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Volume 10, Number 8—August 2004

Serotype III Streptococcus agalactiae from Bovine Milk and Human Neonatal Infections1

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John F. Bohnsack*Comments to Author , April A. Whiting*, Gabriela Martinez†, Nicola Jones‡, Elisabeth E. Adderson§, Shauna Detrick*, Anne J. Blaschke-Bonkowsky*, Naiel Bisharat‡, and Marcelo Gottschalk†
Author affiliations: *University of Utah Health Sciences Center, Salt Lake City, Utah, USA; †Faculté de Médicine Vétérinaire, Université de Montréal, Saint-Hyacinthe, Québec, Canada; ‡John Radcliffe Hospital, Oxford, United Kingdom; §St. Jude Children’s Research Hospital, Memphis, Tennessee, USA

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Streptococcus agalactiae (group B streptococcus [GBS]) causes invasive human infections and bovine mastitis. This study examined the genetic relationship between bovine and human serotype III GBS by using molecular techniques that classify human serotype III GBS into four distinct phylogenetic lineages. Bovine serotype III GBS were largely contained in two lineages, which are distinct from the two major lineages (restriction digest types III-2 and III-3) that infect human neonates. One of the bovine lineages closely resembles the human III-1 lineage, whose members occasionally cause human neonatal infections. The bovine strains in the other lineage characteristically have an initiation factor IF2 gene (infB) H allele and multilocus sequence types that are not found in human GBS strains. Evidence suggests that this “H allele” lineage is related to the human III-3 lineage. These results support the assertion that human and bovine GBS are largely unrelated and provide further insight into the genetic relation between human and bovine GBS.

Streptococcus agalactiae (group B streptococcus [GBS]) is the major etiologic agent of invasive neonatal infections in humans in industrialized countries, causing sepsis, pneumonia, meningitis, osteomyelitis, and soft tissue infections (1). GBS has also been increasingly recognized as an important pathogen in immunocompromised and elderly persons (2,3). GBS emerged as an important cause of neonatal infections in the 1960s; before this time, it was mainly recognized as a cause of bovine mastitis (4). Most data suggest that GBS strains that infect humans are distinct from strains isolated from bovine sources, since bovine strains frequently cannot be typed with antisera to determine capsular polysaccharide serotype, often express protein antigens not found on human isolates, and tend to have different biochemical properties (58). The possibility remains, however, that subgroups of GBS infect both humans and cows. If so, these two closely associated hosts could act as reservoirs for each other and sites for the emergence of novel pathogens.

A number of molecular methods, including multilocus enzyme electrophoresis, pulsed-field gel electrophoresis (PFGE) of restriction enzyme digest products of genomic DNA, randomly amplified polymorphic DNA (RAPD) analysis, and multilocus sequence typing (MLST), have been used to demonstrate that the population of GBS that infects humans is highly clonal and limited to a relatively small number of phylogenetic lineages (913). Martinez and colleagues reported in 2000 that a large sample of GBS isolated from cows in Quebec Province in Canada could be classified into five major RAPD groups, which indicates that this sample of bovine GBS also comprised a limited number of lineages (7).

The Quebec sample is particularly useful for further investigating the relationship between bovine and human GBS because most typeable bovine isolates in the sample were serotype III. Serotype III GBS strains account for a substantial proportion of early-onset neonatal human GBS infections and almost all late-onset neonatal infections (2). Four distinct phylogenetic lineages of human serotype III GBS have been identified by PFGE of restriction digest patterns and designated restriction digest patterns type III-1, III-2, III-3, and III-4 (11). Human GBS strains can also be assigned to each restriction digest pattern type by a distinct set of molecular markers, which include analysis of nucleotide substitutions in the centrally conserved region of the translation infB, the presence or absence of the inserted sequences GBSi1 and IS1548 in three chromosomal loci, and MLST (9,11).

RAPD analysis of human GBS isolates collected with the Quebec bovine isolates suggested that the serotype III bovine strains and human GBS strains were largely unrelated, although a definite conclusion was hindered by the small number of human isolates in the study. The obstacle presented by the small human sample size can now be circumvented by the use of the molecular markers described above that identify human phylogenetic lineages of GBS, but which have not yet been applied to the study of GBS from nonhuman sources. We reexamined the Quebec sample with these molecular markers to better understand the genetic relationship between bovine serotype III GBS and human serotype III GBS.


Bacterial Isolates


Thumbnail of Simplified dendrograms illustrating the genetic relationship between human and bovine group B streptococcus. A) Dendrogram of Quebec sample derived by randomly amplified polymorphic DNA (RAPD) analysis; adapted from (7). All RAPD groups contain bovine serotype III GBS, but those marked by an asterisk also contain human isolates (see Table 2). B) Dendrogram of human restriction digest pattern types (RDP) of serotype III GBS derived by analysis of RDP of genomic DNA created by digesti

Figure. Simplified dendrograms illustrating the genetic relationship between human and bovine group B streptococcus. A) Dendrogram of Quebec sample derived by randomly amplified polymorphic DNA (RAPD) analysis; adapted from (7). All RAPD...

