Genomic insights into antibiotic resistance and mobilome of lactic acid bacteria and bifidobacteria
Open accessAbstract
sp. (bifidobacteria) can carry antimicrobial resistance genes (ARGs), yet data on resistance mechanisms in these bacteria are limited. The aim of our study was to identify the underlying genetic mechanisms of phenotypic resistance in 103 LAB and bifidobacteria using whole-genome sequencing. Sequencing data not only confirmed the presence of 36 acquired ARGs in genomes of 18 strains, but also revealed wide dissemination of intrinsic ARGs. The presence of acquired ARGs on known and novel mobile genetic elements raises the possibility of their horizontal spread. In addition, our data suggest that mutations may be a common mechanism of resistance. Several novel candidate resistance mechanisms were uncovered, providing a basis for further in vitro studies. Overall, 1,314 minimum inhibitory concentrations matched with genotypes in 92.4% of the cases; however, prediction of phenotype based on genotypic data was only partially efficient, especially with respect to aminoglycosides and chloramphenicol. Our study sheds light on resistance mechanisms and their transferability potential in LAB and bifidobacteria, which will be useful for risk assessment analysis.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Probiotic research is increasingly using computational technologies including whole-genome sequencing, in silico functional annotation, comparative genomic analysis, pathway reconstruction, and AI-based predictive models to support analysis and selection of specific strains.
“Probiotic research is increasingly using computational technologies, including whole-genome sequencing, in silico functional annotation, comparative genomic analysis, pathway reconstruction, and AI-based predictive models, to support the analysis and selection of specific strains [132,133,151].”
From Current Concepts in Probiotic Safety and Efficacy (2026) · cites this paper as [133]
The Introduction (page unavailable) says whole-genome sequencing became a requirement for characterising certain food-chain microorganisms in 2018 and notes subsequent studies of resistance genes in probiotic-related bacteria. Materials and Methods (Whole-genome sequencing and assembly; Sequence analysis, pages unavailable) documents sequencing, annotation, and comparative genomic analyses of strains. The paper does not substantiate the full list of technologies: the cited passages do not describe pathway reconstruction or AI-based predictive models for strain selection. (LLM, conf=0.87)
Experimental — accuracy not yet measuredWhole-genome sequencing-based genomic screening allows in silico detection of antibiotic resistance genes, virulence-associated factors, and mobile genetic elements, providing a basis for modern probiotic safety evaluation.
“Whole-genome sequencing-based genomic screening allows for the in silico detection of antibiotic resistance genes, virulence-associated factors, and mobile genetic elements, thus providing a basis for modern probiotic safety evaluation [20,133,155,156].”
From Current Concepts in Probiotic Safety and Efficacy (2026) · cites this paper as [133]
The Introduction (page not provided) links whole-genome analysis of antibiotic resistance genes and mobile genetic elements to the safety of probiotics, and the Sequence analysis methods describe genomic screening for those genes. The cited passages do not establish detection of virulence-associated factors, so that part of the attributed claim is unsupported. (LLM, conf=0.88)
Experimental — accuracy not yet measuredComputational tools such as whole genome sequencing and bioinformatics analysis are increasingly included in probiotic regulatory dossiers as supporting evidence for strain characterization and safety, provided methods are transparent, reproducible, and interpretable alongside phenotypic data.
“Computational tools such as whole genome sequencing and bioinformatics analysis are increasingly being included in probiotic regulatory dossiers as supporting evidence for strain characterization and safety, provided that the methods are transparent, reproducible, and interpretable alongside phenotypic data [31,132,133].”
From Current Concepts in Probiotic Safety and Efficacy (2026) · cites this paper as [133]
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredComputational approaches can result in false positives and false negatives due to annotation thresholds, database bias, fragmented assemblies, or model overfitting.
“These approaches can result in false positives and false negatives due to factors such as annotation thresholds, database bias, fragmented assemblies, or model overfitting, highlighting the need for careful validation against phenotypic data and careful interpretation when assessing the safety and efficacy of probiotics [67,132,133].”
