Divergence and redundancy of 16S rRNA sequences in genomes with multiple rrn operons - PubMed (original) (raw)
Divergence and redundancy of 16S rRNA sequences in genomes with multiple rrn operons
Silvia G Acinas et al. J Bacteriol. 2004 May.
Abstract
The level of sequence heterogeneity among rrn operons within genomes determines the accuracy of diversity estimation by 16S rRNA-based methods. Furthermore, the occurrence of widespread horizontal gene transfer (HGT) between distantly related rrn operons casts doubt on reconstructions of phylogenetic relationships. For this study, patterns of distribution of rrn copy numbers, interoperonic divergence, and redundancy of 16S rRNA sequences were evaluated. Bacterial genomes display up to 15 operons and operon numbers up to 7 are commonly found, but approximately 40% of the organisms analyzed have either one or two operons. Among the Archaea, a single operon appears to dominate and the highest number of operons is five. About 40% of sequences among 380 operons in 76 bacterial genomes with multiple operons were identical to at least one other 16S rRNA sequence in the same genome, and in 38% of the genomes all 16S rRNAs were invariant. For Archaea, the number of identical operons was only 25%, but only five genomes with 21 operons are currently available. These considerations suggest an upper bound of roughly threefold overestimation of bacterial diversity resulting from cloning and sequencing of 16S rRNA genes from the environment; however, the inclusion of genomes with a single rrn operon may lower this correction factor to approximately 2.5. Divergence among operons appears to be small overall for both Bacteria and Archaea, with the vast majority of 16S rRNA sequences showing <1% nucleotide differences. Only five genomes with operons with a higher level of nucleotide divergence were detected, and Thermoanaerobacter tengcongensis exhibited the highest level of divergence (11.6%) noted to date. Overall, four of the five extreme cases of operon differences occurred among thermophilic bacteria, suggesting a much higher incidence of HGT in these bacteria than in other groups.
Figures
FIG. 1.
Distribution of different rrn operon numbers among bacterial (gray bars) and archaeal (black bars) isolates. Data were obtained from complete genome sequences from the NCBI and TIGR genome databases, the rrndb database, and the literature.
FIG. 2.
Numbers (bars) and percentages of the total (line) of genomes with all identical 16S rRNA sequences among operons. Data were retrieved from the NCBI and TIGR genome databases and the rrndb database.
FIG. 3.
Secondary structure model of the helices that differ in length between operons in Thermoanaerobacter tengcongensis. Nucleotide positions 444 to 490 (A) and 1,447 to 1,456 (B) are given according to Escherichia coli reference numbering.
Similar articles
- Reprint of New opportunities for improved ribotyping of C. difficile clinical isolates by exploring their genomes.
Gürtler V, Grando D. Gürtler V, et al. J Microbiol Methods. 2013 Dec;95(3):425-40. doi: 10.1016/j.mimet.2013.09.009. Epub 2013 Sep 16. J Microbiol Methods. 2013. PMID: 24050948 Review. - Assembly of a complete genome sequence for Gemmata obscuriglobus reveals a novel prokaryotic rRNA operon gene architecture.
Franke JD, Blomberg WR, Todd RT, Thomas RW, Selmecki AM. Franke JD, et al. Antonie Van Leeuwenhoek. 2018 Nov;111(11):2095-2105. doi: 10.1007/s10482-018-1102-0. Epub 2018 May 21. Antonie Van Leeuwenhoek. 2018. PMID: 29785674 - First complete nucleotide sequence and heterologous gene organization of the two rRNA operons in the phytoplasma genome.
Jung HY, Miyata S, Oshima K, Kakizawa S, Nishigawa H, Wei W, Suzuki S, Ugaki M, Hibi T, Namba S. Jung HY, et al. DNA Cell Biol. 2003 Mar;22(3):209-15. doi: 10.1089/104454903321655837. DNA Cell Biol. 2003. PMID: 12804119 - Distinct types of rRNA operons exist in the genome of the actinomycete Thermomonospora chromogena and evidence for horizontal transfer of an entire rRNA operon.
Yap WH, Zhang Z, Wang Y. Yap WH, et al. J Bacteriol. 1999 Sep;181(17):5201-9. doi: 10.1128/JB.181.17.5201-5209.1999. J Bacteriol. 1999. PMID: 10464188 Free PMC article. - New opportunities for improved ribotyping of C. difficile clinical isolates by exploring their genomes.
Gürtler V, Grando D. Gürtler V, et al. J Microbiol Methods. 2013 Jun;93(3):257-72. doi: 10.1016/j.mimet.2013.02.013. Epub 2013 Mar 29. J Microbiol Methods. 2013. PMID: 23545446 Review.
Cited by
- Groundtruthing next-gen sequencing for microbial ecology-biases and errors in community structure estimates from PCR amplicon pyrosequencing.
Lee CK, Herbold CW, Polson SW, Wommack KE, Williamson SJ, McDonald IR, Cary SC. Lee CK, et al. PLoS One. 2012;7(9):e44224. doi: 10.1371/journal.pone.0044224. Epub 2012 Sep 6. PLoS One. 2012. PMID: 22970184 Free PMC article. - Considerations For Optimizing Microbiome Analysis Using a Marker Gene.
de la Cuesta-Zuluaga J, Escobar JS. de la Cuesta-Zuluaga J, et al. Front Nutr. 2016 Aug 8;3:26. doi: 10.3389/fnut.2016.00026. eCollection 2016. Front Nutr. 2016. PMID: 27551678 Free PMC article. Review. - Use of 16S rRNA and rpoB genes as molecular markers for microbial ecology studies.
Case RJ, Boucher Y, Dahllöf I, Holmström C, Doolittle WF, Kjelleberg S. Case RJ, et al. Appl Environ Microbiol. 2007 Jan;73(1):278-88. doi: 10.1128/AEM.01177-06. Epub 2006 Oct 27. Appl Environ Microbiol. 2007. PMID: 17071787 Free PMC article. - Culture-dependent and culture-independent diversity within the obligate marine actinomycete genus Salinispora.
Mincer TJ, Fenical W, Jensen PR. Mincer TJ, et al. Appl Environ Microbiol. 2005 Nov;71(11):7019-28. doi: 10.1128/AEM.71.11.7019-7028.2005. Appl Environ Microbiol. 2005. PMID: 16269737 Free PMC article. - Novel and unexpected prokaryotic diversity in water and sediments of the alkaline, hypersaline lakes of the Wadi An Natrun, Egypt.
Mesbah NM, Abou-El-Ela SH, Wiegel J. Mesbah NM, et al. Microb Ecol. 2007 Nov;54(4):598-617. doi: 10.1007/s00248-006-9193-y. Epub 2007 Apr 21. Microb Ecol. 2007. PMID: 17450395
References
- Alm, R. A., L.-S. L. Ling, D. T. Moir, B. L. King, E. D. Brown, P. C. Doig, D. R. Smith, B. Noonan, B. C. Guild, B. L. deJonge, G. Carmel, P. J. Tummino, A. Caruso, M. Uria-Nickelsen, D. M. Mills, C. Ives, R. Gibson, D. Merberg, S. D. Mills, Q. Jiang, D. E. Taylor, G. F. Vovis, and T. J. Trust. 1999. Genomic-sequence comparison of two unrelated isolates of the human astric pathogen Helicobacter pylori. Nature 397:176-180. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources