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1 School of Veterinary Medicine, Azabu University, 1-17-71 Fuchinobe, Sagamihara, Kanagawa 229-8501, Japan
2 Microbial Genome Research Group, Japan Agency of Marine-Earth Science and Technology, 2-15 Natsushima, Yokosuka, Kanagawa 237-0061, Japan
3 Nodai Culture Collection Center, Department of Brewing, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya, Tokyo 156-8502, Japan
4 Northern Farm, 275 Hayakita-genbu, Abira-cho, Yufutsu-gun, Hokkaido 059-1432, Japan
5 Clossfield-Bio Inc., 1-1-20, Higashi Nihonbashi, Chuo, Tokyo 103-0004, Japan
Correspondence
Hidetoshi Morita
morita{at}azabu-u.ac.jp
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Trees showing the phylogenetic relationship, based on the 16S rRNA gene sequence, of the isolate in comparison to species of the Lactobacillus salivarius phylogenetic group constructed by the maximum-parsimony and maximum-likelihood methods are available with the online version of this paper.
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; Morotomi et al., 2002). In our study, we isolated the following lactobacilli present in the intestinal tract of healthy thoroughbreds: Lactobacillus gasseri, Lactobacillus johnsonii, Lactobacillus ruminis, Lactobacillus reuteri, Lactobacillus salivarius, Lactobacillus crispatus and Lactobacillus agilis. These species are well-known species isolated from mammalian gastrointestinal tracts. Lactobacillus equi was also found during our study, which is a dominant and indigenous species in equine gastrointestinal tracts (Morotomi et al., 2002). As part of a study on the intestinal microbiota in thoroughbreds, two strains, KBL13T and GBL13, were isolated from different thoroughbreds. A polyphasic taxonomic study of these strains was performed using phenotypic characterization and phylogenetic as well as genetic methods; the results obtained by using these methods consistently revealed the isolates, KBL13T and GBL13, to represent a novel Lactobacillus species, from intestines of thoroughbreds, for which the name Lactobacillus hayakitensis sp. nov. is proposed.
Bacterial strains, KBL13T and GBL13, were isolated from fresh faeces of different healthy thoroughbreds of the same farm where they were born in Hokkaido, Japan. The fresh faeces of each thoroughbred were transferred under anaerobic conditions by AnaeroPack (Mitsubishi Gas Chemical) at 4 °C to our laboratory within 24 h. The initial processing and subsequent weighing and dilution of the specimens were carried out under anaerobic conditions. Each dilution was then spread on to BL agar plates (Eiken Chemical) and incubated anaerobically at 37 °C for 2 days. All further cultivation was performed at 37 °C in ABCM broth (Eiken Chemical). The 16S rRNA gene sequences of the isolates were determined as described previously (Endo & Okada, 2005). The 1484 bp of the 16S rRNA gene sequence of KBL13T was consistent with those of GBL13. DNA–DNA hybridization was carried out by using the microdilution-well technique, with photobiotin for labelling of the DNA (Ezaki et al., 1989). KBL13T and GBL13 shared high levels of DNA–DNA relatedness (99.5–100.0 %). The closest known relatives of the isolates were determined by performing database searches, and the sequences of closely related species were retrieved from the DDBJ database. Multiple alignments of the sequences were carried out with the CLUSTAL_X program, version 1.18 (Thompson et al., 1997). Distance matrices for the aligned sequences were calculated by using the two-parameter method of Kimura (1980). The neighbour-joining method was used to construct a phylogenetic tree (Saitou & Nei, 1987). The robustness of individual branches was estimated by using bootstrapping with 1000 replicates (Felsenstein, 1985). Phylogenetic trees were also constructed by using the maximum-likelihood (Cavalli-Sforza & Edwards, 1967) and maximum-parsimony (Kluge & Farris, 1969) methods with PHYLIP version 3.65 (Felsenstein, 2005).
