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Int J Syst Evol Microbiol 57 (2007), 2259-2261; DOI  10.1099/ijs.0.64915-0
© 2007 International Union of Microbiological Societies

EzTaxon: a web-based tool for the identification of prokaryotes based on 16S ribosomal RNA gene sequences

Jongsik Chun1,2, Jae-Hak Lee1, Yoonyoung Jung1, Myungjin Kim2, Seil Kim2, Byung Kwon Kim2 and Young-Woon Lim2

1 Interdisciplinary Program in Bioinformatics, Seoul National University, 56-1 Shillim-dong, Kwanak-gu, Seoul 151-742, Republic of Korea
2 School of Biological Sciences and Institute of Microbiology, Seoul National University, 56-1 Shillim-dong, Kwanak-gu, Seoul 151-742, Republic of Korea

Correspondence
Jongsik Chun
jchun{at}snu.ac.kr


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS AND DISCUSSION
 REFERENCES
 
16S rRNA gene sequences have been widely used for the identification of prokaryotes. However, the flood of sequences of non-type strains and the lack of a peer-reviewed database for 16S rRNA gene sequences of type strains have made routine identification of isolates difficult and labour-intensive. In the present study, we generated a database containing 16S rRNA gene sequences of all prokaryotic type strains. In addition, a web-based tool, named EzTaxon, for analysis of 16S rRNA gene sequences was constructed to achieve identification of isolates based on pairwise nucleotide similarity values and phylogenetic inference methods. The system developed provides users with a similarity-based search, multiple sequence alignment and various phylogenetic analyses. All of these functions together with the 16S rRNA gene sequence database of type strains can be successfully used for automated and reliable identification of prokaryotic isolates. The EzTaxon server is freely accessible over the Internet at http://www.eztaxon.org/


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS AND DISCUSSION
 REFERENCES
 
It is undisputed that information held in 16S rRNA gene sequences has played a vital role in microbiology (Rosselló-Mora & Amann, 2001Go) and that it can be utilized in many ways in various disciplines, notably taxonomy and ecology. Pairwise nucleotide similarity values of 16S rRNA gene sequences have been used routinely for the delineation of prokaryotic species (Stackebrandt & Goebel, 1994Go) and have been widely accepted. When a 16S rRNA gene sequence is applied for the identification of prokaryotic isolates, the general process includes: (i) similarity search against public domain nucleotide databases, (ii) retrieval of sequences for type strains with validly published names, (iii) calculation of pairwise nucleotide similarity values between sequences of the isolate and phylogenetically neighbouring type strains and (iv) phylogenetic analysis. This process requires expertise in prokaryotic taxonomy and can be complicated and labour-intensive, as public databases have been flooded with sequences of non-type strains including environmental clones and may contain erroneous and mislabelled sequences. Furthermore, there are no curated databases for 16S rRNA gene sequences of type strains of prokaryotic species. In this study, we present a database containing 16S rRNA gene sequences of all prokaryotic type strains and a web-based tool for analysis of 16S rRNA gene sequences, allowing automation of the process indicated above.


    METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS AND DISCUSSION
 REFERENCES
 
Construction of 16S rRNA gene sequence database.
The validly published names of prokaryotic species were obtained from the Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ) website (http://www.dsmz.de/). 16S rRNA gene sequences of type strains were extracted from the NCBI GenBank database. The validity and authenticity of sequence entries were checked by manual inspection by reviewing culture collection catalogues and relevant publications. Sequences that are a part of longer sequences (e.g. genome sequence) were trimmed to obtain only the 16S rRNA gene coding region. The names and corresponding 16S rRNA gene sequences will be updated on a monthly basis following the publication of the Validation and Notification Lists of the International Journal of Systematic and Evolutionary Microbiology.

Inputs for sequence similarity search.
The formats of input data for sequence similarity searches are either text or tracer files generated from automated sequencers. The PHRED program was used for the base-calling and trimming of uploaded tracer files (Ewing & Green, 1998Go; Ewing et al., 1998Go).

Finding phylogenetic neighbours using the EzTaxon server.
The BLAST program (Altschul et al., 1997Go) was employed for the initial similarity search. The parsed BLAST hits are stored and can be sorted by BLAST scores or e values.

