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n
1
a Zorec2ek-Logar2
1 Institute of Animal Physiology and Genetics, Czech Academy of Sciences, P
átelství 560, 104 00, Prague 10, Uhín
ves, Czech Republic
2 University of Ljubljana, Biotechnical Faculty, Zootechnical Dept, Dom
ale, Slovenia
3 Hokkaido University, Graduate School of Agriculture, Sapporo 060-8589, Japan
Correspondence
Jan Kopen
kopecny{at}iapg.cas.cz
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONMETHODSRESULTS AND DISCUSSIONREFERENCES |
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-endoglucanase was also detected in the culture medium. The bacterium utilized a wide range of carbohydrates. Glucose was fermented to formate, butyrate, lactate, succinate and ethanol. The DNA G+C content was 42·1 mol%. The complete 16S rDNA sequence was obtained and phylogenetic relationships were determined. Strain Mz 5T and related isolates were located in clostridial cluster XIVa and were closely related to Pseudobutyrivibrio ruminis, Butyrivibrio crossotus, Roseburia cecicola and Eubacterium rectale. The name proposed for this novel bacterium is Pseudobutyrivibrio xylanivorans; the type strain is Mz 5T (=DSM 14809T =ATCC BAA-455T). Strain JK 615T produced no fibrolytic activity, but utilized a wide range of carbohydrates. Glucose was fermented to formate, acetate, butyrate and ethanol. The DNA G+C content was 44·8 mol%. The complete 16S rDNA sequence was obtained and phylogenetic relationships were determined. Strain JK 615T was located in clostridial cluster XIVa and was closely related to Clostridium proteoclasticum, Butyrivibrio fibrisolvens and Eubacterium halii. The name proposed for this novel bacterium is Butyrivibrio hungatei; the type strain is JK 615T (=DSM 14810T =ATCC BAA-456T).
The EMBL accession numbers for the 16S rDNA sequences of Pseudobutyrivibrio xylanivorans Mz 5T, Pseudobutyrivibrio ruminis JK 626, Pseudobutyrivibrio xylanivorans JK 23/2, Pseudobutyrivibrio xylanivorans JK 633, Clostridium proteoclasticum UC 142 and Butyrivibrio hungatei JK 615T are AJ428548–AJ428553, respectively.
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTS AND DISCUSSIONREFERENCES |
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, 1997; Stewart et al., 1997) and have been observed in DNA samples of uncultivated rumen bacteria (Tajima et al., 1999). A large number of Butyrivibrio strains contributes to fibre degradation in the rumen. Most isolates synthesize xylanase, amylase and cellodextrinase, but few strains produce 1,4--endoglucanase (Stewart et al., 1997). Butyrivibrio isolates are usually able to utilize a wide spectrum of sugar monomers and oligomers.
Up to now, most butyrate-producing isolates have been assigned to Butyrivibrio fibrisolvens on the basis of common phenotypic and metabolic characteristics, despite their vast diversity and genetic unrelatedness. Great variation between B. fibrisolvens strains has been observed in reactions with polyclonal (Margherita et al., 1964) and monoclonal (Hazlewood et al., 1986) antibodies, fermentation products and utilization of sugars (Diez-Gonzalez et al., 1999; Van der Toorn & Van Gylswyk, 1985), cell-wall composition (Hespell et al., 1993), sugar composition of extracellular polysaccharides (Stack, 1988), and DNA–DNA hybridization (Hudman & Gregg, 1989; Mannarelli et al., 1990). 16S rDNA sequencing has confirmed the vast genetic heterogeneity of and great phylogenetic distances between different isolates in the Butyrivibrio group (Forster et al., 1996; Willems et al., 1996; Kopen et al., 2001). Similar variations have been observed in butyrate-producing bacteria from the human gut (Barcenilla et al., 2000).
Recently, three species have been described that are genetically related to B. fibrisolvens: lophotrichous Butyrivibrio crossotus from the human gut (Moore et al., 1976); proteolytic Clostridium proteoclasticum (Attwood et al., 1996); and lactate-producing Pseudobutyrivibrio ruminis (Van Gylswyk et al., 1996) from the rumen. Descriptions of these species have significantly improved the taxonomy of butyrate-producing anaerobic bacteria from the digestive tract.
The aim of this study was to collect taxonomic data for the possible classification of novel species of butyrate-producing anaerobic bacteria from the animal digestive tract.
