is maximum for yellow colour and declines with the increase or decrease in the wavelength of maximum light transmission. Red and bluish-green colours repel the larvae.     

Dithyreanitrile: an unusual insect antifeedant from Dithyrea wislizenii

Dithyreanitrile, a novel sulfur-containing indole alkaloid, was isolated from the seeds of Dithyrea wislizenii (Cruciferae). Dithyreanitrile inhibits feeding of fall armyworm (Spodoptera frugiperda) and European corn borer (Ostrinia nubilalis) larvae. Dithyreanitrile, the first natural product with two sulfur atoms and a nitrile attached to the same carbon, was characterized by X-ray diffraction, spectroscopy, and chemical synthesis.     

Free amino acids of the haemolymph of the cotton leaf-worm,Spodoptera littoralis Boisduval full-grown larvae,infected with nuclear-polyhedrosis virus

Summary Free amino acids in the haemolymph ofSpodoptera littoralis full-grown larvae infected with a nuclearpolyhedrosis virus were compared with those in the haemolymph of normal insects. Amino acids were separated by 2-dimensional paper chromatography and quantified colorimetrically. Most of the amino acids in the haemolymph of diseased full-grown larvae decreased markedly in concentration but proline, lysine, aspartic acid and histidine occurred in greater concentration in the haemolymph of diseased full-grown larvae than in the haemolymph of healthy insects.     

Dithyreanitrile: an unusual insect antifeedant fromDithyrea wislizenii

Summary Dithyreanitrile, a novel sulfur-containing indole alkaloid, was isolated from the seeds ofDithyrea wislizenii (Cruciferae). Dithyreanitrile inhibits feeding of fall armyworm (Spodoptera frugiperda) and European corn borer (Ostrinia nubilalis) larvae. Dithyreanitrile, the first natural product with two sulfur atoms and a nitrile attached to the same carbon, was characterized by X-ray diffraction, spectroscopy, and chemical synthesis.     

Transcriptome profiling of lung schistosomula,in vitro cultured schistosomula and adult Schistosoma japonicum

The schistosomulum is the main target of vaccine-induced protective immunity; however, most studies have utilized schistosomula produced by mechanical transformation of infective larvae followed by in vitro culture rather than larvae isolated directly from the lungs of infected mammals. Using transmission electron microscopy, we demonstrated that there was little difference in the ultrastructure of Schistosoma japonicum schistosomula obtained by the two methods. However, significant differences in gene expression profiles were apparent when we used an oligonucleotide microarray to compare the gene expression profiles of schistosomula obtained in vivo from lung tissue with those maintained in vitro, and with adult worms of S. japonicum. It is likely that host environmental factors, which cannot be reliably reproduced in vitro, do influence the growth, development and overall biology of schistosomes. Thus caution is urged when using in vitro-cultured schistosomes and mechanically transformed/cultured schistosomula in molecular, biochemical and immunological studies.     

The effect of actinomycin D on the production of viruses by the protoplasts of Chinese cabbage infected in vitro by the yellow mosaic virus of turnips]

Chinese Cabbage (Brassica sinensis L. var. Cantonner) protoplasts were infected by Turnip yellow mosaic virus (TYMV) and inoculated in the presence or absence of actinomycin D. Virus production was determined 40 hrs. after inoculation, the time required for the virus replication cycle to be terminated. While actinomycin D had no effect on TYMV production when present at a concentration of 1 microng/ml, a 50 to 80% inhibition of virus production was noticed at concentrations of the order of 5 to 10 microng/ml, and the inhibition reached 90% with 25 microng/ml.     

