Advaita Acarya Singh1,2
Priyen Pillay1
Previn Naicker3Kabamba Alexandre3Kanyane Malatji3
Lukas Mach4
Herta Steinkellner4
Juan Vorster2Rachel Chikwamba1
Tsepo L. Tsekoa1*- 1Future Production: Chemicals Cluster, Council for Scientific and Industrial Research, Pretoria, South Africa
- 2Department of Plant and Soil Sciences, University of Pretoria, Pretoria, South Africa
- 3NextGen Health Cluster, Council for Scientific and Industrial Research, Pretoria, South Africa
- 4Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna, Austria
A Corrigendum on
Transient proteolysis reduction of Nicotiana benthamiana-produced CAP256 broadly neutralizing antibodies using CRISPR/Cas9
By Singh AA, Pillay P, Naicker P, Alexandre K, Malatji K, Mach L, Steinkellner H, Vorster J, Chikwamba R and Tsekoa TL (2022) Front. Plant Sci. 13:953654. doi: 10.3389/fpls.2022.953654
In the published article, there was an error. In the original article, we did not have the Addgene repository numbers and hyperlinks available so we could not refer to them and so that information was omitted from the original article.
A correction has been made to Materials and methods, The sgRNA cloning. This sentence previously stated:
“Vectors were transformed into E. coli DH10β and sequenced by Inqaba Biotechnical Industries (Pty) Ltd (ZA) using sequencing primers listed in Supplementary Table 2.”
The corrected sentence appears below:
“Vectors were transformed into E. coli DH10β and sequenced by Inqaba Biotechnical Industries (Pty) Ltd (ZA) using sequencing primers listed in Supplementary Table 2. Plasmids were deposited in Addgene under the following names and IDs:pICH86966::AtU6p::sgRNA: NbCysP6 (223217) and pICH86966::AtU6p::sgRNA: NbVPE1a/b (223218).”
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.
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.
Keywords: plant biotechnology, CRISPR/Cas9, genome editing, Nicotiana benthamiana, proteases, immunoglobulin G, human immunodeficiency virus
Citation: Singh AA, Pillay P, Naicker P, Alexandre K, Malatji K, Mach L, Steinkellner H, Vorster J, Chikwamba R and Tsekoa TL (2025) Corrigendum: Transient proteolysis reduction of Nicotiana benthamiana-produced CAP256 broadly neutralizing antibodies using CRISPR/Cas9. Front. Plant Sci. 16:1568756. doi: 10.3389/fpls.2025.1568756
Received: 30 January 2025; Accepted: 24 February 2025;
Published: 19 March 2025.
Edited and Reviewed by:
Giuseppe Dionisio, Aarhus University, DenmarkCopyright © 2025 Singh, Pillay, Naicker, Alexandre, Malatji, Mach, Steinkellner, Vorster, Chikwamba and Tsekoa. 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) and the copyright owner(s) 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: Tsepo L. Tsekoa, dHRzZWtvYUBjc2lyLmNvLnph