Effects of marital/dependency status on reenlistment behavior of second-term enlisted females.

This thesis investigates the relationship of reenlistment decisions of second-term enlisted women in the military to their marital and dependent status, using individual-level data from the 1985 DoD Survey of Officer and Enlisted Personnel. Actual reenlistment status (December 1988) of each survey respondent was merged with the data set. Logit analysis was used to estimate the likelihood of a respondent choosing to reenlist given her set of individual characteristics. Separate logit models were estimated for the following groups of second-term personnel: single women without children, single women with children, married women without children, and married women with children. Certain variables affected all groups similarly (pay grade, minority status, perception of civilian job alternatives). Others exerted differential impact on subgroups (job satisfaction, traditionality of job). Results illustrated differential reenlistment behavior based upon the presence of children. Results may be used to target reenlistment incentives for specified marital/dependent status groups.http://archive.org/details/effectsofmarital00edwaLieutenant, United States NavyApproved for public release; distribution is unlimited

Glycoprotein gene truncation in avian metapneumovirus subtype C isolates from the United States

The length of the published glycoprotein (G) gene sequences of avian metapneumovirus subtype-C (aMPV-C) isolated from domestic turkeys and wild birds in the United States (1996–2003) remains controversial. To explore the G gene size variation in aMPV-C by the year of isolation and cell culture passage levels, we examined 21 turkey isolates of aMPV-C at different cell culture passages. The early domestic turkey isolates of aMPV-C (aMPV/CO/1996, aMPV/MN/1a-b, and 2a-b/97) had a G gene of 1,798 nucleotides (nt) that coded for a predicted protein of 585 amino acids (aa) and showed >97% nt similarity with that of aMPV-C isolated from Canada geese. This large G gene got truncated upon serial passages in Vero cell cultures by deletion of 1,015 nt near the end of the open reading frame. The recent domestic turkey isolates of aMPV-C lacked the large G gene but instead had a small G gene of 783 nt, irrespective of cell culture passage levels. In some cultures, both large and small genes were detected, indicating the existence of a mixed population of the virus. Apparently, serial passage of aMPV-C in cell cultures and natural passage in turkeys in the field led to truncation of the G gene, which may be a mechanism of virus evolution for survival in a new host or environment

Different Domains of the RNA Polymerase of Infectious Bursal Disease Virus Contribute to Virulence

BACKGROUND: Infectious bursal disease virus (IBDV) is a pathogen of worldwide significance to the poultry industry. IBDV has a bi-segmented double-stranded RNA genome. Segments A and B encode the capsid, ribonucleoprotein and non-structural proteins, or the virus polymerase (RdRp), respectively. Since the late eighties, very virulent (vv) IBDV strains have emerged in Europe inducing up to 60% mortality. Although some progress has been made in understanding the molecular biology of IBDV, the molecular basis for the pathogenicity of vvIBDV is still not fully understood. METHODOLOGY, PRINCIPAL FINDINGS: Strain 88180 belongs to a lineage of pathogenic IBDV phylogenetically related to vvIBDV. By reverse genetics, we rescued a molecular clone (mc88180), as pathogenic as its parent strain. To study the molecular basis for 88180 pathogenicity, we constructed and characterized in vivo reassortant or mosaic recombinant viruses derived from the 88180 and the attenuated Cu-1 IBDV strains. The reassortant virus rescued from segments A of 88180 (A88) and B of Cu-1 (BCU1) was milder than mc88180 showing that segment B is involved in 88180 pathogenicity. Next, the exchange of different regions of BCU1 with their counterparts in B88 in association with A88 did not fully restore a virulence equivalent to mc88180. This demonstrated that several regions if not the whole B88 are essential for the in vivo pathogenicity of 88180. CONCLUSION, SIGNIFICANCE: The present results show that different domains of the RdRp, are essential for the in vivo pathogenicity of IBDV, independently of the replication efficiency of the mosaic viruses

