ABSTRACT
We here report the draft genome sequences of 8 Yersinia pestis subsp. microtus bv. caucasica strains isolated from the East Caucasian (previous name, Dagestan) mountain focus (no. 39), representing the most ancient branch of the 0.PE2 phylogroup circulating in populations of common voles (Microtus arvalis).
GENOME ANNOUNCEMENT
Yersinia pestis, the etiologic agent of plague, includes several phylogenetic groups (1). Strains of Y. pestis subsp. pestis are virulent for a broad spectrum of mammal species and were the causes of the three pandemics (Plague of Justinian, the Black Death, and the Third Plague pandemic). Other endemic strains (Y. pestis subsp. microtus) circulating in populations of different species of voles are characterized by high virulence to their main natural hosts and laboratory mice; as a rule, however, they were of low virulence or were avirulent for guinea pigs and caused only occasional disease in humans that was not accompanied by outbreaks of human-to-human transmission of infection (2). Our understanding of the population structure, origin, and spread of this major pathogen has increased using whole-genome sequencing to investigate isolates of Y. pestis.
The study of distal branches of the plague tree can give additional data for comparative analysis of transformation from the enteropathogenic bacterium Yersinia pseudotuberculosis with a fecal-oral route of transmission into hypervirulent vector-borne Y. pestis that, as a rule, causes a generalized highly lethal septic infection.
The data of 25-locus multiple-locus variable-number tandem-repeat analysis (MLVA25) typing of Y. pestis subsp. microtus bv. caucasica strains (3) suggest that the strains from the East Caucasian (previous name, Dagestan) mountain focus (no. 39) represent the most ancient branch of the 0.PE2 phylogroup circulating in populations of common voles (Microtus arvalis). To date, only one whole-genome sequence of the strains from this ancient plague focus, which is characterized by a polymorphism of circulating their strains, has been deposited in GenBank (accession number LIYP00000000 [4]). In this study, we sequenced eight additional strains isolated in different years from different parts of this focus.
DNA samples were extracted using conventional SDS lysis and phenol-chloroform extraction methods.
Whole-genome sequencing was performed using the Illumina MiSeq instrument, according to the manufacturer’s instruction. DNA libraries were prepared using a Nextera DNA laboratory preparation kit. The MiSeq reagent kit version 2 was used for sequencing. For each genome, reads were assembled de novo using SPAdes version 3.8.1 (http://cab.spbu.ru/software/spades/). Finally, we obtained from 166 to 191 contigs for each genome (Table 1). The genome sizes ranged from 4.50 to 4.57 Mb. Each genome contains 3,927 to 4,215 coding sequences. Each of the strains has two plasmids (pMT and pCD). The pPCP plasmid is absent, as in all other 0.PE2 (Y. pestis subsp. microtus bv. caucasica) strains. A detailed report of a full comparative genomic analysis will be included in a future publication.
TABLE 1 .
Strain name | Alternative strain name | Raw data accession no. | GenBank assembly accession no. | Size (bp) | No. of contigs | No. of genes |
No. of CDSsa |
||
---|---|---|---|---|---|---|---|---|---|
Total | Coding | Total | Coding | ||||||
SCPM-O-B-7111 | C-746 | SRR3501107 | MTZY00000000 | 4,567,036 | 191 | 4,466 | 4,215 | 4,381 | 4,215 |
SCPM-O-B-7005 | C-824 | SRR3529493 | MTZZ00000000 | 4,569,487 | 190 | 4,466 | 4,214 | 4,381 | 4,214 |
SCPM-O-B-6994 | С-739 | SRR3529496 | MTZX00000000 | 4,558,616 | 188 | 4,451 | 4,200 | 4,366 | 4,200 |
SCPM-O-B-7042 | C-712 | SRR3529526 | MTZW00000000 | 4,567,750 | 182 | 4,456 | 4,205 | 4,371 | 4,205 |
SCPM-O-B-7037 | C-370 | SRR4017164 | MIDX00000000 | 4,558,520 | 176 | 4,235 | 3,985 | 4,149 | 3,985 |
SCPM-O-B-6176 | C-535 | SRR4017165 | MIDY00000000 | 4,562,336 | 176 | 4,234 | 4,020 | 4,147 | 4,020 |
SCPM-O-B-7040 | C-678 | SRR4017166 | MIDZ00000000 | 4,564,996 | 186 | 4,244 | 4,012 | 4,157 | 4,012 |
SCPM-O-B-6992 | C-700 | SRR4017171 | MIEA00000000 | 4,503,787 | 166 | 4,164 | 4,080 | 3,927 | 3,927 |
CDSs, coding sequences.
Accession number(s).
The GenBank accession numbers for the eight genome sequences are listed in Table 1.
ACKNOWLEDGMENTS
This work was supported by the Russian Science Foundation (grant 14-15-00599).
The bacterial strains were obtained from the State Collection of Pathogenic Microbes and Cell Cultures on the base of the State Research Center for Applied Microbiology and Biotechnology (http://obolensk.org/center/state-collection.htm).
Footnotes
Citation Kislichkina AA, Bogun AG, Kadnikova LA, Maiskaya NV, Solomentsev VI, Platonov ME, Dentovskaya SV, Anisimov AP. 2017. Eight whole-genome assemblies of Yersinia pestis subsp. microtus bv. caucasica isolated from the common vole (Microtus arvalis) plague focus in Dagestan, Russia. Genome Announc 5:e00847-17. https://doi.org/10.1128/genomeA.00847-17.
REFERENCES
- 1.Platonov ME, Evseeva VV, Dentovskaya SV, Anisimov AP. 2013. Molecular typing of Yersinia pestis. Mol Genet Microbiol Virol 28:41–51. doi: 10.3103/S0891416813020067. [DOI] [PubMed] [Google Scholar]
- 2.Anisimov AP, Lindler LE, Pier GB. 2004. Intraspecific diversity of Yersinia pestis. Clin Microbiol Rev 17:434–464. doi: 10.1128/CMR.17.2.434-464.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Platonov ME, Evseeva VV, Svetoch TE, Efremenko DV, Kuznetsova IV, Dentovskaya SV, Kulichenko AN, Anisimov AP. 2012. Phylogeography of Yersinia pestis vole strains isolated from natural foci of the Caucasus and South Caucasus. Mol Genet Microbiol Virol 27:108–111. doi: 10.3103/S089141681203007X. [DOI] [PubMed] [Google Scholar]
- 4.Kislichkina AA, Bogun AG, Kadnikova LA, Maiskaya NV, Platonov ME, Anisimov NV, Galkina EV, Dentovskaya SV, Anisimov AP. 2015. Nineteen whole-genome assemblies of Yersinia pestis subsp. microtus, including representatives of biovars caucasica, talassica, hissarica, xilingolensis, and ulegeica. Genome Announc 3(6):e01342-15. doi: 10.1128/genomeA.01342-15. [DOI] [PMC free article] [PubMed] [Google Scholar]