Treatment of the repeat breeder cow syndrome in Kenya

Summary One hundred repeat breeder dairy cows have been studied in detail. Although clinically 60 per cent of them were normal bacteria were isolated from the uteri of the majority (90 per cent). Thirty per cent of these isolates were mixed.Intra-uterine infusion of the uteri with diluted Lugol's Iodine solution, supplemented in a few cases by antibiotic therapy, resulted in a 62 per cent conception rate compared with 26 per cent in the control group. It is concluded that dilute Lugol's Iodine is a useful treatment for repeat breeder cows under conditions similar to those described.

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Tratamiento Del Sindrome De Vacas Repetidoras En Kenya

Resumen Se estudíaron en detalle 100 vacas repetidoras destinadas a la producción de leche, en Kenya. Aunque el 60 por ciento de ellas parecía normal clinicamente, se aislaron bacterias del útero de la mayoría (90 por ciento). El 30 por ciento de los aislamientos fue mixto.La infusión intrauterina de una solución diluída de Lugol, combinada en algunos casos con antibióticos, resultó en una proporción del 62 por ciento de concepciones, comparada con el 26 por ciento del grupo control. Se concluye, que la solución de Lugol diluída es útil para el tratamiento del síndrome de vacas repetidoras, bajo condiciones similares a las aquí descritas.

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Traitement Du Syndrome De L'Accouplement Repete Chez La Vache Au Kenya

Résumé Cent vaches laitières ont été examinées avec soin. Bien que 60 p. 100 d'entre elles aient été considérées comme normales, des germes ont été isolés de l'utérus de la majorité d'entre elles (90 p. 100). Dans 30 p. 100 des cas, la population microbienne était mixte.Des injections intra-utérines d'une solution diluée de Lugol accompagnée dans quelques cas par de l'antibiothérapie ont fait que le groupe traité à un taux de fécondité de 62 p. 100 contre 26 p. 100 dans le groupe témoin. Les auteurs concluent que la solution iodée de Lugol constitute un traitement utile chez les vaches contre ce syndrome, dans les conditions semblables à celles décrites.

     

Serological evidence of the occurrence of bluetongue in Iraq.

Precipitating antibodies against bluetongue were detected in sheep and goat serum samples collected from animals slaughtered in Baghdad abattoir. Out of 294 sheep serum samples and 110 goat serum samples examined, 28 and 18 samples respectively showed precipitating activity. In addition, examination of sheep serum samples collected from localities where clinical cases similar to bluetongue were previously reported revealed the presence of bluetongue precipitating antibodies in 101 sera out of 198 samples examined. This is the first report confirming the occurrence of bluetongue in Iraq.     

Kinetics of NDV specific antibodies in chickens—V. Analysis of frequency distributions of antibody titers against Newcastle disease virus by investigation of random samples in chicken flocks

Chicks and chickens maintained under commercial conditions were vaccinated against Newcastle Disease via drinking water. Prior and after different times of vaccination blood samples were drawn from different numbers of birds and checked for HI antibodies. The modes of distribution of the antibody titers within the random sample were assayed. The following results were obtained:

1. 1. On the basis of the distribution of the serum titers can be concluded whether the antibody level within a flock is increasing or decreasing.

◦ —A right steep asymmetry can be observed up to 20 days post vaccination.

◦ —In the phase of maximal antibody levels an almost symmetric distribution of the titers is present.

◦ —In later times (more than three weeks p. vacc.) the distribution shows a left steep asymmetry (Poisson distribution).

2. 2. A poisson distribution is also observable during the elimination of maternal antibodies of chicks until complete elimination.

3. 3. The mode of distribution of the HI titers in sera of day-old chicks correlates with the mode of distribution of the dams. Therefore, conclusions are possible from the status of the chicks to the dams and reverse.

4. 4. Factors which interfere with the mode of distribution are:

◦ —Two or more peaks after vaccination of chickens. This indicates an uneven immune response within the flock.

◦ —Distributions with several peaks may also occur if flocks are composed of day-old chicks from parent flocks with different levels of antibody titers.

Some characteristics of a natural infection by parainfluenza-3 virus in a group of calves.

Parainfluenza-3 (Pi3) virus infection in a group of 25 calves is described. The virus was isolated from the lungs of four calve at days 6, 7, 13 and 55 after they were housed together at birth. Intracytoplasmic inclusion bodies were seen by light microscopy in bronchial and bronchiolar epithelial cells of two of these calves. Virus infected cells were detected by electron microscopy in three of the four calves. Haemagglutination inhibition antibodies to Pi3 virus were found in the sera of the calves. Despite the virus being present in the group from one week, a significant increase in antibody titre was found in only two animals although all the calves were in contact with each other during the study period. The pulmonary lesions in the four infected calves consisted of a bronchitis and bronchiolitis with infiltration of the walls and lumena of these structures by neutrophils and an adjacent neutrophil infiltration of alveoli some of which were collapsed.     

