scholarly journals Pituitary Extracts and the Virus of Foot-Andmouth Disease—the Effect on the Virus of Certain Chemical Methods Employed in Their Preparation

1939 ◽  
Vol 39 (6) ◽  
pp. 597-614 ◽  
Author(s):  
I. A. Galloway

THe experiments recorded here were initiated following upon the occurrence in this country of foot-and-mouth disease in a cow, which a short time previously had been injected for the purpose of inducing oestrus with a pituitary extract imported from the Continent. Mr D. A. E. Cabot, M.R.C.V.S., Chief Veterinary Officer of the Ministry of Agriculture, made reference to this interesting case in a discussion on foot-and-mouth disease at the First Imperial Veterinary Conference held in London (1938). Confirmation of the nature of the infection was obtained by the inoculation of test animals under experimental conditions with suitable material collected from the injected animal. Further investigations were made. Three ampoules containing pituitary extract were obtained from the distributors in London of the imported commercial preparation under discussion. These ampoules belonged to the same batch as the ampoule with the extract from which the cow had been inoculated. Messrs A. Eccles, M.R.C. V.S. and A. M. Graham, M.R.C.V.S., at the Experimental Station of the Foot-and-Mouth Disease Research Committee at Pirbright, tested this material for virus infectivity by the inoculation of cattle and guinea-pigs. They reported that all three samples of pituitary extract were contaminated with the virus of footand-mouth disease. In addition they produced evidence that the immunological type of the virus recovered from the extract in the ampoules was the same as that of the virus recovered from the cow, viz. Vallée and Carré 0. This and additional information left no doubt that the outbreak of the disease had been produced by the inoculation of the pituitary extract, and further that this extract had been prepared from the pituitary glands of cattle, which were very probably in the early stages of infection with foot-and-mouth disease at the time of slaughter.

PLoS ONE ◽  
2012 ◽  
Vol 7 (7) ◽  
pp. e41382 ◽  
Author(s):  
Teodoro Fajardo ◽  
Maria Flora Rosas ◽  
Francisco Sobrino ◽  
Encarnacion Martinez-Salas

2019 ◽  
Author(s):  
Jonathan Arzt ◽  
Ian Fish ◽  
Steven J. Pauszek ◽  
Shannon L. Johnson ◽  
Patrick S. Chain ◽  
...  

AbstractFoot-and-mouth disease (FMD) is a highly contagious viral disease that severely impacts global food security and is one of the greatest constraints on international trade of animal products. Extensive viral population diversity and rapid, continuous mutation of circulating FMD viruses (FMDVs) pose significant obstacles to the control and ultimate eradication of this important transboundary pathogen. The current study investigated mechanisms contributing to within-host evolution of FMDV in a natural host species (cattle). Specifically, vaccinated and non-vaccinated cattle were infected with FMDV under controlled, experimental conditions and subsequently sampled for up to 35 days to monitor viral genomic changes as related to phases of disease and experimental cohorts. Consensus-level genomic changes across the entire FMDV coding region were characterized through three previously defined stages of infection: early, transitional, and persistent. The overall conclusion was that viral evolution occurred via a combination of two mechanisms: emergence of full-genomic minority haplotypes from within the inoculum super-swarm, and concurrent continuous point mutations. Phylogenetic analysis indicated that individuals were infected with multiple distinct haplogroups that were pre-existent within the ancestral inoculum used to infect all animals. Multiple shifts of dominant viral haplotype took place during the early and transitional phases of infection, whereas few shifts occurred during persistent infection. These insights into FMDV population dynamics have important implications for virus sampling methodology and molecular epidemiology.


2004 ◽  
Vol 85 (8) ◽  
pp. 2289-2297 ◽  
Author(s):  
Carmen M. Ruiz-Jarabo ◽  
Nonia Pariente ◽  
Eric Baranowski ◽  
Mercedes Dávila ◽  
Gema Gómez-Mariano ◽  
...  

Foot-and-mouth disease virus (FMDV) variants adapted to BHK-21 cells showed an expanded host-cell tropism that extended to primate and human cell lines. Virus replication in human HeLa and Jurkat cells has been documented by titration of virus infectivity, quantification of virus RNA, expression of a virus-specific non-structural antigen, and serial passage of virus in the cells. Parallel serial infections of human Jurkat cells with the same variant FMDVs indicates a strong stochastic component in the progression of infection. Chimeric viruses identified the capsid as a genomic region involved in tropism expansion. These results indicate that, contrary to theoretical predictions, replication of an RNA virus in a constant cellular environment may lead to expansion of cellular tropism, rather than to a more specialized infection of the cellular type to which the virus has been adapted.


2019 ◽  
Vol 93 (10) ◽  
Author(s):  
Silvia López-Argüello ◽  
Verónica Rincón ◽  
Alicia Rodríguez-Huete ◽  
Encarnación Martínez-Salas ◽  
Graham J. Belsham ◽  
...  

