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Previous Article | Next Article 
Applied and Environmental Microbiology, November 2007, p. 6819-6828, Vol. 73, No. 21
0099-2240/07/$08.00+0 doi:10.1128/AEM.00786-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan 48824-4320
Received 9 April 2007/ Accepted 25 August 2007
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Early measurements of the redox potential of hindguts, together with the presence of strictly anaerobic microbes, led to the hypothesis that termite guts were devoid of oxygen (7, 53). By contrast, other data suggested that some portion(s) of the hindgut must contain O2. For example, aerotolerant, facultative, and even O2-requiring microorganisms were frequently represented among isolates (13, 43, 51, 53), and degradation of lignin model compounds in vivo was found to be O2 dependent (14). It was not until direct measurements were made with microelectrodes that fine-scale profiles of O2 gradients within intact hindguts were obtained (13, 17). The results demonstrated the presence of a peripheral hypoxic zone, with O2 occurring at partial pressures of about 20 x 102 to 30 x 102 Pa (ca. 20 to 30% air saturation) at the gut wall, which decreased steeply to anoxia a distance of 150 to 200 µm inward. This indicated that a majority (approximately 60%) of the hindgut contained significant levels of O2, undoubtedly a result of its small size and relatively large surface-to-volume ratio (12). Such results also implied that some members of the microbiota on and/or near the hindgut wall constituted an important "oxygen sink" (12, 13, 17). Consistent with this interpretation were earlier experiments showing that hindguts rapidly became completely oxic (implied by the color of redox dyes) when termites were fed antibacterial drugs (53); and exposure of termites to hyperbaric levels of O2 resulted in the death of hindgut spirochetes and protozoans (both groups have been reported to be anaerobes) but led to a 6- to 10-fold increase in overall hindgut bacterial colony counts on culture plates incubated in air (53). However, such treatments decreased the ability of termites to survive on a diet of wood or cellulose.
It now seems clear that O2-consuming members of the peripheral hindgut microbiota are critical in creating and maintaining anoxic conditions in the luminal region for an essentially homoacetic conversion of wood polysaccharides by carbohydrate fermenters and CO2-reducing acetogens (27, 50). However, our understanding of this O2-consuming microbiota is meager, as is the nature of the substrate(s) that fuels their respiratory activity, although acetate itself is a likely candidate given its abundance and high rate of oxidation to CO2 in termite hindguts (50), as well as the abundance of (not-yet-characterized) acetate oxidizers inferred from most-probable-number enumerations (51). Accordingly, we sought to explore the nature of O2 consumers in more detail by using acetate as a substrate in isolation media, as well as in incubation atmospheres that included hypoxia (2% O2) to accommodate the possibility that some members of the O2-consuming microbiota might be so highly adapted to life in hypoxia that they do not grow in air (21% O2). The results of this effort led to the isolation of several previously uncultivated bacteria from termite guts, including a microaerophilic, acetate-oxidizing member of the ß-Proteobacteria, Stenoxybacter acetivorans gen. nov., sp. nov., which is a significant member of the O2-consuming bacterial microbiota and whose description is the subject of this paper. A companion paper (55) reports on the physiological ecology of S. acetivorans, including the expression of relevant genes in situ.
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Isolation and cultivation of bacteria.
Guts from 50 worker larvae were extracted with sterile forceps under an hypoxic, CO2-enriched atmosphere (2% O2, 5% CO2, 93% N2) within a vinyl chamber (Coy Laboratory Products, Grass Lake, MI). Extracted guts were transferred to and homogenized in a sterile glass tissue homogenizer containing 2 ml of a buffered salts solution (BSS) composed of (per liter) 0.2 g KH2PO4, 0.25 g NH4Cl, 0.5 g KCl, 0.15 g CaCl2·2H2O, 1.0 g NaCl, 0.62 g MgCl2·6H2O, 2.84 g Na2SO4, and 10 mM 3-(N-morpholino)propanesulfonic acid (MOPS). The pH of the BSS was adjusted to pH 7.0, and the solution was preincubated under the CO2-enriched hypoxic atmosphere for at least 12 h before use, during which time the pH decreased to about 6.5, which was close to the pH of the hindgut fluid (pH 6.4) (13). Serial 10-fold dilutions of gut homogenate were prepared in BSS, and 0.1-ml aliquots of each dilution were spread onto six plates of ACY medium, which consisted of BSS amended with 10 mM sodium acetate, 0.05% (wt/vol) Bacto Casamino Acids, 0.05% (wt/vol) Bacto yeast extract, 0.01% (vol/vol) each of a trace element solution and a vitamin solution (49), and 1.5% (vol/vol) Bacto agar. The pH of ACY medium was adjusted to 7.0. Three plates from each dilution were retained within the hypoxic chamber, and the remaining plates were placed in glass desiccator jars containing CO2-enriched air (5% [vol/vol] CO2, 95% air). Every 2 days, the atmosphere in the jars was replenished. All incubations were at 22 to 23°C.
