Literature DB >> 25792040

Draft Genome Sequences of 33 Salmonella enterica Clinical and Wildlife Isolates from Chile.

Magaly Toro, Patricio Retamal1, Marc Allard2, Eric W Brown2, Peter Evans2, Narjol Gonzalez-Escalona3.   

Abstract

Salmonella enterica causes health problem worldwide. The relationships among strains that are from the same serotype but different hosts, countries, and continents remain elusive. Few genome sequences are available from S. enterica isolates from South America. Therefore, we sequenced the genomes of 33 strains from diverse sources isolated in Chile and determined that they were of different serotypes. These genomes will improve phylogenetic analysis of Salmonella strains from Chile and the rest of South America.
Copyright © 2015 Toro et al.

Entities:  

Year:  2015        PMID: 25792040      PMCID: PMC4395066          DOI: 10.1128/genomeA.00054-15

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Salmonella enterica is a major pathogen in the world, and it causes >1,000,000 cases of foodborne disease in the United States every year (1). In Chile, Salmonella is the most frequently involved foodborne pathogen in outbreaks in recent years (2). More than 2,500 Salmonella serovars are described (3), and they associate with a wide range of hosts. The pathogen causes infection not only in humans and domestic animals, but it also can infect wildlife; recent studies demonstrated the presence of Salmonella in pinnipeds, penguins, and waterfowl (4–6). Currently, only one genome sequence from Salmonella isolated in Chile is available (7). Here, we announce 33 draft genome sequences from a collection of S. enterica strains isolated in Chile from 2010 to 2012 and from different hosts and geographical locations, including 12 human clinical samples and wildlife samples. DNA from each strain was isolated from overnight cultures with the DNeasy blood and tissue kit (Qiagen, Valencia, CA). Libraries were prepared using 1 ng of genomic DNA with the Nextera XT kit (Illumina, San Diego, CA), and the genomes were sequenced using MiSeq Illumina with the V2 kit (2 × 250 bp), according to the manufacturer’s instructions, at 40 to 190× coverage. The genomic sequence contigs for each strain were de novo assembled using CLC Genomics Workbench version 7.6.1 (CLC bio, Germantown, MD, USA). Ridom Seqsphere+ was used for in silico multilocus sequence type (MLST) analysis, and the sequences were annotated using the NCBI Prokaryotic Genomes Automatic Annotation Pipeline (PGAAP) (http://www.ncbi.nlm.nih.gov/genome/annotation_prok). The average G+C mol% of these strains was 52.1%, similar to the reported G+C content for other Salmonella strains (8). The genome length was also within the range described for Salmonella (4.6 Mb to almost 5.1 Mb) (9). The number of contigs per assembly for each isolate ranged from 32 to 92 (Table 1). While the samples were isolated from different hosts and geographical locations, in silico analysis determined that they belong to only 11 sequence types (ST), most of which were already reported in the S. enterica MLST database (http://mlst.warwick.ac.uk/mlst/dbs/Senterica) (Table 1). S. enterica strain serotype Havana presented different STs (ST588 and ST1524); the remaining 9 serotypes displayed a single ST each (Table 1). Those STs agreed with the serotyping results reported for the same strains in previous studies (4, 5, 10). Moreover, we found a new ST for S. enterica serovar Paratyphi B, with a hemD gene differing from previously described allele 24 by one new substitution at position 270 (T instead of C). Additionally, a preliminary analysis for detecting the presence of plasmids indicated that 13 of these isolates carry plasmids (Table 1) (11). We used two approaches, PlasmidFinder and pMLST (https://cge.cbs.dtu.dk/services); the first detects plasmid replication origins, and the second determines incompatibility types, both allowing mining for contigs with those characteristics.
TABLE 1 

Metadata for S. enterica subsp. enterica strains isolated in Chile from different hosts