From Current Concepts in Probiotic Safety and Efficacy (2026) · cites this paper as [133]
The Results (Phenotype–genotype agreement; page unavailable) report imperfect prediction from genomic data, and the Discussion says that detection methods and similarity cut-offs may explain discrepancies. The paper does not attribute false positives or false negatives to database bias, fragmented assemblies, or model overfitting. (LLM, conf=0.86)
Experimental — accuracy not yet measuredAbsence of ARG identified by WGS does not imply absence of resistance mechanisms in probiotic lactic acid bacteria, as intrinsic or non-canonical resistance determinants may remain undetected due to database and methodological limitations.
“The absence of ARG identified by WGS does not imply the absence of resistance mechanisms in probiotic lactic acid bacteria, as intrinsic or non-canonical resistance determinants may remain undetected due to database and methodological limitations, highlighting the need for cautious interpretation of safety assessments based on genomic data [132,133,134].”
From Current Concepts in Probiotic Safety and Efficacy (2026) · cites this paper as [133]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Trimmomatic: a flexible trimmer for Illumina sequence data
Bolger, A. M., Lohse, M., & Usadel, B. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu170 · Cited by 65,548 · see citing works
Fast gapped-read alignment with Bowtie 2
Langmead, B., & Salzberg, S. L. (2012) · Nature Methods · doi:10.1038/nmeth.1923 · Cited by 56,400 · see citing works
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
Stamatakis, A. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu033 · Cited by 32,291 · see citing works
SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing
Bankevich, A., Nurk, S., Antipov, D., Gurevich, A. A., Dvorkin, M. V., Kulikov, A. S., Lesin, V. M., Nikolenko, S., Pham, S., Prjibelski, A. D., et al. (2012) · Journal of Computational Biology · doi:10.1089/cmb.2012.0021 · Cited by 25,691 · see citing works
BLAST+: architecture and applications
Camacho, C., Coulouris, G., Avagyan, V., Ma, N., Papadopoulos, J., Bealer, K., & Madden, T. L. (2009) · BMC Bioinformatics · doi:10.1186/1471-2105-10-421 · Cited by 22,074 · see citing works
Prokka: rapid prokaryotic genome annotation
Seemann, T. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu153 · Cited by 18,512 · see citing works
FLASH: fast length adjustment of short reads to improve genome assemblies
Magoč, T., & Salzberg, S. L. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr507 · Cited by 15,366 · see citing works
QUAST: quality assessment tool for genome assemblies
Gurevich, A., Saveliev, V., Vyahhi, N., & Tesler, G. (2013) · Bioinformatics · doi:10.1093/bioinformatics/btt086 · Cited by 11,172 · see citing works
Database resources of the National Center for Biotechnology Information: update
Wheeler, D. L. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkh073 · Cited by 10,691 · see citing works
KEGG as a reference resource for gene and protein annotation
Kanehisa, M., Sato, Y., Kawashima, M., Furumichi, M., & Tanabe, M. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkv1070 · Cited by 7,387 · see citing works
Accelerated Profile HMM Searches
Eddy, S. R. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002195 · Cited by 6,975 · see citing works
Shifting the genomic gold standard for the prokaryotic species definition
Richter, M., & Rossello-Mora, R. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906412106 · Cited by 6,343 · see citing works
Roary: rapid large-scale prokaryote pan genome analysis
Page, A. J., Cummins, C. A., Hunt, M., Wong, V. K., Reuter, S., Holden, M. T. G., Fookes, M., Falush, D., Keane, J. A., & Parkhill, J. (2015) · Bioinformatics · doi:10.1093/bioinformatics/btv421 · Cited by 5,736 · see citing works
Identification of acquired antimicrobial resistance genes