Hemorragic enteritis of Turquey: culture of virus in vitro; replication on receptive animais

Des essais de réplication du virus de l'entérite hémorragique du dindon sur cultures cellulaires de rate de dindon sont décrits. L’observation en microscopic électronique des surnageants de cultures cellulaires ainsi que leur inoculation à des animaux sensibles, permettent d’affirmer que le virus s'est multiplié in vitro dans ce système. Cependant, aucun effet cyto- pathogène caractéristique n'a encore été observé.The replication of the virus of hémorragie enteritis of turkeys is descri bed using spleen cells. The observation of the supernatants with electron microscop and their inoculation to sensible young turkeys give indication of a viral multiplication on this system. No cytopathic effect was observed

Activ immunization of the breeding common pheasant (Phasianus Colchicus) against the disease of the mottled spleen virus

Une expérience d'immunisation de faisandeaux contre le virus de la Maladie de la Rate Marbrée a été réalisée en laboratoire. L'antigène utilisé est le virus de l'Entérite Hémorragique du dindon, multiplié sur dindon neaux et administré per os. Les auteurs décrivent les protocoles de production de cet antigène, son contrôle, les résultats cliniques et séro- logiques obtenus sur les faisandeaux ainsi immunisés.An experiment was done concerning experimental immunisation of young pheasants against Marble Spleen Disease Virus. The antigen used was an Hémorragie Enteritis Virus of Turkey and it was produced on turkeys. Immunisation was done by putting this antigen by oral route. Authors are describing methods for producing this antigen, controles, and clinical and serological results obtained

Infectious bursal disease (Gumboro disease).

&lt;p&gt;Infectious bursal disease (IBD) (Gumboro disease) has been described throughout the world, and the socio-economic significance of the disease is considerable world-wide. Various forms of the disease have been described, but typing remains unclear, since antigenic and pathotypic criteria are used indiscriminately, and the true incidence of different types is difficult to determine. Moreover, the infection, when not fatal, leads to a degree of immunosuppression which is often difficult to measure. Finally, the control measures used are subject to variations, and seldom follow a specific or standardised plan. In the context of expanding international trade, the authors provide an overview of existing knowledge on the subject to enhance available information on the epidemiology of IBD, the identification of reliable viral markers for diagnosis, and the implementation of specific control measures to ensure a global and co-ordinated approach to the disease.&lt;/p&gt;</p

Chicken recombinant antibodies specific for very virulent infectious bursal disease virus.

&lt;p&gt;A phage-displayed single chain variable fragment (scFv) antibody library was constructed from the immune spleen cells of chickens immunized with very virulent infectious bursal disease virus (vvIBDV) strain CS89. A library consisting of around 9.2 x 10(7) clones was subjected to 3 rounds of panning against captured CS89 virus. Analysis of individual clones by nucleotide sequencing revealed at least 22 unique scFv antibodies binding to vvIBDV in ELISA. Testing of the scFv antibody panel in ELISA against classical, variant or vaccine strains and a wide variety of vvIBDV isolates from the UK, China, France, Belgium, Africa, Brazil, Indonesia and the Netherlands identified one antibody, termed chicken recombinant antibody 88 (CRAb 88) that was specific for vvIBDV. CRAb 88 was capable of recognizing all vvIBDV strains tested regardless of their country of origin and showed no reactivity with classical, variant or vaccine strains, lending support to the use of this scFv as a powerful diagnostic tool for the differentiation of vvIBDV strains. Immunoprecipitation studies revealed that CRAb 88 was directed towards a highly conformational epitope located within the major neutralizing protein VP2. Sequence analysis of the hypervariable region of VP2 of the IBDV strains tested indicate that Ile(256) and Ile(294) may play roles in binding of CRAb 88. This is the first reagent of its type capable of positively distinguishing vvIBDV from other IBDV strains.&lt;/p&gt;</p