Konstantin V Kuleshov

Dr. Konstantin V Kuleshov

Central Research Institute of Epidemiology
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orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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21 March 2016 in Nature Microbiology
Verified
Journal Article
Open access
ENElisabeth Njamkepo
Elisabeth Njamkepo
NFNizar Fawal
Nizar Fawal
ATAlicia Tran-Dien
Alicia Tran-Dien
JHJane Hawkey
Jane Hawkey
NSNancy Strockbine
Nancy Strockbine
FWFrançois-Xavier Weill
François-Xavier Weill
Together with plague, smallpox and typhus, epidemics of dysentery have been a major scourge of human populations for centuries1. A previous genomic study concluded that Shigella dysenteriae type 1 (Sd1), the epidemic dysentery bacillus, emerged and spread worldwide after the First World War, with no clear pattern of transmission2. This is not consistent with the massive cyclic dysentery epidemics reported in Europe during the eighteenth and nineteenth centuries1,3,4 and the first isolation of Sd1 in Japan in 18975. Here, we report a whole-genome analysis of 331 Sd1 isolates from around the world, collected between 1915 and 2011, providing us with unprecedented insight into the historical spread of this pathogen. We show here that Sd1 has existed since at least the eighteenth century and that it swept the globe at the end of the nineteenth century, diversifying into distinct lineages associated with the First World War, Second World War and various conflicts or natural disasters across Africa, Asia and Central America. We also provide a unique historical perspective on the evolution of antibiotic resistance over a 100-year period, beginning decades before the antibiotic era, and identify a prevalent multiple antibiotic-resistant lineage in South Asia that was transmitted in several waves to Africa, where it caused severe outbreaks of disease.

6 January 2020 in BMC Genomics
Verified
Journal Article
Open access
PDF file
KKKonstantin V Kuleshov
Konstantin V Kuleshov
Gabriele MargosGabriele Margos
Gabriele Margos
VFVolker Fingerle
Volker Fingerle
JKJoris Koetsveld
Joris Koetsveld
IGIrina A. Goptar
Irina A. Goptar
APAlexander E. Platonov
Alexander E. Platonov
Background: The genus Borrelia comprises spirochaetal bacteria maintained in natural transmission cycles by tick vectors and vertebrate reservoir hosts. The main groups are represented by a species complex including the causative agents of Lyme borreliosis and relapsing fever group Borrelia. Borrelia miyamotoi belongs to the relapsing fever group of spirochetes and forms distinct populations in North America, Asia, and Europe. As all Borrelia species B. miyamotoi possess an unusual and complex genome consisting of a linear chromosome and a number of linear and circular plasmids. The species is considered an emerging human pathogen and an increasing number of human cases are being described in the Northern hemisphere. The aim of this study was to produce a high quality reference genome that will facilitate future studies into genetic differences between different populations and the genome plasticity of B. miyamotoi. Results: We used multiple available sequencing methods, including Pacific Bioscience single-molecule real-time technology (SMRT) and Oxford Nanopore technology (ONT) supplemented with highly accurate Illumina sequences, to explore the suitability for whole genome assembly of the Russian B. miyamotoi isolate, Izh-4. Plasmids were typed according to their potential plasmid partitioning genes (PF32, 49, 50, 57/62). Comparing and combining results of both long-read (SMRT and ONT) and short-read methods (Illumina), we determined that the genome of the isolate Izh-4 consisted of one linear chromosome, 12 linear and two circular plasmids. Whilst the majority of plasmids had corresponding contigs in the Asian B. miyamotoi isolate FR64b, there were only four that matched plasmids of the North American isolate CT13–2396, indicating differences between B. miyamotoi populations. Several plasmids, e.g. lp41, lp29, lp23, and lp24, were found to carry variable major proteins. Amongst those were variable large proteins (Vlp) subtype Vlp-α, Vlp-γ, Vlp-δ and also Vlp-β. Phylogenetic analysis of common plasmids types showed the uniqueness in Russian/Asian isolates of B. miyamotoi compared to other isolates. Conclusions: We here describe the genome of a Russian B. miyamotoi clinical isolate, providing a solid basis for future comparative genomics of B. miyamotoi isolates. This will be a great impetus for further basic, molecular and epidemiological research on this emerging tick-borne pathogen.

4 January 2018 in Microbiology Resource Announcements
Verified
Journal Article
Open access
KKKonstantin V Kuleshov
Konstantin V Kuleshov
JKJoris Koetsveld
Joris Koetsveld
IGIrina A. Goptar
Irina A. Goptar
MMMikhail L. Markelov
Mikhail L. Markelov
NKNadezhda M. Kolyasnikova
Nadezhda M. Kolyasnikova
APAlexander Platonov
Alexander Platonov
Here, we report the whole-genome sequence of six clinical Borrelia miyamotoi isolates from the Russian Federation. Using two independent next-generation sequencing platforms, we determined the complete sequence of the chromosome and several plasmids. All strains have an Asian genotype with 99.8% chromosome nucleotide similarity with B. miyamotoi strain FR64b.

12 December 2019 in Microbiology Resource Announcements
Verified
Journal Article
Open access
PDF file
KKKonstantin V Kuleshov
Konstantin V Kuleshov
DHDieuwertje Hoornstra
Dieuwertje Hoornstra
HSHein Sprong
Hein Sprong
APAlexander E. Platonov
Alexander E. Platonov
JHJoppe W. Hovius
Joppe W. Hovius
We report the draft whole-genome sequences of two Borrelia miyamotoi strains isolated in The Netherlands. Using next-generation sequencing, we determined the complete sequence of the chromosomes and several plasmids. The two strains show a genotype typical of European strains, distinct from the genomes of strains from Asia or the United States.

1 November 2016 in Emerging Infectious Diseases
Verified
Journal Article
Open access
KKKonstantin V Kuleshov
Konstantin V Kuleshov
SVSergey O. Vodop’ianov
Sergey O. Vodop’ianov
VDVladimir George Dedkov
Vladimir George Dedkov
MMMikhail L. Markelov
Mikhail L. Markelov
ADAndrei A Deviatkin
Andrei A Deviatkin
GSGerman Shipulin
German Shipulin

1 May 2016 in Journal of Clinical Virology
Verified
Journal Article
Closed access
VDVladimir George Dedkov
Vladimir George Dedkov
ALA.N. Lukashev
A.N. Lukashev
ADAndrei A Deviatkin
Andrei A Deviatkin
KKKonstantin V Kuleshov
Konstantin V Kuleshov
MSM.V. Safonova
M.V. Safonova
GSGerman Shipulin
German Shipulin