Evidence map›Paper›PMID 26370680›Full record

ArticleBMC genomics2015

Next generation genome sequencing reveals phylogenetic clades with different level of virulence among Salmonella Typhimurium clinical human isolates in Hong Kong.

Chi Keung Cheng, Man Kit Cheung, Wenyan Nong, Patrick Tik Wan Law, Jing Qin, Julia Mei-Lun Ling, Kai Man Kam, William Man Wai Cheung, Hoi Shan Kwan

Abstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Chi Keung ChengSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China. billyc801@yahoo.com.hk.
Man Kit CheungSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China. mkcheung@cuhk.edu.hk.
Wenyan NongSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China. nongwenyan@cuhk.edu.hk.
Patrick Tik Wan LawSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China. patricklaw@cuhk.edu.hk.
Jing QinSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China. qin0jing0@hotmail.com.
Julia Mei-Lun LingDepartment of Microbiology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong SAR, China. meilunling@cuhk.edu.hk.
Kai Man KamCentre for Health Protection, Department of Health, Hong Kong SAR, China. kmkam1@gmail.com.
William Man Wai CheungSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China. mwcheung@cuhk.edu.hk.
Hoi Shan KwanSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China. hoishankwan@cuhk.edu.hk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSalmonella Typhimurium is frequently isolated from foodborne infection cases in Hong Kong, but the lack of genome sequences has hindered in-depth epidemiological and phylogenetic studies. In this study, we sought to reconstruct the phylogenetic relationship and investigate the distribution and mutation patterns of virulence determinants among local S. Typhimurium clinical isolates using their genome sequences.

resultsWe obtained genome sequences of 20 S. Typhimurium clinical isolates from a local hospital cluster using a 454 GS FLX Titanium sequencing platform. Phylogenetic analysis was performed based on single nucleotide polymorphism positions of the core genome against the reference strain LT2. Antimicrobial susceptibility was determined using minimal inhibitory concentration for five antimicrobial agents and analyses of virulence determinants were performed through referencing to various databases. Through phylogenetic analysis, we revealed two distinct clades of S. Typhimurium isolates and three outliers in Hong Kong, which differ remarkably in antimicrobial susceptibility and presentation and mutations of virulence determinants. The local isolates were not closely related to many of the previously sequenced S. Typhimurium isolates, except LT2. As the isolates in the two clades spanned over 10 years of isolation, they probably represent endemic strains. The outliers are possibly introduced from outside of Hong Kong. The close relatedness of members in one of the clades to LT2 and the Japanese stool isolate T000240 suggests the potential reemergence of LT2 progeny in regions nearby.

conclusionsOur study demonstrated the utility of next-generation sequencing coupled to traditional microbiological testing method in a retrospective epidemiological study involving multiple clinical isolates. The evolution of multidrug- and ciprofloxacin-resistant strains among the more virulent clade is also an increasing concern.

Indexed as

Genome, BacterialGenotypePhylogenyAdolescentAdultAgedAged, 80 and overAnti-Bacterial AgentsChildChild, PreschoolDrug Resistance, BacterialFemaleHigh-Throughput Nucleotide SequencingHong KongHumansInfantAnti-Bacterial Agents

Identifiers

PMID26370680
PMCPMC4570558

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