After ca. 20 days, when new colony formation was subsiding, plates containing well-separated colonies were selected for colony enumeration, isolation, and identification. The number of colonies having a similar morphology on each plate was noted, and an effort was made to have at least one pure culture representative of each colony type. For each colony, duplicate plates of homologous medium were streaked; one plate was incubated under hypoxia, and the companion plate was incubated in CO2-enriched air. In addition, specific groups of organisms were targeted for isolation by using a "plate wash PCR" (49) with the following 16S rRNA gene forward primers: Acd31f (5'-GAT CCT GGC TCA GAA TC-3') for Acidobacteria (4), End197f (5'-GCA GCA ATG CGT TTT GAG-3') for Endomicrobia (this study), Pla40f (5'-CGG RTG GAT TAG GCA TG-3') for Planctomycetes (K. Huizinga, personal communication), and Ver53f (5'-TGG CGG CGT GGW TAA GA-3') for Verrucomicrobia (49). The reverse primer in all cases was the general bacterial reverse primer 1492r (see below). The purity of isolates was based on uniform colony and cell morphology; the latter was determined by phase-contrast microscopy. Preliminary screening of isolates for acetate utilization was done by streaking onto plates of ACY medium with and without acetate. Conspicuously better growth on acetate-containing ACY medium was a presumptive indicator of acetate utilization. Isolated strains of the novel acetate-oxidizing, microaerophilic member of the ß-Proteobacteria described here (S. acetivorans gen. nov., sp. nov.) were assigned designations with the prefix "TAM."
DNA extraction and PCR-related procedures.
For rapid phylogenetic identification of isolates, a portion of colony material was removed with a sterile inoculating loop, suspended in 500 µl of sterile BSS, and centrifuged for 10 min at 4,000 x g. The supernatant liquid was removed, and total DNA in the cell pellet was extracted and purified by using a Bactozol DNA extraction kit as recommended by the manufacturer (Molecular Research Center, Cincinnati, OH). The precipitated DNA was dissolved in 250 to 500 µl of sterile water (pH 7.5), occasionally aided by incubation at 60°C for 1 to 12 h.
For each isolate, the 16S rRNA gene was amplified by PCR using the general primers 8f (5'-AGA GTT TGA TCC TGG CTC AG-3') and 1492r (5'-GGT TAC CTT GTT ACG ACT T-3'), which target regions of the gene common to most Bacteria (54). Each 25-µl reaction mixture contained 25 to 100 ng DNA template, 1x reaction buffer (Invitrogen, Carlsbad, CA), 1.5 mM MgCl2, 0.25 mM of each deoxynucleoside triphosphate, 0.2 µM of each primer, and 0.625 U Taq polymerase (Invitrogen). The PCR mixtures were subject to (i) 3 min at 95°C, (ii) 30 cycles of 45 s at 95°C, 45 s at 56°C, and 45 s at 72°C, and (iii) 5 min at 72°C. A 5-µl sample of each PCR mixture was analyzed by electrophoresis on 1.0% agarose gels prepared in 0.5x Tris-borate-EDTA with 10 µg/ml ethidium bromide (39). PCR products were visualized by UV transillumination, and images were captured by using a Kodak 290 electrophoresis documentation and analysis system (Eastman Kodak).