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METHODS |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTS AND DISCUSSIONREFERENCES |
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). We greatly appreciate the gifts of G. T. Attwood (Palmerston, New Zealand), K. Gregg (Perth, WA, Australia), N. O. van Gylswyk (Uppsala, Sweden) and C. S. Stewart (Aberdeen, UK). Bacterial cultures were kept in 15 % (v/v) glycerol at -70 °C. For further analyses, strains were grown in medium M10 with 10 % rumen fluid and 4 g cellobiose l-1 (Kopen et al., 2001) or in DSM medium no. 330 without rumen fluid.
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) on a Shimadzu GC-14A chromatograph equipped with an FID detector and Supelcowax 10 capillary column (Supelco).
Substrate utilization and degradation of biopolymers.
Substrate utilization and enzyme activities were tested with kits for anaerobic bacteria: API 20 and ID 32 (bioMérieux). Separate analyses were carried out on extracellular activities of amylase, xylanase, laminarinase (1,3--glucanase), proteinase, pectin hydrolase and DNase (Kopen & Barto, 1990; Avgutin et al., 1997).
GC determination of cellular fatty acid composition.
Cells cultured in DSM medium no. 330 without rumen fluid were harvested by centrifugation at 3000 r.p.m. at 4 °C for 10 min. Pellets were washed twice in sodium phosphate buffer (50 mM, pH 6·5). Preparation of fatty acid methyl esters by saponification, methylation and extraction into hexane and sample clean-up were done following the procedure of Moore et al. (1994). Methyl esters were analysed on an HP fused silica capillary column Ultra2 (HP 19091B-102) using a Shimadzu GC-14 A chromatograph equipped with an FID detector and Chromatopac C-R6A for data processing. A calibration standard kit (fatty acid methyl esters in hexane, HP 19298-60500) was used for identification of fatty acids and equivalent chain length factors were calculated for unknown peaks (Moore et al., 1994). Relative concentrations of individual fatty acids were calculated as percentages. Bacterial strains were grouped according to the similarity of their cellular fatty acid profiles.
Transmission electron microscopy.
Bacterial colonies were resuspended in filtered water, transferred onto grids covered with Formvar support film (Robards & Wilson, 1993) and negatively stained with an equal volume of 0·5 % (w/v) aqueous uranyl acetate (Robards & Wilson, 1993). Stained bacteria were air-dried at room temperature and examined with a Philips CM 100 EM. The images were recorded by a Gatan Bioscan CCD camera using DIGITALMICROGRAPH software.
RFLP analyses.
DNA of selected strains was isolated (Gregg et al., 1994) and 16S rDNA regions (1490 bp) were amplified by PCR with the aid of primers fD1 and rP2 (Weisburg et al., 1991; Barcenilla et al., 2000). Obtained fragments were digested at 37 °C for 2 h with restriction endonucleases HaeIII and AluI and then analysed by electrophoresis in 2 % agarose gels (Sambrook et al., 1989).
DNA sequencing and phylogenetic tree construction.
16S rDNA fragments were obtained after amplifying 500 bp regions of bacterial DNA with primers FP27/515R, FP3/RP16 and FP19/rP2 (Forster et al., 1996) on a thermocycler. These fragments were sequenced with an ABI 310 capillary sequencer (Perkin-Elmer). After editing, full 16S rDNA sequences were compared with published sequences of related bacteria from the EMBL and GenBank nucleotide databases using BLAST and with data from the Ribosomal Database Project (Maidak et al., 1994). The sequences were aligned using CLUSTAL W (Thompson et al., 1994) in the BIOEDIT program (Hall, 1999) and a phylogenetic tree was generated with the PHYLIP package (Felsenstein, 1989). Sequence data for distance matrices and analysis were subjected to bootstrap resampling (resampled 1000 times) using the SEQBOOT program. The DNADIST program analysed distances using the Kimura–Nei correction (Kimura, 1980) trees produced from distance matrices that used the neighbour-joining method (Saitou & Nei, 1987). A consensus tree was generated by the CONSENSE program (Felsenstein, 1985).
DNA G+C content.
Estimation of the G+C contents in bacterial chromosomal DNAs was done after extraction and enzymic hydrolysis by HPLC on a C18 reversed-phase column (Supelcosil LC18; Supelco) with the same guard column (Mesbah et al., 1989). DNAs from Escherichia coli strain B (50 mol%) and calf thymus (42 mol%) were used as reference samples for G+C content.
Genera-specific PCR.