Calculation of pairwise sequence similarity values.
The phylogenetically closest neighbours identified by BLAST search were then selected for the calculation of pairwise nucleotide sequence similarity using the algorithm of Myers & Miller (1988)Go. The alignment gap was not considered in the similarity calculation.

Multiple sequence alignment and phylogenetic inference.
The current version of the EzTaxon server provides multiple sequence alignment by CLUSTAL W (Thompson et al., 1994Go). The resultant sequence alignment can then be used for the neighbour-joining (Saitou & Nei, 1987Go), maximum-parsimony (Fitch, 1971Go), and maximum-likelihood (Felsenstein, 1981Go) methods using the PHYLIP package (Felsenstein, 2005Go); all were implemented within the server. The alignment can be exported for use by external programs including jPHYDIT (Jeon et al., 2005Go), PAUP (Swofford, 2002Go), PHYLIP, MEGA (Kumar et al., 2004Go) and MrBayes (Ronquist & Huelsenbeck, 2003Go).

Operating system and programming languages.
All databases and computer programs were generated using MySQL, JSP and JAVA under Linux operating system.

Availability.
The EzTaxon server is freely accessible over the Internet at http://www.eztaxon.org/


    RESULTS AND DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS AND DISCUSSION
 REFERENCES
 
The database, named TYP16S, consisted of more than 7000 sequence entries together with the validly published names of the taxa concerned, GenBank/EMBL/DDBJ accession numbers and type strain designations. We have found that there are still more than 250 species with validly published names for which 16S rRNA gene sequences are not available.

The overall process for the identification of isolates using the EzTaxon server is given in Fig. 1Go. The final goal of the system is to find taxonomically meaningful phylogenetic relatives from either sequences or raw tracers (chromatograms). The BLAST search is based on local alignment that cannot be used for the calculation of overall sequence similarity. On the other hand, pairwise global sequence alignment using the algorithm of Myers & Miller (1988)Go guarantees the identification of the most similar sequence, but requires a higher computing cost. The EzTaxon server utilizes two methods sequentially to obtain accurate search results at reasonable computing cost. Such a combinatory strategy should guarantee the identification of the closest phylogenetic neighbour to the query sequence.


Figure 1
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Fig. 1. Overview of the process for analysing 16S rRNA gene sequences using the EzTaxon server (http://www.eztaxon.org/). The websites from which the programs can be obtained are jPHYDIT (http://plaza.snu.ac.kr/~jchun/jphydit/), PAUP (http://paup.csit.fsu.edu/), PHYLIP (http://evolution.genetics.washington.edu/phylip.html), MEGA (http://www.megasoftware.net/) and MrBayes (http://mrbayes.csit.fsu.edu/).

 
The 16S rRNA gene sequence similarity value has played an important role in delineating novel taxa and in the identification of isolates. Stackebrandt & Goebel (1994)Go suggested that a 16S rRNA gene sequence similarity of 97 % should become the boundary for delineation of prokaryotic species, which has been well accepted among microbiologists. More recently, Stackebrandt & Ebers (2006)Go proposed a more relaxed cut-off value of 98.7–99 %, after inspection of a large amount of recently published data. Even though this new proposal requires further validation and discussion, it is evident that high quality of sequencing should be the prerequisite to the use of lower similarity cut-off values for the identification of prokaryotes.

Similarity values tend to vary depending on the alignment algorithms employed and how gaps are considered. In addition, calculations based on multiple sequence alignment might produce different similarity values depending on the sequences included in the analysis. Therefore, to achieve a reliable and conservative measure of pairwise similarity values, we propose that the calculation should be carried out using rigorous pairwise global alignment algorithms such as that developed by Myers & Miller (1988)Go, and that alignment gaps should not be considered. The calculation of pairwise sequence similarity values from multiple alignments should be avoided.

EzTaxon was successfully developed to include the collection of all reference sequences, and to provide various functions, including a similarity search engine, calculation of pairwise similarity, multiple sequence alignment and phylogenetic treeing algorithms at the server side. This would allow users in places where only poor computing facilities are available to carry out most of the necessary bioinformatic analyses of 16S rRNA gene sequences. It could also be useful in various levels of classes for educational purposes.

In future, the EzTaxon server will be upgraded to include more analysis tools for phylogenetics, taxonomy and ecology of prokaryotes. We also plan to implement parallel computing versions of time-consuming methods such as multiple sequence alignment and maximum-likelihood inference of phylogenetic trees.