Zankari, E., Hasman, H., Cosentino, S., Vestergaard, M., Rasmussen, S., Lund, O., Aarestrup, F. M., & Larsen, M. V. (2012) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dks261 · Cited by 4,980 · see citing works
Carattoli, A., Zankari, E., García-Fernández, A., Voldby Larsen, M., Lund, O., Villa, L., Møller Aarestrup, F., & Hasman, H. (2014) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02412-14 · Cited by 4,877 · see citing works
progressiveMauve: Multiple Genome Alignment with Gene Gain, Loss and Rearrangement
Darling, A. E., Mau, B., & Perna, N. T. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011147 · Cited by 3,848 · see citing works
PHASTER: a better, faster version of the PHAST phage search tool
Arndt, D., Grant, J. R., Marcu, A., Sajed, T., Pon, A., Liang, Y., & Wishart, D. S. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw387 · Cited by 3,496 · see citing works
SeqKit: A Cross-Platform and Ultrafast Toolkit for FASTA/Q File Manipulation
Shen, W., Le, S., Li, Y., & Hu, F. (2016) · PLOS ONE · doi:10.1371/journal.pone.0163962 · Cited by 3,380 · see citing works
Mash: fast genome and metagenome distance estimation using MinHash
(2016) · Genome biology · doi:10.1186/s13059-016-0997-x · Cited by 3,373 · see citing works
BLAST Ring Image Generator (BRIG): simple prokaryote genome comparisons
Alikhan, N.-F., Petty, N. K., Zakour, N. L. B., & Beatson, S. A. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-402 · Cited by 3,274 · see citing works
CARD 2017: expansion and model-centric curation of the comprehensive antibiotic resistance database
Jia, B., Raphenya, A. R., Alcock, B. P., Waglechner, N., Guo, P., Tsang, K. K., Lago, B. A., Dave, B. M., Pereira, S. K., Sharma, A. N., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw1004 · Cited by 2,671 · see citing works
CD-HIT Suite: a web server for clustering and comparing biological sequences
Huang, Y., Niu, B., Gao, Y., Fu, L., & Li, W. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btq003 · Cited by 2,618 · see citing works
Genomics and taxonomy in diagnostics for food security: soft-rotting enterobacterial plant pathogens
Pritchard, L., Glover, R. H., Humphris, S. N., Elphinstone, J. G., & Toth, I. K. (2015) · Analytical Methods · doi:10.1039/c5ay02550h · Cited by 1,597 · see citing works
ARG-ANNOT, a new bioinformatic tool to discover antibiotic resistance genes in bacterial genomes
Gupta, S. K., Padmanabhan, B. R., Diene, S. M., Lopez-Rojas, R., Kempf, M., Landraud, L., & Rolain, J.-M. (2014) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01310-13 · Cited by 1,476 · see citing works
Feldgarden, M., Brover, V. V., Haft, D. H., Prasad, A. B., Slotta, D. J., Tolstoy, I., Tyson, G. H., Zhao, S., Hsu, C.-H., McDermott, P. F., et al. (2019) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00483-19 · Cited by 1,436 · see citing works
Robertson, J. A., & Nash, J. H. E. (2018) · Microbial Genomics · doi:10.1099/mgen.0.000206 · Cited by 1,033 · see citing works
Guidance on the characterisation of microorganisms used as feed additives or as production organisms
(FEEDAP), E. P. O. A. A. P. O. S. U. I. A. F., Rychen, G., Aquilina, G., Azimonti, G., Bampidis, V., Bastos, M. D. L., Bories, G., Chesson, A., Cocconcelli, P. S., Flachowsky, G., et al. (2018) · EFSA Journal · doi:10.2903/j.efsa.2018.5206 · Cited by 1,009 · see citing works
Database resources of the National Center for Biotechnology Information
Sayers, E. W., Beck, J. D., Bolton, E., Bourexis, D., Brister, J. R., Canese, K., Comeau, D. C., Funk, K., Kim, S., Klimke, W. A., et al. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa892 · Cited by 960 · see citing works
Brodersen, D. E., Clemons, W. M., Carter, A. P., Morgan-Warren, R. J., Wimberly, B. T., & Ramakrishnan, V. (2000) · Cell · doi:10.1016/s0092-8674(00)00216-6 · Cited by 950 · cited 1× · see citing works
“We believe that a novel A1197T polymorphism leads to tetracycline resistance because this nucleotide is involved in hydrogen bonding with the drug (45).”