Specific forward PCR primers developed previously for the genera Butyrivibrio (71f; 5'-CGG AGA ATT TAC GCT GAT GAA G) and Pseudobutyrivibrio (F2; 5'-AAT TTT CTA CGA TCC CTT CGG GG) were used with reverse primer 515R (Mrázek & Kopen, 2001) to distinguish both genera.
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RESULTS AND DISCUSSION |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTS AND DISCUSSIONREFERENCES |
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; Willems et al., 1996; Forster et al., 1996). To characterize our isolates, RFLP analysis (with restriction endonucleases AluI and HaeIII) of the 16S rDNA fragments from 42 Butyrivibrio isolates (Table 1
), obtained from the digestive tract of ruminants, was used. According to variable fragment size in fingerprints, restriction patterns isolates clustered into five groups. Three of these groups corresponded with three previously described species: B. fibrisolvens, P. ruminis and C. proteoclasticum. Two other homogeneous groups of bacteria with different restriction profiles were observed (Table 2).
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). All strains tested were located in the XIVa cluster of the Gram-positive bacteria (Collins et al., 1994). For two groups of isolates, the assignment of two novel species, Butyrivibrio hungatei and Pseudobutyrivibrio xylanivorans, is proposed. The proposed novel species were significantly different from previously described species. All Butyrivibrio isolates formed two large groups.
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16S rDNA sequence similarities of B. hungatei with B. fibrisolvens (93·7 %), C. proteoclasticum (95·7 %) and B. crossotus (90·6 %) were estimated. Similarly, sequence similarities of P. xylanivorans with P. ruminis (96·4 %), B. fibrisolvens (89·5 %) and B. crossotus (89·6 %) were also determined.
DNA G+C content data are summarized in Table 3. The mean values for most isolates are in the range 40–44 mol%. This range is in agreement with values described for the genera Butyrivibrio and Pseudobutyrivibrio (Stewart et al., 1997; Van Gylswyk et al., 1996). The G+C content data of novel strains resembling C. proteoclasticum were in the same range, contrary to the published value (28 mol%) for the type strain of C. proteoclasticum, which was significantly lower (Attwood et al., 1996). The mean values for G+C contents of the novel species were 41·6 mol% for B. hungatei and 42·7 mol% for P. xylanivorans.
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). High production of lactate by Butyrivibrio isolates was connected with the presence of butyryl-CoA/acetate CoA transferase (Diez-Gonzalez et al., 1999). In agreement with that, in our P. ruminis strains, lactate production was associated with acetate utilization. Roche et al. (1973) described these isolates as acetate-utilizing butyrivibrios. Lactate was also produced by B. fibrisolvens D1T. Isolates of C. proteoclasticum and B. hungatei did not produce lactate at all or did so in small quantities (less than 0·5 mmol l-1). Production of acetate was observed in most cultures of C. proteoclasticum and B. hungatei. Ethanol was produced by most strains of P. xylanivorans and B. hungatei.
Hungate (1966) preliminarily classified isolates producing butyrate and acetate but not producing lactate and ethanol as ‘Butyrivibrio alactacidigens’.
Substrate utilization
The substrate utilization of our 42 Butyrivibrio and Pseudobutyrivibrio strains was tested with API 20A test kits. No strains produced catalase or indole. All strains used glucose, cellobiose, maltose and aesculin. Only strains JK 633 and JK 730 did not use sucrose and mannose. Results obtained with all other substrates tested were variable. These facts are in agreement with previous attempts to reclassify Butyrivibrio isolates (Hungate, 1966; Hudman & Gregg, 1989).
Polysaccharidase activities
Amylase production was observed in many Butyrivibrio isolates (McAllister et al., 1990). This activity was characteristic for most of the P. xylanivorans isolates (Table 3). Other existing and proposed species did not produce any significant amylase activity at all. Xylanase activity was typical of B. fibrisolvens D1T and isolates of P. xylanivorans. P. ruminis did not produce any xylanase activity. In C. proteoclasticum and B. hungatei, the xylanase activity varied (Table 3). Laminarinase activity was observed in several isolates of C. proteoclasticum, B. hungatei and P. xylanivorans only; B. fibrisolvens and P. ruminis isolates did not produce this enzyme activity at all.
-Endoglucanase was characteristic of B. fibrisolvens D1T and several isolates of P. ruminis and P. xylanivorans. No activity was observed in strains of C. proteoclasticum and B. hungatei. Pectin hydrolase was not produced by strains of B. fibrisolvens, P. ruminis or B. hungatei. In the rest of the tested species, the activity differed. The presence of pectin hydrolase was observed only in C. proteoclasticum isolates. Activity of 
-fucosidase was characteristic of B. fibrisolvens D1T and C. proteoclasticum. -Fucosidase was not detected in P. ruminis or in most of the P. xylanivorans isolates. -Fucosidase activity was not observed in all isolates of B. hungatei.
