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Journal of Clinical Microbiology, August 1998, p. 2314-2321, Vol. 36, No. 8
Laboratory of Enteric Pathogens, Central
Public Health Laboratory, London NW9 5HT, United Kingdom
Received 17 February 1998/Returned for modification 15 April
1998/Accepted 15 May 1998
Pulsed-field gel electrophoresis (PFGE) was used to resolve
XbaI and SpeI macrorestriction fragments from
60 defined phage type (PT) reference strains of Salmonella
enteritidis. The level of discrimination was compared to that
afforded by plasmid profile analysis and ribotyping. Twenty-eight
distinct XbaI pulsed-field profiles (PFPs) were observed,
although a single type, PFP X1, predominated. Absence of the 57-kb
spv-associated fragment was observed for three PT reference
strains, and the profile was designated PFP X1A. The XbaI
macrorestriction profiles of a further four PT reference strains were
altered by the presence of plasmid-associated bands. Twenty-six
SpeI-generated PFPs (plus one subtype) were observed for
the same strains. No SpeI fragment corresponding to the
38-MDa serovar-specific plasmid was detected. The distribution of
XbaI and SpeI profiles did not always
correspond, producing a total of 32 combined PFPs for the 60 PT
reference strains. This compared with a total of 18 different plasmid
profiles and three PvuII ribotypes generated by the same
strains. The results of this study indicate that PFGE may offer an
improved level of discrimination over other genotypic typing methods
for the epidemiological typing of S. enteritidis.
Salmonella enteritidis
remains the most common Salmonella serotype recovered from
humans in England and Wales (1), with 18,968 isolates
referred to the Laboratory of Enteric Pathogens in 1996. Although phage
type (PT) 4 has predominated for some time, the number of isolates
involving this PT appears to be declining, with a corresponding
increase in isolations of PTs 6, 1, 8, and 6a being recorded. Of
isolates of S. enteritidis received during 1996, five
PTs (4, 1, 6, 6a, and 8) accounted for 88%, and specifically, 72% of
the strains belonged to PT 4, 5% to PT 6, 4% to PT 1, 3% to PT 8, and 3% to PT 6a.
Strain identification is essential for the effective investigation of
common-source outbreaks, and phage typing is the method of choice for
the primary differentiation of S. enteritidis. The scheme of
Ward and colleagues (28) defined 27 PTs for this serovar (22), and this has subsequently been extended to 60 types
(28a). However, this method has limited applicability for
epidemiological studies, as the majority of isolates from cases of
human infection in the United Kingdom since 1987 have belonged to PT 4. Further subdivision by DNA-based methods may therefore be required for investigation of outbreaks. Plasmid profiling has been shown to be of
limited use for the subdivision of S. enteritidis PT 4, as
many strains carry a single 38-MDa plasmid (23, 24). DNA probes based on insertion sequence IS200 (7)
generate only two fragments with the majority of S. enteritidis PTs (21), consequently limiting the
discriminatory potential. Probes based on rRNA, including rRNA (4,
10), the cloned rrn operon of Escherichia
coli (2), and an intragenic fragment of the 16S rrn gene amplified by PCR (18), have been applied
to the analysis and elucidation of phylogenetic relationships in
several Salmonella serotypes. Probes based on known
(20) or randomly cloned (25) sequences have also
been used with varying degrees of success. These methods have led to
the conclusion that S. enteritidis falls into three clonal
lines, with the prevalent PTs, PT 4 and PT 6, falling in the first
group (14).
Pulsed-field gel electrophoresis (PFGE) has become established as a
method for the analysis of large DNA fragments generated by restriction
endonuclease digestion of genomic DNA (17). The procedure
has been used successfully for the estimation of genomic size and the
determination of the physical map of S. enteritidis SSU7998
(9). PFGE has also recently been applied to epidemiological investigation of Salmonella serovars and provides a useful
indicator of the level of genotypic diversity existing between strains
(12, 14). Preliminary studies have demonstrated that strains
of S. enteritidis PT 4 can be subdivided by PFGE
(15). However, to further evaluate the potential of the
method for all S. enteritidis PTs, it is important that
phylogenetic relationships between the different PTs of S. enteritidis be elucidated in relation to the relationships
provided by chromosomal fingerprinting methods, such as pulsed-field
profile (PFP) patterns and restriction fragment length polymorphism
(RFLP) at 16S rRNA gene loci.