Background(FEEDAP), E. P. O. A. A. P. O. S. U. I. A. F. (2012) · EFSA Journal · doi:10.2903/j.efsa.2012.2740 · Cited by 904 · see citing works
Metagenome-wide analysis of antibiotic resistance genes in a large cohort of human gut microbiota
Hu, Y., Yang, X., Qin, J., Lü, N., Cheng, G., Wu, N., Pan, Y., Li, J., Zhu, L., Wang, X., et al. (2013) · Nature Communications · doi:10.1038/ncomms3151 · Cited by 777 · see citing works
Tetracycline Antibiotics and ResistancePreprint
Grossman, T. H. (2016) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a025387 · Cited by 737 · see citing works
Pärnänen, K. M. M., Karkman, A., Hultman, J., Lyra, C., Bengtsson‐Palme, J., Larsson, D. G. J., Rautava, S., Isolauri, E., Salminen, S., Kumar, H., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06393-w · Cited by 682 · see citing works
(EFSA), E. F. S. A. (2007) · EFSA Journal · doi:10.2903/j.efsa.2007.587 · Cited by 479 · see citing works
ICEberg 2.0: an updated database of bacterial integrative and conjugative elements
Liu, M., Li, X., Xie, Y., Bi, D., Sun, J., Li, J., Tai, C., Deng, Z., & Ou, H. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky1123 · Cited by 473 · see citing works
Klare, I., Konstabel, C., Werner, G., Huys, G. R. B., Vankerckhoven, V., Kahlmeter, G., Hildebrandt, B., Müller-Bertling, S., Witte, W., & Goossens, H. (2007) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkm035 · Cited by 365 · see citing works
Genus-Wide Assessment of Antibiotic Resistance in <i>Lactobacillus</i> spp
Campedelli, I., Mathur, H., Salvetti, E., Clarke, S., Rea, M. C., Torriani, S., Ross, R. P., Hill, C., & O’Toole, P. W. (2019) · Applied and Environmental Microbiology · doi:10.1128/aem.01738-18 · Cited by 343 · see citing works
Mechanisms of quinolone action and resistance: where do we stand?
Correia, S., Poeta, P. A. C. Q. D., Hébraud, M., Capelo, J. L., & Igrejas, G. (2017) · Journal of Medical Microbiology · doi:10.1099/jmm.0.000475 · Cited by 332 · see citing works
Zaheer, R., Cook, S. R., Barbieri, R., Goji, N., Cameron, A., Petkau, A., Polo, R. O., Tymensen, L., Stamm, C., Song, J., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-61002-5 · Cited by 262 · see citing works
RNA Sequence Determinants for Aminoglycoside Binding to an A-site rRNA Model Oligonucleotide
Recht, M. I., Fourmy, D., Blanchard, S. C., Dahlquist, K. D., & Puglisi, J. D. (1996) · Journal of Molecular Biology · doi:10.1006/jmbi.1996.0526 · Cited by 252 · see citing works
Rosander, A., Connolly, E., & Roos, S. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.00991-08 · Cited by 239 · see citing works
Roberts, A. P., & Mullany, P. P. (2011) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2011.00283.x · Cited by 238 · see citing works
Update of probiotics in human world: A nonstop source of benefactions till the end of time
Zommiti, M., Feuilloley, M. G. J., & Connil, N. (2020) · Microorganisms · doi:10.3390/microorganisms8121907 · Cited by 225 · see citing works
(EFSA), E. F. S. A. (2021) · EFSA Journal · doi:10.2903/j.efsa.2021.6506 · Cited by 222 · see citing works
Canu, A., Malbruny, B., Coquemont, M., et al. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.1.125-131.2002 · Cited by 218 · see citing works
The hidden life of integrative and conjugative elements
Delavat, F., Miyazaki, R., Carraro, N., Pradervand, N., & van der Meer, J. R. (2017) · FEMS Microbiology Reviews · doi:10.1093/femsre/fux008 · Cited by 207 · see citing works
Antibiotic resistant enterococci-tales of a drug resistance gene trafficker.
