Characterization of a Bacteroides Mobilizable Transposon, NBU2

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also integrated in Escherichia coli, but integration was much less site specific than in B. ... whether they carry resistance genes. ... and infections caused by them are becoming more difficult to ... in Luria broth (LB) or plated on Luria agar (LA) plates. .... Nal, nalidixic acid; Rif, rifampin; Sm, streptomycin; Tp, trimethoprim. Other.

JOURNAL OF BACTERIOLOGY, June 2000, p. 3559–3571 0021-9193/00/$04.00⫹0 Copyright © 2000, American Society for Microbiology. All Rights Reserved.

Vol. 182, No. 12

Characterization of a Bacteroides Mobilizable Transposon, NBU2, Which Carries a Functional Lincomycin Resistance Gene JUN WANG, NADJA B. SHOEMAKER, GUI-RONG WANG,

AND

ABIGAIL A. SALYERS*

Department of Microbiology, University of Illinois, Urbana, Illinois 61801 Received 20 October 1999/Accepted 24 March 2000

The mobilizable Bacteroides element NBU2 (11 kbp) was found originally in two Bacteroides clinical isolates, Bacteroides fragilis ERL and B. thetaiotaomicron DOT. At first, NBU2 appeared to be very similar to another mobilizable Bacteroides element, NBU1, in a 2.5-kbp internal region, but further examination of the full DNA sequence of NBU2 now reveals that the region of near identity between NBU1 and NBU2 is limited to this small region and that, outside this region, there is little sequence similarity between the two elements. The integrase gene of NBU2, intN2, was located at one end of the element. This gene was necessary and sufficient for the integration of NBU2. The integrase of NBU2 has the conserved amino acids (R-H-R-Y) in the C-terminal end that are found in members of the lambda family of site-specific integrases. This was also the only region in which the NBU1 and NBU2 integrases shared any similarity (28% amino acid sequence identity and 49% sequence similarity). Integration of NBU2 was site specific in Bacteroides species. Integration occurred in two primary sites in B. thetaiotaomicron. Both of these sites were located in the 3ⴕ end of a serine-tRNA gene NBU2 also integrated in Escherichia coli, but integration was much less site specific than in B. thetaiotaomicron. Analysis of the sequence of NBU2 revealed two potential antibiotic resistance genes. The amino acid sequences of the putative proteins encoded by these genes had similarity to resistances found in gram-positive bacteria. Only one of these genes was expressed in B. thetaiotaomicron, the homolog of linA, a lincomycin resistance gene from Staphylococcus aureus. To determine how widespread elements related to NBU1 and NBU2 are in Bacteroides species, we screened 291 Bacteroides strains. Elements with some sequence similarity to NBU2 and NBU1 were widespread in Bacteroides strains, and the presence of linAN in Bacteroides strains was highly correlated with the presence of NBU2, suggesting that NBU2 has been responsible for the spread of this gene among Bacteroides strains. Our results suggest that the NBU-related elements form a large and heterogeneous family, whose members have similar integration mechanisms but have different target sites and differ in whether they carry resistance genes. Bacteroides spp. are gram-negative obligate anaerobes that comprise 20 to 30% of the normal microbiota of the human colon. Some Bacteroides species are opportunistic pathogens, and infections caused by them are becoming more difficult to treat successfully due to increasing antibiotic resistance in this genus. Bacteroides spp. have been shown to carry a plethora of self-transmissible and mobilizable elements, which are probably responsible for the spread of antibiotic resistance genes. Antibiotic resistance genes have been found on conjugative and mobilizable plasmids (21, 34, 43), conjugative transposons (CTns) and integrated elements that are mobilized by CTns (33, 35, 37). In particular, a family of CTns, exemplified by CTnDOT and CTnERL, appears to be playing an important role in transferring resistance genes among Bacteroides strains. CTns of this family not only transfer themselves but also mobilize coresident plasmids. In addition, proteins encoded on these CTns trigger in trans the excision and circularization of mobilizable integrated elements called NBUs, and they mobilize these circular forms to Bacteroides or Escherichia coli recipients (35, 49, 57). They may also mobilize other integrated elements that have been given transposon designations, such as Tn4399 (14), Tn4555 (51), and Tn5520 (60). To distinguish mobilizable elements that have been given a transposon designation from nonmobilizable Bacteroides transposons such as

Tn4351 or Tn4551, we will designate them as MTns, e.g., MTn5520. So far, the MTns of Bacteroides species seem to be falling into two distinct groups. MTn5520 (60), the smallest of the MTns (5 kbp) and the only other MTn besides NBU1 (48) to be sequenced completely, integrates almost randomly and does not duplicate the target site. By contrast, the NBU1 integration was highly site specific, at least in Bacteroides spp., and the target site was duplicated when NBU1 was inserted. We had noted that the integrase of NBU1, IntN1, was very different at the amino acid sequence level from the integrase of MTn5520, although both were distantly related to the phage lambda integrase (46, 60). Since NBU2 seems to have the same general integration features of NBU1, we wanted to identify the integrase of NBU2 and determine whether it was more closely related to that of NBU1 than to that of MTn5520. Previously, we obtained the entire sequence of NBU1 (10.3 kbp) and identified its integrase gene (46). Subsequently, we have identified three other genes that appear to be essential for NBU1 excision (48). In earlier surveys of Bacteroides clinical isolates for NBU1-like elements, we had identified a second NBU-type element that appeared at first to be very closely related to NBU1. A 2.5-kbp region of NBU2 that contained the transfer origin (oriT) and mobilization gene (mobN2) was sequenced and found to be ⬎85% identical to a similarly sized segment from NBU1 (19, 20, 44). However, results of further hybridization experiments suggested that outside this region, NBU2 might be quite different from NBU1. We report here the complete DNA sequence of NBU2 and the characteristics of its integrase gene. NBU1 carried no antibiotic resistance

* Corresponding author. Mailing address: Department of Microbiology, B103 CLSL, 601 S. Goodwin, Urbana, IL 61801. Phone: (217) 333-7378. Fax: (217) 244–8485. E-mail: [email protected] 3559

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J. BACTERIOL. TABLE 1. Strains and plasmids

Bacterial strain or plasmid

Relevant phenotypea

Description and/or source

Bacterial strains E. coli DH5␣MCR EM24NR BW19851

RecA RecA Nalr Rifr, Pir⫺ RecA, ⍀RP4 tra, uidA::pir⫹

Gibco-BRL RecA derivative of LE392 (39), used as recipient for integrative Pir requiring vectors R6K pir integrated into the uidA of S17-1 (50); host strain for R6K replicons (23)

B. thetaiotaomicron BT5482 BT4001 BT4004 BT4004N3 BT4004N6

Rifr Rifr Tcr Rifr Tcr Lnr Rifr Tcr Lnr

Spontaneous rifampin resistant isolate of BT5482 BT4001 containing the conjugative transposon, CTnERL BT4004 with single copy of NBU2 in site 2 BT4004 containing two copies of NBU2, one in site 1 and one in site 2