Detection of caprine arthritis-encephalitis- and maedi-visna viruses using the polymerase chain reaction

Summary The polymerase chain reaction (PCR) was used to demonstrate proviral DNA of lentiviruses of small ruminants in cultured cells. Primers for the Taq polymerase were selected in the GAG gene of Icelandic maedi-visna virus and POL gene of caprine arthritis-encephalitis (CAE) virus. Using PCR, proviral DNA of CAE virus was detected at 1 day post infection, 4 days beforeviral protein could be demonstrated using a sensitive immunoblotting protocol and 6 days before the appearance of syncytia. Primers derived from the published sequence of CAE virus successfully primed for the synthesis of homologous virus and Icelandic maedi-visna viruss but not for maedi-visna virus isolated in The Netherlands. In contrast, primers derived from the GAG region of Icelandic maedi-visna virus allowed the amplification of DNA of homologous virus, maedi-visna virus isolated in The Netherlands as well as CAE virus.     

Detection of human cytomegalovirus (HCMV) DNA from cell-free plasma of immunosuppressed patients by nested PCR: influence of nucleic acid extraction method

Conclusions Blood cells and plasma preparations from HCMV-seropositive healthy blood donors were all nPCR negative. Detection of HCMV DNA from PBMC and granulocytes (DNAemia) of immunosuppressed patients by nPCR did not correlate with the isolation of infectious virus from these cell populations in cell culture (viremia). However HCMV could be isolated in 60% of cases from other materials of the same patient. HCMV DNA detected in blood cells persisted for up to one year in an asymptomatically infected individual after NTX. The sensitivity of HCMV DNA detection in cell-free plasma (up to 5 fg) depended on the method used for DNA isolation. The rate of HCMV DNA detection in plasma was lower than in leukocytes. In all cases of positive plasma PCR infectious virus could be isolated from any other material of the symptomatically infected patients. Therefore HCMV DNA PCR from plasma of immunosuppressed patients seems to be a suitable and easy alternative to HCMV RT/PCR for routine diagnosis of HCMV disease.     

Studies on experimental ancylostomiasis: transfer of acquired immunity to Ancylostoma caninum in mice through sensitized thymus and bone marrow cells.

An attempt has been made to transfer acquired immunity to Ancylostoma caninum infective larvae from infected Swiss albino female mice to nonimmune, isologous recipients of same sex, through immunized thymus and bone marrow cells. Immunized cells from donors infected with a single high dose of 1000 larvae were found to be more immunocompetent than cells from donors infected with a single, but low dose of 500 larvae.     

Course of fever response to repeated administration of sublethal doses of lipopolysaccharides, polyinosinic:polycytidylic acid and muramyl dipeptide to rabbits

The purpose of the present study was to examine the development of tolerance to three structurally dissimilar pyrogens, i.e., lipopolysaccharide (LPS), muramyl dipeptide (MDP) and polyinosinic:polycytidylic acid (poly I:C) in rabbits. The possibility of pyrogenic cross-tolerance among these agents has also been studied. It was observed that repeated injection of sublethal doses of LPS and MDP was connected with the changing of biphasic fever to monophasic. The consequence of this was a drop in the fever index. In contrast to LPS and MDP, the repeated administration of poly I:C did not result in such changes. Successive injections of this pyrogen always evoked biphasic fever. We also demonstrated that pyrogenic cross-tolerance between LPS and MDP did not occur. The cross-tolerance between LPS and MDP did not occur. The cross-tolerance among pyrogens was possible if they originated from the same class, for example endotoxin from Salmonella abortus eq. and endotoxin from Escherichia coli.     

Insect antifeedant properties of withanolides and related steroids from Solanaceae

Summary Physalis peruviana shrubs were not attacked by larvae ofSpodoptera littoralis. It was demonstrated that withanolide E, a steroid isolated fromP. peruviana, as well as several related steroids, have insect antifeedant properties.     

Distribution of tunichrome and vanadium in sea squirt blood cells sorted by flow cytometry

Specialized blood cells of many tunicates accumulate high concentrations of vanadium and phenolic peptide pigments called tunichromes (TC). In order to determine whether V and TC reside in the same cells, Ascidia nigra and Ascidia ceratodes blood cell subpopulations were isolated by fluorescence-activated cell sorting (flow cytometry) and chemically analyzed. V was found in the spherical, green/grey signet ring cells, and to a lesser degree in the mulberry-shaped, yellow/green morula cells (MRs), whereas free TC was detected mainly in MRs.