CFSAN no.Isolate nameWGS accession no.aSourceSerotypeNo. of contigsSTPlasmidFinder/pMLSTb
CFSAN024756SAG1JWQW00000000PenguinAgona5513−/−
CFSAN024757SAG2JWQV00000000Kelp gullAgona5513−/−
CFSAN024758SAG3JWQU00000000PenguinAgona6413−/−
CFSAN024759SAG4JWQT00000000ClinicalAgona6013−/−
CFSAN024760SAG5JWQS00000000ClinicalAgona4813−/−
CFSAN024761SAG6JWQR00000000PenguinAgona5213−/−
CFSAN024763SAN3JWQP00000000ClinicalAnatum3264−/−
CFSAN024764SAN4JWQO00000000ClinicalAnatum6064−/−
CFSAN024765SBR1JWQN00000000Sea lionBrandenburg3865−/−
CFSAN024767SDU1JWQM00000000Kelp gullDublin4710+/+
CFSAN024768SDU2JWQL00000000ClinicalDublin3710+/+
CFSAN024769SDU3JWQK00000000ClinicalDublin3510+/+
CFSAN024770SHA1JWQJ00000000Sea lionHavana491524+/+
CFSAN024771SHA2JWQI00000000Gray gullHavana41588+/−
CFSAN024773SHE2JWQG00000000Kelp gullHeidelberg3515+/−
CFSAN024774SHE3JWQF00000000Kelp gullHeidelberg4415+/+
CFSAN024776SHE5JWQE00000000ClinicalHeidelberg3815+/−
CFSAN024777SHE6JWQD00000000ClinicalHeidelberg3915+/−
CFSAN024778SIN1JWQC00000000Kelp gullInfantis4132−/−
CFSAN024779SIN2JWQB00000000Kelp gullInfantis4732−/−
CFSAN024780SIN3JWQA00000000Kelp gullInfantis4232−/−
CFSAN024781SIN6JWPZ00000000ClinicalInfantis4432−/−
CFSAN024715SIN7JWRH00000000ClinicalInfantis3932−/−
CFSAN024716SLI1JWRG00000000Sea lionLivingstone32457−/−
CFSAN024717SLI2JWRF00000000Sea lionLivingstone41457−/−
CFSAN024718SSE1JWRE00000000Kelp gullSenftenberg3214−/−
CFSAN024719SSE2JWRD00000000Kelp gullSenftenberg4314−/−
CFSAN024720SSE3JWRC00000000Kelp gullSenftenberg5614−/−
CFSAN024721SSE4JWRB00000000ClinicalSenftenberg5214+/+
CFSAN024722SSE5JWRA00000000ClinicalSenftenberg4514+/−
CFSAN024723SSE6JWQZ00000000Kelp gullSenftenberg7214−/−
CFSAN024724SSE7JWQY00000000Kelp gullSenftenberg9214−/−
CFSAN024725SGB1JWQX00000000Kelp gullParatyphi B58New−/−

WGS, whole-genome shotgun.

PlasmidFinder/pMLST, presence of plasmids. +, positive; −, negative.

Metadata for S. enterica subsp. enterica strains isolated in Chile from different hosts WGS, whole-genome shotgun. PlasmidFinder/pMLST, presence of plasmids. +, positive; −, negative. The data provided will help in understanding the differences between Salmonella strains isolated from different countries and continents, improving traceback investigations for foodborne-related outbreak events. Moreover, these new draft genome sequences will contribute to the analysis of host-associated differences among Salmonella strains and provide phylogenetic insights into their evolution on different continents. A detailed report of these genomic features will be addressed in a future publication.

Nucleotide sequence accession numbers.

The draft genome sequences for these 33 Salmonella isolates are available in GenBank and are listed in Table 1.
  10 in total

1.  [Foodborne disease outbreaks around the urban Chilean areas from 2005 to 2010].