The total number of S. acetivorans, Acidobacteria, or Verrucomicrobia cells in R. flavipes and their primary anatomical location were estimated by a dilution-to-extinction PCR approach. DNA was extracted from 50 to 100 freshly collected intact termites, termite hindguts (from which the midgut had been detached at the midgut-hindgut junction with a sterile scalpel), and degutted termite bodies by using a MoBio Ultraclean soil DNA extraction kit (MoBio Laboratories, Carlsbad, CA) after homogenization in a Mini-BeadBeater-8 (BioSpec Products, Inc., Bartlesville, OK) operating at full speed for 45 s according to the DNA isolation protocol. Purified DNA was normalized on a per-termite-equivalent basis and was serially diluted in buffer (10 mM Tris-HCl [pH 8.0] containing 50 ng/µl calf thymus DNA as a carrier). As a control, 100 ng purified DNA from S. acetivorans TAM-DN1 or Verrucomicrobia strain TAV-1 (49) was also serially diluted in buffer. Each dilution was used as the template in a PCR with forward primer TAM203f (5'-GCT TCG CAA GGA CCT CAC-3'; targeting the 16S rRNA gene of S. acetivorans strains [see below]), Ver53f, or Acd31f combined with reverse primer 1492r (see above). The PCR mixture was identical to that described above, and a total of 30 PCR cycles was used. Five-microliter samples of each PCR mixture were analyzed by electrophoresis on a 1.0% agarose-0.5x Tris-borate-EDTA gel stained with 1x Gelstar nucleic acid stain (Cambrex, East Rutherford, NJ). Fluorescent bands of PCR products were visualized, captured, and analyzed as described above. An estimate of the in situ abundance of the organisms was then made by comparing the extinction point (i.e., the smallest amount of template DNA yielding a visible amplimer) of purified TAM-DN1 or TAV-1 DNA to that of homologous target DNA in serially diluted termite samples, as well as the determined genome sizes and 16S rRNA gene copy numbers of S. acetivorans (3.2 Mb and four copies, respectively [see below]) and Verrucomicrobia strain TAV-1 (4.0 Mb and one copy, respectively [see below]) and a presumed 3.0-Mb genome and one 16S rRNA gene copy for Acidobacteria (18).
To evaluate the autochthony (i.e., indigenousness) of S. acetivorans for R. flavipes, termites were freshly collected from a forested area in Dansville, MI, along with termite "nest soil" (i.e., soil at the interface of a fallen log on which termites were feeding and through which they were actively tunneling) and separate "nonnest soil" that showed no evidence of termite activity. Soil samples were collected with sterile spatulas and placed in sterile Whirl-Pak bags (Nasco, Fort Atkinson, WI) kept on ice, and DNA was extracted from termite guts (100 guts) and soil samples (1 g) within hours of collection by using the MoBio Ultraclean soil DNA extraction kit as described above. The purified DNA was used in PCRs performed as described above with the S. acetivorans-targeting 16S rRNA gene forward primer TAM203f and general reverse primer 1492r. PCR-amplified DNA was cloned into Escherichia coli TOP10 using the plasmid vector pCR2.1 (TA clone kit; Invitrogen). The partial sequences of randomly selected clones were determined using the TAM203f primer. Only sequences longer than 500 bp were used for subsequent analyses. Sequences were imported into the ARB software package (30) and aligned, and phylogenetic trees were constructed (see below) using 503 shared nucleotide positions. The statistical program LIBSHUFF was used to determine relatedness of the clones, and a nonparametric estimate of library similarity was obtained using the method of Yue and Clayton as implemented by SONS (40, 41).
Sequencing and phylogenetic analysis.
Before amplimers were sequenced, unreacted deoxynucleoside triphosphates and PCR primers were digested and dephosphorylated using ExoSap-IT by following the supplier's instructions (USB, Cleveland, OH).
Partial 16S rRNA gene sequences for each isolate were determined with Applied Biosystems cycle sequencing technology (Applied Biosystems, Foster City, CA), using the general bacterial primer 8f. Sequence chromatograms were checked for quality, and the initial identity of each isolate was determined by using the BLAST search tool in GenBank (2) or the Ribosomal Database Project (http://cme.rdp.msu.edu) (16). A total of 29 strains of S. acetivorans were obtained from R. flavipes collected in Dansville and Spring Arbor, MI, Raleigh, NC, Woods Hole, MA, and Janesville, WI, as well as from R. santonensis. Of these 29 strains, a subset of 15 strains representing the apparent phylogenetic breadth of the group was chosen for nearly full-length sequencing of the 16S rRNA gene. Fourfold coverage of each nucleotide position was obtained by using the method described previously (49) but omitting primers F2, R4*, Acd31f, and Ver53f and adding primer 8f. Individual 16S rRNA gene sequence reads for each isolate were manually edited and assembled by using the Contig Assembly Program contained within BioEdit (http://www.mbio.ncsu.edu/BioEdit/bioedit.html).
For phylogenetic analyses, the partial or nearly full-length 16S rRNA gene sequence of each isolate or clone was aligned in ARB (http://www.arb-home.de/) (30). Ambiguities in sequence alignments were corrected manually, where possible, and only unambiguously aligned positions were used for phylogenetic analyses. Maximum likelihood phylogenetic trees were constructed and estimates of internal branch support were obtained in ARB using the TREE-PUZZLE routine (30, 42).
Termite microsatellite DNA analysis.