    ACKNOWLEDGEMENTS
 
This work was supported by the Korea Science and Engineering Foundation (KOSEF) through the National Research Lab. Program funded by the Ministry of Science and Technology (no. M10500000110-06J0000-11010). We are grateful to the Korea Bioinformatics Center (http://www.kobic.re.kr/) for supporting hardware.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS AND DISCUSSION
 REFERENCES
 
Altschul, S. F., Madden, T. L., Schaffer, A. A., Zhang, J., Zhang, Z., Miller, W. & Lipman, D. J. (1997). Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25, 3389–3402.[Abstract/Free Full Text]

Ewing, B. & Green, P. (1998). Base-calling of automated sequencer traces using phred. II. Error probabilities. Genome Res 8, 186–194.[Abstract/Free Full Text]

Ewing, B., Hillier, L., Wendl, M. C. & Green, P. (1998). Base-calling of automated sequencer traces using phred. I. Accuracy assessment. Genome Res 8, 175–185.[Abstract/Free Full Text]

Felsenstein, J. (1981). Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 17, 368–376.[CrossRef][Medline]

Felsenstein, J. (2005). PHYLIP (Phylogeny Inference Package), version 3.6. Distributed by the author. Department of Genome Sciences, University of Washington, Seattle, USA.

Fitch, W. M. (1971). Toward defining the course of evolution: minimum change for a specific tree topology. Syst Zool 20, 406–416.[Abstract]

Jeon, Y. S., Chung, H., Park, S., Hur, I., Lee, J. H. & Chun, J. (2005). jPHYDIT: a JAVA-based integrated environment for molecular phylogeny of ribosomal RNA sequences. Bioinformatics 21, 3171–3173.[Abstract/Free Full Text]

Kumar, S., Tamura, K. & Nei, M. (2004). MEGA3: Integrated software for molecular evolutionary genetics analysis and sequence alignment. Brief Bioinform 5, 150–163.[Abstract/Free Full Text]

Myers, E. W. & Miller, W. (1988). Optimal alignments in linear space. Comput Appl Biosci 4, 11–17.[Abstract/Free Full Text]

Ronquist, F. & Huelsenbeck, J. P. (2003). MrBayes 3: bayesian phylogenetic inference under mixed models. Bioinformatics 19, 1572–1574.[Abstract/Free Full Text]

Rosselló-Mora, R. & Amann, R. (2001). The species concept for prokaryotes. FEMS Microbiol Rev 25, 39–67.[Medline]

Saitou, N. & Nei, M. (1987). The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4, 406–425.[Abstract]

Stackebrandt, E. & Ebers, J. (2006). Taxonomic parameters revisited: tarnished gold standards. Microbiol Today 33, 152–155.

Stackebrandt, E. & Goebel, B. M. (1994). Taxonomic note: a place for DNA-DNA reassociation and 16S rRNA sequence analysis in the present species definition in bacteriology. Int J Syst Bacteriol 44, 846–849.[Abstract/Free Full Text]

Swofford, D. L. (2002). PAUP*: Phylogenetic analysis using parsimony (*and other methods), version 4. Sunderland, MA: Sinauer Associates.

Thompson, J. D., Higgins, D. G. & Gibson, T. J. (1994). CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 22, 4673–4680.[Abstract/Free Full Text]