Plasmids pUC19 pGEM-T pBR328::NBU2

Apr Apr Cmr Tcr

E. coli cloning vector (62) Promega PCR product cloning vector Circular intermediate of NBU2 digested with PstI and cloned into the PstI site of the ColE1 replicon vector pBR328 (11), this study 1.2-kbp HincII of NBU2 containing the joined ends cloned into the HincII site of pUC19, this study A 5-kbp HindIII fragment containing the left junction of NBU2 in one of the chromosomal targets (site 1) in BT4004N6 cloned into the HindIII site of pUC19, this study Cloning vector that requires pir product in trans for replication; contains the RP4 oriT for mobilization (24) 1.8-kbp ermG PCR product from CTn7853 (10) cloned into the NsiI site of pEP185.2 to create a suicide vector that is selectable in both Bacteroides and E. coli hosts, this study 1.8-kbp PCR product from NBU2 circular form containing the attN2 and intN2 region cloned into ApaI/SstII site of pEPE (Fig. 1); integrates into the chromosomes of Bacteroides and E. coli hosts, this study 0.9-kbp internal deletion of intN2 in pEPIntN2 cloned into pEPE, this study EcoRV clone of both NBU2-chromosomal junctions from pEPIntN2 insertions in BT4001 chromosome in sites 1 (J1) and 2 (J2), this study Bacteroides-E. coli shuttle vector (38) 3.5-kbp HindIII fragment of NBU2 containing mefEN2-linAN2 cloned into pNLY1, this study

pUC19::attN2

Apr

pUC19::LJ1

Apr

pEP185.2

Cmr, R6KoriV

pEPE

Cmr R6KoriV (Emr)

pEPIntN2

Cmr R6KoriV Int⫹ (Emr Int⫹)

pEPIntN2D pEPE::N2-J1 and pEPE::N2-J2 pNLY1 pNLY-ML

Cmr, R6KoriV, Int- (Emr Int⫺) Cmr (Emr) Apr Cmr (Cmr) Apr Cmr (Cmr Lnr)

a The phenotypes in parentheses are expressed Bacteroides hosts, and the phenotypes outside the parentheses are expressed E. coli. Abbreviations used for antibiotics resistances: Ap, ampicillin; Cm, chloramphenicol; Em, erythromycin; Ln, lincomycin; Nal, nalidixic acid; Rif, rifampin; Sm, streptomycin; Tp, trimethoprim. Other phenotype abbreviations: int⫹ or int⫺ for the ability to integrate and R6KoriV for the pir-dependent replication origin of R6K.

genes, but an MTn that seems to be related to NBU1, MTn4555, carries a cefoxitin resistance gene (28). Accordingly, we were interested in determining whether NBU2 carried any resistance genes. Finally, we wanted to learn more about the distribution of NBU-type elements in Bacteroides strains. Virtually all work to date on CTns and MTns of Bacteroides species has focused on a small number of strains, most of which are clinical isolates. We have a collection of Bacteroides strains that includes a variety of clinical and community isolates, including strains of Bacteroides isolated before 1970, as well as strains isolated in recent years. We were interested in determining not only how prevalent NBUs are today but also whether carriage of these elements has changed with time. Information obtained by comparing NBU2 with NBU1 allowed us for the first time to design probes that would distinguish NBU1 from NBU2 and thus allow us to determine how widely each was distributed in Bacteroides strains. MATERIALS AND METHODS Bacterial strains and growth conditions. The bacterial strains and plasmids used in this study are shown in Table 1. The E. coli strains were grown aerobically in Luria broth (LB) or plated on Luria agar (LA) plates. The Bacteroides strains labeled BT (e.g., BT4001 and BT4004) are derivatives of the B. thetaiotaomicron 5482 strain (Virginia Polytechnical Institute [VPI] Anaerobe Laboratory, Blacksburg, Va.). The source and time period of isolation of the Bacteroides strains used in the survey are described, along with the results of the NBU survey (see Table 4). The Bacteroides strains are grown anaerobically in prereduced Trypticase-

yeast extract-glucose (TYG [15]) or on TYG agar plates incubated in BBL GasPak jars. Preparation of plasmid and total cellular DNA. Plasmid preparations from either Bacteroides or E. coli strains were done using the alkaline lysis procedure (39). Total DNA was prepared by a modification of the method of Saito and Miura (32). A quick method for preparing total DNA from 2 ml of an overnight culture was used routinely. The cells were pelleted in a microfuge tube, washed one time in 0.5 ml of saline-EDTA (0.5 M NaCl, 0.1 M EDTA; pH 8). The cells were resuspended in 0.5 ml of saline-EDTA and frozen in a ⫺80°C freezer until solid. Then, 0.5 ml of Tris-SDS (0.1 M Tris, 1% sodium dodecyl sulfate [SDS]; pH 9.0 to 9.3) was added to the frozen cells. The tubes were agitated constantly until the cells thawed and lysed completely. The lysate was mixed with 0.5 ml of phenol saturated with saline-EDTA, mixed well, and placed on ice for 20 min with occasional mixing. The mixture was centrifuged at 12,000 rpm in a microfuge for 10 min. The supernatant was removed and put into a fresh tube. Then, 0.8 ml of isopropanol was added, the tubes were inverted several times for complete mixing, and the DNA was allowed to precipitate at room temperature for at least 30 min. The tubes were centrifuged for 10 min at 12,000 rpm. The pellets were rinsed with 70% ethanol and then dried. The DNA was resuspended in 0.2 to 0.4 ml of TE (0.01M Tris, 0.001 M EDTA; pH 8) containing 50 ␮g of RNase per ml. Cloning and sequencing of NBU2. NBU2 was induced to excise from the chromosome of B. thetaiotaomicron BT4104N3-1 by growing the strain in medium containing tetracycline. Exposure to tetracycline induces the regulatory functions on the conjugative transposon required to induce the excision of NBU2 (55). The circular intermediate of NBU2 was isolated by using a plasmid preparation procedure described previously (44) and then digested with PstI and cloned into the PstI site of pBR328 (11). This clone was stable enough to allow subcloning for sequencing and for other analysis (Table 1). Various regions were subcloned into pUC19 (62) and sequenced using the M13 universal and reverse primers. Primer walking and sequencing of PCR products across restriction sites was done to get the total sequence of both strands. The sequencing was performed by the University of Illinois Biotechnology Facility using the Applied Biosystems model 373A version 2.0 dye terminator sequencing system.

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TABLE 2. Primers used for PCR amplification Primer, sequencea (5⬘ to 3⬘)

Purpose (size [bp])

Joined ends of NBU2 (455) or to amplify the cloned chromosomal DNA between the ends (2,122–2,574)

RN2end, CTT TCA GGA CGA TGT AAA GTC CTG LN2end, GTA CGT CTC CTA CGA TTG GCA CAC

Target site 1 in BT4001 (466)

TRN2, TCC AAG AGC AAC AAG TCA AGA TGC TLN2, TTA GAG CGC ACA AAG TTA CAA TCA

intN2-attN2 (1,882); minimal integrative region and probe (7,420–8,391)

IntFN2, TGT AAT TGC CTA TCT TCC AGT GAT G IntRN2, AAC AAA TAC TTT CAG GAC GAT GTA A

ermG; erythromycin-clindamycin resistance marker for Bacteroides spp.

ErmGF, GAA CAC CTG CAG1 AAA AGT CGG GGA TTG GTG AAC ErmGR, GAC AGA CTG CAG1 ACA CCT TGT TAT TGG ACG CCT AC

prmN1 (974); NBU1 sequence (7,420–8,391).

