In this study, we report on the full genome phylogenetic analysis of four ASFV isolates obtained from wild boars in Russia. These samples originated from two eastern and two western regions of Russia in 2019. Phylogenetic analysis indicated that the isolates were assigned to genotype II and grouped according to their geographical origins. The two eastern isolates shared 99.99% sequence identity with isolates from China, Poland, Belgium, and Moldova, whereas the western isolates had 99.98% sequence identity with isolates from Lithuania and the original Georgia 2007 isolate. Based on the full genome phylogenies, we identified three single locus targets, MGF-360-10L, MGF-505-9R, and I267L, that yielded the same resolving power as the full genomes. The ease of alignment and a high level of variation make these targets a suitable selection as additional molecular markers in future ASFV phylogenetic practices.
Literature data concerning research organosilicon ion-exchangers and complexing agents have been summarized and systematized. Data on organophilic organosilicon adsorbents and sorption systems for chromatography are not considered here.
At present no effective measures for specific prevention and treatment of African swine fever have been developed. The control strategy for the disease is designed for rapid diagnosis of infected animals with subsequent slaughter and decontamination (stamping out). The present review deals with current epidemic situation for African swine fever and examines features of the virus genomics and genetic differentiation of the isolates. The Russian Federation has been ASF-infected since 2007. Since that time the disease has been one of the key problems in pig farming of this country inflicting great economic losses, both directly and indirectly. The disease continues to spread. In January 2014 African swine fever was introduced to Lithuania, then pervaded Poland, Latvia, Estonia, Romania, Belgium and Moldova. Since 2018 the disease outbreaks have been reported in Asia (China, Vietnam, and Mongolia). Specific structure of the virus and long genome, encoding genes with unknown function, and circulation of 24 genotypes and 9 serotypes of the virus hinder the development of ASF vaccine. The article shows that the use of many specific genetic markers during determination of relationship and study of pathways of ASF virus global spread is the most accurate method.
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