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Int. J. Syst. Evol. Microbiol.Home page
X. Luo, L. Zhang, J. Dai, M. Liu, K. Zhang, H. An, and C. Fang
Mucilaginibacter ximonensis sp. nov., isolated from Tibetan soil
Int J Syst Evol Microbiol, June 1, 2009; 59(6): 1447 - 1450.
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Int. J. Syst. Evol. Microbiol.Home page
H. An, L. Zhang, Y. Tang, X. Luo, T. Sun, Y. Li, Y. Wang, J. Dai, and C. Fang
Skermanella xinjiangensis sp. nov., isolated from the desert of Xinjiang, China
Int J Syst Evol Microbiol, June 1, 2009; 59(6): 1531 - 1534.
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Int. J. Syst. Evol. Microbiol.Home page
K. Watanabe, H. Makino, M. Sasamoto, Y. Kudo, J. Fujimoto, and S. Demberel
Bifidobacterium mongoliense sp. nov., from airag, a traditional fermented mare's milk product from Mongolia
Int J Syst Evol Microbiol, June 1, 2009; 59(6): 1535 - 1540.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
J.-H. Qu, H.-L. Yuan, J.-S. Yang, H.-F. Li, and N. Chen
Lacibacter cauensis gen. nov., sp. nov., a novel member of the phylum Bacteroidetes isolated from sediment of a eutrophic lake
Int J Syst Evol Microbiol, May 1, 2009; 59(5): 1153 - 1157.
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Int. J. Syst. Evol. Microbiol.Home page
Y.-Y. Huo, X.-W. Xu, Y. Cao, C.-S. Wang, X.-F. Zhu, A. Oren, and M. Wu
Marinobacterium nitratireducens sp. nov. and Marinobacterium sediminicola sp. nov., isolated from marine sediment
Int J Syst Evol Microbiol, May 1, 2009; 59(5): 1173 - 1178.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
C. Sanchez-Porro, V. Gallego, H.-J. Busse, P. Kampfer, and A. Ventosa
Transfer of Teichococcus ludipueritiae and Muricoccus roseus to the genus Roseomonas, as Roseomonas ludipueritiae comb. nov. and Roseomonas rosea comb. nov., respectively, and emended description of the genus Roseomonas
Int J Syst Evol Microbiol, May 1, 2009; 59(5): 1193 - 1198.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
M. Halpern, T. Shaked, R. Pukall, and P. Schumann
Leucobacter chironomi sp. nov., a chromate-resistant bacterium isolated from a chironomid egg mass
Int J Syst Evol Microbiol, April 1, 2009; 59(4): 665 - 670.
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Int. J. Syst. Evol. Microbiol.Home page
F. Peng, L. Zhang, X. Luo, J. Dai, H. An, Y. Tang, and C. Fang
Deinococcus xinjiangensis sp. nov., isolated from desert soil
Int J Syst Evol Microbiol, April 1, 2009; 59(4): 709 - 713.
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Int. J. Syst. Evol. Microbiol.Home page
D. Tappe, R. Pukall, P. Schumann, S. Gronow, M. Spiliotis, H. Claus, K. Brehm, and U. Vogel
Streptococcus merionis sp. nov., isolated from Mongolian jirds (Meriones unguiculatus)
Int J Syst Evol Microbiol, April 1, 2009; 59(4): 766 - 770.
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Int. J. Syst. Evol. Microbiol.Home page
Y. Wang, J. Dai, L. Zhang, X. Luo, Y. Li, G. Chen, Y. Tang, Y. Meng, and C. Fang
Lysobacter ximonensis sp. nov., isolated from soil
Int J Syst Evol Microbiol, April 1, 2009; 59(4): 786 - 789.
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Int. J. Syst. Evol. Microbiol.Home page
S. W. Roh, Y.-D. Nam, H.-W. Chang, K.-H. Kim, M.-S. Kim, K.-S. Shin, J.-H. Yoon, H.-M. Oh, and J.-W. Bae
Paracoccus aestuarii sp. nov., isolated from tidal flat sediment
Int J Syst Evol Microbiol, April 1, 2009; 59(4): 790 - 794.
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Int. J. Syst. Evol. Microbiol.Home page
C.-S. Wang, Y. Wang, X.-W. Xu, D.-S. Zhang, Y.-H. Wu, and M. Wu
Microbulbifer donghaiensis sp. nov., isolated from marine sediment of the East China Sea
Int J Syst Evol Microbiol, March 1, 2009; 59(3): 545 - 549.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
M. Arenas, P. I. Banon, J. L. Copa-Patino, C. Sanchez-Porro, A. Ventosa, and J. Soliveri
Halomonas ilicicola sp. nov., a moderately halophilic bacterium isolated from a saltern
Int J Syst Evol Microbiol, March 1, 2009; 59(3): 578 - 582.
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Int. J. Syst. Evol. Microbiol.Home page
Y. Tang, J. Dai, L. Zhang, Z. Mo, Y. Wang, Y. Li, S. Ji, C. Fang, and C. Zheng
Dyadobacter alkalitolerans sp. nov., isolated from desert sand
