CORRECTION article

Front. Immunol., 08 November 2022

Sec. Microbial Immunology

Volume 13 - 2022 | https://doi.org/10.3389/fimmu.2022.932151

Corrigendum: Escape of TLR5 recognition by Leptospira spp.: A rationale for atypical endoflagella

  • 1. Institut Pasteur, Unité Biologie et Génétique de la Paroi Bactérienne, Paris, France

  • 2. CNRS, UMR 2001 Microbiologie Intégrative et Moléculaire, Paris, France

  • 3. Institut National de la Santé et de la Recherche Médicale, Equipe Avenir, Paris, France

  • 4. Sorbonne Paris Cité, Université de Paris, Paris, France

  • 5. Institut Pasteur de Nouvelle Calédonie, Immunity and Inflammation Group, Institut Pasteur International Network, Noumea, France

  • 6. Unité Histopathologie Humaine et Modèles Animaux, Institut Pasteur, Paris, France

  • 7. Leptospirosis Research and Expertise Unit, Institut Pasteur International Network, Institut Pasteur de Nouvelle Calédonie, Noumea, France

  • 8. Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Brazilian Ministry of Health, Salvador, Brazil

  • 9. Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, United States

  • 10. Unité Biologie des Spirochètes, Institut Pasteur, Paris, France

  • 11. Department of Pathobiology and Population Sciences, Royal Veterinary College, Hatfield, United Kingdom

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In the original article, there was a mistake in Figure 8A, as published. We showed that we did not get expression of the FLaB1 subunit in Manilae L495 strain. In fact, the forward primer (designed according to the Fiocruz sequence) used to amplify the FlaB1 subunit has two mismatches within the Manilae sequence. We did the RT-PCR with the good primer and found an amplification, showing an enhanced expression at the stationary phase compared to the exponential phase, likewise the other FlaB subunits. The corrected Figure 8 appears below.

A correction has been made to Results, “FlaB mRNA Are Upregulated in Stationary Phase”.

Of note, and different from other strains, the Manilae L495 flaB1 mRNA was undetectable and a paragraph in the Discussion, Furthermore, in Manilae L495… are not accurate and should be both omitted.

In the original article, there was also mistake in Figure 6, Supplementary Figure 3, Supplementary Figure 4 and Supplementary Figure 6 and their legends as published. We realized a “slipping” of the names of FlaB subunits only in the figures of alignments and comparison of sequences (Figure 6, Sup Figure 3, Sup Figure 4 and Sup Figure 6). What we called FlaB1 in figures and respective legends is in fact FlaB4, FlaB2 is FlaB1, FlaB3 is FlaB2, and FlaB4 is FlaB3 (see corrected annotation in Additional table provided).

Figure 6

Figure 6

(A) Amino acid sequence homology average percentage between Salmonella typhimurium FliC (P06179) and Leptospira interrogans strain Fiocruz FlaB (LIC11890, LIC11889, LIC 11532 and LIC11531) and FlaAs (LIC10788 and LIC10787) and primary structures of the flagellin proteins with TLR5 binding consensus. (B)In silico (Phyre2 and Chimera softwares) prediction of Salmonella typhimurium FliC (P06179) structure with the four described domains and with positions of the TLR5 binding consensus: 1 (red), 2 (yellow) and 3 (light blue) and stabilization region (light green) highlighted. (C)In silico (Phyre2 and Chimera softwares) prediction of Leptospira interrogans strain Fiocruz FlaB4 (LICI1531) with the positions of the TLRS binding consensus and stabilization region highlighted, FlaA1 (LIC10788), FlaA2 (LICI0787). (D) Clustal (MEGA software) alignment of the amino acid sequences for the TLR5 binding consensus regions of: Salmonella enterica FliC (GeneBank QDQ31983.1), L. bifleva (strain Patoc) FlaB1 (LEPBla2133), FlaB2 (LEPBIa2132), FlaB3 (LEPBla1872) and FlaB4 (LEPBla1589), L. interrogans (strain Fiocruz L1-130) FlaB1 (LIC18890), FlaB2 (LICIT889), FlaB3 (LICI1532) and FlaB4 (LIC11531), L. interrogans (strain L495) FlaB1 (LMANv2 260016), FlaB2 (LMANv2 260015). FlaB3 (LMANv2 590024) and FlaB4 (LMANv2 590023), and L. interrogans (strain Verdun) FlaB1 (AKWP_v1_110429), FlaB2 (AKWP_v1_110428) and FlaB3 (AKWP_v1_110068) and FlaB4 (AKWP_v1_110067).