PrmN2F, CGC AAG ACC ATG G2CA ATA GAA GAA PrmN2R, AGT GGG AGA TCT3 CCG AAA GCC GTT TTT

a

The underlined sequences are restriction sites inserted in the primers: 1, PstI; 2, NcoI; 3, BglII.

The resulting nucleotide sequences and the derived amino acid sequences of the potential open reading frames (ORFs) were used to search a variety of data bases for possible identification using Gapped BLAST and Psi-BLAST programs (1). Southern blot and dot blot analysis. Southern blot analysis of restriction enzyme-digested DNA was performed as outlined in Sambrook et al. (39). The probes were made from isolated DNA fragments or purified PCR products labeled with fluorescein-dUTP using random primers according to the protocol in the Renaissance kit from NEN Life Sciences. The Southern blots were incubated with a chemiluminescence substrate for exposure to film as directed by the manufacturer. Dot blot analyses of bacterial strains were done by spotting 3 ␮l of a 2-ml (total) DNA preparation onto GeneScreen (NEN-Dupont) in a grid configuration. The spotted membranes were then treated as in colony or plaque hybridizations and were hybridized with NBU1- and NBU2-specific probes using the same protocol used for Southern blots. The NBU probes used for the dot blots were the 4.5-kbp HindIII fragment of NBU1 (C-terminal of IntegraseN1 to the N-terminal of MobN1), the PCR product of the prmN2, oriT⬘-mobN1 (1.6kbp AvaI-PvuII), intN1-attN1 (2.4-kbp PstI-ScaI), intN2-attN2 (1.8-kbp PCR product), and a 1.3-kbp HincII-EcoRV NBU2 fragment containing the C-terminal end of mefEN2 and the N-terminal end of linAN2. Primers used to produce specific PCR products to make the probes or for cloning are shown in Table 2. Construction of minimal integration vector, pEPIntN2. A mobilizable shuttle vector which could be used to follow the integration of cloned regions of NBU2 in either Bacteroides or E. coli recipients was constructed using the pir-dependent R6KoriV vector, pEP185.2 (Fig. 1) (24). The ermG gene from the conjugative transposon CTn7853 was PCR amplified (10) (Table 2) with PstI sites in the primers and then cloned into the PstI-compatible unique NsiI site of pEP185.2 to produce pEPE (Fig. 1). The sequences of the ends of the integrated form of NBU2 were used to design primers for PCR amplification of the joined ends of NBU2 (attN2) plus the adjacent ORF, intN2. The 1.8-kbp fragment was first cloned into the pGEM-T (Promega) PCR product cloning vector to form pGEM::IntN2 and was sequenced. The attN2-intN2 or IntN2 region was then isolated on a 1.8-kbp ApaI-SstII fragment and cloned into the corresponding sites on pEPE to form pEPIntN2 (Fig. 1). This vector can be mobilized out of the Pir⫹ S17-1 derivative, BW19851 (23), either to Bacteroides or to E. coli recipients, by filter matings to select for possible integration due to the NBU2 IntN2 region. Filter matings. The procedure for filter matings between E. coli donors and E. coli or Bacteroides recipients has been previously described (42, 59). BW19851 (pEPIntN2) was filter mated with BT4001. BT4001 transconjugants containing insertions of pEPIntN2 in the chromosome were selected as gentamicin-resistant (Genr, 200 ␮g/ml) and erythromycin-resistant (Emr, 10 ␮g/ml) isolates. Integration into the chromosome via the NBU2 ends was verified by Southern blot analysis using the 1.8-kbp ApaI-SstII fragment of NBU2 cloned in pEPIntN2 (Fig. 1) as the probe. In matings between BW19851(pEPIntN2) and the E. coli recipient EM24NR, the transconjugants were isolated as rifampin-resistant (Rifr, 10 ␮g/ml), chloramphenicol-resistant (Cmr, 20 ␮g/ml), trimethoprim-sensitive (Tps) isolates. Integration was verified by Southern blot analysis using the 1.8kbp ApaI-SstII NBU2 attN2-intN2 fragment as the probe. Cloning and sequencing of NBU2 target sites in Bacteroides and E. coli hosts. A left junction of NBU2 was obtained from BT4004N6 (Table 1) on a 5.0-kbp HindIII fragment, which was cloned into the HindIII site of pUC19 to produce pUC19::LJ1, and was then sequenced. The sequence identified the crossover region on NBU2 attN2. In the process of cloning the ends of NBU2, we learned that BT4004N6 had two copies of ⍀NBU2. Both junctions of both integration sites were cloned simultaneously from the BT4001⍀pEPIntN2 transconjugants, all of which contained only single insertions. First, the DNA from a BT4001⍀pEPIntN2 transconjugant was digested with EcoRV, which does not cut within the integrated pEPIntN2 vector. The digested DNA was cleaned, diluted, and ligated. The ligation reaction was then used to transform competent

BW19851 cells selecting for Cmr. The Cmr transformants obtained from the two observed insertion sites on the Southern blots contained the chromosomal sequences adjacent to both ends of the integrated NBU2 derivative cloned on pEPIntN2-J1 (site 1) or pEPIntN2-J2 (site 2). The R6KoriV-based vector has a copy number too low for good template preparation for sequencing. Therefore, the cloned chromosomal DNA between the NBU2 ends on the resultant J-clones were amplified by PCR using the NBU2 end primers (Table 2). The PCR products were cloned into the high-copy-number pGEM-T and sequenced using the M13 forward and reverse primers. The sequences obtained for the chromosomal junctions allowed primers to be designed (Table 2) to PCR amplify and sequence the Bacteroides target sites. A similar strategy was used to obtain target sites in E. coli. DNA amplification and cloning. The primers used for the DNA amplifications are shown in Table 2. A 2 ␮l sample of genomic DNA or 10 to 100 ng of plasmid DNA was mixed with 200 ng of each primer in 100 ␮l of reaction buffer (1⫻ Gibco-BRL PCR buffer, 1.5 mM MgCl2, 0.2 mM deoxyribonucleoside triphosphate mixture) and amplified with Taq polymerase. Amplification was preceded by denaturation for 5 min at 95°C, followed by the addition of polymerase and 25 cycles of 95°C for 1 min, annealing at 50 to 55°C for 1 min, and extension at 72°C for 2 min. Then, 5 ␮l of the PCR product was checked on agarose gels for production, size, and concentration. The PCR products were gel purified and sequenced directly using the PCR primers, used to prepare probes for the dot blot hybridization survey, or cloned on the PCR cloning vector pGEM-T as specified by the manufacturer (Promega). Expression of the mefEN2 and linAN2. The BT4004, BT4004N3, BT4004N6, and BT4004(pNLY-ML) strains (Table 1) were tested for their ability to grow in TYG broth containing erythromycin or lincomycin. Fresh overnight cultures of each strain were inoculated in triplicate into media containing 0, 3, 5, 10, 20, 30, or 40 ␮g of the respective antibiotic per ml. The cultures were incubated at 37°C, and growth was checked after 24 and 48 h. Nucleotide sequence accession numbers. The GenBank accession number (L42370) for the prmN2-oriT-mobN2 region has been previously reported (20). The nucleotide sequences for the entire NBU2 and the Bacteroides targets, BT2-1 and BT2-2, containing the Ser-tRNAUGA genes have been deposited in GenBank under accession numbers AF251288.