Int J Syst Evol Microbiol, January 1, 2009; 59(1): 60 - 64.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
P. Kampfer, N. Lodders, B. Huber, E. Falsen, and H.-J. Busse
Deinococcus aquatilis sp. nov., isolated from water
Int J Syst Evol Microbiol, December 1, 2008; 58(12): 2803 - 2806.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
Y. Wang, Y.-H. Wu, C.-S. Wang, X.-W. Xu, A. Oren, X.-F. Zhu, and M. Wu
Halomonas salifodinae sp. nov., a halophilic bacterium isolated from a salt mine in China
Int J Syst Evol Microbiol, December 1, 2008; 58(12): 2855 - 2858.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
S. W. Roh, Z.-X. Quan, Y.-D. Nam, H.-W. Chang, K.-H. Kim, S.-K. Rhee, H.-M. Oh, C. O. Jeon, J.-H. Yoon, and J.-W. Bae
Marinobacter goseongensis sp. nov., from seawater
Int J Syst Evol Microbiol, December 1, 2008; 58(12): 2866 - 2870.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
M. C. Gutierrez, A. M. Castillo, M. Kamekura, and A. Ventosa
Haloterrigena salina sp. nov., an extremely halophilic archaeon isolated from a salt lake
Int J Syst Evol Microbiol, December 1, 2008; 58(12): 2880 - 2884.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
K. S. Baik, S. C. Park, M. S. Kim, E. M. Kim, C. Park, J. Chun, and C. N. Seong
Luteimonas marina sp. nov., isolated from seawater
Int J Syst Evol Microbiol, December 1, 2008; 58(12): 2904 - 2908.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
Y.-H. Wu, M. Wu, C.-S. Wang, X.-G. Wang, J.-Y. Yang, A. Oren, and X.-W. Xu
Microbacterium profundi sp. nov., isolated from deep-sea sediment of polymetallic nodule environments
Int J Syst Evol Microbiol, December 1, 2008; 58(12): 2930 - 2934.
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Int. J. Syst. Evol. Microbiol.Home page
A. Valverde, A. Peix, R. Rivas, E. Velazquez, S. Salazar, I. Santa-Regina, C. Rodriguez-Barrueco, and J. M. Igual
Paenibacillus castaneae sp. nov., isolated from the phyllosphere of Castanea sativa Miller
Int J Syst Evol Microbiol, November 1, 2008; 58(11): 2560 - 2564.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
F.-L. Lee, C.-J. Tien, C.-J. Tai, L.-T. Wang, Y.-C. Liu, and L.-L. Chern
Paenibacillus taichungensis sp. nov., from soil in Taiwan
Int J Syst Evol Microbiol, November 1, 2008; 58(11): 2640 - 2645.
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Appl. Environ. Microbiol.Home page
S. W. Roh, Y.-D. Nam, H.-W. Chang, K.-H. Kim, M.-S. Kim, J.-H. Ryu, S.-H. Kim, W.-J. Lee, and J.-W. Bae
Phylogenetic Characterization of Two Novel Commensal Bacteria Involved with Innate Immune Homeostasis in Drosophila melanogaster
Appl. Envir. Microbiol., October 15, 2008; 74(20): 6171 - 6177.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
S. H. Ryu, J. H. Park, J. C. Moon, Y. Sung, S.-S. Lee, and C. O. Jeon
Flavobacterium resistens sp. nov., isolated from stream sediment
Int J Syst Evol Microbiol, October 1, 2008; 58(10): 2266 - 2270.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
B.-S. Kim, Y. W. Lim, and J. Chun
Sphingopyxis marina sp. nov. and Sphingopyxis litoris sp. nov., isolated from seawater
Int J Syst Evol Microbiol, October 1, 2008; 58(10): 2415 - 2419.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
S.-K. Tang, X.-P. Tian, X.-Y. Zhi, M. Cai, J.-Y. Wu, L.-L. Yang, L.-H. Xu, and W.-J. Li
Haloactinospora alba gen. nov., sp. nov., a halophilic filamentous actinomycete of the family Nocardiopsaceae
Int J Syst Evol Microbiol, September 1, 2008; 58(9): 2075 - 2080.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
M. Wang, M. Yang, G. Zhou, X. Luo, L. Zhang, Y. Tang, and C. Fang
Paenibacillus tarimensis sp. nov., isolated from sand in Xinjiang, China
Int J Syst Evol Microbiol, September 1, 2008; 58(9): 2081 - 2085.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
J.-H. Qu, H.-F. Li, J.-S. Yang, and H.-L. Yuan
Flavobacterium cheniae sp. nov., isolated from sediment of a eutrophic reservoir
Int J Syst Evol Microbiol, September 1, 2008; 58(9): 2186 - 2190.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
J.-H. Qu and H.-L. Yuan
Sediminibacterium salmoneum gen. nov., sp. nov., a member of the phylum Bacteroidetes isolated from sediment of a eutrophic reservoir
Int J Syst Evol Microbiol, September 1, 2008; 58(9): 2191 - 2194.
[Abstract] [Full Text] [PDF]


