CORRECTION article

Front. Microbiol., 24 April 2025

Sec. Food Microbiology

Volume 16 - 2025 | https://doi.org/10.3389/fmicb.2025.1583946

Corrigendum: Pseudomonas aeruginosa detection using conventional PCR and quantitative real-time PCR based on species-specific novel gene targets identified by pangenome analysis

  • 1. College of Food Science, South China Agricultural University, Guangzhou, China

  • 2. Guangdong Provincial Key Laboratory of Microbial Safety and Health, State Key Laboratory of Applied Microbiology Southern China, Institute of Microbiology, Guangdong Academy of Sciences, Guangzhou, China

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In the published article, there were errors in Figures 2, 3, page 8 as published.

The purpose of both Figures 2, 3 was to explore the sensitivity of the novel identified target detection between genomic DNA and pure culture of P. aeruginosa. Unfortunately, during the final uploading of the data, the Figures 2, 3 were pasted incorrectly.

The corrected Figures 2, 3 and their captions appear below.

Figure 2

Figure 3

In the published article, there was an error in Supplementary Figure 1. During the assembling of different Figures, we mistakenly pasted Figure S1.d at the position of Figure S1.h.

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

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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.

Summary

Keywords

novel target gene, Pseudomonas aeruginosa, pangenome analysis, PCR, ready-to-eat vegetables

Citation

Wang C, Ye Q, Jiang A, Zhang J, Shang Y, Li F, Zhou B, Xiang X, Gu Q, Pang R, Ding Y, Wu S, Chen M, Wu Q and Wang J (2025) Corrigendum: Pseudomonas aeruginosa detection using conventional PCR and quantitative real-time PCR based on species-specific novel gene targets identified by pangenome analysis. Front. Microbiol. 16:1583946. doi: 10.3389/fmicb.2025.1583946

Received

26 February 2025

Accepted

24 March 2025

Published

24 April 2025

Volume

16 - 2025

Edited and reviewed by

Filipa Grosso, University of Porto, Portugal

Updates

Copyright

*Correspondence: Qingping Wu Juan Wang

†These authors have contributed equally to this work

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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