RESULTS Sequence analysis of NBU2. The 2.5-kbp mobilization region of NBU2, which has high sequence identity to NBU1, had been previously sequenced and characterized by Li et al. (20). This region had been cloned from the excised circular form of NBU2 using an NBU1-derived hybridization probe to detect it. To determine the sequence of the rest of NBU2, we first cloned the entire circular intermediate from plasmid preparations of a tetracycline-induced B. thetaiotaomicron strain that contained both the conjugative transposon CTnERL and NBU2. Sequence analysis of NBU2 revealed that the element was 11,123 bp in size, slightly larger than NBU1 (10,276 bp [48]). The sizes of the predicted ORFs and the sizes of the proteins they could encode are shown in Table 3. In Fig. 2A the location of the ORFs are shown on the circular intermediate form of NBU2. Genes on the integrated form of NBU2 are compared to genes on integrated NBU1 in Fig. 2B. Compari-

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FIG. 1. Construction of the integration vector, pEPIntN2. An insertional vector that could be used in either Bacteroides or in E. coli was constructed from the pir-dependent mobilizable pEP185.2 (24). The erythromycin-clindamycin resistance gene, ermG, from CTn7853 was PCR amplified with PstI sites encoded in the primers and cloned into the PstI-compatible unique NsiI site on pEP185.2 to form pEPE. pEPE, a Pir-dependent vector, has selectable markers for both E. coli and Bacteroides hosts. The NBU2 integration region, IntN2, consisting of the joined ends, attN2, from the circular form of NBU2 and the adjacent gene, intN2, was PCR amplified from the induced circular form of NBU2. The PCR product was first cloned into pGEM-T (Promega) and sequenced. The 1.8-kbp ApaI-SstII fragment was isolated from pGEM-T and cloned into the ApaI and SstII sites of pEPE to form the NBU2 integration vector, pEPIntN2.

sons of these genes at the nucleic acid and amino acid sequence level showed clearly that, outside of the prmN-oriTmob region, NBU2 differed appreciably from NBU1. Like NBU1, most of the NBU2 genes were transcribed in the same

direction, but there was little sequence similarity to the other NBU1 genes. Examination of the sequences at the edges of the highly conserved internal prmN-oriT-mob region revealed that the transition from nearly identical sequences to very dissimilar

TABLE 3. NBU2 ORFs and the characteristics of the putative proteinsa Range 5⬘–3⬘ (bp)

% G⫹C

Length (aa)

Size (kDa)

pI

Search results and comments

769–237

40.5

171

19.8

4.5

mefEN2

2,000–804

41.3

403

44.3

9.1

attN2

2,000–2,400

intN2

2,499–3,782

45.8

427

50.4

8.9

orf2 orf3 prmN2

3,846–6,194 6,736–7,815 8,028–8,984

42.9 46.3 48.1

783 360 319

91.3 41.5 36.8

5.4 8.6 9.1

oriTN2 mobN2

880–910 9,137–10,543

44.0

469

55.1

9.3

52% identity and 70–72% similarity to LinA⬘ from S. aureus BM4611 and LinA on pIP855 in S. haemolyticus (5, 6) 33–34% identity and 52–54% similarity to MefE of S. pneumoniae and MefA of S. pyogenes (8, 58) Two target sites: 13-bp identity to attN2 at the 3⬘ end of two Ser-tRNAUGA genes, followed by inverted repeats 26–28% identity and 44–49% similarity to the C-terminal ends of MTn5520 IntBIP and NBU1 IntN1 (46, 60); member of the lambda family of site-specific integrases 26% identity and 45% similarity to an E. coli hypothetical protein 37% identity and 52% similarity to sigma 70 of Rhizobium sp. ⬎85% sequence identity to prmN1 of NBU1 and sequence on MTn4399 (20); 30–33% identity and 52–57% identity to the N-terminal ends of DNA primases from L. monocytogenes and B. subtilis dnaE. Gram-positive family of nick sites also shared by NBU1, MTn4555, pBI143 and pIP421 (53) 88% nucleotide identity to NBU1 mobN1 and 84% nucleotide identity to MTn4555 mobATn; 44, 48, and 55% aa sequence similarity to pIP421 Mob421, pBI143 MobA143, and MTn5520 MobBMP, respectively (20, 52, 60)

ORF

linAN2

a

aa, amino acids.

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FIG. 2. Circular and integrated forms of NBU2. (A) Partial restriction map of the excised circular form of NBU2. The location and orientation of the possible ORFs derived from the NBU2 sequence are indicated. The region containing the joined ends of the NBU2 (attN2) is indicated. The attN2 is contained within a 1.2-kbp HincII fragment. (B) The integrated form of NBU2 is compared to the integrated form of NBU1. The double-headed arrows indicate the region of high sequence identity between NBU2 and NBU1 (see Fig. 3). The attN-left sequences of the integrated NBUs are the same sequence as the attN on the elements, and the attN-right sequences are the attBT sequences of the target sites. Both elements integrate site specifically into the 3⬘ end of tRNA genes: Ser-tRNAUGA for NBU2 and Leu-tRNACAA for NBU1.

sequences was not an abrupt one, as might be expected if these genes are on a gene cassette (Fig. 3). There were some inverted repeat sequences that flanked prmN on one side and mob on the other, but these were outside the region of high identity. The fact that the inverted repeat sequences seen on NBU1 were in approximately the same sites relative to the region of identity as those on NBU2 could mean that they play a role, either in the assembly of the NBUs or in the current function of the intact element. However, there was no indication that the region of identity was a gene cassette in an integron or some other mobile gene cassette. MTn4555 has pairs of inverted repeats flanking its oriT-mobATN region, a region that exhibits sequence identity to the corresponding region of NBU1 and NBU2, and the mobilizable Bacteroides

plasmid, pBI143, has 56-bp inverted repeats that separate its NBU-related mobilization region and its replication region (52, 54). Thus, the inverted repeats may prove to have some significance in the future, but their role is not evident from work done to date. Comparisons of the known Bacteroides mobilizable transposons, including the NBUs, and mobilizable Bacteroides plasmids suggest that these are modular elements with mix-and-match components, but it is not clear how this modular assembly was achieved. Localization of the integration region (attN2) on NBU2. DNA from strains of B. thetaiotaomicron that contained insertions of NBU2 (⍀NBU2) were probed on Southern blots and the ends of the NBU2 were determined to be within the 1.2kbp HincII fragment indicated in Fig. 2 that is also called

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FIG. 3. Sequence comparison of NBU2 and NBU1. The prmN-oriT-mobN regions of NBU1 and NBU2 have more than 85% identity. Outside of this mobilization region the sequence identity drops to ⬍30%. Near the borders of the sequence identities both elements have inverted repeat sequences (underlined) of 11 to 12 bp indicated by arrows above the sequences for NBU1 (IR1) and dotted arrows below the sequences for NBU2 (IR2). The start and stop codons for the prmN (PrmN) and mobN (MobN) are indicated in boldface. The oriT nick sites as determined by sequence identity to MTn4555 (53) are at the end of the TAG codon (⍀ Stop) of the prmN genes and are indicated by the arrows.

attN2. The Southern blots and previous pulse field analysis of B. thetaiotaomicron strains revealed that NBU2 had two primary target sites (3), and some of our isolates contained copies of ⍀NBU2 in both sites (e.g., Fig. 4A). In Fig. 4A, the chromosomal DNAs from BT4004N3 (lane 1), BT4004N6 (lane 2), and BT4004N6 grown in tetracycline to induce the excision of NBU2 (lane 3) were digested with HincII. The Southern blot of the agarose gel was probed with the 1.2-kbp HincII NBU2 fragment (Fig. 2). BT4004N3 has one ⍀NBU2 (two junction

bands) and BT4004N6 had two copies of ⍀NBU2 in two different sites (four junction bands). One of the ⍀NBU2 insertions in BT4004N6 is the same as the ⍀NBU2 in BT4004N3, as is evident from the fact that two junction bands of the same size appear in both lanes 1 and 2. The arrow in lane 3 indicates an additional 1.2-kbp HincII band that runs just above one of the junction bands. This band is formed when tetracycline stimulation of the coresident CTnERL leads to excision of NBU2. No 1.2-kbp band is observed if the cells are not grown

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FIG. 4. Southern blot analysis of the NBU2 insertions in Bacteroides attB2 sites. (A) Southern blot of two B. thetaiotaomicron BT4001 transconjugants from BT ERL that received both CTnERL and NBU2. The DNAs of the two strains were digested with HincII, and Southern blots were probed with the labeled 1.2-kbp HincII fragment containing attN2 (Fig. 2). BT4004N3 in lane 1 has a single insertion (two junction bands), and BT4004N6 in lane 2 has two insertions of NBU2 (four junction bands). In lane 3, BT4004N6 was grown in tetracycline to induce the circular excised form of NBU2. The 1.2-kbp fragment from the excised circular form of NBU2 is indicated by the arrow. (B) Southern blot showing 6 of 10 independent insertions of the minielement vector, pEPIntN2, into the B. thetaiotaomicron BT4001 chromosome. The DNAs from the strains were digested with ApaI-SstII, and the Southern blot was probed with the labeled 1.8-kbp ApaI-SstII fragment containing the intN2-attN2 region of NBU2 cloned on pEPIntN2 (Fig. 1). The sequence obtained for the cloned targets sites (see Materials and Methods) indicated that the insertion site of pEPIntN2 in lanes 1, 2, and 4 were the same as the wild-type element in BT4004N3 (panel A, lane 1). In BT4004N6, one of the ⍀NBU2 copies was integrated into this site and the other copy of ⍀NBU2 was integrated into the site represented by lanes 3, 5, and 6 of panel B. The locations of the HindIII lambda size fragments in kilobase pairs are marked on the left of each panel.

in medium containing tetracycline (lanes 1 and 2). To determine the exact region on NBU2 where the crossovers occurred, a 5-kbp HindIII fragment containing one end of NBU2 in BT4004N6 was cloned and sequenced and compared to the sequence of the 1.2-kbp HincII fragment. The HindIII fragment was later determined to be the left junction of NBU2, as shown in Fig. 2B, and the chromosome from site 1. The single insertion of NBU2 in BT4004N3 (Fig. 4A, lane 1) was later shown to be in site 2. The ORF immediately adjacent to the right end junction of the integrated NBU2 encoded a protein with 28% identity and 44 to 49% similarity to the C-terminal ends of the NBU1 integrase (IntN1) and the integrase of MTn5520 (IntBIP), respectively. All three of the Bacteroides MTn integrases have some sequence similarity to the lambda family of site-specific integrases. This similarity is confined to the C-terminal end of the proteins. C-terminal alignments of IntN2 to some of the closest sequences identified in BLASTP (1) searches are shown in Fig. 5. The three MTn integrases were 40 to 50 amino acids larger than other integrases, including the integrases of bacteriophage P21 and the E14 prophage of E. coli. The MTn integrases all contained the conserved amino acids in lambdoid phage domain I and domain II (2, 27), except that MTn5520 had an alanine (A) instead of arginine (R) in domain I. The highly conserved amino acids in the two domains are boxed, highlighted, and indicated with a number sign (#) in Fig. 5. All of the MTn integrases also had the glycine (G)-histidine (H) doublet in domain II in addition to the H-R-Y conserved amino acids. There are clearly similarities between NBU1 and NBU2 integrases other than those highlighted. In an alignment of the entire MTn integrase proteins with each other (not shown), IntN2 did not align with first 50 amino acids of MTn5520 integrase-transposase or with the first 200 amino acids for IntN1. This indicates that the N-terminal ends encoded the domains responsible for the element specific func-

tions of the integrases. It was somewhat surprising that IntN2 had more sequence similarity in its N-terminal end to IntBIP than to IntN1, since NBU1 and NBU2 integrate site specifically, whereas MTn5520 inserts more randomly in AT-rich sites (3, 46, 60). A simple unrooted tree depicting the relationship of the integrases included in Fig. 5 is shown in Fig. 6. The entire sequences of the integrases were used to form the tree and not just the conserved regions in the C-terminal ends. The three MTn integrases clustered with IntN2 closer to MTn5520 Int than to IntN1. From this, it is evident that there is quite a range of integrase sequences in Bacteroides MTns, including NBUs. Our earlier picture, based on traits of the MTns, which had the elements falling into two groups represented by NBU1 and MTn5520, is clearly too simplistic. The integrase-resolvase-like genes identified by sequence on the cyanobacterial plasmid, pDU1, and the plasmid, ece1, from the marine hyperthermophile Aquiflex aeolicus have not been characterized but were included because they were two of the closer relatives identified in the database searches. The similarity between these genes and proven integrases from NBU1 and NBU2 provides further evidence that these genes might well encode integrases. The integrases of pDU1 and ece1 clustered with the integrase from the site-specific CTn5276 found in the gram-positive L. lactis (30). The bacteriophage integrases from the proteobacter group of gram-negative bacteria formed the third cluster. The Bacteroides MTns are adding new branches to the lambda family of site-specific integrase tree. Note, however, that the branch lengths that separate the integrases of the NBUs and MTn5520 are, if anything, longer than those separating the integrases of the CTn5276 group, which come from three different phylogenetic groups. This observation underscore the extent of the diversity within the NBU-MTn5520 group of integrases found in a single genus of gram-negative bacteria.

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FIG. 5. C-terminal alignment of IntN2 and related members in the lambda family of site-specific integrases. The similarity of IntN2 to members of the lambda family of site-specific integrases was in the C-terminal end. The alignment of IntN2 and the integrases with the highest similarities is shown. Domain I and domain II in the C-terminal ends of this family of integrases contain conserved amino acids for the active sites of the integrases (2, 27). The conserved amino acids are labeled (#) and boxed for these active site domains. The total size of each integrase is shown at the end of its sequence as COOH-, with the number of amino acids in parentheses. The accession numbers for the integrases shown here are as follows: Bacteroides MTns NBU2 (L42370), NBU1 (L13840), and MTn5520 (AF038866) and cyanobacterial plasmid pDU1 (L23221), A. aeolicus plasmid, ece1, (C55205), L. lactis CTn5276 (L27649), bacteriophage P21 (P27077), and prophage E14 (M61865).

Use of a special vector to study integration and the targets sites of NBU2. An insertional shuttle vector, pEPE, was constructed to locate the integration gene of NBU2 and to clone chromosomal target sites (Fig. 1). This vector can be mobilized out of E. coli BW19851 to Bacteroides or E. coli recipients. In E. coli strains that contain the R6K pir gene the vector replicates but in Bacteroides recipients and E. coli recipients such as EM24NR, pEPE cannot replicate and transconjugants are only obtained if the vector contains regions that allow it to integrate (24, 47). Since we suspected that the first ORF at the right end of NBU2 was the integrase gene, we PCR amplified this gene together with the joined ends of the circular form and cloned it into pEPE to form pEPIntN2 (Fig. 1 and 2A). In matings between BW19851(pEPIntN2) and BT4001, erythromycin-resistant transconjugants occurred at a frequency of 10⫺4 to 10⫺5 per recipient at the end of the mating. All of the transconjugants were contained insertions of pEPIntN2 (Fig. 4B). Transfer of a plasmid that replicates in Bacteroides spp. and has the same oriT occurred at a frequency of 10⫺3 to 10⫺4 transconjugants per recipient. Thus, the integration efficiency of pEPIntN2 was close to 10⫺1 integrants per circular form introduced into the cell. This integration frequency is similar to that calculated for NBU1 (24, 46, 47, 49). Southern blot analysis of 10 independent BT4001 ⍀pERIntN2 transconjugants demonstrated that the pEPIntN2 had integrated with equal frequency (6 to 4) into one of two sites. The Southern blot of six of the transconjugants is shown in Fig. 4B. Chromosomal DNA from each of these strains was digested with ApaI-SstII, and the Southern blot was probed with the 1.8-kbp ApaI-SstII NBU2 region, cloned on the pEPE vector. Analysis of the Southern blot pattern showed that all of the insertions occurred within the 1.8-kbp NBU2 region and there were no double insertions. To test whether intN2 was essential for in-

tegration, a 0.9-kbp internal deletion was made in intN2 on pEPIntN2 to produce pEPIntN2D. This plasmid did not integrate into the BT4001 chromosome (⬍10⫺9). Therefore, there were no cryptic elements in BT4001 that were providing the integration function in trans, and IntN2 was required for integration. Integration occurred equally well in a Bacteroides

FIG. 6. Unrooted tree of the NBU2 integrase and related integrases. The entire sequences of the lambda family of site-specific integrases, including the IntN2 of NBU2, that were aligned in Fig. 5 were grouped on a cladogram or unrooted tree to show their relationships using the Bioinformatics analyses conducted on BioNavigator.com provided by eBioinformatics. The tree showed three clusters: the three Bacteroides MTn integrases [NBU1 (IntN1), NBU2 (IntN2) and MTn5520 (IntBIP)], the two bacteriophage integrases from P21 and prophage E14, and the group containing the putative integrase-recombinases on plasmids from Nostoc (pDU1) and A. aeolicus plasmid ece1 (pAquifex) and the integrase from the L. lactis conjugative transposon CTn5276. Accession numbers are given in Fig. 5.

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FIG. 7. NBU2 attN2 and chromosomal target sites. The attN2 region of NBU2, shown at the top of the figure, has two regions that have identity or similarity to its target sites. The crossovers occurred within or adjacent to a 13-bp sequence in highlighted capital letters that has sequence identity to the two attBT2 Bacteroides target sites. The second region of attN2 has a 14-bp sequence, boxed and highlighted, that has partial sequence identity to the attBT2 sites, and is located at the 5⬘ end of a pair of IRs. The IRs are indicated by arrows and the bases which could pair in a stem and loop structure are capitalized. The two attBT2 sites are located at the 3⬘ ends of Ser-tRNAUGA genes that differ from each other by only a single base pair. The crossovers occurred within or adjacent to the 13-bp sequence of identity to attN2. Both attBT2-1 and attBT2-2 also had 15-bp sequences with partial identity, boxed and highlighted, to the 14-bp sequence of attN2 that were located 5⬘ to IRs. The sequence for one of the pEPintN2 insertion sites in E. coli (attBEc) is shown at the bottom. The insertion occurred in the 3⬘ end of fecI. The crossover occurred adjacent to or within the triplet (CCT) at the beginning of a sequence with partial identity (8 of 13) to the 13-bp region on attN2. The crossover region for attBEc was followed by a set of IRs indicated by arrows which had no sequence identity to the NBU2 IR region.

strain not carrying a CTn as it did in one carrying a CTn. Thus, although NBU2 excision and mobilization require trans-acting CTn functions, integration is independent of CTn functions. To determine whether the NBU1 integrase might be able to act on the joined ends of NBU2, we transferred pEPIntN2D, which contained the joined ends but not the integrase of NBU2, into a strain that contained a copy of NBU1. No transconjugants were obtained, indicating that the NBU1 integrase could not replace NBU2 integrase in trans. Junction regions of ⍀pEPIntN2 integrated in both of the two target sites were cloned and sequenced. Analysis of the sequence of the junctions showed that integration had occurred via the ends of NBU2. Using this sequence information, we were also able to PCR amplify and sequence the integration site. The sequences of the two NBU2 integration sites are shown Fig. 7. There was a 13-bp sequence of identity between the attN2 formed by the joined ends of NBU2 and the two BT4001 target sites, attBT2-1 and attBT2-2. The integration event occurred within or adjacent to this 13-bp sequence, duplicating the 13-bp target site. Immediately downstream of the 13-bp region there were inverted repeats that contained a second region of partial identity between attN2 and the two attBT2 sites. In both attBT2 sites the 13-bp sequence was at the 3⬘ end of a Ser-tRNA gene, Ser-tRNAUGA, and Ser-tRNAUGA2. There was only one mismatch between the sequences of the

two Ser-tRNA genes. Yet the regions outside the tRNA gene differed considerably. The ability of NBU2 to integrate into the E. coli chromosome was tested by mating BW19851(pEPIntN2) with the nonpermissive E. coli recipient, EM24NR. EM24NR is RecA deficient and lacks pir which is required for replication of the vector. Transconjugants were isolated at frequencies of 10⫺6 to 10⫺7 per recipient. Since transfer of pEPIntN2 to permissive hosts was 10⫺1 (24, 47), the efficiency of integration was lower (⬍10⫺5) than what was observed in the Bacteroides recipient, BT4001 (10⫺1). The integration of pEPIntN2 in EM24NR was RecA independent, which was expected since the integration of NBU1 was previously shown to be RecA independent in both Bacteroides and E. coli recipients (9). A Southern blot analysis of EM24NR ⍀pEPIntN2 transconjugants showed that the insertions E. coli were not site specific (data not shown). The sequence of a representative target site is shown at the bottom of Fig. 7. The insertion occurred in the 3⬘ end of fecI. There was limited sequence identity to the 13-bp region, and the crossover occurred within or adjacent to the CCT indicated. The E. coli insertion site shown in Fig. 7 had a possible inverted-repeat (IR) set, but there was no sequence identity to the attN2 IR region. Expression of the putative NBU2-encoded antibiotic resistance genes, mefEN2 and linAN2. The sequence of NBU2 re-

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FIG. 8. Alignment of the NBU2 lincosamide resistance, LinAN2, with LinA⬘ and LinA from Staphylococcus spp. The amino acid sequence of the lincosamide resistance on NBU2, LinA(N2), was aligned with the sequences of LinA⬘ from S. aureus and LinA from pIP855 in S. haemolyticus (5, 6) using the BLASTP search program. LinA(N2) has 52% identity and 70 to 72% identity to LinA⬘ and LinA. The regions of identity are indicated in boldface. The total number of amino acids for each protein is indicated at the ends of the respective sequences. The accession numbers for LinA⬘ and LinA are J03947 and A25633, respectively.