We describe the genotypic characterization of S. enteritidis
PT reference strains by PFGE and ribotyping. The epidemiological applicability of these methods is also assessed.
Bacterial strains.
Sixty strains representing the currently
defined PT reference strains of S. enteritidis, listed in
Table 1, were stored on nutrient agar
slopes and grown overnight in nutrient broth at 37°C. The strains
were maintained in the culture collection of the Laboratory of Enteric
Pathogens and had been phage typed by standard methods (28).
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Genotypic Characterization of Salmonella
enteritidis Phage Types by Plasmid Analysis, Ribotyping,
and Pulsed-Field Gel Electrophoresis
ABSTRACT
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
INTRODUCTION
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
MATERIALS AND METHODS
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
TABLE 1.
Characteristics of the 60 S. enteritidis PT
reference strains
Plasmid analysis. Plasmid DNA was isolated by the method of Kado and Liu (6) and analyzed by agarose gel electrophoresis with E. coli 39R861 as a plasmid molecular mass marker (24). Plasmid sizes were determined with reference to 39R861 and the 38-MDa S. enteritidis serovar-specific plasmid (SSP). Plasmid DNA was transferred to Hybond N hybridization membranes (Amersham International, Amersham, United Kingdom) by capillary blotting. The presence of the Salmonella plasmid virulence (spv) region was determined by hybridization to a digoxigenin-labelled probe comprising a 437-bp fragment encoding the spvC virulence gene, prepared by PCR with oligonucleotide primers (Boehringer Mannheim, Lewes, United Kingdom) (4a). Detection of the hybridization signal was done according to the manufacturer's recommendations.
Ribotyping.
Genomic DNA was extracted by the method of
Wilson (29). Approximately 2 µg was digested with
PvuII (Boehringer Mannheim) and electrophoresed, together
with digoxigenin-labelled HindIII digest of
bacteriophage 
(Boehringer Mannheim), on a 0.8% agarose (Med EEO;
Sigma, Poole, United Kingdom) gel. The DNA was transferred to Hybond N
hybridization membranes as described above and hybridized to a 550-bp
rrnB probe (3) prepared by PCR amplification and incorporating 11-dUTP-digoxigenin (Boehringer Mannheim) label. Immunological detection was done by standard protocols (Boehringer Mannheim), and restriction fragment patterns were compared visually. The level of discrimination provided was assessed by calculation of
Simpsons' index as described by Hunter and Gaston (5).
PFGE. The method of strain preparation was essentially that described by Powell and colleagues (15). Chromosomal DNA contained in the agarose plugs was digested with 10 to 20 U of XbaI, NotI (Boehringer Mannheim), AvrII (BlnI), SpeI, or NheI (New England Biolabs, Hitchin, United Kingdom). PFGE was performed with CHEF DRII systems (Bio-Rad, Hemel Hempstead, United Kingdom) in 0.5× Tris-borate-EDTA. DNA macrorestriction fragments were resolved on 1.0% agarose gels (PFGE certified; Bio-Rad). Lambda ladders, comprising 48.5-kb concatemers (Sigma), were used as size standards. Electrophoresis conditions used as standard in this study were 6 V/cm for 40 h. Pulse times were ramped from 15 to 40 s during the run for XbaI-generated macrorestriction fragments. Runs comprising 4.8 V/cm for 66 h ramped at 10 to 100 s were also employed in some cases to ensure that alterations to very high molecular weight fragments were not overlooked. The preferred pulse time employed for a 40-h PFGE analysis of SpeI macrorestriction fragments was 5 to 20 s.