Scanning electron microscope study of Sendai virus fusion between HeLa cells and chick erythrocytes.

Chick erythrocytes were fused with HeLa cells by Sendai virus and preparations examined by scanning electron microscopy at different times after fusion. Heterokaryons were usually formed by fusion of erythrocyte ghosts with HeLa cells. Occasionally whole erythrocytes were engulfed but there was no evidence that free nuclei fused. Initial inter-cell attachments were usually, and possibly always, made at the site of an attached virus particle. This study helps to correlate topographical findings with previous two-dimensional studies with the transmission electron microscope and may also provide a model system for the fusion of parasitised erythrocytes with eukaryotic cells.     

Relative persistence of di-and tri-chlorophenoxyalkanoic acid herbicides in Saskatchewan soils

The persistence of 2,4-D, 2,4-DB, dichlorprop, 2,4,5-T, and fenoprop at the 2 ppm level was studied in the laboratory on three prairie soils at 85% of field capacity and 20°C. Following extraction of the soils with aqueous acetonitrile containing acetic acid, the herbicidal acids remaining were analysed gas chromatographically. Breakdown was rapid on all soils and the average half-lives for 2,4-D, 2,4-DB, dichloroprop, 2,4,5-T, and fenoprop were < 7, < 7, 10, 12, and 12 days respectively. Degradation on air-dried soils (15% of field capacity) was negligible with over 85% of the applied herbicides being recoverable after incubation periods during which the herbicides remaining in the moist soils accounted for less than 30% of the original treatments. Persistance relative des acides di et tri-chlorophénoxy-alkanoï-ques herbicides dans des sols du Saskatchewan. La persistance du 2,4-D, du 2,4-DB, du dichlorprop, du 2,4,5-T et du fénoprop, à la concentration de 2 ppm, a étéétudiée au laboratorire, sur trois sols de prairie, a 85% de la capacité au champ et a 20°C. Après leur extraction des sols par l'acétonitrile aqueux contenant de l'acide acétique, les acides herbicides restants ont été analysés par chromatographie en phase gaseuse. La dégradation a été rapide pour tous les sols et les demi-vies moyennes du 2,4-D, du 2,4-DB, du dichlorprop, du 2,4,5-T, et du fénoprop ont été respectivement de <7, <7, 10, 12 et 12 jours. La dégradation sur des sols séchés a l'air (15% de la capacité au champ), a été négligeable, plus de 85% des quantités d'herbicides appliquées étant récupérables après des périodes d'incubation durant lesquelles les herbicides restant dans les sols humides ne représentaient plus que moins de 30% des quantités apportées à l'origine. Relative Persistenz von Di-und Trichlorphenoxyalkansäure-Her-biziden in Böden Saskatchewan In Laborversuchen wurde die Persistenz von 2,4-D, 2,4-DB, Dichlorprop, 2,4,5-T und Fenoprop in drei Prärieböden festgestellt. Die Versuche wurden bei 20°C, 85 % der Feldkapazität und einem anfänglichen Herbizidgehalt der Böden von 2 ppm durchgeführt. Die Extraktion der Böden erfolgte mit wässerigem Acetonitril mit einem geringen Anteil an Essigsäure. Die Herbizide wurden gaschromatographisch nachgewiesen. In allen Böden wurde ein schneller Abbau festgestellt. Die Halbwertszeiten betrugen für 2,4-D, 2,4-DB, Dichlorprop, 2,4,5-T und Fenoprop < 7, < 7,10, 12 bzw. 12Tage. Der Abbau im lufttrockenen Boden (15% der Feldkapazität) war zu vernachlässigen. Hier waren noch mehr als 85% der ausgebrachten Herbizidmenge vorhanden, wenn in den feuchten Böden die Konzentration bereits weniger als 30% betrug.     

