The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
454 Pyrosequencing reveals bacterial diversity of activated sludge from 14 sewage treatment plants
Open accessAbstract
Activated sludge (AS) contains highly complex microbial communities. In this study, PCR-based 454 pyrosequencing was applied to investigate the bacterial communities of AS samples from 14 sewage treatment plants of Asia (mainland China, Hong Kong, and Singapore), and North America (Canada and the United States). A total of 259 K effective sequences of 16S rRNA gene V4 region were obtained from these AS samples. These sequences revealed huge amount of operational taxonomic units (OTUs) in AS, that is, 1183–3567 OTUs in a sludge sample, at 3% cutoff level and sequencing depth of 16 489 sequences. Clear geographical differences among the AS samples from Asia and North America were revealed by (1) cluster analyses based on abundances of OTUs or the genus/family/order assigned by Ribosomal Database Project (RDP) and (2) the principal coordinate analyses based on OTUs abundances, RDP taxa abundances and UniFrac of OTUs and their distances. In addition to certain unique bacterial populations in each AS sample, some genera were dominant, and core populations shared by multiple samples, including two commonly reported genera of Zoogloea and Dechloromonas, three genera not frequently reported (i.e., Prosthecobacter, Caldilinea and Tricoccus) and three genera not well described so far (i.e., Gp4 and Gp6 in Acidobacteria and Subdivision3 genera incertae sedis of Verrucomicrobia). Pyrosequencing analyses of multiple AS samples in this study also revealed the minority populations that are hard to be explored by traditional molecular methods and showed that a large proportion of sequences could not be assigned to taxonomic affiliations even at the phylum/class levels.
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A human gut microbial gene catalogue established by metagenomic sequencing
MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624
UniFrac: a New Phylogenetic Method for Comparing Microbial Communities
Lozupone, C., & Knight, R. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.12.8228-8235.2005 · Cited by 8,227
Environmental genome shotgun sequencing of the sargasso sea
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Ironing out the wrinkles in the rare biosphere through improved OTU clustering
Huse, S. M., Welch, D. M., Morrison, H. G., & Sogin, M. L. (2010) · Environmental Microbiology · doi:10.1111/j.1462-2920.2010.02193.x · Cited by 1,346
Cited by
Rizzo, L., Manaia, C., Merlin, C., Schwartz, T., Dagot, C., Ploy, M. C., Michael, I., & Fatta-Kassinos, D. (2013) · Science of The Total Environment · doi:10.1016/j.scitotenv.2013.01.032 · Cited by 2,493
Bacterial communities in full-scale wastewater treatment systems
Cydzik-Kwiatkowska, A., & Zielińska, M. (2016) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-016-2012-9 · Cited by 426
Combining 16S rRNA gene variable regions enables high-resolution microbial community profiling
(2017) · doi:10.1186/s40168-017-0396-x · Cited by 266
Antimicrobial usage and resistance in beef production
Cameron, A., & McAllister, T. A. (2016) · Journal of Animal Science and Biotechnology · doi:10.1186/s40104-016-0127-3 · Cited by 207
Sarvajith, M., Reddy, G. K. K., & Nancharaiah, Y. V. (2018) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2017.08.064 · Cited by 131
Metadata
- Authors
- Zhang, T., Shao, M.-F., & Ye, L.
- Venue
- The ISME Journal
- Publisher
- Oxford University Press (OUP)
- Published
- 2011-12-15
- Volume
- 6
- Issue
- 6
- Pages
- 1137-1147
- ISSN
- 1751-7362 (ISSN-L)
- 1751-7370
- OpenAlex
- W2091333662
- Cited by
- 1,131
- References
- 5
- FWCI
- 33.00
- Type
- journal article
- Language
- en
- Open access
- bronze
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