CORRECTION article

Front. Microbiol., 08 August 2023

Sec. Antimicrobials, Resistance and Chemotherapy

Volume 14 - 2023 | https://doi.org/10.3389/fmicb.2023.1221779

Corrigendum: Pathogen genomics and phage-based solutions for accurately identifying and controlling Salmonella pathogens

  • 1. Department of Bacteriology, Animal and Plant Health Agency, Weybridge, United Kingdom

  • 2. Department of Veterinary and Animal Science, Scotland's Rural College, Inverness, United Kingdom

  • 3. Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom

  • 4. Department of Immunology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand

  • 5. Department of Microbiology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand

  • 6. Department of Chemical Engineering, Loughborough University, Loughborough, United Kingdom

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In the published article, there was an error in the Figure 3 and its legend as published. Figure 3B was removed from the manuscript; however, the associated legend text still needs to be removed and the key was not completely included in the original picture. The corrected Figure 3 and its caption appear below.

Figure 3

Figure 3

Percentages of UK and Thai MDR, non-MDR, and sensitive isolates harboring virulence determinants. MDR isolates from the UK (green), non-MDR isolates from the UK (grey), sensitive isolates from the UK (blue), MDR isolates from Thailand (pink), non-MDR isolates from Thailand (yellow), and sensitive isolates from Thailand (orange) have been included.

In the published article, there was an error in Table 1 as published. strA, strB and tetA(B) genes were misspelt as straA, straB and tet-AB. The corrected Table 1 and its caption appear below.

Table 1

ClassesAntimicrobialGenesUK (n isolates)PercentageThai (n isolates)Percentage
PenicillinAmpicillinblaCARB−24 of 884.55%0 of 550%
blaTEM−1350 of 880%3 of 555.45%
blaTEM−1b11 of 8812.50%13 of 5523.64%
blaTEM−1D1 of 881.14%0 of 550%
MacrolidesAzithromycinmphB1 of 881.14%0 of 550%
PhenicolChloramphenicolcmlA14 of 884.55%1 of 551.82%
floR4 of 884.55%0 of 550%
FluoroquinoloneCiprofloxacinmutation gyrA4 of 884.55%15 of 5527.27%
qnrS10 of 880%4 of 557.27%
Nalidixic acidmutation gyrA4 of 884.55%15 of 5527.27%
AminoglycosideGentamicinaac(3)-Id1 of 881.14%0 of 550%
aac(3)-IVa2 of 882.27%1 of 551.82%
StreptomycinstrA7 of 887.95%7 of 5512.73%
strB9 of 8810.23%7 of 5512.73%
SulfonamideSulfamethoxazolesul14 of 884.55%1 of 551.18%
sul26 of 886.82%8 of 5514.55%
sul37 of 887.95%5 of 559.09%
TetracyclineTetracyclinetetA(B)7 of 887.95%5 of 559.09%
tet(A)6 of 886.82%2 of 553.64%
tet(G)4 of 884.55%0 of 550%
tet(M)0 of 880%1 of 551.82%
DiaminopyrimidineTrimethoprimdfrA124 of 884.55%1 of 551.82%

AMR genotypes of 143 isolates identified by the APHA Seqfinder.

AMR genes were grouped according to antimicrobial classes, and they are shown alongside the percentage of isolates per country harboring the AMR gene.

In the published article, the reference for the virulence genes safBCD, srfJ, lpfD, and fhuA were present in both MDR S. Kentucky isolates, which were identified as clones of a ST198 S. Kentucky global lineage (Martínez and Baquero, 2002; Beceiro et al., 2013) was incorrectly written as (Martínez and Baquero, 2002; Beceiro et al., 2013). It should be deleted.

In the published article, there was an error to Materials and methods, Phylogenetic and SNP analysis. The reference name should not contain commas.

This sentence previously stated:

“Snippy version v4.6.0 (Seemann, 2015) was used to detect SNPs in the core genome of S. Kentucky isolates BL700 and BL800, and two S. Kentucky MDR ST198 isolates from earlier research [SAMN08784244 and SAMN08784253; (Hawkey et al., 2019)], aligning them against the reference 201,001,922 (CP028357).”

The corrected sentence appears below:

“Snippy version v4.6.0 (Seemann, 2015) was used to detect SNPs in the core genome of S. Kentucky isolates BL700 and BL800, and two S. Kentucky MDR ST198 isolates from earlier research [SAMN08784244 and SAMN08784253; (Hawkey et al., 2019)], aligning them against the reference 201001922 (CP028357).”

In the published article, there was an error in Results, Antimicrobial resistance characterization. The Thai S.1,4,12:i:- isolate does not present resistance to streptomycin.

This sentence previously stated:

“One Thai isolate, serotyped as S. 1,4,12:i:-, was resistant to seven antimicrobial classes (ampicillin, chloramphenicol, ciprofloxacin-nalidixic acid, gentamicin-streptomycin, sulfamethoxazole, tetracycline, and trimethoprim).”

The corrected sentence appears below:

“One Thai isolate, serotyped as S. 1,4,12:i:-, was resistant to seven antimicrobial classes (ampicillin, chloramphenicol, ciprofloxacin-nalidixic acid, gentamicin, sulfamethoxazole, tetracycline, and trimethoprim).”

In the published article, there was an error in Results, Characterization of MDR isolates with distinct virulence profiles, 3rd Paragraph. The tetA(B) gene was misspelt.

This sentence previously stated:

“From the resolved genome of MDR isolate BL708 S. 1,4,[5],12:i:-, we identified SGI-4 in the chromosome with genes showing resistance to copper, arsenic, mercury, and antimicrobials [blaTem−1b, sul2, tet(AB), strA, strB].”

The corrected sentence appears below:

“From the resolved genome of MDR isolate BL708 S. 1,4,[5],12:i:-, we identified SGI-4 in the chromosome with genes showing resistance to copper, arsenic, mercury, and antimicrobials [blaTEM−1B, sul2, tetA(B), strA, strB].”

In the published article, there was an error with the percentage of MDR isolates reported in the Author's Summary.

The sentence previously stated:

“The results indicated genes harboring resistance to antimicrobials differed between the countries, possibly due to differing farming practices; however, 17–18% of all isolates were multidrug resistant.”

The corrected sentence appears below:

“The results indicated genes harboring resistance to antimicrobials differed between the countries, possibly due to differing farming practices; however, 14%−15% of all isolates were multidrug resistant.”

In the published article, there was an error in Supplementary Table S5. The tet-AB gene was misspelt and should be replaced by tetA(B). The supplementary table with the error typo amended has been submitted.

The authors apologize for these errors and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Statements

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

  • 1

    HawkeyJ.Le HelloS.DoubletB.GranierS. A.HendriksenR. S.FrickeW. F.et al. (2019). Global phylogenomics of multidrug-resistant Salmonella enterica serotype Kentucky ST198.Microb. Genom. 5. 10.1099/mgen.0.000269

  • 2

    SeemannT. (2015). Snippy: Fast bacterial variant calling from NGS reads.

Summary

Keywords

antimicrobial resistance, Salmonella, virulence genes, genomics, bacteriophages, serovar

Citation

Lopez-Garcia AV, AbuOun M, Nunez-Garcia J, Nale JY, Gaylov EE, Phothaworn P, Sukjoi C, Thiennimitr P, Malik DJ, Korbsrisate S, Clokie MRJ and Anjum MF (2023) Corrigendum: Pathogen genomics and phage-based solutions for accurately identifying and controlling Salmonella pathogens. Front. Microbiol. 14:1221779. doi: 10.3389/fmicb.2023.1221779

Received

12 May 2023

Accepted

26 July 2023

Published

08 August 2023

Approved by

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Volume

14 - 2023

Updates

Copyright

*Correspondence: Muna F. Anjum

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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