Embryo transfer: a discussion on its potential for infectious disease control based on a review of studies on infection of gametes and early embryos by various agents

Studies on laboratory animals have shown that viruses vary as to whether or not they are transmissible by the gametes or are capable of passing through the zona pellucida and infecting the embryo.

Methods of studying early embryos for the presence of infectious agents include electron microscopy, immunocytochemistry and cell cultivation.

Determination that early bovine embryos do not become infected by certain agents might allow for easing of restrictions in the current import and export regulations for cattle embryos.

Embryo transfer could be used as a means of controlling or eliminating disease in a herd or flock if the causal agent does not infect the early embryo via the gametes or by penetrating the zona pellucida.

     

Field studies with convalescent serum and infectious bursal disease vaccine to control turkey coryza

Convalescent serum given to 1-day-old poults delayed clinical signs of turkey coryza by several days and reduced mortality on infected farms. Turkey breeders immunized with cell-culture-adapted infectious bursal disease virus (IBDV) or turkey infectious bursal disease virus (TIBDV) had a marked increase in virus-neutralization (VN) antibody titers. The VN antibody titer was significantly higher in progeny poults than in poults from unimmunized breeders. Clinical turkey coryza and mortality was considerably less in poults from IBD- or TIBD-vaccinated breeders than in control poults. They also responded more favorably to hemorrhagic enteritis and fowl cholera vaccination.     

Preliminary investigation of a possible lung worm (Parafilaroides decorus), fish (Girella nigricans), and marine mammal (Callorhinus ursinus) cycle for San Miguel sea lion virus type 5

Colostrum-deprived neonatal Northern fur seal pups (Callorhinus ursinus) were exposed to San Miguel sea lion virus type 5 (SMSV-5) by feeding them fish (Girella nigricans) infected with virus or fish infected with both the sea lion lung worm larvae (Parafilaroides decorus) and virus. Virus infection was demonstrated in 8 of 9 pups, and 1 of these developed a vesicular lesion on the flipper. In this sequence, P decorus larvae exposed to SMSV-5 were fed to G nigricans held at 15 C in a salt water aquarium; 32 days later, these fish were killed, then fed to the fur seal pups. The vesicle developed 22 days subsequent to this and SMSV-5 was reisolated from the lesion. The SMSV-5 was shown to persist for at least 23 days in infected neonatal fur seals. Attempts to establish P decorus infection in Northern fur seal pups were apparently unsuccessful.     

Tests of soil fertility following repeated applications of MCPA, tri-allate, simazine and linuron

The following herbicides were applied annually from 1963 to experimental plots of appropriate crops grown in monoculture: MCPA 1.7 kg ha^?1, triallate 1.7 kg ha^?1, simazine 1.7 kg ha^?1 and linuron 0.84 kg ha^?1 (applied twice per year). Before the eighth treatment in 1970, nutrient status, pH and growth in greenhouse tests of a range of plants were similar in soils from treated and control plots. There were no significant differences in yield when several test crops were grown in the field plots in 1977. In a similar experiment which ran for 6 years, the same herbicides were applied twice per year at twice the above rates on each occasion (three times a year at 1.7 kg ha^?1 in the case of linuron) to uncropped plots. Three years after the last treatment, there were no differences in extractable nutrients, pH, soil structure and crop yield on treated or control plots. These results support the conclusion from the main monitoring of the experiments reported elsewhere that annual treatments with these herbicides have had no adverse affect on the soil.     

The use of separate root and shoot tests in the screening of herbicides for strawberries

The tolerance of strawberries to herbicides was tested by applications to the roots of plants growing in sand and by foliage applications to plants grown in compost, and compared with tolerance in the field. Dimefuron was safe as a foliar application but much more toxic than simazine when applied in sand or in the field. Metamitron caused slight injury as a foliar spray; in sand and in the field it was intermediate in toxicity between simazine and lenacil. At normal rates propachlor was safe as a foliar spray and much safer than lenacil when applied in sand. High rates had no adverse effect in the field. Ethofumesate and pendimethalin caused some temporary stunting when applied to foliage, but were less toxic than lenacil when applied to roots in sand. Field applications of both herbicides at 1–1.5 kg/ha were safe. Foliage sprays of bentazone, oxadiazon and oxyfluorfen severely damaged the sprayed leaves, but these herbicides were less active than lenacil when applied to the roots. In the field they caused severe leaf damage, but by the end of the growing season the plants had recovered. The experiments demonstrated the value of separate root and shoot activity tests for indicating which herbicides merit further field testing.     

Translocation of 14C-glyphosate in johnsongrass (Sorghum halepense L. Pers.) as affected by growth stage and rhizome length