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J. Clin. Microbiol.Home page
S. Y. Shin, M. Y. Lee, J.-H. Song, and K. S. Ko
New Erwinia-Like Organism Causing Cervical Lymphadenitis
J. Clin. Microbiol., September 1, 2008; 46(9): 3156 - 3158.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
S. G. Dastager, J.-C. Lee, Y.-J. Ju, D.-J. Park, and C.-J. Kim
Rubellimicrobium mesophilum sp. nov., a mesophilic, pigmented bacterium isolated from soil
Int J Syst Evol Microbiol, August 1, 2008; 58(8): 1797 - 1800.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
R. Rivas, P. Garcia-Fraile, J. L. Zurdo-Pineiro, P. F. Mateos, E. Martinez-Molina, E. J. Bedmar, J. Sanchez-Raya, and E. Velazquez
Saccharibacillus sacchari gen. nov., sp. nov., isolated from sugar cane
Int J Syst Evol Microbiol, August 1, 2008; 58(8): 1850 - 1854.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
S. G. Dastager, J.-C. Lee, Y.-J. Ju, D.-J. Park, and C.-J. Kim
Frigoribacterium mesophilum sp. nov., a mesophilic actinobacterium isolated from Bigeum Island, Korea
Int J Syst Evol Microbiol, August 1, 2008; 58(8): 1869 - 1872.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
H.-W. Chang, S. W. Roh, K.-H. Kim, Y.-D. Nam, C. O. Jeon, H.-M. Oh, and J.-W. Bae
Vibrio areninigrae sp. nov., a marine bacterium isolated from black sand
Int J Syst Evol Microbiol, August 1, 2008; 58(8): 1903 - 1906.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
M. C. Marquez, I. J. Carrasco, Y. Xue, Y. Ma, D. A. Cowan, B. E. Jones, W. D. Grant, and A. Ventosa
Aquisalibacillus elongatus gen. nov., sp. nov., a moderately halophilic bacterium of the family Bacillaceae isolated from a saline lake
Int J Syst Evol Microbiol, August 1, 2008; 58(8): 1922 - 1926.
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Int. J. Syst. Evol. Microbiol.Home page
S. G. Dastager, J.-C. Lee, Y.-J. Ju, D.-J. Park, and C.-J. Kim
Leifsonia bigeumensis sp. nov., isolated from soil on Bigeum Island, Korea
Int J Syst Evol Microbiol, August 1, 2008; 58(8): 1935 - 1938.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
I. J. Carrasco, M. C. Marquez, Y. Xue, Y. Ma, D. A. Cowan, B. E. Jones, W. D. Grant, and A. Ventosa
Sediminibacillus halophilus gen. nov., sp. nov., a moderately halophilic, Gram-positive bacterium from a hypersaline lake
Int J Syst Evol Microbiol, August 1, 2008; 58(8): 1961 - 1967.
[Abstract] [Full Text] [PDF]