Eight degutted Reticulitermes worker larvae from each of the six collection sites were placed individually in 550 µl Bead solution (MoBio Ultraclean soil DNA kit; MoBio Labs) in separate Bead tubes and were homogenized in a Mini-BeadBeater-8 operating at full speed for 1 min. Purified DNA was obtained using the MoBio Ultraclean soil DNA kit protocol. The resulting DNA was used in individual, nonmultiplexed PCRs with 5'-Hex-labeled PCR primers 5-10, 6-1, 11-1, 11-2, and 21-1 (52). Each 50-µl reaction mixture contained 10 ng of termite DNA, 1x reaction buffer (Invitrogen, Carlsbad, CA), 1.5 mM MgCl2, 0.25 mM of each deoxynucleoside triphosphate, 0.2 µM of each primer, and 0.625 U Taq polymerase (Invitrogen). The PCR was performed as follows: (i) 3 min at 94°C; (ii) 35 cycles of 30 s at 94°C, 50 s at 60°C, and 1.0 min at 72°C; and (iii) 5 min at 72.0°C. PCR products were precipitated by adding 0.1 volume of 3 M sodium acetate (pH 5.0) and 2 volumes of 100% ethanol. The DNA pellet was washed in 75% ethanol, air dried, and dissolved in 50 µl sterile water (pH 7.0). Two hundred to 300 ng of the purified PCR product(s) was separated by using an ABI Prism 3100 genetic analyzer (Applied Biosystems, Foster City, CA). Peak sizes were determined with the Genotyper software (Applied Biosystems), and alleles at each locus were binned according to fragment size (±1.5 bp to accommodate variability during electrophoretic separation). The number of alleles at each locus was categorized using a Microsoft Excel spreadsheet. For all possible alleles, "1" was used when an allele was present in a given termite and "0" was used when an allele was absent. Based on this table, the Jaccard coefficient (Jc) was calculated for all pairwise comparisons by using EstimateS (15). A distance matrix was created by using Microsoft Excel, where the Jaccard distance was calculated as follows: 1 – Jc. This matrix was uploaded into MEGA (26) for cluster analysis.
Genomic properties.
The genome sizes of S. acetivorans TAM-DN1 and Verrucomicrobia strain TAV-1 were estimated by pulsed-field gel electrophoresis of restriction endonuclease-digested total DNA (genomic DNA kit; QIAGEN Inc., Chatsworth, CA) (8, 22). The 16S rRNA gene copy number was determined by methods described previously (25), using the restriction enzymes Sma2 and Hae2 (New England Biolabs, Ipswich, MA). The G+C content was determined by high-performance liquid chromatography (HPLC) analysis (31), as modified by Graber et al. (22).
Cultivation, nutrition, and physiological studies.
Routine cultivation of TAM strains was in BYA medium consisting of BSS (see above), 0.05% (wt/vol) Bacto yeast extract, and 10 mM sodium acetate. Isolates were typically grown in 50-ml sterile Erlenmeyer flasks containing 15 ml BYA medium and were incubated at 22 to 23°C with shaking (250 rpm) in the CO2-enriched hypoxic atmosphere of the vinyl glove box (see above). The pH of uninoculated BYA medium kept in the CO2-enriched hypoxic atmosphere was 6.5.
Substrate utilization by TAM-DN1 was tested by using 18-mm anaerobe tubes (catalog no. 2048-00150; Bellco) with butyl rubber stoppers containing 5 ml of BYA medium in which acetate was replaced by the test substrate at a concentration of 10 mM. The tube headspace (ca. 22 ml) contained 2% O2, 5% CO2, and 93% N2. Test cultures were inoculated (1%, vol/vol) with an exponential-phase culture growing in BYA medium and then were incubated at 22 to 23°C with the tubes held horizontally in a reciprocal shaker operating at 150 rpm. Cell yields were determined by measuring the optical density of cultures at 600 nm with a Milton Roy Spectronic 20 colorimeter and converting the value to cell density by means of an experimentally determined standard curve. An increase of at least 50% in the cell yield above the "no-substrate" control yield after two successive transfers was considered evidence of substrate utilization.
The ability of TAM-DN1 to utilize acetate and succinate simultaneously was tested by using 500-ml screw-cap bottles (catalog no. 5636-00533; Bellco) to which an 18-mm anaerobe tube (see above) was fused. The bottles contained 100 ml of BYA medium supplemented with 10 mM succinate and were inoculated (1%, vol/vol) with an exponential-phase culture growing in BYA medium. Incubation was at 22 to 23°C in the CO2-enriched hypoxic chamber (see above) with shaking at 250 rpm. Concurrent with growth measurements (see above), 1-ml samples of culture fluid were removed and centrifuged at 12,000 x g for 10 min, and the supernatant was filtered through a 0.2-µm-pore-size filter and stored at –20°C until analysis. Organic acids were analyzed by HPLC (Waters, Milford, MA) on an Aminex HPX-87H column (300 by 7.8 mm; Bio-Rad, Hercules, CA) at 23°C, with 4 mM H2SO4 as the eluent (0.6 ml/min). Organic acids were detected and quantified with a Waters 2487 UV detector operating at 210 nm and calibrated with homologous standards.