The preparation of DNA from selected strains was repeated, and preparations of all strains were digested and electrophoresed under the same conditions on at least two occasions to assess the reproducibility of the method and the stabilities of strains. Macrorestriction fragment patterns were compared visually in order to obtain schematic representations of all profiles observed. PFPs were assigned to types in accordance with those obtained in a previous study (15). Simpson's index of discrimination was calculated as described above (5). Selected gels were blotted onto nylon membranes and hybridized to Digoxigenin-labelled spvC, as described above, in order to determine the macrorestriction fragments encoding the S. enteritidis SSP.| |
RESULTS |
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Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
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Plasmid profile and spv analysis. Plasmid masses, in megadaltons, obtained for each S. enteritidis PT reference strain are shown in Table 1. Of the 60 PT reference strains, 42 carried the 38-MDa S. enteritidis SSP, and of these 42 strains, 13 carried additional plasmids. Five PT reference strains were plasmid free, and the remainder carried at least one plasmid of 33 MDa or greater (Table 1 and Fig. 1). The reference strain for PT 6 (P99327) carried a 50-MDa plasmid, which hybridized to spvC, plus additional plasmids of 4.6 and 2.6 MDa, a profile which differed from that previously reported (24). Plasmids of approximately 59, 4.0, and 3.0 MDa were observed for the PT 6a reference strain, E2408 (Table 1). Both the 59-MDa plasmids of PTs 6a, 9a, 9b, 11, and 20 and the 33-MDa plasmids of PTs 9c, 37, and 40 hybridized to spvC. In contrast, the single 65-MDa plasmid carried by the reference strain of PT 10 (E3945) failed to hybridize to this probe, as did 65-MDa plasmids carried in addition to the 38-MDa SSP in the PT 5a and PT 22 reference strains.
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Ribotyping. Three distinct PvuII profiles were observed among the 60 S. enteritidis PT reference strains examined after hybridization with the 16S rrnB riboprobe (Fig. 2). Ribotyping with PvuII as the sole restriction enzyme was not particularly helpful in discriminating within S. enteritidis, as the majority (50 of 60) of the reference strains belonged to PvuII type A (Table 1 and Fig. 2, lanes 2 to 4, 6, 7, and 12 to 14); five strains generated each of the other ribotypes, B (Fig. 2, lanes 5 and 9) and C (Fig. 2, lanes 8, 10, and 11). The numerical index of discrimination (DI) for PvuII ribotyping of the 60 PT reference strains was low (DI = 0.259).
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PFGE analysis and identification of profile types. (i) XbaI. PFGE permitted the resolution of XbaI macrorestriction fragments of the 60 PT reference strains into 28 distinct types (Fig. 3). XbaI PFPs typically comprised 13 to 16 resolvable bands (usually 14) between 40 and 600 kb under the conditions used in the study (Fig. 4A), correlating well with the XbaI genomic cleavage map of S. enteritidis SSU7998, which revealed 16 fragments ranging from 19 to 900 kb in size (9). The predominant XbaI profile was identical to PFP 1 described by Powell et al. (15) and was accordingly designated PFP X1 (Fig. 4A, lane 2). A variation of PFP X1, designated PFP X1A, from which a single 57-kb fragment representing the 38-MDa plasmid was absent (Fig. 4A, lane 5), was observed for three strains, of which two (P221267 and P124191) were plasmid free. The 57-kb XbaI fragment corresponded to the 38-MDa plasmid encoding the common virulence region, which contains a single XbaI site, and appeared as a linear fragment of approximately 57 kb after resolution by PFGE. The PT 37 reference strain (P267187) carried a single 33-MDa plasmid, which was not visible by PFGE analysis under the conditions employed. In contrast, for the reference strains of S. enteritidis PTs 6 and 30, the 57-kb XbaI fragment was absent but plasmid-associated fragments of approximately 70 (PFP X1B) and 63 kb (PFP X1E) were generated, corresponding to the observed carriage of plasmids of 50 and 45 MDa, respectively (Table 1 and Fig. 4A, lane 4). The 70-, 63-, and 57-kb XbaI fragments, corresponding to the 50-, 45-, and 38-MDa plasmids, contained spv, as all hybridized to the spvC probe (not shown). The XbaI-generated PFPs X1, X12, X11, and X1A were the most commonly observed profiles among the S. enteritidis PT reference strains; PFP X1 was generated by the type strains of S. enteritidis PTs 1c, 4, 4a, 5a, 5b, 7a, 14b, 21, 24, 25, 27, 31, 36, and 39; PFP X12 was generated by PTs 2, 8, 8a, 13a, 23, and 28 (X12A by PT 7); PFP X11 was generated by PTs 1, 1b, 32, and 35 (X11A by PT 5); and PFP X1A was generated by reference strains of PTs 1a, 29, and 37 (Table 1). There were two instances of reference strains generating PFPs which were almost identical to those of an already-defined type but which differed by the appearance of a single XbaI-generated band in each case, which was reproducible for different preparations of the same strains and did not appear to be plasmid associated (not shown). The affected PTs were designated subtypes of the PFP from which they are likely to have been derived (PFP X11A from X11 and PFP X12A from X12 [Table 1]). PFPs X13 and X13A were differentiated by a positional change of a single plasmid-associated band (57 to 63 kb). The discrimination index calculated for XbaI macrorestriction profiles of S. enteritidis PTs analyzed by PFGE was 0.874.
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(ii) SpeI. Macrorestriction fragments of the 60 S. enteritidis PT reference strains generated by SpeI were resolved into 25 individual profiles by PFGE by using pulse times of 5 to 20 s (Fig. 4B and 5). Differences in profiles ranged from the loss of a single fragment of 70 to 75 kb to profiles which comprised five common resolvable bands in a macrorestriction profile which typically comprised 21 clearly resolvable bands of between 30 and 450 kb, some of which were observed as doublets (Fig. 4B).
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(iii) Combined XbaI and SpeI profiles. When the results of macrorestriction with SpeI and XbaI were combined there were six groups comprising two or more type strains of S. enteritidis PTs generating identical combined profiles. The remaining PT type strains generated unique combined PFPs. The largest group comprised 12 S. enteritidis PTs (1c, 4, 4a, 5a, 5b, 7a, 14b, 21, 24, 25, 36, and 39) and displayed a PFP XS1 macrorestriction profile, resulting from the combination of the predominant XbaI- and SpeI-generated profiles (Table 1). The second most prevalent combined type (PFP XS7) was generated by five PT type strains (PTs 2, 8, 13a, 23, and 28) and resulted from a combination of PFP X12 and PFP S3 (Table 1). There was a significant amount of overlap between PFPs generated by XbaI and SpeI, resulting in only a small increase in the number of types (to 32) and a corresponding improvement in discrimination (DI = 0.902).
(iv) Other restriction endonucleases. Macrorestriction analysis of S. enteritidis with NotI and NheI generated too many fragments below 100 kb for practical analysis, particularly as fragments below 70 kb were poorly resolved and could comprise digested extrachromosomal DNA. In contrast, AvrII, an isoschizomer of BlnI, generated a maximum of 10 resolvable fragments, compared with the 12 BlnI fragments reported for the genomic cleavage map of S. enteritidis SSU7998 (9), but did not offer improved discrimination over that of XbaI.
Reproducibility. Minor variations between different preparations of the same strains were not observed within the confines of the study, with the exception of a weak fragment of >700 kb appearing in occasional preparations (not shown). This was considered to be due to the presence of incompletely digested DNA and was usually removed by further treatment with proteinase K and subsequent washing steps.
Reduction of the electrophoresis time, from 64 to 40 h, with a corresponding increase in voltage, was applied in order to reduce the overall time required to generate a PFP. This was achieved, but with loss of resolution of very large fragments (>600 kb). However, profiles containing differences in bands of this size also had variations in smaller fragments.Comparison of PFGE, ribotyping, and plasmid profile types. S. enteritidis PT reference strains generating the predominant PFGE combined type, PFP XS1, carried the 38-MDa SSP. Some strains were observed to carry additional plasmids (Table 1), none of which showed homology to spvC. With a single exception, this group of strains generated the predominant PvuII ribotype (A). Only P118526 (PT 14b) generated ribotype B, which differed by the increase in size (from approximately 8.8 to 10.5 kb) of the second largest PvuII-generated band (Fig. 2, lane 9). Strains belonging to the second most common combined PFP (XS7) generally carried a single plasmid of 38 MDa. Only P125363 (PT 28) carried an additional plasmid, of 8 MDa, which did not appear to affect either the ribotype or PFP. Of the S. enteritidis PT strains found to be plasmid-free (PTs 1a, 11b, 16, 26, and 29), only those of PTs 1a and 29 generated PFP XS1A. The remaining strains belonging to this group generated unique XbaI and SpeI PFPs.
S. enteritidis PT reference strains generating ribotypes B and C did not carry the 38-MDa SSP and, with a single exception (PT 14b), generated combined PFPs unique to each strain (Table 1). Reference strains generating PvuII ribotype B varied in plasmid profiles (Table 1). In contrast, four of the five strains generating PvuII ribotype C possessed a single 59-MDa plasmid which showed homology to spvC, while P187803 (PT 11b) was plasmid free (Table 1).| |
DISCUSSION |
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Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
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Genotypic analysis of Salmonella by molecular typing methods has proved to be helpful in the characterization of strains from a range of Salmonella serovars (4, 11-16, 19-21, 26, 27). In this study, the 38-MDa SSP was not common to all S. enteritidis PTs but was present in the reference strains of most of the PTs commonly causing human infection. Notable exceptions were the reference strains of PT 6 (P99327) and PT 6a (E2408), each of which carried a plasmid of >38 MDa but also carried the common virulence region. However, examination of recent human strains belonging to PTs 6 and 6a indicates the presence of the 38-MDa SSP and the absence of the 59-MDa plasmid in the majority of strains (16, 16a). Although plasmid analyses have not been included in combination with other genotyping methods in previous studies involving typing of S. enteritidis, it was useful to correlate the presence of particular plasmids with fragments obtained by PFGE analyses. Typically, plasmids were observed as intensely stained fragments on PFGE gels, although this was less apparent for the 57-kb XbaI fragment corresponding to the S. enteritidis SSP.
This study has extended the molecular typing of S. enteritidis to 60 PTs. Plasmid-free strains did not hybridize to spvC, and the XbaI profiles were distinguished by the absence of a 57-kb fragment, which when present hybridizes to spvC. A corresponding fragment was not detected in SpeI macrorestriction profiles analyzed by PFGE, and it is presumed that the lack of a SpeI site in the SSP allows it to remain supercoiled and hence to migrate off the end of the gel. The results have provided a useful indicator as to how plasmids may affect PFGE profiles.