Proteinase and peptidase activities
It has been accepted that Butyrivibrio strains have an important role in protein degradation in the rumen (Attwood & Reilly, 1995). Proteinase activity (Table 3) was characteristic for all strains of C. proteoclasticum and most isolates (12 out of 14 strains tested) of P. xylanivorans. Azocasein was not hydrolysed by all strains of B. hungatei, P. ruminis or B. fibrisolvens D1T. The distribution of proteolytic activity estimated with azocasein did not fully correlate with the gelatin hydrolysing activity observed in API 20 tests. Glycine arylamidase and leucyl-glycine arylamidase activity was observed in B. fibrisolvens D1T and in a few isolates of P. xylanivorans. Similar distribution of enzyme activity was observed in the case of histidine arylamidase; this activity was also observed in one isolate of B. hungatei.
Deoxyribonuclease (DNase) activity
Nuclease activity (Table 3) was observed in most strains of P. xylanivorans and P. ruminis, and also in some strains of B. hungatei. No DNase activity was detected in the culture media of B. fibrisolvens or C. proteoclasticum strains.
Cellular fatty acids
Cellular fatty acid profiles have been used to establish taxonomic relationships among anaerobic bacteria (Holdeman et al., 1977; Mayberry et al., 1982; Moore et al., 1994) and have also proven to be useful in the classification of anaerobic Gram-negative bacteria (Stoakes et al., 1991). The most extensive work on 21 different Butyrivibrio strains was done by Miyagawa (1982). Moore et al. (1994) determined the fatty acid composition only in B. fibrisolvens D1T (=ATCC 19171T). Miyagawa (1982) found that the cellular fatty acid composition varied considerably among strains and divided the Butyrivibrio isolates into two major groups based on fatty acid and fatty aldehyde composition: Group 1 contained branched-chain fatty acids as major components, whereas Group 2 contained only straight-chain fatty acids as major components. Although it is difficult to compare directly our results with those of other authors (different growth media and analyses conditions used), our data (Table 4) in general confirm those of Miyagawa (1982). The fatty acids of P. xylanivorans and B. fibrisolvens contained a low proportion of branched-chain fatty acids and the other three groups of isolates contained the same branched-chain fatty acids as the major ones previously detected by Miyagawa (1982): iso-C14 : 0 and anteiso-C15 : 0, which are the discriminating fatty acids of C. proteoclasticum isolates; iso-C15 : 1, a major, characteristic fatty acid of isolates of P. ruminis; and anteiso-C17 : 0, found in C. proteoclasticum, B. hungatei and B. fibrisolvens D1T. Our results also confirmed that among straight-chain fatty acids, C16 : 0 was generally the major fatty acid in Butyrivibrio and Butyrivibrio-like isolates. The two Pseudobutyrivibrio species (P. ruminis and P. xylanivorans) and B. fibrisolvens contained C16 : 0 fatty acid in the highest proportion (Van Gylswyk et al., 1996). Other major straight-chain saturated and unsaturated fatty acids detected were C14 : 0, C15 : 0, C16 : 1 and C18 : 1, which is in total accordance with the results of Miyagawa (1982). The different relative proportions of these fatty acids and the detection of some fatty acids unique to some groups of isolates enabled us to cluster our isolates into five separate species.
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; Hespell et al., 1993; Forster et al., 1996). Our data fully support the proposal of two novel bacterial species: the non-proteolytic and non-fibrolytic species B. hungatei and the fibrolytic species P. xylanivorans. Both species are common in the rumen content of sheep and cow.
Description of Butyrivibrio hungatei sp. nov.
Butyrivibrio hungatei (hun.ga'te.i.N.L. gen. n. hungatei named after Robert E. Hungate, an American microbiologist, who isolated similar strains in the 1960s).