ABSTRACTInfection by viruses depends on a balance between capsid stability and dynamics. This study investigated biologically and biotechnologically relevant aspects of the relationship in foot-and-mouth disease virus (FMDV) between capsid structure and thermostability and between thermostability and infectivity. In the FMDV capsid, a substantial number of amino acid side chains at the interfaces between pentameric subunits are charged at neutral pH. Here a mutational analysis revealed that the essential role for virus infection of most of the 8 tested charged groups is not related to substantial changes in capsid protein expression or processing or in capsid assembly or stability against a thermally induced dissociation into pentamers. However, the positively charged side chains of R2018 and H3141, located at the interpentamer interfaces close to the capsid 2-fold symmetry axes, were found to be critical both for virus infectivity and for keeping the capsid in a state of weak thermostability. A charge-restoring substitution (N2019H) that was repeatedly fixed during amplification of viral genomes carrying deleterious mutations reverted both the lethal and capsid-stabilizing effects of the substitution H3141A, leading to a double mutant virus with close to normal infectivity and thermolability. H3141A and other thermostabilizing substitutions had no detectable effect on capsid resistance to acid-induced dissociation into pentamers. The results suggest that FMDV infectivity requires limited local stability around the 2-fold axes at the interpentamer interfaces of the capsid. The implications for the mechanism of genome uncoating in FMDV and the development of thermostabilized vaccines against foot-and-mouth disease are discussed.IMPORTANCEThis study provides novel insights into the little-known structural determinants of the balance between thermal stability and instability in the capsid of foot-and-mouth disease virus and into the relationship between capsid stability and virus infectivity. The results provide new guidelines for the development of thermostabilized empty capsid-based recombinant vaccines against foot-and-mouth disease, one of the economically most important animal diseases worldwide.


2002 ◽  
Vol 128 (2) ◽  
pp. 301-312 ◽  
Author(s):  
S. ALEXANDERSEN ◽  
I. BROTHERHOOD ◽  
A. I. DONALDSON

Foot-and-mouth disease virus (FMDV) can spread by a variety of mechanisms, including, under certain circumstances, by the wind. Simulation models have been developed to predict the risk of airborne spread of FMDV and have played an important part in decision making during emergencies. The minimal infectious dose of FMDV for different species by inhalation is an important determinant of airborne spread. Whereas the doses for cattle and sheep have been quantified, those for pigs are not known. The objective of the study was to obtain that data in order to enhance the capability of simulation models. Under experimental conditions, forty pigs were exposed individually to naturally generated aerosols of FMDV, strain O1 Lausanne. The results indicated that doses under 100 TCID50 failed to infect pigs but doses of approximately 300 TCID50 caused short-term sub-clinical infection. The calculations suggested that a dose of more than 800 TCID50 is required to cause infection and typical disease.


2004 ◽  
Vol 78 (18) ◽  
pp. 9773-9781 ◽  
Author(s):  
Hernando Duque ◽  
Michael LaRocco ◽  
William T. Golde ◽  
Barry Baxt

ABSTRACT At least four members of the integrin family of receptors, αVβ1, αVβ3, αVβ6, and αVβ8, have been identified as receptors for foot-and-mouth disease virus (FMDV) in vitro. Our investigators have recently shown that the efficiency of receptor usage appears to be related to the viral serotype and may be influenced by structural differences on the viral surface (H. Duque and B. Baxt, J. Virol. 77:2500-2511, 2003). To further examine these differences, we generated soluble αVβ3 and αVβ6 integrins. cDNA plasmids encoding the individual complete integrin αV, β3, and β6 subunits were used to amplify sequences encoding the subunits' signal peptide and ectodomain, resulting in subunits lacking transmembrane and cytoplasmic domains. COS-1 cells were transfected with plasmids encoding the soluble αV subunit and either the soluble β3 or β6 subunit and labeled with [35S]methionine-cysteine. Complete subunit heterodimeric integrins were secreted into the medium, as determined by radioimmunoprecipitation with specific monoclonal and polyclonal antibodies. For the examination of the integrins' biological activities, stable cell lines producing the soluble integrins were generated in HEK 293A cells. In the presence of divalent cations, soluble αVβ6 bound to representatives of type A or O viruses, immobilized on plastic dishes, and significantly inhibited viral replication, as determined by plaque reduction assays. In contrast, soluble αVβ3 was unable to bind to immobilized virus of either serotype; however, virus bound to the immobilized integrin, suggesting that FMDV binding to αVβ3 is a low-affinity interaction. In addition, soluble αVβ3 did not neutralize virus infectivity. Incubation of soluble αVβ6 with labeled type A12 or O1 resulted in a significant inhibition of virus adsorption to BHK cells, while soluble αVβ3 caused a low (20 to 30%), but consistent, inhibition of virus adsorption. Virus incubated with soluble αVβ6 had a lower sedimentation rate than native virus on sucrose density gradients, but the particles retained all of their structural proteins and still contained bound integrin and, therefore, were not exhibiting characteristics of a picornavirus A particle.


2016 ◽  
Vol 189 ◽  
pp. 39-45 ◽  
Author(s):  
C. Colenutt ◽  
J.L. Gonzales ◽  
D.J. Paton ◽  
J. Gloster ◽  
N. Nelson ◽  
...  

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