Although plasmid analysis appeared to exhibit a variety of profiles, the majority contained the 38-MDa S. enteritidis SSP, and many of the differences observed were due to carriage of additional small plasmids. In this study plasmids in addition to the 38-MDa SSP failed to hybridize to the spvC gene probe, and it was concluded that they were unrelated. Carriage of 4.0-MDa plasmids, as found in the type strains of S. enteritidis PTs 6a, 19, and 25, has been associated with resistance to ampicillin (3). The plasmids of 33, 50, 59, and 65 MDa carried by PT type strains not possessing the 38-MDa SSP hybridized to the spvC probe, generating XbaI fragments of 50, 75, 85, and 100 kb, respectively. This suggests that they are related to the SSP and contrasts with the findings of Liebisch and Schwartz (8), which suggested that large plasmid bands do not account for the RFLP detected by PFGE. The reference strain of PT 6 originally contained plasmids of 65, 38, 2.6, and 1.0 MDa (24), compared with the 50-, 4.0-, and 2.6-MDa plasmids observed for the same strain in this study. It may be that a segment of DNA has been lost from the 65-MDa plasmid and taken up by the 38-MDa SSP, thereby increasing its size to 50 MDa (Table 1). The 50-MDa plasmid was observed to hybridize to spvC, confirming the presence of the common virulence region in this plasmid. This study also reports the presence of a single 38-MDa SSP, corresponding to a 57-kb XbaI fragment, in the reference strain of PT 3 (P66040), a finding in contrast with those of Threlfall et al. (24), who observed a 59-MDa plasmid in the same strain. Although useful for strain discrimination in some outbreaks involving S. enteritidis, plasmid profiling does not generally convey strain-specific information.
Genotypic diversity between phenotypically related PTs.
PFGE
analysis demonstrates that some S. enteritidis PT reference
strains generating similar phage typing reactions are genotypically distinct. This observation was most pronounced for reference strains of
S. enteritidis PTs 11, 11a, and 11b for both XbaI
and SpeI macrorestriction fragments (Fig. 4, lanes 13 to
15). The reference strains of PT 11 and 11a XbaI PFPs (X19
and X20) contained 14 band differences, for a total of 13 to 14 resolvable bands of 
40 kb (Fig. 4A, lanes 13 to 15). The
SpeI PFPs (S11 and S12) for the same strains resulted in 12 differences, for a total of 16 to 17 resolvable bands of 48.5 kb,
where 8 bands were common to both PFPs (Fig. 4B, lanes 13 to 15). The
SpeI PFP generated by the PT 11b reference strain (S13)
shared six common fragments with each of the S11 and S12 PFPs, with
between 9 and 17 band differences observed. Five XbaI
fragments of 40 kb were observed to be shared between the PFPs of PTs
11a and 11b, and four were shared between PFPs of PTs 11 and 11b.
48.5 kb. Such observations indicate that strains
grouped according to phenotypic reactions may be genotypically diverse.
Less extensive variation in XbaI and SpeI
macrorestriction profiles was observed between the reference strains of
PTs 13 and 13a and for PTs 7 and 7a (up to three band differences),
indicating a closer genotypic relationship. The type strains of PTs 1 and 1b shared both XbaI and SpeI PFPs. The
SpeI PFPs generated by PTs 1a and 1c were indistinguishable
from each other but differed in the positions of two bands from those
of PTs 1 and 1b, while the XbaI PFPs differed by the absence
of the 57-kb SSP. The type strains of S. enteritidis PTs 24 and 24a and those of PTs 20 and 20a revealed three and four band
differences, respectively. In contrast, the type strains of PTs 4 and
4a shared both XbaI and SpeI PFPs (Table 1) and
hence also shared a combined macrorestriction profile (PFP XS1). Minor
differences in a single fragment size, leading to the designation of
PFPs X11A, X12A, and S3A, were reproducible for different preparations
of the same strains. Such variation may have resulted from a slight
shift in migration of the fragment, the significance of which is
unclear.
Several strains generating different phage reactions shared a common
genotype. This was especially noticeable for the nine PT reference
strains generating identical combined XbaI and
SpeI macrorestriction profiles (PFP XS1). Although the phage
reactions of the reference strains of S. enteritidis PTs 4 and 4a appeared to be similar, those of the reference strains of PTs
12, 21, and 36 and PTs 4, 5a, and 7a were markedly different. Only the
PT 5a reference strain, which carried a 65-MDa plasmid in addition to
the 38-MDa SSP, generated a distinct plasmid profile. Additional plasmids of this size have not been associated with changes to phage
lysis patterns (22). The predominance of PFPs X1 and S1, generated by 14 and 22 PT reference strains, respectively, even among
those type strains not commonly implicated in human infection suggests
that this genotype may confer an as yet unknown selective advantage.
