Publications by authors named "V Gavrilova"

Article Synopsis
  • * Between 1996 and 2022, there was a general decline in pollutant concentrations, but notable spikes in less persistent PCBs were observed in 2017 and 2022, indicating recent pollution entry.
  • * Compared to other Asia-Pacific countries, the levels of DDT and PCBs in mollusks from the Sea of Japan are lower, although Peter the Great Bay shows relatively high levels of HCH isomers.
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Isolation of African swine fever virus (ASFV) is a critical step towards the identification, titration, characterization, and even modification of the virus. Therefore, it is important to identify a suitable cell line that supports the efficient replication of ASFV for these purposes. This should be achieved even when starting with a low virus load, as in the case of isolating the virus from field samples.

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The vast majority of commercial sunflower hybrids worldwide are produced using cytoplasmic male sterility (CMS) of the PET1 type, resulting from the interspecific hybridization of Helianthus petiolaris with Helianthus annuus. Due to the fact that CMS-PET1 was not previously detected in wild sunflower, it was believed that this cytotype could arise during interspecific hybridization and is specific solely for cultivated sunflower. In this study, the open reading frame, orfH522, associated with the CMS-PET1 phenotype, was revealed for the first time in the 3'-flanking region of the mitochondrial atpA gene in wild H.

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Interspecific hybridization is widespread for sunflowers, both in wild populations and commercial breeding. One of the most common species that can efficiently cross with is the Silverleaf sunflower-. The current study carried out structural and functional organization analyses of mitochondrial DNA in and the interspecific hybrid, (VIR114A line) × .

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Introduction: The causative agent of African swine fever (Asfarviridae: Asfivirus: African swine fever virus) (ASF) is a double-stranded DNA virus of 175-215 nm. To date, 24 of its genotypes are known. Clustering of ASF genotype II isolates is carried out by examining a limited number of selected genome markers.

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