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Proc. Natl. Acad. Sci. USAHome page
L. Ponnusamy, N. Xu, S. Nojima, D. M. Wesson, C. Schal, and C. S. Apperson
Identification of bacteria and bacteria-associated chemical cues that mediate oviposition site preferences by Aedes aegypti
PNAS, July 8, 2008; 105(27): 9262 - 9267.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
M. Cai, X.-Y. Zhi, S.-K. Tang, Y.-Q. Zhang, L.-H. Xu, and W.-J. Li
Streptomonospora halophila sp. nov., a halophilic actinomycete isolated from a hypersaline soil
Int J Syst Evol Microbiol, July 1, 2008; 58(7): 1556 - 1560.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
S. W. Roh, Z.-X. Quan, Y.-D. Nam, H.-W. Chang, K.-H. Kim, M.-K. Kim, W.-T. Im, L. Jin, S.-H. Kim, S.-T. Lee, et al.
Pedobacter agri sp. nov., from soil
Int J Syst Evol Microbiol, July 1, 2008; 58(7): 1640 - 1643.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
S. Jit, M. Dadhwal, O. Prakash, and R. Lal
Flavobacterium lindanitolerans sp. nov., isolated from hexachlorocyclohexane-contaminated soil
Int J Syst Evol Microbiol, July 1, 2008; 58(7): 1665 - 1669.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
K. H. Cho, S. G. Hong, H. H. Cho, Y. K. Lee, J. Chun, and H. K. Lee
Maribacter arcticus sp. nov., isolated from Arctic marine sediment
Int J Syst Evol Microbiol, June 1, 2008; 58(6): 1300 - 1303.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
S. G. Dastager, J.-C. Lee, Y.-J. Ju, D.-J. Park, and C.-J. Kim
Marmoricola bigeumensis sp. nov., a member of the family Nocardioidaceae
Int J Syst Evol Microbiol, May 1, 2008; 58(5): 1060 - 1063.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
L.-J. Yuan, Y.-Q. Zhang, Y. Guan, Y.-Z. Wei, Q.-P. Li, L.-Y. Yu, W.-J. Li, and Y.-Q. Zhang
Saccharopolyspora antimicrobica sp. nov., an actinomycete from soil
Int J Syst Evol Microbiol, May 1, 2008; 58(5): 1180 - 1185.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
J.-T. Wang, Y.-J. Chou, J.-H. Chou, C. A. Chen, and W.-M. Chen
Tenacibaculum aiptasiae sp. nov., isolated from a sea anemone Aiptasia pulchella
Int J Syst Evol Microbiol, April 1, 2008; 58(4): 761 - 766.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
M. Pineiro-Vidal, C. G. Carballas, O. Gomez-Barreiro, A. Riaza, and Y. Santos
Tenacibaculum soleae sp. nov., isolated from diseased sole (Solea senegalensis Kaup)
Int J Syst Evol Microbiol, April 1, 2008; 58(4): 881 - 885.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
Y.-J. Chou, J.-H. Chou, K.-Y. Lin, M.-C. Lin, Y.-H. Wei, A. B. Arun, C.-C. Young, and W.-M. Chen
Rothia terrae sp. nov. isolated from soil in Taiwan
Int J Syst Evol Microbiol, January 1, 2008; 58(1): 84 - 88.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
J.-H. Kim, K.-Y. Kim, Y.-T. Hahm, B.-S. Kim, J. Chun, and C.-J. Cha
Actibacter sediminis gen. nov., sp. nov., a marine bacterium of the family Flavobacteriaceae isolated from tidal flat sediment
Int J Syst Evol Microbiol, January 1, 2008; 58(1): 139 - 143.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
M. Okamoto, Y. Benno, K.-P Leung, and N. Maeda
Bifidobacterium tsurumiense sp. nov., from hamster dental plaque
Int J Syst Evol Microbiol, January 1, 2008; 58(1): 144 - 148.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
M. E. Trujillo, R. M. Kroppenstedt, C. Fernandez-Molinero, P. Schumann, and E. Martinez-Molina
Micromonospora lupini sp. nov. and Micromonospora saelicesensis sp. nov., isolated from root nodules of Lupinus angustifolius
Int J Syst Evol Microbiol, December 1, 2007; 57(12): 2799 - 2804.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
S.-C. Chang, W.-M. Chen, J.-T. Wang, and M.-C. Wu
Chitinilyticum aquatile gen. nov., sp. nov., a chitinolytic bacterium isolated from a freshwater pond used for Pacific white shrimp culture
Int J Syst Evol Microbiol, December 1, 2007; 57(12): 2854 - 2860.
[Abstract] [Full Text] [PDF]


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Int. J. Syst. Evol. Microbiol.Home page
J.-H. Chou, K.-Y. Lin, M.-C. Lin, S.-Y. Sheu, Y.-H. Wei, A. B. Arun, C.-C. Young, and W.-M. Chen
Brachybacterium phenoliresistens sp. nov., isolated from oil-contaminated coastal sand
Int J Syst Evol Microbiol, November 1, 2007; 57(11): 2674 - 2679.
[Abstract] [Full Text] [PDF]


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