General Commentary ARTICLE
Commentary: Clinical utilization of genomics data produced by the international Pseudomonas aeruginosa consortium
- Laboratório de Genética Molecular de Microrganismos, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brasil
by Freschi, L., Jeukens, J., Kukavica-Ibrulj, I., Boyle, B., Dupont, M-J., Laroche, J., et al. (2015) Front. Microbiol. 6:1036. doi: 10.3389/fmicb.2015.01036
The robust study on Pseudomonas aeruginosa genome evolution, epidemiology, antimicrobial resistance mechanisms, and pathogenesis performed by Freschi et al. (2015) will offer a huge contribution to clinicians to improve the management of infections caused by this organism. Moreover, it is a big step toward the application of such genomic data to understand cystic fibrosis infections and to establish a powerful surveillance system in the clinical routine. This study also presented the first snapshot of the P. aeruginosa resistome by performing searches on 389 P. aeruginosa genomes using the Resistance Gene Identifier tool from the Comprehensive Antibiotic Resistance Database (CARD) (McArthur et al., 2013). The resistome comprises all genes that are direct or indirectly involved with antimicrobial resistance emergence, which includes intrinsic and acquired resistance genes, distinct resistance mechanisms as well as new determinants not yet identified in the clinical environment (Wright, 2007). Freschi and Colleagues have applied an interesting strategy to recover the resistome information, however, we would like to highlight here that some methodological limitations can compromise this type of screening due to the resistome complexity. For example, they included in the resistome screening three P. aeruginosa genomes (9BR, 19BR, and 213BR; Boyle et al., 2012) that belong to the pandemic high-risk clone SP/ST277 (Fonseca et al., 2015) however, some relevant resistance genes that characterize this clone were not identified. The blaSPM-1 gene codes for a metallo-β-lactamase that confers resistance to all β-lactams antibiotics, including carbapenems, which is the first line antibiotic class in the treatment of infections caused by Gram-negative bacteria. This gene characterizes the P. aeruginosa clone SP/ST277, being recognized as a genetic marker of this lineage. Recently, it was demonstrated that the blaSPM-1 is carried by the ICETn43716061, which also harbors the byciclomycin resistance bcr-1 gene (Fonseca et al., 2015). ICEs (Integrative and Conjugative Elements) are genetic mobile platforms that can have a major impact in the spread and resistance emergence (Carraro and Burrus, 2014). However, neither blaSPM-1 nor bcr-1 resistance genes were identified by Resistance Gene Identifier tool as part of the 19BR, 213BR, and 9BR resistome. Similarly, the IslandViewer, a specific tool to identify genomic islands, was not able to identify the ICETn43716061 in none of these three genomes. In order to verify whether this finding resulted from a bias imposed by any parameters used by Freschi et al. (2015) to perform the analyzes or if it was a methodological limitation of the approach used, we applied the Resistance Gene Identifier tool on one genome of clone SP/ST277, extensively studied by our group (PS106), as well as on 9BR, 19BR, and 213BR. A previous BLASTn search using ICETn43716061 as query revealed its presence in these genomes (Fonseca et al., 2015) however, they were not recognized in our analysis using Resistance Gene Identifier tool, showing some limitations of this approach in the resistome mining. Therefore, we provided here an evidence of an underestimated scenario of the antimicrobial resistance potential, which could also affect the efficient establishment of antimicrobial therapy strategies in the clinical routine. In conclusion, in spite of the valuable contribution of Freschi's study, we would like to stress here that, although the bioinformatics comprehend an important tool to study the overall biology of microorganisms and to assess specific genomic information, they all have limitations that are ameliorated when distinct in silico approaches are performed.
All authors listed, have made substantial, direct and intellectual contribution to the work, and approved it for publication.
Conflict of Interest Statement
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.
This work was supported by CNPq grant.
Boyle, B., Fernandez, L., Laroche, J., Kukavica-Ibrulj, I., Mendes, C. M., Hancock, R. W., et al. (2012). Complete genome sequences of three Pseudomonas aeruginosa isolates with phenotypes of polymyxin B adaptation and inducible resistance. J. Bacteriol. 194, 529–530. doi: 10.1128/JB.06246-11
Fonseca, E. L., Marin, M. A., Encinas, F., and Vicente, A. C. (2015). Full characterization of the integrative and conjugative element carrying the metallo-β-lactamase blaSPM-1 and bicyclomycin bcr1 resistance genes found in the pandemic Pseudomonas aeruginosa clone SP/ST277. J. Antimicrob. Chemother. 70, 2547–2550. doi: 10.1093/jac/dkv152
Freschi, L., Jeukens, J., Kukavica-Ibrulj, I., Boyle, B., Dupont, M.-J., Laroche, J., et al. (2015). Clinical utilization of genomics data produced by the international Pseudomonas aeruginosa consortium. Front. Microbiol. 6:1036. doi: 10.3389/fmicb.2015.01036
McArthur, A. G., Waglechner, N., Nizam, F., Yan, A., Azad, M. A., Baylay, A. J., et al. (2013). The comprehensive antibiotic resistance database. Antimicrob. Agents Chemother. 57, 3348–3357. doi: 10.1128/AAC.00419-13
Keywords: SPM-1, metallo-beta-lactamase, integrative and conjugative elements (ICEs), Pseudomonas aeruginosa genomics, clone SP/ST277, byciclomycin resistance, BCR-1
Citation: Fonseca EL and Vicente ACP (2016) Commentary: Clinical utilization of genomics data produced by the international Pseudomonas aeruginosa consortium. Front. Microbiol. 7:770. doi: 10.3389/fmicb.2016.00770
Received: 18 March 2016; Accepted: 06 May 2016;
Published: 23 May 2016.
Edited by:Eric Altermann, AgResearch Ltd., New Zealand
Reviewed by:Pierre Cornelis, Vrije Universiteit Brussel, Belgium
Hongwei David Yu, Joan C. Edwards School of Medicine at Marshall University, USA
George Tsiamis, University of Patras, Greece
Copyright © 2016 Fonseca and Vicente. 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: Erica L. Fonseca, firstname.lastname@example.org