Differentiation of strains of bean common mosaic virus

Pathogenicity and symptom expression of seventeen described isolates of bean common mosaic virus (BCMV) and five previously unreported isolates were compared on many bean cultivars (Phaseolus vulgaris L.). From these cultivars, a standard set of differentials were assigned to nine groups with different disease reactions. The twenty-two virus isolates comprised seven strain (pathotype) groups, three of which were divided into two subgroups each. To promote international standardization in BCMV research, recommendations are given for test conditions and procedures, criteria for strain differentiation, and maintenance of differential cultivars and virus strains.Samenvatting Zeventien beschreven stammen van het bonerolmozaïekvirus en vijf niet geïdentificeerde isolaten (Tabel 1) werden bestudeerd op een uitgebreide reeks van toetsrassen. De meeste van deze toetsrassen waren in de literatuur als zodanig vermeld, maar door de desbetreffende onderzoekers waren vaak verschillende series toetsrassen gebruikt, hetgeen de onderlinge vergelijking van de stammen bemoeilijkte.De bedoeling van dit onderzoek was: vergelijking en indeling van de virusstammen, samenstelling van een standaard-toetsrassenserie en het ontwerpen en beschrijven van werden zowel in Wageningen als in Prosser, Washington, USA, uitgevoerd met dezelfde virusisolaten en dezelfde zaadmonsters van de toetsrassen.De toetsrassen konden op grond van hun differentiële reacties na inoculatie met de virusstammen worden ingedeeld in negen groepen. De rassen binnen een groep hebben hetzelfde resistentiespectrum t.o.v. een standaardserie virusstammen. Uit elke groep werden op grond van hun geschiktheid (duidelijkheid en reproduceerbaarheid van de symptomen) één of meer vertegenwoordigers gekozen, waaruit een standaardserie van toetsrassen werd samengesteld (Tabel 2).De 22 stammen en isolaten werden op grond van hun pathogeniteitsspectrum t.o.v. de standaardserie van toetsrassen ingedeeld in tien groepen en subgroepen (Tabel 1). De stammen en isolaten binnen een groep of subgroep hebben eenzelfde pathogeniteitsspectrum (Tabellen 4 en 6) en worden op grond daarvan als identiek beschouwd. De differentiële reacties tussen de rassen van de standaardserie en de virusstammen en-isolaten zijn vermeld in de Tabellen 3 en 5. Voorgesteld wordt om de naam van de eerstbeschreven stam van iedere groep te handhaven en de andere stammen in een groep of subgroep op te vatten als isolaten daarvan.De toetsmethodiek wordt uitvoerig beschreven om standaardisatie van de stammenidentificatie te bevorderen. Ter verklaring van de in de literatuur gevonden tegenstrijdigheden in de differentiële reactie van de toetsrassen wordt een negental mogelijke oorzaken genoemd, o.a. het gebruik van planten van toetsrassen die reeds vanuit zaad met een onbekende stam waren besmet en het gebruik van onzuivere virusstammen (mengisolaten).De auteurs stellen zich verantwoordelijk voor het distribueren (op aanvraag) van kleine zaadhoeveelheden van de toetsrassen en, op beperkte schaal, van in zaad aanwezige zuivere virusstammen aan onderzoekers die betrokken zijn bij de identificatie van de stammen van dit virus. Bovendien zal zaad van de standaardserie van toetsrassen worden gedeponeerd in het National Seed Storage Laboratory te Fort Collins, Colorado, USA, terwijl de virusstammen (in zaad) in bewaring worden gegeven bij de American Type Culture Collection te Rockville, Maryland, USA, waar ze beschikbaar zullen blijven voor verder onderzoek.     

Quinone accumulation in S-ethyl dipropylthiocarbamate-treated wheat

Wheat (Triticum aestivum L. cv Holley) was grown for 15 days in sand into which S-ethyl dipropylthiocarbamate (EPTC) (0, 15.6, 31.25, 62.5, or 125.0 μg/kg) had been incorporated. Growth was decreased more by EPTC under high light intensity (270 μein/m²/sec) than under low light (20 μein/m²/sec) intensity. Wheat grown in the dark did not respond to EPTC at these concentrations. In high light intensity, plastoquinone-9, plastohydroquinone-9, α-tocopheroquinone, and α-tocopherol contents (nanomoles per gram fresh weight) increased as EPTC concentration increased. Similar but less marked results occurred at the low light intensity. Plastohydroquinone-9/plastoquinone and α-tocopherol/α-tocopheroquinone ratios increased at both light intensities as EPTC concentration increased. This indicated an EPTC-induced inhibition of plastohydroquinone and α-tocopherol epoxidation. Chlorophyll a and b and total carotenoid contents increased as EPTC concentration increased in plants grown at high light intensities. Changes in the membrane electron carriers contents per unit of chlorophyll or carotenoid (micrograms per milligram of pigment) occurred. As a tentative hypothesis, it is suggested that transmembrane electron transport systems were inhibited, but growth in size (fresh weight per pot) was inhibited more than was synthesis of the various pigments and quinones. Thus, a separation of growth and metabolic response to EPTC was demonstrated.     

Etiology of the stomatitis pneumoenteritis complex in Nigerian dwarf goats.

The causative agent of stomatitis pneumoenteritis complex was isolated in domesticated goats and Vero cell culture. It was identified immunologically and morphologically as identical with the "Peste des Petits Ruminants" virus. There were cross reactions between stomatitis pneumoenteritis complex virus isolate and rinderpest virus by immunodiffusion and complement fixation tests but no cross neutralization. Goats recovered from stomatitis pneumoenteritis complex were protected against a challenge with rinderpest virus that was lethal to control goats. Ultrastructural morphology revealed intracytoplasmic and intranuclear inclusions made up of random arrays of fibrillar strands. Pleomorphic particles budded from the plasma membrane of infected cells and enveloped virions were seen extracellularly. Specific ferritin tagging was demonstrated in the stomatitis pneumoenteritis complex virus infected cells treated with homologous and peste des petits ruminants viral antibody systems but little, if any, tagging in the heterologous rinderpest system.