Studies were conducted in the green house on ¹⁴C-methyllabelled glyphosate translocation in johnsongrass as affected by rhizome length and growth stage. The amount of ¹⁴C measured by the liquid scintillation technique in the rhizomes (2-8%) increased with rhizome length (10, 20 or 30 cm) and tended to increase with growth stage (15-30 cm tall, 45-60 cm tall, or at seedhead), but the amount of ¹⁴C per g fresh rhizome weight was almost similar in all cases. Of the total amount applied per plant (0·2 μCi) about 1/3 or less remained on the treated leaf area, while another 1/3 was a absorbed into the treated leaves. Autoradiographs showed that the ¹⁴C label moved to all plant parts, basipetally and acropetally. Migration du glyphosate ¹⁴ C chez le sorgho d'Alep (Sorghum halepense L. Pers.) en relation avec le stage de croissance et la longueur du rhizome Des recherches ont été effectuées en serru sur la migration du glyphosate marqué au ¹⁴C sur le méthyle, chez le sorgho d'Alep, en relation avec la longueur du rhizome et le stade de croissance. La quantité de ¹⁴C mesurée par la technique de scintillation liquide dans les rhizomes (2 à 8%) s'est accrue avec la longueur du rhizome (10, 20 ou 30 cm) et elle a eu tendance à augmenter avec le stade de croissance (Hauteur 15-30 cm, hauteur 45-60 cm ou épiaison), mais la quantité de ¹⁴C par gramme de poids frais de rhizome est restée Presque identique dans tous les cas. Environ 1/3, ou moins, de la quantitéà la surface des feuilles traitées par plante (0,2 μCi), est restéà la surface des feuilles traitées cependant qu'un autre 1/3 a été absorbé dans less feuilles traitées Les autoradiographies ont montré que le ¹⁴C marqueur a migré dans toutes les parties de la plante, dans le sens basipète et dans le sens acropète. Translokation von ¹⁴C-Glyphosat in Johnsongras (Sorghum halepense L. Pers.) in Abhängigkeit vom Wachstumsstadium der Pflanzen und der Rhizomlänge Im Gewächshaus wurden Versuche über die Translokation von ¹⁴C-Glyphosat in Johnsongras (Sorghum halepense L. Pers.) in Abhängigkeit vom Wachstumsstadium der Pflanzen und der Rhizomlänge durchgeführt. An den Rhizomen stieg der Gehalt von ¹⁴C(2–8%), gemessen mit der Flüssig-Szintillationstechnik, mit zunehmender Rhizomlänge (10, 20 oder 30 cm) an und nahm tendenziell auch mit fortschreitendem Pflanzenwachstum zu (15–30 cm und 45–60 cm Sprosslänge oder nach dem Rispenschieben); jedoch blieb die Menge pro g Rhizomfrischgewicht beinahe konstant. Von der insgesamt ausgebrachten Menge pro Pflanze (0.2 μCi) blieben bis zu 1/3 auf der behandelten Blättern absorbiert wurde. Die Autoradiographie zeigte, dass der ¹⁴C markierte Teil in alle Pflanzenteile sowohl basipetal wie auch akropetal transportiert wurde.     

Melanin biosynthesis in Pyricularia oryzae: Site of tricyclazole inhibition and pathogenicity of melanin-deficient mutants

Tricyclazole (5-methyl-1,2,4-triazolo[3,4-b]benzothiazole) inhibits melanin synthesis in Pyricularia oryzae at concentrations less than 0.01 μg/ml. The primary site of inhibition in the biosynthetic pathway occurs between scytalone and vermelone. Accumulation of several metabolites derived from melanin precursors along branch pathways is associated with inhibition of melanin biosynthesis. At low tricyclazole concentrations (0.01–1 μg/ml), predominant accumulation of 2-hydroxyjuglone and 3,4-dihydro-3,4,8-trihydroxy-1-(2H)-naphthalenone (3,4,8-DTN) occurs as a result of the primary block between 1,3,8-trihydroxynaphthalene and vermelone. As the concentration of tricyclazole is increased from 1 to 10 μg/ml, flaviolin accumulation is markedly enhanced, whereas that of 3,4,8-DTN and 3,4-dihydro-4,8-dihydroxy-1-(2H)-naphthalenone is depressed, indicating possible secondary sites of inhibition in the main and branch pathways. Five melanin-deficient mutants of P. oryzae that phenotypically resemble the tricyclazole-treated wild-type strain were nonpathogenic or rarely infected two rice varieties. Three of the mutants studied were genetically defective in the melanin biosynthetic pathway at the site blocked by tricyclazole in the wild type. The wild-type strain converted both scytalone and vermelone to melanin; whereas the three mutants and the tricyclazole-treated wild type converted only vermelone to melanin. The data suggest a relationship between melanin biosynthesis and pathogenicity in P. oryzae.     

Comparative inhibition of the juvenile hormone esterases from Trichoplusia ni,Tenebrio molitor, and Musca domestica

Twenty-seven compounds were screened as potential inhibitors of juvenile hormone esterases. Of these compounds O-ethyl-S-phenyl phosphoramidothiolate provided the best inhibition for the cabbage looper, Trichoplusia ni (Hubner), and the yellow mealworm, Tenebrio molitor L., while the juvenile hormone esterases of the house fly, Musca domestica L., were best inhibited by a juvenoid carbamate (1-(m-phenoxy-N-ethyl carbamate)-3,7-dimethyl-7-methoxy-2E-octene). The inhibition patterns of T. ni and T. molitor are similar, while those of M. domestica are relatively different. Further studies on the juvenile hormone and α-napthyl acetate esterases of T. ni showed that they could be differentially inhibited. Diisopropyl phosphorofluoridate and an alkyl trifluoromethyl ketone selectively inhibit the hydrolysis of α-naphthyl acetate and juvenile hormone, respectively, while O-ethyl-S-phenyl phosporamidothiolate inhibits both enzymes. The juvenile hormone esterases of T. ni also appear to be unique enzymes that are selective for juvenile-hormone-like molecules. The in vivo inhibition of T. ni juvenile hormone esterases by O-ethyl-S-phenyl phosphoramidothiolate slows the in vivo hydrolysis of juvenile hormone and results in delayed pupation and malformed larvae that resemble larval-pupal intermediates. Thus, the esterases involved in juvenile hormone metabolism appear to be important in juvenile hormone regulation.