vealed two ORFs whose derived amino acid sequences were related to those of known antibiotic resistance genes previously found in the gram-positive bacteria. The deduced amino acid sequence of mefEN2 had 34% identity and 54% similarity to MefE of Streptococcus pneumoniae (58), a protein that is thought to be a macrolide pump. Although the sequence identity was low, it extended throughout the protein. This is the first mefE homolog seen in Bacteroides species. The deduced amino acid sequence of linAN2, LinA(N2), had 50 to 52% identity and 70 to 72% similarity to the LinA⬘ of Staphylococcus aureus (5) and LinA on pIP855 in S. haemolyticus (6). An alignment of the three resistances is shown in Fig. 8. LinA is an O-nucleotidyltransferase which inactives lincosamides including lincomycin and clindamycin (6). Clindamycin resistance is a clinical problem because clindamycin is still a drug of choice for treating anaerobic infections, including those caused by Bacteroides spp. This is also the first sighting of a linA type gene in Bacteroides species. The erythromycin and clindamycin resistances in the Bacteroides spp. have previously been associated exclusively with MLS (ribosome methylation)-type resistances, e.g., ermF and ermG. ermF and ermG have been found on transposons, conjugative and mobilizable plasmids, and conjugative transposons (10, 21, 33, 35). Neither of these genes, however, has yet been seen on a MTn. The possible expression of the putative antibiotic resistance genes carried on NBU2 was tested in the B. thetaiotaomicron 5482, since the original clinical isolates, B. thetaiotaomicron DOT and B. fragilis ERL, both contained CTns that carried the ermF gene. Therefore two B. thetaiotaomicron BT4001 transconjugants from B. fragilis ERL, BT4004N3 (single copy of ⍀NBU2) and BT4004N6 (2 copies ⍀NBU2), were both tested for their ability to grow in TYG containing erythromycin or lincomycin. The MICs for BT4004N3 and BT4004N6 were 40 ␮g/ml, but BT4004N6 grew faster in medium containing higher concentrations of the antibiotic than BT4004N3. Neither strain could grow in medium containing 3 ␮g of erythromycin per ml. Thus, the linAN2 gene is expressed in B. thetaiotaomicron, and the resistance phenotype it confers is the same as the linA of gram-positive bacteria. By contrast, since mefEN2 did not confer resistance to erythromycin, it appears that this gene is not expressed in Bacteroides species.

J. BACTERIOL.

Since the mefEN2 gene appeared to be nonfunctional in single copy, we cloned the 3.7-kbp HindIII fragment of NBU2 that included mefEN2-linAN2 into the shuttle vector pNLY1 to provide 10 to 20 copies of the gene per cell. There was still no growth in erythromycin (3 ␮g/ml). Thus, the mefEN2 appears not to be capable of conferring macrolide resistance on B. thetaiotaomicron even if multiple copies are provided. We also checked for tetracycline resistance in BT4001(pNLY-ML) since there was some similarity between MefEN2 and tetracycline resistance efflux proteins such as TetL (22, 29), but the strain remained susceptible (MIC, ⬍1 ␮g/ml). The percent G⫹C content of mefE in S. pneumoniae is 38% and of linA⬘ in S. aureus is 31%, whereas the genes carried on NBU2 had a G⫹C content of 41%, which is within the normal range of 40 to 45% G⫹C for Bacteroides spp. (16). Thus, the linAN2 and mefEN2 genes on NBU2 probably did not come into the Bacteroides spp. from the low-GC gram-positive bacteria. Our results show that the mefE and linA type genes are not exclusively gram-positive resistances, as was once thought, but have a much wider distribution. NBU2 is only the second MTn found that carries a functional antibiotic resistance gene. MTn4555 carries a cefoxitin resistance gene (cfxA [28]), and there undoubtedly are other uncharacterized MTn elements that are carrying antibiotic resistance genes in the Bacteroides spp. Prevalence of NBU genes in community and clinical Bacteroides isolates. We have seen NBU-like elements in several Bacteroides clinical isolates and were interested in determining how widespread these elements were in Bacteroides species. To this end, we surveyed community and clinical isolates for the presence of NBU-type elements in general and for NBU1 and NBU2, separately. The probe used to detect NBU-type elements was the 4.5-kbp HindIII fragment of NBU1 that contains the highly conserved prmN1-oriT-mobN1 region. The probes used to detect NBU1 and NBU2 specifically were the integrase genes of these two elements. Since earlier data had shown that the highly conserved region might be modular, we also probed the strains separately with prmN1- and mobN1specific probes to learn how often these genes were found together. Finally, we probed the strains with the mefE-linA region of NBU2. We were interested in answering three different questions. First, are NBUs widely distributed in Bacteroides species and, if so, are they as widely distributed in community as well as clinical isolates? Second, has the prevalence of NBUs in Bacteroides species changed over the past few decades? Finally, how prevalent are the mefE-linA homologs in Bacteroides species and are they always associated with NBU-positive strains? Some of the strains were isolated in the 1960s and 1970s by the Anaerobe Laboratory at VPI in Blacksburg, Va. (16), and some strains were isolated in the 1990s, so we were able to look at prevalence data from older and more recently isolated strains. A summary of the results is provided in Table 4. The number of strains in each category is shown in the row with column headings, and the probes used are in the first column (see Materials and Methods). The percentage of the strains that hybridized to the general NBU probe was similar in clinical and community isolates and seems to have nearly doubled in the newer strains compared to the older strains. Both the mobN1- and prmN1-specific probes showed an even greater rise in prevalence. This may have been due to an increase in prevalence of the NBU-type elements, as indicated by a slight rise in prevalence of NBU2 in the modern strains and a large increase in the prevalence of mefE-linA carrying elements. A total of 70% of the strains tested positive for hybridization with the conserved region of NBU1 and NBU2, but only 53% of these strains hybridized to either or both of the NBU1- and

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TABLE 4. Summary of the results using NBU probes on Bacteroides isolates

Probe

% Bacteroides strains before 1970a

% Bacteroides strains from 1980 to 1990sb

Summary totals (n ⫽ 291)

Community (n ⫽ 75)

Clinical (n ⫽ 23)

Community (n ⫽ 105)

Loyola, Va. clinicals (n ⫽ 65)

Other clinicals (n ⫽ 26)

4.5-kbp HindIII (NBU1)c IntN1 IntN2 IntN1 and IntN2d

48 (36) 17 22 6

35 (8) 62 37 33

75 (79) 39 39 19

92 (60) 20 47 10

91 (21) 38 52 25

70 (204) 30 40 17

MObN1N2

24

55

66

69

50

PrmN1N2

28

58

74

74

52

37

43

39

28

(MefE-LinA)N2

5.3

8.7 13 8.7

a

Community and clinical isolates from the VPI anaerobe laboratory isolated in the 1960s and 1970s (16). The community isolates were isolated by participants in the Microbial Diversity Course at Woods Hole, Mass., in 1996 and 1997. The majority of the clinical isolates are from the VA Hospital at Loyola of Chicago Medical Center (65 isolates) and the Wadsworth Anaerobe Laboratory in Los Angeles, Calif. (14 isolates). The remaining isolates were requested and received from different hospitals and laboratories. c Four ORFs from the C-terminal end of intN1 through the N-terminal end of mobN1, including prmN and the oriT region (Fig. 2B). The percentages of the strains that hybridized to the HindIII fragment of NBU1 that also hybridized to the intN1 or intN2 probes are given. The numbers of strains tested are indicated in parentheses. d A total of 17% of the strains hybridized to both IntN1 and IntN2, which means that the overall percentage of the strains that hybridized to the HindIII probe and the IntN in hybridization pattern was: 17% N1-N2 ⫹ 13% N1 only ⫹ 23% N2 only ⫽ 53%, or 108 of the 204 strains. b