Small differences in a single fragment size, leading to PFPs X11A (PT
5) and X12A and S3A (PT 7), were reproducible for different preparations of the same strains. The altered fragments may have resulted from a shift in migration, the significance of which has not
yet been evaluated.
The results of this study correlate well with those of previous studies
by Olsen and colleagues (14), who reported that the
convergence of PTs occurred between those which generated the same
SmaI ribotype and the same NotI PFGE and
PstI RFLP profiles, although some generated different
IS200 profiles. Type strains from several PTs not previously
typed by molecular methods were included in the present investigation.
Of these, PTs 1c, 5a, 5b, 7a, 36, and 39 were indistinguishable from
the predominant combined PFP XS1, ribotype A. Only PTs 1c, 5a, and 5b
carried plasmids in addition to the 38-MDa SSP. XbaI and
SpeI were chosen, as their discrimination between fragments
of >48 kb was greater than that of other enzymes (NotI,
NheI, and AvrII) evaluated. Olsen and colleagues
(14) employed NotI and reported 10 different
macrorestriction profiles for 33 S. enteritidis PT reference
strains. However, the PT 16 reference strain (E866) was refractory to
digestion by this enzyme. In addition, the numerous small
NotI fragments of <100 kb were excluded for discriminatory
purposes, as they were not clearly resolved. This study employed
XbaI, generating 28 PFPs, with a further four subtypes of
the predominant PFP X1, and SpeI, generating 25 PFPs for the
60 S. enteritidis PT type strains examined. This does not
include additional PFPs identified for clinical isolates of S. enteritidis (15, 15a, 16). Furthermore, no strains were
found to be refractory to digestion by the enzymes chosen for this
study. A recent study demonstrated that ribotyping and plasmid
profiling provided insufficient discriminatory power for
epidemiological subdivision of a set of 31 unrelated strains of
S. enteritidis of several different PTs (8). PFGE
analysis provided improved typing of these strains; however, more than one enzyme was required to separate strains belonging to PTs 1, 4, 6, 7, and 8 (8). PTs of S. enteritidis predominantly
causing infection in the United Kingdom include PTs 1, 4, 6, 6a, 8, and 13. By using PFGE analysis of macrorestriction fragments, the PT
reference strains can be successfully differentiated. However, studies
in this (16) and in other (14, 27) laboratories have demonstrated that some strains causing infection generate PFPs
which may be markedly different from those observed for that particular
PT reference strain, suggesting that strains causing infections in
humans have a higher degree of genotypic homogeneity than is indicated
by phage typing.
The level of discrimination permitted by combined XbaI and
SpeI macrorestriction fragment analysis by PFGE
(DI = 0.902) is superior to that obtained by ribotyping
(DI = 0.259) and correlates well with a recent study of 31 isolates of S. enteritidis, for which an overall
discrimination index for PFGE, calculated for a combination of three
different enzymes, was 0.815 (8).
In this study we have addressed the framework of XbaI and
SpeI macrorestriction fragments, analyzed by using PFGE for
S. enteritidis by characterization of the 60 defined PT
reference strains. The results suggest that PFGE analysis is
potentially a valuable tool for the characterization of S. enteritidis. Furthermore, by combining results obtained for two or
more enzymes, the discriminatory power of the method may be enhanced
for several of the most common PTs causing infections in humans.
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ACKNOWLEDGMENTS |
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We thank Anna New for technical assistance.
This study was supported by a grant from the Department of Health (DH code 217) for the differentiation of S. enteritidis PT 4.
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FOOTNOTES |
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* Corresponding author. Mailing address: Laboratory of Enteric Pathogens, Central Public Health Laboratory, 61 Colindale Ave., London NW9 5HT, United Kingdom. Phone: 0181 200 4400. Fax: 0181 905 9929. E-mail: jthrelfall{at}phls.co.uk.
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REFERENCES |
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Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
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