Biomathematical system of relationship and dominance for the classification of foot-and-mouth disease strains

1972 ◽  
Vol 37 (4) ◽  
pp. 357-364 ◽  
Author(s):  
C. Stellmann ◽  
Y. Moreau ◽  
M. Roumiantzeff
Keyword(s):  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Foot And Mouth

scholarly journals John Burns Brooksby. 25 December 1914 — 17 December 1998

2007 ◽  
Vol 53 ◽  
pp. 77-92
Author(s):  
R. F. Sellers
Keyword(s):  
Disease Virus ◽  
International Organizations ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Virus Diseases ◽  
Animal Virus ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
The Uk

John Brooksby was an outstanding veterinary virologist, who worked at the Animal Virus Diseases Research Institute, Pirbright, for 40 years, for 16 of which he was Director of the Institute. He will be remembered for his contributions to the diagnosis of foot-and-mouth disease, for his discovery of four new types, for the classification of subtypes and for fundamental studies of the virus. As Deputy Director and Director he was responsible for programmes on fundamental investigations of foot–and–mouth disease virus and other viruses exotic to the UK and for the application of the results both in the UK and worldwide. His advice on the distribution and the control of foot–and–mouth disease was sought by international organizations and by individual countries and was responsible for reducing the risk of spread of disease.

scholarly journals A Proposal for the Classification and Nomenclature of Hand, Foot and Mouth Disease-Related Enteroviruses

2020 ◽  
Author(s):  
Yajuan Dong ◽  
Zhenzhou Wan ◽  
Shenwei Li ◽  
Jian-Hua Wang ◽  
Xia Jin ◽  
...  
Keyword(s):  
Vaccine Development ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Epidemiological Surveillance ◽  
Subtype B ◽  
Current Classification ◽  
Foot And Mouth ◽  
The Mean ◽  
Phylogenic Relationship

Abstract Background: Enterovirus has diverged into many types, some of which cause hand, foot and mouth disease (HFMD) in children. The predominant enterovirus types associated with HFMD are EVA71, CVA16, CVA6 and CVA10. Subtyping of these enteroviruses is crucial to HFMD surveillance. Because of lacking proper and uniform criteria and being based on partial VP1 sequences, however, current classification resulted in some confusing and conflicting results. Method: We reclassified EVA71, CVA16, CVA6 and CVA10 using a combined criteria of phylogenic relationship and genetic distance. Results: Using the combined criteria, we classified EVA71 into seven genotypes of A–G, CVA16 and CVA6 into three subtypes of A-C, and CVA10 into nine subtypes/sub-subtypes of A-G, H1 and H2, and identified eight unclassified subtypes that lack genomic sequences. The mean genetic divergence was 15.5-33.8% between subtypes, 12-15% between sub-subtypes, and less than 12% within subtypes/sub-subtypes. In addition, we identified two new EVA71 inter-subtype recombinants RF01_CG and RF02_CG and demonstrated that EVA71 subtypes D and F and CVA10 subtype B experienced inter-subtype recombination events during early evolution. Conclusions: The new nomenclature proposal provides a reasonable framework for proper classification of enteroviruses, which will be useful for epidemiological surveillance of HFMD, disease management, and vaccine development.

scholarly journals The sub-type classification of strains of foot-and-mouth disease virus

1975 ◽  
Vol 74 (2) ◽  
pp. 227-232 ◽  
Author(s):  
A. J. Forman
Keyword(s):  
Disease Virus ◽  
Antigenic Variation ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Sat 1 ◽  
Reference Strains ◽  
Type Classification

SUMMARYSixteen foot-and-mouth disease virus (FMDV) strains of type SAT 1 were compared in complement-fixation tests. With the test used, the range of antigenic variation within a type appeared to be greater than previously described. The concept of a sub-type group within which all strains are more closely related to each other than to any strain outside the group was not supported. Considering the group of strains studied, it is suggested that the classification of strains is best achieved by nominating a reference strain for each sub-type. Others are classified as related strains in one or more sub-type groups according to their relationships with the reference strains.

Biophysical Measurement of Molecular Weight of Foot-and-Mouth Disease RNA Fragments

1974 ◽  
Vol 32 ◽  
pp. 262-263
Author(s):  
Sydney S. Breese ◽  
Howard L. Bachrach
Keyword(s):  
Chemical Properties ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Distilled Water ◽  
Bovine Plasma ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Carbon Coated ◽  
Rna Fragments ◽  
Physical And Chemical

Continuing studies on the physical and chemical properties of foot-and-mouth disease virus (FMDV) have included electron microscopy of RNA strands released when highly purified virus (1) was dialyzed against demlneralized distilled water. The RNA strands were dried on formvar-carbon coated electron microscope screens pretreated with 0.1% bovine plasma albumin in distilled water. At this low salt concentration the RNA strands were extended and were stained with 1% phosphotungstic acid. Random dispersions of strands were recorded on electron micrographs, enlarged to 30,000 or 40,000 X and the lengths measured with a map-measuring wheel. Figure 1 is a typical micrograph and Fig. 2 shows the distributions of strand lengths for the three major types of FMDV (A119 of 6/9/72; C3-Rezende of 1/5/73; and O1-Brugge of 8/24/73.

High resolution surface structure of foot-and-mouth disease virus

1978 ◽  
Vol 36 (2) ◽  
pp. 376-377
Author(s):  
S. S. Breese ◽  
H. L. Bachrach
Keyword(s):  
Electron Microscopy ◽  
High Resolution ◽  
Surface Structure ◽  
Disease Virus ◽  
Potassium Phosphate ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Physical Measurements ◽  
Mouth Disease Virus ◽  
Foot And Mouth

Models for the structure of foot-and-mouth disease virus (FMDV) have been proposed from chemical and physical measurements (Brown, et al., 1970; Talbot and Brown, 1972; Strohmaier and Adam, 1976) and from rotational image-enhancement electron microscopy (Breese, et al., 1965). In this report we examine the surface structure of FMDV particles by high resolution electron microscopy and compare it with that of particles in which the outermost capsid protein VP3 (ca. 30, 000 daltons) has been split into smaller segments, two of which VP3a and VP3b have molecular weights of about 15, 000 daltons (Bachrach, et al., 1975).Highly purified and concentrated type A12, strain 119 FMDV (5 mg/ml) was prepared as previously described (Bachrach, et al., 1964) and stored at 4°C in 0. 2 M KC1-0. 5 M potassium phosphate buffer at pH 7. 5. For electron microscopy, 1. 0 ml samples of purified virus and trypsin-treated virus were dialyzed at 4°C against 0. 2 M NH4OAC at pH 7. 3, deposited onto carbonized formvar-coated copper screens and stained with phosphotungstic acid, pH 7. 3.

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