Werner, G., Coque, T., Franz, C., Grohmann, E., Hegstad, K., Jensen, L., van Schaik, W., & Weaver, K. (2013) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2013.03.001 · Cited by 182 · see citing works
Dale, G. E., Broger, C., Arcy, A. D., HARTMAN, P. G., DeHoogt, R., Jolidon, S., Kompis, I. M., Labhardt, A. M., Langen, H., Locher, H. H., et al. (1997) · Journal of Molecular Biology · doi:10.1006/jmbi.1996.0770 · Cited by 177 · see citing works
de Vries, L. E., Vallès, Y., Agersø, Y., Vaishampayan, P., García-Montaner, A., Kuehl, J. V., Christensen, H. K., Barlow, M., & Francino, M. P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021644 · Cited by 145 · see citing works
Mutations in gidB Confer Low-Level Streptomycin Resistance in Mycobacterium tuberculosis
Wong, S. Y., Lee, J. S., Kwak, H.-K., Via, L. E., Boshoff, H. I., & Barry, C. E. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01814-10 · Cited by 138 · see citing works
The human microbiome: A hot spot of microbial horizontal gene transfer
Liu, L., Chen, X., Skogerbø, G., Zhang, P., Chen, R., He, S., & Huang, D.-W. (2012) · Genomics · doi:10.1016/j.ygeno.2012.07.012 · Cited by 131 · see citing works
SecReT4: a web-based bacterial type IV secretion system resource
Bi, D., Liu, L., Tai, C., Deng, Z., Rajakumar, K., & Ou, H. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks1248 · Cited by 118 · see citing works
Li, J., Tai, C., Deng, Z., Zhong, W., He, Y. O., & Ou, H. (2016) · Briefings in Bioinformatics · doi:10.1093/bib/bbw141 · Cited by 117 · see citing works
Castanheira, M., Watters, A. A., Mendes, R. E., et al. (2010) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkq094 · Cited by 111 · see citing works
Prevalence of antibiotic resistance genes among human gut-derived bifidobacteria
Duranti, S., Lugli, G. A., Mancabelli, L., Turroni, F., Milani, C., Mangifesta, M., Ferrario, C., Anzalone, R., Viappiani, A., van Sinderen, D., et al. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.02894-16 · Cited by 103 · see citing works
Nishimura, K. J., Hosaka, T., Tokuyama, S., et al. (2007) · Journal of Bacteriology · doi:10.1128/jb.01776-06 · Cited by 102 · see citing works
Phage-inducible islands in the Gram-positive cocci
Martínez‐Rubio, R., Quiles‐Puchalt, N., Martí, M., Humphrey, S., Ram, G., Smyth, D. S., Chen, J. Y.-S., Novick, R. P., & Penadés, J. R. (2016) · The ISME Journal · doi:10.1038/ismej.2016.163 · Cited by 100 · see citing works
Rozman, V., Lorbeg, P. M., Accetto, T., & Matijašić, B. B. (2019) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2019.108388 · Cited by 93 · see citing works
Self-citationDégrange, S., Renaudin, H., Charron, A., et al. (2008) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkn118 · Cited by 59 · see citing works
Whole-genome sequencing based characterization of antimicrobial resistance in Enterococcus
Tyson, G. H., Sabo, J. L., Rice-Trujillo, C., Hernandez, J., & McDermott, P. F. (2018) · Pathogens and Disease · doi:10.1093/femspd/fty018 · Cited by 58 · see citing works
Cammarata, M. B., Thyer, R. T., Lombardo, M. N., Anderson, A., Wright, D. L., Ellington, A. D., & Brodbelt, J. S. (2017) · Chemical Science · doi:10.1039/c6sc05235e · Cited by 57 · see citing works
Teuber, M., Schwarz, F., & Perreten, V. (2003) · International Journal of Food Microbiology · doi:10.1016/s0168-1605(03)00195-8 · Cited by 54 · see citing works
Montealegre, M. C., Roh, J. H., Rae, M. M., Davlieva, M. G., Singh, K. V., Shamoo, Y. E., & Murray, B. E. (2016) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02034-16 · Cited by 54 · see citing works
Distribution of glutathione transferases in Gram-positive bacteria and Archaea
