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CORRECTION article
Front. Plant Sci., 09 March 2017
Sec. Plant Pathogen Interactions
Volume 8 - 2017 | https://doi.org/10.3389/fpls.2017.00325
This article is part of the Research TopicPlant Pathogenic Ralstonia spp. From the Field to the Lab and Back Again: mechanisms of pathogen virulence and host resistance, population biology, community ecology and strategies for bacterial wilt disease management.View all 34 articles
This article is a correction to:
Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Ralstonia solanacearum Phylotype I Mulberry Strains in China
A corrigendum on
Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Ralstonia solanacearum Phylotype I Mulberry Strains in China
by Huang, W., Zhang, H., Xu, J., Wang, S., Kong, X., Ding, W., et al. (2017). Front. Plant Sci. 8:76. doi: 10.3389/fpls.2017.00076
There were mistakes regarding the phylotype of strain Po35, Po40, and PoYN. Those strains belong to Phylotype II, not Phylotype III.
In the Results section, sub-section Specificity, paragraph one, samples 35–38 and 41 were allocated to Phylotype II and samples 39–40 and 42 to Phylotype III. The correct paragraph should be:
The specificity of the LAMP for detecting R. solanacearum phylotype I mulberry strains was analyzed using genomic DNA isolated from 46 representative R. solanacearum strains that belonged to Phylotypes I (sample 1–34; 43–46), II (sample 35–42), and 7 other pathogens.
In addition, in the fourth paragraph of the Discussion, it was suggested that Phylotype III was also covered when it was not. The correct paragraph should be:
To evaluate the specificity of the LAMP-based method, 53 strains were used in this study, including 46 R. solanacearum strains covering Phylotypes I, II and seven other soil- borne bacteria strains.
Finally, in Table 1, the Phylotype of No. 39 (III), 40 (III), and 42 (III) are incorrect. The corrected table appears below.
The authors apologize for these errors and state that they do not affect the conclusion of the article in any way.
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Keywords: Ralstonia solanacearum, phylotype I mulberry strains, loop-mediated isothermal amplification, detection, bacterial wilt
Citation: Huang W, Zhang H, Xu J, Wang S, Kong X, Ding W, Xu J and Feng J (2017) Corrigendum: Loop-Mediated Isothermal Amplification Method for the Rapid Detection of Ralstonia solanacearum Phylotype I Mulberry Strains in China. Front. Plant Sci. 8:325. doi: 10.3389/fpls.2017.00325
Received: 19 February 2017; Accepted: 23 February 2017;
Published: 09 March 2017.
Edited and reviewed by: Brigitte Mauch-Mani, University of Neuchâtel, Switzerland
Copyright © 2017 Huang, Zhang, Xu, Wang, Kong, Ding, Xu and Feng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jin Xu, amlueHVAaXBwY2Fhcy5jbg==
Jie Feng, amZlbmdAaXBwY2Fhcy5jbg==
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