The oxygen tolerance of TAM-DN1 was determined from the ability of cells to grow in liquid medium or on plates under defined headspace concentrations of O2. For growth in liquid, 5 ml of anoxic BYA medium was dispensed into 18-mm anaerobe tubes with butyl rubber stoppers containing a headspace consisting of air (21% [vol/vol] O2) or 100% N2. Into the tubes containing 100% N2, air or pure oxygen was injected to obtain a final headspace concentration of O2 of 0.5, 1, 2, 4, or 8% (after release of overpressure). The tubes were sterilized by autoclaving, inoculated (5%, vol/vol) with exponential-phase TAM-DN1 cells growing in BYA medium, and then incubated horizontally at 22 to 23°C with shaking at 150 rpm. Growth was monitored spectrophotometrically (see above). The duration of the lag phase was estimated as described by Lenski et al. (28). For growth on plates, 1.5% agar was incorporated into liquid BYA medium, which was then dispensed into Wolfe anaerobic agar bottle plates (4 ml/bottle) fitted with screw caps (catalog no. 2535-S0020; Bellco). The bottle plates were autoclaved and then placed on their sides to allow the medium to solidify. The bottle plates were then transferred into an anoxic chamber (10% H2, 5% CO2, 85% N2; PlasLabs, Lansing, MI), uncapped, and streaked with an exponential-phase culture of TAM-DN1. Each bottle plate was then closed with a butyl rubber stopper held in place by a screw cap having a hole as an injection port. Pure, sterile O2 was then injected into the bottle plates (average headspace volume, 60 ml) to obtain final concentrations of O2 of 0.5, 1, 2, 4, 6, 8, 12, 16, and 21% in the headspace (after release of overpressure), after which the bottle plates were incubated in an upright position at 22 to 23°C.
The ability of strain TAM-DN1 to grow under anoxic conditions by fermentation or anaerobic respiration was tested by using 5 ml BYA medium that had been deoxygenated under a vacuum and added to 18-mm anaerobe tubes with butyl rubber stoppers under 100% N2. After autoclaving, the BYA medium was supplemented with 10 mM (final concentration) glucose or one of the following potential electron acceptors from a sterile stock solution: potassium nitrate, potassium nitrite, sodium sulfate, or sodium fumarate. For some of the tubes containing fumarate, 30% hydrogen was included in the headspace. The positive controls were tubes of BYA medium supplemented with 2% O2 by injection of air. The tubes were inoculated (2%, vol/vol) with an exponential-phase culture growing in BYA medium under hypoxia and then incubated at 22 to 23°C horizontally with shaking at 150 rpm.
Enzyme assays.
S. acetivorans TAM-DN1 was grown in 100 ml BYA medium in 500-ml sidearm bottles (see above) under an hypoxic atmosphere with shaking at 250 rpm. At mid-log phase (at which growth was known to be acetate dependent, with ca. 5 x 108 cells/ml), cells from an entire culture were harvested by centrifugation at 10,000 x g for 10 min at 4°C, washed with 20 ml sonication buffer (10 mM EDTA, 50 mM Tris-HCl; pH 7.0), recentrifuged, and then resuspended in 10 ml of the same buffer. Cells were disrupted in an ice water bath by sonication (three 30-s treatments) with a Branson model 450 Sonifier (power setting, 5; 50% duty cycle) equipped with a 0.5-in. threaded-body step horn with a flat tip. The sonicate was centrifuged at 12,000 x g for 60 min at 4°C, and the resulting supernatant liquid, considered to be the crude cell extract, was transferred into a Slide-A-Lyzer dialysis cassette (capacity, 3 to 12 ml; 3,500-molecular-weight cutoff; Pierce, Rockford, IL) and dialyzed for 12 h in 2 liters of dialysis buffer (50 mM Tris-HCl, pH 7.0). The dialyzed crude extract was removed from the cassette and used immediately for assays of enzyme activities.
Catalase activity was assayed as described by Beers and Sizer (6). Superoxide dismutase activity was measured by the xanthine/xanthine oxidase-cytochrome c reduction method (20). NAD(P)H oxidase and peroxidase activities were assayed as described previously (48). The qualitative, colorimetric test used for cytochrome c oxidase has been described previously (46).
Microscopy.
Phase-contrast micrographs were prepared from wet mounts on agar-coated slides (36). Images were captured with a Zeiss Axioskop microscope (Carl Zeiss, Inc., Thornwood, NY) equipped with a SPOT charge-coupled device digital camera (Diagnostic Instruments, Inc., Sterling Heights, MI).