Allocati, N., Federici, L., Masulli, M., et al. (2011) · Biochimie · doi:10.1016/j.biochi.2011.09.008 · Cited by 53 · see citing works
Isnard, C., Malbruny, B., Leclercq, R., & Cattoir, V. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01030-13 · Cited by 53 · see citing works
Drug resistance-conferring mutations in Mycobacterium tuberculosis from Madang, Papua New Guinea
Ballif, M., Harino, P., Ley, S. D., Coscollá, M., Niemann, S., Carter, R., Coulter, C., Borrell, S., Siba, P., Phuanukoonnon, S., et al. (2012) · BMC Microbiology · doi:10.1186/1471-2180-12-191 · Cited by 48 · see citing works
Singh, K. V., & Murray, B. E. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.49.1.32-39.2005 · Cited by 47 · see citing works
Acquired Gentamicin Resistance by Permeability Impairment in Enterococcus faecalis
Aslangul, E., Massias, L., Meulemans, A., et al. (2006) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00390-06 · Cited by 46 · see citing works
Kiwaki, M., & Sato, T. (2009) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2009.06.011 · Cited by 43 · see citing works
Furneri, P. M., Rappazzo, G., Musumarra, M. P., et al. (2001) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.45.10.2958-2960.2001 · Cited by 42 · see citing works
Enterococcus faecium PBP5-S/R, the Missing Link between PBP5-S and PBP5-R
Pietta, E., Montealegre, M. C., Roh, J. H., et al. (2014) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.03648-14 · Cited by 38 · see citing works
Ridenhour, M. B., Fletcher, H. M., Mortensen, J. E., et al. (1996) · Plasmid · doi:10.1006/plas.1996.0009 · Cited by 37 · see citing works
Ribosomal Mutations Conferring Macrolide Resistance in Legionella pneumophila
Descours, G., Ginévra, C., Jacotin, N., et al. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02188-16 · Cited by 37 · see citing works
Mutation Analysis of the Mycobacterium leprae folP1 Gene and Dapsone Resistance
Nakata, N., Kai, M., & Makino, M. (2010) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01212-10 · Cited by 36 · see citing works
Flórez, A. B., & Mayo, B. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.02608 · Cited by 36 · see citing works
Oh, T., Kwon, A., & Choi, E. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.21.5788-5791.1998 · Cited by 28 · see citing works
Martínez, N., Luque, R., Milani, C., Ventura, M., Bañuelos, Ó., & Margollés, A. (2018) · Applied and Environmental Microbiology · doi:10.1128/aem.02888-17 · Cited by 27 · see citing works
Flórez, A. B., Ladero, V., Álvarez‐Martín, P., Ammor, M. S., Álvarez, M. A., & Mayo, B. (2007) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2007.06.002 · Cited by 24 · see citing works
Antimicrobial resistance of Lactobacillus spp. from fermented foods and human gut
Ma, Q., Fu, Y., Sun, H., Huang, Y. C., Li, L., Yu, Q., Dinnyés, A., & Sun, Q. (2017) · LWT · doi:10.1016/j.lwt.2017.07.059 · Cited by 23 · see citing works
Cao, L., Chen, H., Wang, Q., Li, B., Hu, Y., Zhao, C., Hu, Y., & Yin, Y. (2020) · Current Microbiology · doi:10.1007/s00284-020-02230-w · Cited by 21 · see citing works
Shani, N., Oberhaensli, S., & Arias‐Roth, E. (2020) · Journal of Food Protection · doi:10.4315/jfp-20-363 · Cited by 21 · see citing works
Rozman, V., Mohar Lorbeg, P., Treven, P., Accetto, T., Golob, M., Zdovc, I., & Bogovič Matijašić, B. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2127438 · Cited by 21 · see citing works
Self-citationDeng, F., Chen, Y., Zhou, X., Xiao, H., Sun, T., Deng, Y., & Wen, J. (2021) · Microorganisms · doi:10.3390/microorganisms9040726 · Cited by 19 · see citing works
Different Genetic Supports for the tet (S) Gene in Enterococci