NBU2-specific probes. MTn4399 (prm⫹) and MTn4555 (moboriT⫹) would fall into the non-NBU category, and MTn5520 (⬍60% mobN or intN sequence identity) would not be detected. This suggests that there may still be more NBU-type elements that remain unidentified, possibly due to extensive sequence divergence and/or modular assembly of functional regions. Clearly, however, NBU1 and NBU2 are widespread among Bacteroides isolates, especially those obtained within the past decade. It is important to stress that the isolates surveyed represented a number of different Bacteroides species. These included B. fragilis, B. thetaiotaomicron, B. uniformis, B. vulgatus, B. ovatus, and several other species. Thus, the prevalence of NBU1 and NBU2 is likely due to horizontal transfer of the NBUs and not the prevalence of a single Bacteroides species or strain that happens to carry NBU1 or NBU2. The prevalence of NBU elements in the community isolates paralleled the prevalence in clinical isolates, both in the older and in the newer isolates. This indicates that whatever force is driving the increased acquisition of NBU-like elements and mefEN2linAN2 by Bacteroides species is being experienced in the community rather than being limited to hospitals. The diversity and range of the MTns could be an important component of the gene transfer capabilities of Bacteroides in the ecosystem of the human colon. Gene transfer from Bacteroides donors to members of other genera has already been observed in the laboratory (26, 41, 45). Evidence for transfer of genes in the environment has been indicated by the appearance of the Bacteroides tetracycline resistance gene, tetQ, in other genera, mostly human-associated gram-negative anaerobes (12, 13, 17, 18, 25). It remains to be seen whether transfer is also occurring between Bacteroides species and the gram-positive colonic anaerobes that are also a major component of the colon microflora. DISCUSSION The integrase of NBU2, intN2, has been identified. This gene and the joined ends of NBU2 were all that were required for integration. The NBU2 integrase, like that of the related mobilizable element, NBU1, appears to be a member of the fam-

ily of phage lambda recombinases, in the sense that it has the conserved C-terminal catalytic amino acids that are preserved on all members of the lambda Int family (27). The finding of lamba-type integrases in the NBUs and other nonphage integrating elements suggests that this mode of site-specific integration is more general than was previously realized. NBU2 and NBU1 both have some other phage-like traits. For one thing, they integrate site specifically via a 13-bp att sequence that is identical to the att site in the NBU2 joined ends. For another, they integrate into the 3⬘ ends of tRNA genes. The number of integrating elements that share one or more of these properties is growing and now includes not only bacteriophages and the NBUs but also integrative Streptomyces plasmids, sone pathogenicity islands, and integrative elements in Dichelobacter nodosus (4, 7, 31, 40, 61). The use of tRNA genes as targets for integration may increase the host range of an integrating element because tRNA genes are fairly highly conserved in different species. On the other hand, the use of tRNA genes as target sites could be considered as limiting their movement since such integration sites are unlikely to be found on plasmids or other self-transmissible elements. This limitation, however, does not seem to have prevented the NBUs from spreading extensively among different Bacteroides species in the human colon. Transmissible elements that use tRNA genes as an integration sites could be hazardous to a bacterial recipient if the structure of the tRNA gene was disrupted. In the case of NBU2, the crossover event exchanges the IR at the 3⬘ end of the tRNA with the IR found in the attN site. This change seems not to be deleterious for the recipients, but such a change could possibly influence the processing of the tRNA transcript (61). The importance of the IRs in the attN or the attBT sites for either the integration or the excision of the NBUs is not yet known. At present, there is no information available about Bacteroides host factors that might be involved in NBU integration or excision. Previous work has shown that NBU integration is independent of RecA (10), but whether integration requires a host factor-like IHF remains to be determined. Integration of NBU2 did not require any CTn functions, in contrast to the excision of NBUs, which requires functions provided by a CTn.

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In E. coli, integration was much more random than in B. thetaiotaomicron. This could be due to lack or a suitable primary integration site, because the Ser-tRNA gene of E. coli is not identical to that of B. thetaiotaomicron. It is also possible, however, that the relative lack of NBU2 integration specificity in E. coli, together with the much lower frequency of integration, reflects the absence in E. coli of a host factor that aids accurate alignment of the att sequences and efficient formation of the protein-DNA contacts in Bacteroides species. Excision of NBUs is proving to be a much more complex process than integration. The integrase is required, along with at least three other proteins and the oriT region (48). Moreover, excision requires trans action of CTn regulatory proteins, RteA and RteB. Thus, although the integration process of NBUs may resemble that of lambdoid phages, the excision process seems much different. Integrated elements carrying genes that cross-hybridize with genes on NBU1 and NBU2 are very widespread in Bacteroides species. The fact that their incidence seems to be increasing is a good indication of the efficiency of their transfer and their stability once acquired. Our results suggest that this group of integrated elements is likely to be a very heterogeneous group. Not only were NBU1 and NBU2 quite different outside the prmN-oriT-mob region, but the integrases of NBU1, NBU2, and a related element, MTn5520, had substantially different amino acid sequences (Fig. 6). The differences between the integrases is evident at the functional as well as the amino acid sequence level because the integrase of NBU1 did not substitute for the integrase of NBU2 in an integration assay. Why the prmN-oriT-mob region of NBU1 and NBU2 is so highly conserved at the sequence level, whereas the remainder of the elements are so different, has yet to be determined. This region could be on a cassette but, if so, it has been in the NBUs long enough for its edges to be obscured by mutation. Another possible explanation is that this region of NBU1 is very important for excision (48). Yet, so are the integrase and genes downstream of the integrase, which are quite different on NBU1 and NBU2. Still another possible explanation for the conservation of the prmN-oriT-mob region is that one or more proteins or DNA segments in this region interact with functions supplied by the CTns. This is most likely in the case of the Mob protein, which must interact with transfer functions on encoded on the CTn, which mediate the transfer of the NBU circular form. Both NBU1 and NBU2 also interact in some with the CTn regulatory proteins that trigger excision (RteA, RteB), so the conserved region might also be involved in that interaction. In our survey of Bacteroides isolates, we noted a few isolates that hybridized with prmN but not with mob. It will be interesting to determine whether the NBU-like elements in such isolates are capable of excision and transfer.

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ACKNOWLEDGMENTS We thank the following laboratories for providing strains: former VPI Anaerobe Laboratory, Blacksburg, Va.; David Hecht at the VA Hospital, Loyola Medical Center, Mayfield, Ill.; and S. Feingold and H. Wexler at the Wadsworth Anaerobe Laboratory in Los Angeles, Calif. We also thank the students attending the 1996–1997 Microbial Diversity summer course at the Marine Biological Laboratory, Woods Hole, Mass., for isolating the Bacteroides community isolates. This work was supported by grant AI22383 from the National Institute of Health.

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