For scanning electron microscopy, late-exponential-phase cells of S. acetivorans TAM-DN1 were harvested and then resuspended in 0.1 M sodium phosphate buffer (pH 7.4) and mixed with an equal amount of 4% glutaraldehyde. After fixation for 30 min, 1 drop of the fixed cells was placed on a poly-L-lysine-coated coverslip. The suspension was allowed to settle for 10 min, and the coverslip was washed with distilled water and placed in graded ethanol series (25, 50, 75, and 95% ethanol and then three changes of 100% ethanol) for not less than 5 min for each stage. Samples were then critical point dried in a Balzers critical point dryer (BAL-TEC AG, Liechtenstein) using liquid carbon dioxide as the transitional fluid. The glass coverslips were mounted on aluminum stubs, and samples were coated with gold (thickness, approximately 20 nm) by using an Emscope model SC 500 sputter coater (Quorum Technologies, East Sussex, United Kingdom). Electron micrographs were obtained with a JEOL 6400V scanning electron microscope with a LaB6 emitter (JOEL-USA, Inc., Peabody, MA).
For transmission electron microscopy, exponential-phase cells were harvested and resuspended in 0.1 M cacodylate buffer (pH 7.4) to which an equal amount of 4% glutaraldehyde was added. Following a 30-min fixation, cells were postfixed in 1% osmium tetroxide in 0.1 M phosphate buffer for 1 h and dehydrated using a graded acetone series (30, 50, 70, 85, and 95% acetone for 15 min each and three 15-min 100% acetone steps). The cells were then embedded in Poly/Bed 812 (Polysciences, Warrington, PA), and 70-nm sections were cut. Sections were stained with uranyl acetate, followed by lead citrate (each at a concentration of 2% in 50% ethanol). Electron micrographs were obtained with a JEOL 2200FS 200-kV field emission transmission electron microscope.
Other procedures.
Protein was quantified by the bicinchoninic acid method (47) with bovine serum albumin as a standard, and the final cell yields, expressed as dry weight, were based on the assumption that protein constitutes 55% of cell dry weight (32).
Accession numbers.
The partial 16S rRNA gene sequences of all isolates and clones obtained in this study have been deposited in the EMBL, GenBank, and DDJB nucleotide sequence databases under accession numbers EF212897 through EF213020. Specific accession numbers are given below. S. acetivorans type strain TAM-DN1 has been deposited in the ATCC and DSMZ culture collections under accession numbers BAA-1483 and DSM 19021, respectively.
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With the exception of the TAM strains, the isolates reported above were typical of organisms isolated from termite guts previously or whose 16S rRNA genes were represented in clone libraries prepared from various termite species, including R. flavipes (1, 5, 19, 23, 24, 37, 38, 43, 44, 51, 56). A 16S rRNA gene clone closely related to that of the TAM isolates was obtained from a gut wall fraction prepared from R. santonensis (56). Otherwise, these organisms have not previously been isolated from termite guts, probably because most previous isolation efforts employed incubations in air or under anoxia.
Recent molecular phylogenetic surveys of termite gut microbes have also revealed the presence of organisms grouping within phyla whose members are not well represented in culture, including the phyla Verrucomicrobia, Acidobacteria, and Planctomyces and the candidate phylum Endomicrobia (24, 34). As such organisms might also be important for O2 consumption in situ, we screened for their presence in earlier isolation attempts with gut homogenates of R. flavipes (from Dansville, MI). By using "plate wash PCR," members of the Verrucomicrobia (strain prefix TAV) and the Acidobacteria (strain prefix TAA) were isolated and described (49) and are included in Fig. 3. Results of dilution-to-extinction PCR analyses (data not shown) indicated that members of the Verrucomicrobia were associated entirely with, and presumably reside in, the gut and were not associated with degutted bodies. By contrast, members of the Acidobacteria were associated with guts and degutted bodies at roughly equal levels, suggesting that they may be transients acquired from soil. In any case, the gut-associated members of the Verrucomicrobia and Acidobacteria in R. flavipes appeared to be minor members of the prokaryotic community, representing only about 0.1 and 0.02% of the direct microscopic counts, respectively. Endomicrobia were not detected on isolation plates.
Autochthony of the TAM strain community.