Cells are Gram-negative, straight to slightly curved rods (0·3–0·5x1·5–2·5 µm) that do not form endospores. Motile by means of a single polar or subpolar flagellum (Fig. 2). Growth occurs anaerobically at 39 °C, but not at 25 °C. Limited growth is observed at 45 °C. No growth is observed in the presence of oxygen. Arabinose, cellobiose, aesculin, glucose, lactose, maltose, mannose, raffinose, salicin, sucrose and xylose are utilized by the type strain. Tryptophan, urea and gelatin are not utilized. The following substrates do not support growth of the type strain: glycerol; mannitol; melezitose; sorbitol; rhamnose; trehalose. Medium M10 with glucose (22 mM) is fermented to formate (12 mM), acetate (2·2 mM), butyrate (10·8 mM) and ethanol (3·4 mM). No lactate or succinate production is observed. No growth occurs in the absence of fermentable carbohydrates. Does not show any significant fibrolytic or proteolytic activity, utilizing mainly oligo- and monosaccharides as growth substrates. The type strain does not liquefy gelatin, produce hydrogen sulfide, reduce nitrate or hydrolyse urea and is catalase-negative. -Galactosidase, -arabinosidase, phenylalanine arylamidase and leucine arylamidase are produced. No amylase, xylanase, -endoglucanase, laminarinase, pectin hydrolase, proteinase or DNase activities are detected. The major cellular fatty acid components of strain JK 615T grown in DSM medium no. 330 without rumen fluid are saturated, branched-chain anteiso-C17 : 0 (17·4 %) and iso-C16 : 0 (14·5 %), and unsaturated straight-chain C16 : 1 (13·2 %) fatty acids. Also present are C16 : 0 2-OH (6·9 %), C14 : 0 2-OH (4·3 %) and iso-C17 : 1 (3·4 %). Branched-chain fatty acids represent the prevailing proportion of cellular fatty acids in this species. Strains are common isolates in our set of anaerobic rumen bacteria. In the rumen, they participate in the utilization of intermediates of fibre degradation. Strains belonging to Butyrivibrio hungatei are listed in the footnote of Table 3. The type strain is JK 615T (=DSM 14810T =ATCC BAA-456T). The DNA G+C content of the type strain is 44·8 mol% (as determined by the HPLC method).
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Cells are Gram-negative, straight to slightly curved rods (0·4–0·6x1·5–3·0 µm) that do not form endospores. Cells are motile by means of a single polar or subpolar flagellum (Fig. 3). Growth occurs anaerobically at 39 °C, but not at 25 or 45 °C. No growth is observed in the presence of oxygen. However, exposure of grown liquid culture to air for several hours does not destroy the ability of the species to recover under anaerobic conditions. Substrates that support growth of the type strain are cellobiose, aesculin, glucose, lactose, maltose, mannose, melezitose, salicin, sucrose and xylose. Tryptophan, urea and gelatin are not utilized. The following substrates do not support growth of the type strain: glycerol; mannitol; raffinose; sorbitol; rhamnose; trehalose. Medium M10 with glucose (22 mM) is fermented to formate (15·1 mM), butyrate (17·6 mM), lactate (10·9 mM), succinate (0·3 mM) and ethanol (1·1 mM). Acetate is utilized. No growth occurs in the absence of fermentable carbohydrates. Strain Mz 5T does not liquefy gelatin or produce hydrogen sulfide; neither does it reduce nitrate, hydrolyse urea nor produce catalase. It produces -galactosidase, -arabinosidase, xylanase, amylase, -endoglucanase, pectin hydrolase, proteinase and DNase. The major cellular fatty acid components of strain Mz 5T grown in DSM medium no. 330 without rumen fluid are C16 : 0 (39·2 %) and anteiso-C17 : 1 (6·4 %), followed by iso-C17 : 0 3-OH (3·9 %) and C14 : 0 (4·3 %). This species is characterized by a higher content of straight-chain cellular fatty acids and a lower content of branched-chain fatty acids. Produces high xylanase activity. Most strains also produce amylase, proteinase and DNase. Laminarinase is detected in some species. Strains belonging to Pseudobutyrivibrio xylanivorans are listed in the footnote of Table 3. The most common butyrate-producing anaerobic bacterium in our set of bacteria isolated from the rumen of sheep and cow. The type strain is Mz 5T (=DSM 14809T =ATCC BAA-455T). The DNA G+C content of the type strain is 42·1 mol% (as determined by the HPLC method).
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ACKNOWLEDGEMENTS |
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ek (University of Ljubljana, Department of Biology, Slovenia) for providing the electron micrographs of the type strains Mz 5T and JK 615T and to G. Avgutin (University of Ljubljana, Zootechnical Department, Slovenia) for valuable discussions. This work was funded by The Grant Agency of the Czech Republic (Project No. 524/99/0602) and also supported by The Ministry of Education, Science and Sports of the Republic of Slovenia. |
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