Novais, C., Freitas, A. R., Silveira, E., Baquero, F., Peixe, L. M. S. V., Roberts, A. P., & Coque, T. M. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00758-12 · Cited by 17 · see citing works
Stallings, C. L., Chu, L., Li, L. X., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021807 · Cited by 17 · see citing works
Cultivable Bacteria from Milk from Slovenian Breastfeeding Mothers
Tušar, T., Žerdoner, K., Matijašić, B. B., Paveljšek, D., Benedik, E., Bratanič, B., Mis, N. F., & Rogelj, I. (2014) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 12 · see citing works
Kondo, J., & Koganei, M. (2019) · Molecules · doi:10.3390/molecules25010159 · Cited by 4 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Current Concepts in Probiotic Safety and Efficacy
Churin, A. A., Sokolyanskaya, L. O., Lukina, A. P., & Karnachuk, O. V. (2026) · Nutrients · doi:10.3390/nu18040696 · Cited by 31 · see citing works
“…as whole genome sequencing and bioinformatics analysis are increasingly being included in probiotic regulatory dossiers as supporting evidence for strain characterization and safety, provided that the methods are transparent, reproducible, and interpretable alongside phenotypic data [31,132,133].”
InfluentialExploring the resistome of probiotics, starter cultures, and cheeses via metagenomic analysis
Rozman, V., Stopnišek, N., Lorbeg, P. M., Obermajer, T., Kušar, D., & Matijašić, B. B. (2025) · Food Control · doi:10.1016/j.foodcont.2025.111173 · Cited by 12 · see citing works
“MGEs were detected in the genetic environment of the predicted ARGs (5 coding sequences upstream and downstream) using a custom MGE database (285,059 MGE genes) (Rozman et al., 2022; Rozman Mohar Lorbeg, Treven et al., 2023).”
Self-citationExploring the genomic traits of infant-associated microbiota members from a Zimbabwean cohort
Mudhluli, T. E., Kujawska, M., Mueller, J., Felsl, A., Truppel, B.-A., Hall, L. J., Chitsike, I., Gomo, E., & Zhou, D. T. (2024) · BMC Genomics · doi:10.1186/s12864-024-10618-2 · Cited by 3 · see citing works
- Authors
- Rozman, V., Mohar Lorbeg, P., Treven, P., Accetto, T., Janežič, S., Rupnik, M., & Bogovič Matijašić, B.
- Affiliations
- University of Ljubljana (SI)
- University of Ljubljana
- University of Maribor (SI)
- Corresponding author
- Rozman, Vita
- Venue
- Life Science Alliance
- Publisher
- Life Science Alliance, LLC
- Published
- 2023-02-13
- Volume
- 6
- Issue
- 4
- Pages
- e202201637
- ISSN
- 2575-1077 (ISSN-L)
- PMC
- PMC9930590
- OpenAlex
- W4320486124
- Cited by
- 36
- References
- 87
- Citations by year
- 2026: 12 · 2025: 16 · 2024: 6 · 2023: 2
- FWCI
- 3.08
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Life Science Alliance (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- University of Maribor digital library (University of Maribor) (submittedVersion, cc-by)
- Repository of the University of Ljubljana (University of Ljubljana) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Javna Agencija za Raziskovalno Dejavnost RS (6316-1/2017-273, 603-1/2017-13, J4-1769, P4-0097)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Antibiotic Resistance in Bacteria
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- antibiotic resistance, antimicrobial resistance genes, lactic acid bacteria, Bifidobacterium, mobile genetic elements, horizontal gene transfer, resistance mechanisms, phenotypic resistance, minimum inhibitory concentration, aminoglycosides, chloramphenicol, foodborne bacteria
- MeSH terms
- Anti-Bacterial Agents, Bifidobacterium, Drug Resistance, Microbial, Genomics, Lactobacillales
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review