We are reporting whole-genome sequences of nine Vibrio sp. isolates closely related to the waterborne human pathogen Vibrio cholerae.
ABSTRACT
We are reporting whole-genome sequences of nine Vibrio sp. isolates closely related to the waterborne human pathogen Vibrio cholerae. These isolates were recovered from sources, including human samples, from different regions of the United States. Genome analysis suggests that this group of isolates represents a highly divergent basal V. cholerae lineage or a closely related novel species.
ANNOUNCEMENT
The genus Vibrio is one of the most diverse and ubiquitous groups of marine bacteria, including species with significant clinical importance, such as Vibrio cholerae, which is the causative agent of the pandemic diarrheal disease cholera (1). Surveillance conducted under the Cholera and Other Vibrio Illness Surveillance (COVIS) program ( https://www.cdc.gov/vibrio/surveillance.html) revealed nine isolates indistinguishable from V. cholerae by traditional phenotypic tests but phylogenetically and genotypically divergent from that species.
Cultivation and laboratory identification of these strains based on rpoB sequence determination and phylogenetic reconstruction were done following standard procedures (2). Genomic DNA was extracted from the isolates using an ArchivePure DNA cell/tissue kit (5 PRIME) according to the manufacturer’s instructions. Sequencing libraries were prepared from the genomic DNA using the Nextera XT DNA library preparation kit (Illumina, San Diego, CA, USA) and sequenced using Illumina MiSeq sequencing platforms (2 × 250-bp paired-end reads). Quality control and de novo assembly of the reads were done using default parameters in CLC Genomics workbench 7 (Qiagen). The average genome size was 3.9 Mbp with an average G+C content of 47.3%. Detailed isolate information is outlined in Table 1. Genome annotations were done using RAST 2.0 (3) and the Prokaryotic Genome Annotation Pipeline (PGAP) (https://www.ncbi.nlm.nih.gov/genome/annotation_prok/). Average nucleotide identity (ANI) and in silico DNA-DNA hybridization (dDDH) values in comparison to those of the reference strains were calculated using JSpecies v1.2.1 (4) and Genome-to-Genome Distance Calculator (GGDC), respectively. Whole-genome alignment was performed using Mugsy v1.2.3 (5) with default parameters, and a maximum likelihood tree was built from this alignment using RaxML v8 (6) under the GTR+GAMMA model with 1,000 bootstrap replicates. The core genome phylogenetic tree and strains used for dDDH and ANI have been deposited in publicly available databases.
TABLE 1.
Demographic and genomic features of the isolates
| Isolate | Source | State | Genome size (bp) |
G+C content (%) |
No. of contigs |
N50 (bp) | GenBank accession no. |
NCBI SRA accession no. |
|---|---|---|---|---|---|---|---|---|
| 2017V-1110 | Wound | CO | 3,994,199 | 47.1 | 168 | 48,914 | QKKU00000000 | SRR7962202 |
| 2016V-1091 | Stool | NE | 3,814,331 | 47.3 | 93 | 156,947 | QKKQ00000000 | SRR7962186 |
| 2017V-1176 | Animal feed | IA | 3,896,770 | 47.2 | 110 | 134,986 | QKKW00000000 | SRR7962200 |
| 2016V-1114 | Stool | IL | 3,873,695 | 47.3 | 92 | 150,142 | QKKS00000000 | SRR7962196 |
| 2016V-1111 | Stool | ND | 3,883,261 | 47.3 | 92 | 118,713 | QKKR00000000 | SRR7962199 |
| 2017V-1105 | Wound | FL | 4,080,989 | 47.2 | 90 | 167,992 | QKKT00000000 | SRR7962197 |
| 2014V-1107 | Stool | IA | 3,988,159 | 47.4 | 116 | 114,877 | QKKP00000000 | SRR7962194 |
| 2017V-1144 | Stool | TX | 3,869,006 | 47.2 | 131 | 124,156 | QKKV00000000 | SRR7962203 |
| 07-2425 | NAa | NA | 3,826,909 | 47.4 | 103 | 112,361 | QKKO00000000 | SRR7962192 |
NA, not applicable.
Species delineation values for prokaryotes have been considered 95% or higher for ANI and 70% or higher for dDDH (7). The nine sequenced strains shared 96.5% to 99% ANI and 82% to 85% dDDH values. On the other hand, in comparisons with representative V. cholerae strains, ANI ranged from 94% to 96% and dDDH from 65% to 70%. Core genome phylogeny shows that these strains form a strongly supported monophyletic clade basal to V. cholerae. Taken together, the tree topology and ANI and dDDH values suggest that these nine isolates could belong to a new species representing the closest relative of V. cholerae known to date or a highly divergent lineage within the species.
All nine strains contain the toxin transcriptional regulator gene (toxR), which is the master regulator of virulence genes in V. cholerae, but lack major virulence factor and related genetic elements and/or genes typical of toxigenic V. cholerae, such as ctxAB, tcpA, and the two Vibrio pathogenicity islands VPI-1 and VPI-2. However, eight out of nine strains possessed RTX toxin (8), and two strains possessed genes for the type III secretion system, which is an established virulence factor for V. cholerae (9). The presence of these virulence-related genes, in addition to their isolation from clinical cases, underscores the pathogenic potential of this monophyletic group of strains.
Data availability.
The complete genome sequences were deposited in DDBJ/GenBank and raw reads were deposited in the SRA depository under the accession numbers listed in Table 1. Phylogenetic tree, ANI, and dDDH values were deposited in a publicly available repository under the DOI 10.7939/DVN/OZHLC2 (https://doi.org/10.7939/DVN/OZHLC2).
ACKNOWLEDGMENTS
This work is supported by the Natural Sciences and Engineering Research Council of Canada, the Integrated Microbial Biodiversity program of the Canadian Institute for Advanced Research (to Y.B.), and federal appropriations to the Centers for Disease Control and Prevention through the Advanced Molecular Detection Initiative.
The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.
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Associated Data
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Data Availability Statement
The complete genome sequences were deposited in DDBJ/GenBank and raw reads were deposited in the SRA depository under the accession numbers listed in Table 1. Phylogenetic tree, ANI, and dDDH values were deposited in a publicly available repository under the DOI 10.7939/DVN/OZHLC2 (https://doi.org/10.7939/DVN/OZHLC2).