To determine whether TAM strains were autochthonous members of the R. flavipes community, 16S rRNA gene clone libraries were prepared from termite guts, termite nest soil, and non-termite-associated forest soil by using PCR with TAM strain-targeting primer sets, and the libraries were analyzed by the LIBSHUFF and SONS programs (40, 41). Results revealed that the forward primer TAM203f was not entirely specific for TAM strains; it also supported amplification of 16S rRNA genes from hitherto unknown ß-Proteobacteria present in nest soil and forest soil (Fig. 4). Nevertheless, analyses clearly indicated the presence of a closely related (average 16S rRNA gene identity, 98.4%) TAM strain community in guts that was phylogenetically distinct from 16S rRNA genes amplified from termite nest soil or non-termite-associated forest soil. A Yue-Clayton nonparametric maximum likelihood similarity estimate revealed that clones from the forest and nest soils shared 23% ± 9.7% similarity, clones from forest soil and termite guts shared 7.5% ± 4.5% similarity, and all nest soil and termite gut clones shared 75.8% ± 10.7% similarity (means ± standard errors). Although clones from the termite gut and surrounding nest soil had a relatively high level of similarity, LIBSHUFF revealed they were statistically different (P = 0.001). These results are consistent with the concept that TAM strains in hindguts of R. flavipes (from Dansville, MI) are autochthonous.
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8% [vol/vol] O2), the duration of the lag phase increased linearly with the initial O2 concentration, as did the final cell yield (Fig. 8). This observation indicates that within limits, cells can adapt to deal with elevated concentrations of O2 (or reactive oxygen species generated by metabolism in the presence of elevated concentrations of O2), and the time required for the adaptation is proportional to the O2 concentration to which the cells are initially exposed. Once adapted, however, they apparently are able to consume all of the O2 for energy generation, which is translated into a proportional increase in cell biomass. The biomass yields of TAM-DN1 for initial oxygen concentrations of 2, 4, and 8% were 19.2 ± 1.5, 22.3 ± 4.5, and 20.2 ± 5.2 g per mol oxygen consumed, respectively (means ± standard deviations; n = 3; corrected for the small amount of growth in medium without acetate). These biomass yields are similar to the value reported for other bacteria grown on acetate (21.4 g per mol oxygen consumed) (35).
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Overall, these observations indicate that TAM-DN1 and related strains are obligate microaerophiles and probably reside in the hypoxic region of hindguts, on or near the gut wall. Expression of oxyprotective enzymes, such as catalase and superoxide dismutase, as well as the ability to tolerate and adapt to headspace O2 concentrations up to 16% in liquid media, may be important during trophallactic (termite-to-termite) transfer and colonization of guts of newly hatched larvae and recently molted colony mates, whose microbiota is essentially absent and drastically reduced, respectively, and whose O2 content is almost certainly substantially higher than the O2 content when the termites are fully colonized.
Substrate utilization by, and growth characteristics of TAM-DN1.
The substrates utilized as energy sources by strain TAM-DN1 for growth included acetate, acetyl-acetate, succinate, butyrate, glutamate, glutamine, fumarate, and one or more components present in Casamino Acids (data not shown). Of these, the compounds known to be present in termite hindgut fluid include acetate (in situ concentration, 60 to 80 mM) and butyrate (2 mM) (33), as well as a number of free amino acids, including glutamate (1.7 mM) and glutamine (1.0 mM) (21, 45).
HPLC analysis of substrate utilization by TAM-DN1 revealed that cells were able to utilize acetate and succinate simultaneously when equimolar amounts (10 mM) of these two compounds were present in the culture medium (data not shown), and the final cell yields were twice as high (2.3 x 109 cells/ml) when the strain was grown on both substrates than when it was grown on acetate alone (1.2 x 109 cells/ml). The rate of acetate utilization by TAM-DN1 was 0.09 µmol·min–1·mg protein–1 when succinate was present in the medium and 0.12 µmol·min–1·mg protein–1 without added succinate. These results suggest that in situ, cells do not need to be restricted to the substrate typically present at the highest concentration (acetate) but may simultaneously be able to use other oxidizable substrates available at lower concentrations. This ability may also be important when bacteria are colonizing newly hatched or recently molted colony mates.
The substrates not utilized for growth included cellobiose, maltose, glucose, xylose, arabinose, lactate, pyruvate, citrate, formate, propionate, 2-oxoglutarate, malate, maleic acid, benzoate, threonine, and glycine. Moreover, TAM-DN1 was not able to grow anaerobically on acetate using fumarate (with or without H2 in the headspace), nitrate, nitrite, or sulfate as electron acceptors, nor was TAM-DN1 able to grow fermentatively on glucose.
In BYA liquid medium under 2% O2, TAM-DN1 grew at 22, 30, and 37°C, but the shortest generation time (3.4 h) was observed at 30°C. No growth occurred at 42°C.