10788PatocFiocruz L1-130ManilaeVerdun
flaA1LEPBIa2335LIC10788LMANv2_260046AKWP_v1_210009
flaA2LEPBIa2336LIC10787LMANv2_260045AKWP_v1_210008
flaB1LEPBIa1589LIC11531LMANv2_590023AKWP_v1_110067
flaB2LEPBIa2133LIC11890LMANv2_260016AKWP_v1_110429
flaB3LEPBIa2132LIC11889LMANv2_260015AKWP_v1_110428
flaB4LEPBIa1872LIC11532LMANv2_590024AKWP_v1_110068

Additional Table Old annotations (published Frontiers Immunol 2020).

10788Patoc*Fiocruz L1-130*Manilae*Verdun*
flaA1LEPBIa2335LIC10788LMANv2_260046 / LIMLP_13775AKWP_v1_210009
flaA2LEPBIa2336LIC10787LMANv2_260045
/ LIMLP_13780
AKWP_v1_210008
flaB1LEPBIa2133LIC11890LMANv2_260016
/ LIMLP_09410
AKWP_v1_110429
flaB2LEPBIa2132LIC11889LMANv2_260015
/LIMLP_09405
AKWP_v1_110428
flaB3LEPBIa1872LIC11532LMANv2_590024
/ LIMLP_07480
AKWP_v1_110068
flaB4LEPBIa1589LIC11531LMANv2_590023
/ LIMLP_07475
AKWP_v1_110067

New annotations consistent with studies from M Picardeau.

*Annotation of L. biflexa serovar Patoc strain Patoc 1 (Patoc), L. interrogans serovar Copenhageni strain Fiocruz L1-130 (Fiocruz L1-130), L. interrogans serovar Manilae strain L495 (Manilae), L. interrogans serovar Manilae UP-MMC-NIID LP (Manilae) (ref Satou et al. 2015 ; PMID: 26272567).

L. interrogans serovar Icterohaemorrhagiae Verdun LP (Verdun) in https://mage.genoscope.cns.fr/microscope/home/index.php.

However, the annotations used in Figures 7, 8 were correct and all the mutants used are correct. The corrected Figure 6 and its corrected legend appears below. The corrected Supplementary Figures 3, 4, and 6 can be accessed from the original article.

Figure 8

Figure 8

(A)In vitro FlaBs mRNA expression in L. interrogans Copenhageni Fiocruz L1-130, Icterohaemorrhagiae Verdun and Manilae L495 at the exponential (E) and stationary (S) phase. Data of RT-qPCR are expressed as the relative mRNA quantities normalized to the expression of the lipl41 mRNA. Technical replicates are represented as dots and lines correspond to mean (+/- SD) of replicates (3 < n < 9). Statistically significant differences (Student t-test) are indicated. (B) In vivo FlaAs and (C) FlaBs mRNA expression in blood of infected mice (n=5, light blue) and hamsters (n-5, dark blue), 24 h post intraperitoneal infection with 2x108 virulent L. interrogans Icterohaemorrhagiae strain Verdun, compared with mRNA expression in culture in EMJH at 30° C. Data of RT-gPCR are expressed as the ratio of mRNA quantities relatives to the EMJH control. Individual animals are represented as dots and lines correspond to mean (+/- SD) of all animals. Statistically significant differences (Student t-test) are indicated with corresponding p values: * for p < 0.05; ** for p < 0.01 and *** for p < 0.001.

The authors apologize for these errors and state that they do 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.

Summary

Keywords

Leptospira, toll-like receptor, innate immunity, Flagelin genes, TLR5, mouse model

Citation

Holzapfel M, Bonhomme D, Cagliero J, Vernel-Pauillac F, d’Andon MF, Bortolussi S, Fiette L, Goarant C, Wunder EA Jr., Picardeau M, Ko AI, Werling D, Matsui M, Boneca IG and Werts C (2022) Corrigendum: Escape of TLR5 recognition by Leptospira spp.: A rationale for atypical endoflagella. Front. Immunol. 13:932151. doi: 10.3389/fimmu.2022.932151

Received

29 April 2022

Accepted

25 May 2022

Published

08 November 2022

Volume

13 - 2022

Edited and reviewed by

Melissa Jo Caimano, University of Connecticut Health Center, United States

Updates

Copyright

*Correspondence: Catherine Werts,

‡Present address: Laurence Fiette, IMMR, Paris, France

This article was submitted to Microbial Immunology, a section of the journal Frontiers in Immunology

†These authors share first authorship

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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