In a neighbour-joining dendrogram created based on the sequence of KBL13T and sequences from the GenBank database, the phylogenetic position of KBL13T was determined. KBL13T was placed within the L. salivarius phylogenetic group (Canchaya et al., 2006) and was most closely related to L. salivarius, Lactobacillus aviarius, Lactobacillus saerimneri and Lactobacillus acidipiscis as shown in Fig. 1. Recently, on the basis of a polyphasic analysis, Li et al. (2006) indicated that L. salivarius subsp. salivarius and L. salivarius subsp. salicinicus did not merit separate subspecies status. As the information of the physiological characteristics of L. salivarius JCM 1150 is available to us (previously described as L. salivarius subsp. salicinicus JCM 1150), the physiological characteristics of KBL13T and GBL13 were compared with those of L. salivarius JCM 1231T (=ATCC 11741T; AF089108) and JCM 1150 as shown in Table 1. L. salivarius JCM 1231T and JCM 1150, L. aviarius subsp. aviarius JCM 5666T and L. aviarius subsp. araffinosus JCM 5667T used in the study were obtained from the Japan Collection of Microorganisms. A high similarity of 96.0 % (1425/1484 bp) was observed in the 16S rRNA gene sequences of KBL13T and L. salivarius JCM 1231T. Identical tree topologies were obtained by using the maximum-likelihood and maximum-parsimony methods (see Supplementary Figs S1 and S2 available in IJSEM Online).
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. The DNA G+C content of KBL13T and GBL13 were 34.3 and 34.8 mol%, respectively. The DNA G+C content of their closest relatives, L. salivarius JCM 1231T and L. aviarius subsp. araffinosus JCM 5667T was 34.7 and 41.3 mol%, respectively. The DNA G+C content of KBL13T was found to be within the range of 32.0–55.0 mol%, which is the range reported for Lactobacillus species (Kandler & Weiss, 1986).
The sugar fermentation patterns were determined using the API 50CH system (bioMérieux) according to the manufacturer's instructions. The results were recorded after 48 h at 37 °C. The isomer of lactic acid produced from glucose was determined by using an F-kit (D-lactic acid/L-lactic acid; Roche Diagnostics Corporation). Other biochemical tests, such as those on motility, growth at a fixed temperature and gas production from glucose, were performed by using the methods described by Mitsuoka (1969). Table 1
shows the characteristics most useful in distinguishing the strains studied from closely related lactobacilli. Since KBL13T and GBL13 were found to be the same species, KBL13T was used as a representative strain in the experiments described below.
DNA–DNA hybridization analyses (Ezaki et al., 1989) were performed, including those for the two most closely related species, L. salivarius JCM 1231T and JCM 1150, and L. aviarius subsp. araffinosus JCM 5667T, based on the 16S rRNA gene sequence analysis. DNA–DNA relatedness values between KBL13T and L. salivarius JCM 1231T and JCM 1150, and L. aviarius subsp. araffinosus JCM 5667T were 14.2, 12.1 and 7.9 %, respectively. These values are well below the threshold of 70.0 % that is suggested for species delineation (Stackebrandt & Goebel, 1994), indicating that strain KBL13T represents a separate genomic species. Analysis by high-performance thin-layer chromatography showed that meso-diaminopimelic acid was not contained in the peptidoglycan of the strain KBL13T, and an analysis, by ultraperformance liquid chromatography according to the methods described by Komagata & Suzuki (1987), of the cell wall composition revealed the Lys–Asp peptydoglycan type in the presence of Lys, Glu, Ala and Asp.
DNA–DNA relatedness showed a clear separation of strain KBL13T from its phylogenetic relatives, it is considered that the strain studied represents a novel species belonging to the genus Lactobacillus, for which the name Lactobacillus hayakitensis sp. nov. is proposed.
Description of Lactobacillus hayakitensis sp. nov.
Lactobacillus hayakitensis (ha.ya.ki.ten'sis. N.L. masc. adj. hayakitensis of Hayakita, which is the name of the area where the bacterium was originally isolated).
Cells are Gram-positive, 3.0–5.0 µm long and 1.0–1.5 µm wide, non-motile and non-spore-forming rods. They occur singly or in pairs. Colonies are small (1.5 mm), circular to slightly irregular, convex, with a smooth to rough surface, and white when grown on MRS agar. The optimum growth temperature is 37 °C. Strain KBL13T is not able to grow in 4.5 % NaCl and at 15 °C, but grows in 3.0 % NaCl and at 45 °C. Cells are catalase-negative. Glucose is metabolized homofermentatively and lactate is the sole final product. Strain KBL13T produces L(+)-lactic acid. Acid is produced from glucose, fructose, mannose, mannitol, N-acetyl-D-glucosamine, arbutin, aesculin, salicin, cellobiose, maltose, sucrose and gentiobiose. Amygdalin and raffinose are weakly fermented. In this species, some strains cannot ferment N-acetyl-D-glucosamine, arbutin and raffinose. The DNA G+C content of the type strain is 34.3 %, and the cell wall composition of the strain exhibits the Lys–Asp peptydoglycan type.
The type strain, KBL13T (=JCM 14209T=DSM 18933T), was isolated from the faeces of a thoroughbred.
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ACKNOWLEDGEMENTS |
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REFERENCES |
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