CO2 was not required for growth, but the onset of growth in BYA medium was generally more rapid under a CO2-enriched hypoxic atmosphere (i.e., 2% O2, 5% CO2, 93% N2), such as that provided within the flexible vinyl glove box. However, the effect of CO2 on the growth rate and final cell yield has not been tested yet. Stimulation by CO2 may reflect a biosynthetic need for CO2 fixation, which would be more obvious at low cell densities before the CO2-producing activity per ml of culture is sufficient to satisfy the demand.
Proposal for a new taxon, Stenoxybacter acetivorans gen. nov., sp. nov.
The molecular and physiological properties of TAM-DN1 and related strains are sufficiently distinct from those of any other known bacterium to warrant their classification as a new genus and species within the phylum ß-Proteobacteria. The relatively distant (16S rRNA gene identity, 94.1%) evolutionary relationship to their closest named relative, E. corrodens, coupled with their obligately microaerophilic phenotype, relatively narrow substrate utilization spectrum, and apparent autochthony in guts of Reticulitermes species are fully consistent with this notion. Accordingly, we propose the name Stenoxybacter acetivorans for these bacteria (see below). In a companion paper (55), we report on experiments to test the hypotheses that S. acetivorans cells reside in the peripheral, hypoxic region of hindguts of R. flavipes and use acetate to fuel their O2-consuming respiratory activity in situ.
Description of Stenoxybacter gen. nov.
Stenoxybacter gen. nov. (Sten.o.xy.bac'ter. Gr. adj. stenos, narrow; Gr. adj. oxys, acid or sour and in combined words indicating oxygen [N.L. oxygenium]; N.L. masc. n. bacter, rod or bacterium; N.L. masc. n. Stenoxybacter, rod with a narrow oxygen range). The genus description is, at present, the same as that for the type species, Stenoxybacter acetivorans.
Description of Stenoxybacter acetivorans sp. nov.
Stenoxybacter acetivorans sp. nov. (a.ce.ti.vo'rans. L. neut. n. acetum, vinegar or acetic acid; L. pres. part. vorans, devouring; N.L. pres. part. acetivorans, acetate consuming). Cells are rods (0.5 by 5 µm) with a gram-negative type of cell wall morphology that includes an outer membrane. Nonmotile. Strict aerobe; obligate microaerophile. Growth occurs on solid media in atmospheres containing 0.5 to 4.0% (vol/vol) oxygen (optimum oxygen concentration, 1 to 2%). No growth under 
6% oxygen or under anoxia, either by fermentation or by anaerobic respiration with fumarate, nitrate, nitrite, or sulfate as the electron acceptor. On solid BYA medium, colonies are 4 to 5 mm diameter, have a crenate, low, convex morphology, and have a "ringed" appearance, with a cream-colored center surrounded by a ring of light orange, followed by a light blue edge. In liquid BYA medium, cells can adapt to headspace concentrations of oxygen up to 16%, but there are prolonged lag phases whose durations are proportional to the initial oxygen concentration. Cells possess cytochrome c oxidase (qualitative test), catalase, and superoxide dismutase enzyme activities. Growth occurs in liquid media at temperatures between 22 and 37°C (optimum temperature, 30°C); no growth occurs at 42°C. Growth onset is stimulated by inclusion of 5% CO2 in the incubation atmosphere. Substrates utilized as energy sources include acetate, acetyl-acetate, succinate, butyrate, glutamate, glutamine, fumarate, and one or more components present in Casamino Acids. Cellobiose, maltose, glucose, xylose, arabinose, lactate, pyruvate, citrate, formate, propionate, 2-oxoglutarate, malate, maleic acid, benzoate, threonine, and glycine are not utilized. The size of the genome of strain TAM-DN1 is 3.3 Mb; the genome has a G+C content of 53.7 ± 0.3 mol% and possesses four 16S rRNA gene copies. The nucleotide sequence of the 16S rRNA gene of strain TAM-DN1 has been deposited in the GenBank database under accession number EF212897.
The type strain, isolated from guts of R. flavipes collected in Dansville, MI, is TAM-DN1; it has been deposited in the American Type Culture Collection, Manassas, VA, as strain BAA-1483 and in the Deutsche Sammlung von Mikroorganismen und Zellkulturen, Braunschweig, Germany, as strain DSM 19021. Similar strains have also been isolated from R. flavipes collected in Spring Arbor, MI, Janesville, WI, and Raleigh, NC, as well as from R. santonensis collected in Forêt de la Coubre, France.
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ACKNOWLEDGMENTS |
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This research was supported by grants from the National Science Foundation (grant IBN-0114505) and Michigan State University Agricultural Experiment Station to J.A.B. and by an MSU College of Natural Science Recruiting Fellowship to J.T.W.
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FOOTNOTES |
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Published ahead of print on 7 September 2007.
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