Authors:  Viller Alerte; Sandra Cortés A; Janepsy Díaz T; Jeannette Vollaire Z; M Eugenia Espinoza M; Verónica Solari G; Jaime Cerda L; Marisa Torres H
Journal:  Rev Chilena Infectol       Date:  2012-04-10       Impact factor: 0.520

2.  Serotype-associated polymorphisms in a partial rpoB gene sequence of Salmonella enterica.

Authors:  Marcela Fresno; Marlen Barreto; Sindy Gutierrez; Catherine Dougnac; Pedro Abalos; Patricio Retamal
Journal:  Can J Microbiol       Date:  2014-01-22       Impact factor: 2.419

3.  In silico detection and typing of plasmids using PlasmidFinder and plasmid multilocus sequence typing.

Authors:  Alessandra Carattoli; Ea Zankari; Aurora García-Fernández; Mette Voldby Larsen; Ole Lund; Laura Villa; Frank Møller Aarestrup; Henrik Hasman
Journal:  Antimicrob Agents Chemother       Date:  2014-04-28       Impact factor: 5.191

4.  Identification of diverse Salmonella serotypes, virulotypes, and antimicrobial resistance phenotypes in waterfowl from Chile.

Authors:  Marcela Fresno; Violeta Barrera; Vanessa Gornall; Pilar Lillo; Natalia Paredes; Pedro Abalos; Alda Fernández; Patricio Retamal
Journal:  Vector Borne Zoonotic Dis       Date:  2013-10-09       Impact factor: 2.133

5.  Foodborne illness acquired in the United States--major pathogens.

Authors:  Elaine Scallan; Robert M Hoekstra; Frederick J Angulo; Robert V Tauxe; Marc-Alain Widdowson; Sharon L Roy; Jeffery L Jones; Patricia M Griffin
Journal:  Emerg Infect Dis       Date:  2011-01       Impact factor: 6.883

6.  Salmonella enterica in pinnipeds, Chile.

Authors:  Natalie Sturm; Pedro Abalos; Alda Fernandez; Guillermo Rodriguez; Pilar Oviedo; Viviana Arroyo; Patricio Retamal
Journal:  Emerg Infect Dis       Date:  2011-12       Impact factor: 6.883

7.  Detection of Salmonella enterica in Magellanic penguins (Spheniscus magellanicus) of Chilean Patagonia: evidences of inter-species transmission.

Authors:  C Dougnac; C Pardo; K Meza; C Arredondo; O Blank; P Abalos; R Vidal; A Fernandez; F Fredes; P Retamal
Journal:  Epidemiol Infect       Date:  2014-08-22       Impact factor: 4.434

8.  Phylogenetics and differentiation of Salmonella Newport lineages by whole genome sequencing.

Authors:  Guojie Cao; Jianghong Meng; Errol Strain; Robert Stones; James Pettengill; Shaohua Zhao; Patrick McDermott; Eric Brown; Marc Allard
Journal:  PLoS One       Date:  2013-02-11       Impact factor: 3.240

9.  Draft Genome Sequences of Two Salmonella Strains from the SARA Collection, SARA64 (Muenchen) and SARA33 (Heidelberg), Provide Insight into Their Antibiotic Resistance.

Authors:  Brenda S Kroft; Eric W Brown; Jianghong Meng; Narjol Gonzalez-Escalona
Journal:  Genome Announc       Date:  2013-10-03

10.  Draft Genome Sequence of Salmonella enterica Serovar Typhi Strain STH2370.

Authors:  Camila Valenzuela; Juan A Ugalde; Guido C Mora; Sergio Alvarez; Inés Contreras; Carlos A Santiviago
Journal:  Genome Announc       Date:  2014-02-20
  10 in total
  2 in total

1.  Atypical Salmonella enterica Serovars in Murine and Human Macrophage Infection Models.

Authors:  Daniel Hurley; Maria Hoffmann; Tim Muruvanda; Marc W Allard; Eric W Brown; Marta Martins; Séamus Fanning
Journal:  Infect Immun       Date:  2020-03-23       Impact factor: 3.441

2.  Transduction as a Potential Dissemination Mechanism of a Clonal qnrB19-Carrying Plasmid Isolated From Salmonella of Multiple Serotypes and Isolation Sources.

Authors:  Andrea I Moreno-Switt; David Pezoa; Vanessa Sepúlveda; Iván González; Dácil Rivera; Patricio Retamal; Paola Navarrete; Angélica Reyes-Jara; Magaly Toro
Journal:  Front Microbiol       Date:  2019-11-07       Impact factor: 5.640

  2 in total

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