Alexandra Beliavskaia

Mrs. Alexandra Beliavskaia

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 July 2023 in Microbial Genomics
Verified
Journal Article
Open access
ABAlexandra Beliavskaia
Alexandra Beliavskaia
Kim Kee TanKim Kee Tan
Kim Kee Tan
Amit SinhaAmit Sinha
Amit Sinha
NHNurul Aini Husin
Nurul Aini Husin
FLFang Shiang Lim
Fang Shiang Lim
JKJing Jing Khoo
Jing Jing Khoo
While fleas are often perceived simply as a biting nuisance and a cause of allergic dermatitis, they represent important disease vectors worldwide, especially for bacterial zoonoses such as plague (transmitted by rodent fleas) and some of the rickettsioses and bartonelloses. The cosmopolitan cat (Ctenocephalides felis) and dog (Ctenocephalides canis) fleas, as well as Ctenocephalides orientis (restricted to tropical and subtropical Asia), breed in human dwellings and are vectors of cat-scratch fever (caused by Bartonella spp.) and Rickettsia spp., including Rickettsia felis (agent of flea-borne spotted fever) and Rickettsia asembonensis , a suspected pathogen. These Rickettsia spp. are members of a phylogenetic clade known as the ‘transitional group’, which includes both human pathogens and arthropod-specific endosymbionts. The relatively depauperate flea microbiome can also contain other endosymbionts, including a diverse range of Wolbachia strains. Here, we present circularized genome assemblies for two C. orientis-derived pathogens ( Bartonella clarridgeiae and R. asembonensis ) from Malaysia, a novel Wolbachia strain (wCori), and the C. orientis mitochondrion; all were obtained by direct metagenomic sequencing of flea tissues. Moreover, we isolated two Wolbachia strains from Malaysian C. felis into tick cell culture and recovered circularized genome assemblies for both, one of which (wCfeF) is newly sequenced. We demonstrate that the three Wolbachia strains are representatives of different major clades (‘supergroups’), two of which appear to be flea-specific. These Wolbachia genomes exhibit unique combinations of features associated with reproductive parasitism or mutualism, including prophage WO, cytoplasmic incompatibility factors and the biotin operon of obligate intracellular microbes. The first circularized assembly for R. asembonensis includes a plasmid with a markedly different structure and gene content compared to the published plasmid; moreover, this novel plasmid was also detected in cat flea metagenomes from the USA. Analysis of loci under positive selection in the transitional group revealed genes involved in host–pathogen interactions that may facilitate host switching. Finally, the first B. clarridgeiae genome from Asia exhibited large-scale genome stability compared to isolates from other continents, except for SNPs in regions predicted to mediate interactions with the vertebrate host. These findings highlight the paucity of data on the genomic diversity of Ctenocephalides-associated bacteria and raise questions regarding how interactions between members of the flea microbiome might influence vector competence.

16 April 2018 in Frontiers in Microbiology
Verified
Journal Article
Open access
SGSofya K. Garushyants
Sofya K. Garushyants
ABAlexandra Beliavskaia
Alexandra Beliavskaia
DMDmitry B. Malko
Dmitry B. Malko
MLMaria D. Logacheva
Maria D. Logacheva
MRMaria S. Rautian
Maria S. Rautian
MGMikhail S. Gelfand
Mikhail S. Gelfand
While most endosymbiotic bacteria are transmitted only vertically, Holospora spp., an alphaproteobacterium from the Rickettsiales order, can desert its host and invade a new one. All bacteria from the genus Holospora are intranuclear symbionts of ciliates Paramecium spp. with strict species and nuclear specificity. Comparative metabolic reconstruction based on the newly-sequenced genome of Holospora curviuscula, a macronuclear symbiont of Paramecium bursaria, and known genomes of other Holospora species shows that even though all Holospora spp. can persist outside the host, they cannot synthesize most of the essential small molecules, such as amino acids, and lack some central energy metabolic pathways, including glycolysis and the citric acid cycle. As the main energy source, Holospora spp. likely rely on nucleotides pirated from the host. Holospora-specific genes absent from other Rickettsiales are possibly involved in the lifestyle switch from the infectious to the reproductive form and in cell invasion.

1 April 2014 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Closed access
STSebastian Tarcz
Sebastian Tarcz
MRMaria S. Rautian
Maria S. Rautian
Alexey PotekhinAlexey Potekhin
Alexey Potekhin
NSNatalia Sawka-Gądek
Natalia Sawka-Gądek
ABAlexandra Beliavskaia
Alexandra Beliavskaia
EPEwa Przyboś
Ewa Przyboś

15 May 2020 in Diversity
Verified
Journal Article
Open access
PDF file
ABAlexandra Beliavskaia
Alexandra Beliavskaia
APAlexander V Predeus
Alexander V Predeus
SGSofya K. Garushyants
Sofya K. Garushyants
MLMaria Logacheva
Maria Logacheva
Jun GongJun Gong
Jun Gong
MRMaria S. Rautian
Maria S. Rautian
Holospora-like bacteria (HLB) are obligate intracellular Alphaproteobacteria, inhabiting nuclei of Paramecium and other ciliates such as “Candidatus Hafkinia” is in Frontonia. The HLB clade is comprised of four genera, Holospora, Preeria, “Candidatus Gortzia”, and “Candidatus Hafkinia”. These bacteria have a peculiar life cycle with two morphological forms and some degree of specificity to the host species and the type of nucleus they inhabit. Here we describe a novel species of HLB—“Candidatus Gortzia yakutica” sp. nov.—a symbiont from the macronucleus of Paramecium putrinum, the first described HLB for this Paramecium species. The new endosymbiont shows morphological similarities with other HLB. The phylogenetic analysis of the SSU rRNA gene places it into the “Candidatus Gortzia” clade.

5 February 2021 in G3: Genes, Genomes, Genetics
Verified
Journal Article
Open access
PDF file
YBYury Barbitoff
Yury Barbitoff
AMAndrew G. Matveenko
Andrew G. Matveenko
AMAnton Matiiv
Anton Matiiv
EMEvgeniia M Maksiutenko
Evgeniia M Maksiutenko
SMSvetlana E Moskalenko
Svetlana E Moskalenko
GZGalina A. Zhouravleva
Galina A. Zhouravleva
Thousands of yeast genomes have been sequenced with both traditional and long-read technologies, and multiple observations about modes of genome evolution for both wild and laboratory strains have been drawn from these sequences. In our study, we applied Oxford Nanopore and Illumina technologies to assemble complete genomes of two widely used members of a distinct laboratory yeast lineage, the Peterhof Genetic Collection (PGC), and investigate the structural features of these genomes including transposable element content, copy number alterations, and structural rearrangements. We identified numerous notable structural differences between genomes of PGC strains and the reference S288C strain. We discovered a substantial enrichment of mid-length insertions and deletions within repetitive coding sequences, such as in the SCH9 gene or the NUP100 gene, with possible impact of these variants on protein amyloidogenicity. High contiguity of the final assemblies allowed us to trace back the history of reciprocal unbalanced translocations between chromosomes I, VIII, IX, XI, and XVI of the PGC strains. We show that formation of hybrid alleles of the FLO genes during such chromosomal rearrangements is likely responsible for the lack of invasive growth of yeast strains. Taken together, our results highlight important features of laboratory yeast strain evolution using the power of long-read sequencing.