The serotype III GBS were isolated from bovine milk or from vaginal and rectal swab specimens from asymptomatic pregnant women in Quebec Province, Canada, during 1996 and 1997, as previously described (7). RAPD analysis of the 224 bovine GBS isolates had assigned 210 of the isolates to four RAPD groups (I–IV); the remaining 14 isolates were ungrouped (Figure). A total of 70 of the 82 original serotype III GBS strains were recovered for this study. The remaining GBS in this collection were not serotype III or were nontypeable. Bovine isolates were studied from all RAPD groups except RAPD group I, which contained a single bovine serotype III GBS isolate that could not be recovered. Genomic DNA was extracted with the Qiagen DNeasy Tissue Kit (Qiagen, Valencia, CA) from individual colonies grown overnight in broth.

Molecular Analyses

The central portion of infB was amplified from bacterial DNA by polymerase chain reaction (PCR) with oligonucleotide primers, as described by Hedegaard et al. (14). Each amplicon was purified and sequenced.

The presence or absence of the inserted sequences GBSi1 and IS1548 in the respective chromosomal loci was determined by using PCR of bacterial DNA with primer pairs flanking each of three sites, as previously described (11). In human serotype III GBS, the first locus is an internal region of hylB, the gene encoding hyaluronidase, which is either interrupted by IS1548 or is intact. The second locus is the region between scpB and lmb, the genes encoding streptococcal C5a-ase and a laminin-binding protein, which either contains GBSi1, IS1548, or no insert. The third locus lies between ftsY and sag0728, two open reading frames (ORFs) with gene products of unknown function, which contains GBSi1 or no insert. The latter locus is either referred to as the AW-10 locus (as we refer to it) or the Y locus, according to Luan et al. (15).

MLST was carried out on 46 selected strains as previously described, and a sequence type was assigned to each strain (9). The sequences of the alleles that make up the novel MLST sequence types described in this manuscript can be found at (9). DNA dot blots were performed by using a 96-chamber vacuum manifold and [32P]-dCTP labeled probes as previously described (16).

The complete sequences of the infB gene H allele and the novel IS1563-like insertion sequence described in this article are available in the GenBank database under accession nos. AY429663 and AY437915, respectively.


Analysis of infB Alleles in Bovine GBS

All human serotype III GBS have either the A or C allele of the gene encoding translation-initiation factor IF2 (infB allele, Table 1). Twenty-five of the 62 Quebec bovine isolates carried the A allele, and 2 carried the C allele, which raises the possibility that these 27 bovine GBS could be closely related to human GBS (Table 2). No strains bearing the B allele were identified, and only one strain carried the D allele. Serotype III GBS that bear the D allele are unlikely to be isolated from humans because all human GBS strains bearing the D allele have thus far been serotype Ia. The remaining 34 strains contained a previously unidentified infB allele, which we have designated the H allele. The infB H allele differs from other previously identified infB alleles (designated A–G) by two, three, or five nucleotide substitutions within the central conserved portion of the infB gene and most closely resembles the infB A allele (11,14). All 34 of the strains bearing the H alleles are bovine in origin (Table 2). The infB H allele has not been previously encountered in approximately 700 GBS isolates isolated from human sources studied in our laboratory, including over 150 serotype III strains (unpub. data; [11]). These observations suggest that GBS bearing the infB H allele rarely, if ever, colonize or infect humans.

Relationship between infB Allele and RAPD Group

The possibility that the A or C allele bovine strains could be related to human GBS was investigated by examining the distribution of the bovine A or C allele isolates among the groups previously determined by RAPD analysis (Figure) (7). Of the 25 bovine A allele isolates, 19 were found in RAPD group IV-A, and 2 were found in RAPD group IV-C, which suggests that at least some of the bovine A allele isolates could be genetically related to human GBS since human A allele isolates are also found in these two RAPD clusters (Table 2, Figure). The two bovine C allele isolates are in RAPD group IV-C clustered with two human C allele isolates and thus appear closely related to human C allele isolates based on RAPD analysis. As expected, neither the single bovine D allele isolate nor the 34 bovine H allele isolates cluster with human isolates by RAPD analysis (Table 2).

Identification of Bovine Serotype III GBS Related to Type III-1 GBS

The bovine A and C allele isolates were further examined by using techniques that distinguish the four known human serotype III GBS lineages. These techniques include determining the presence or absence of inserted sequences in three previously identified loci and determining the strains’ sequence types by MLST (Table 1). Twenty-three of the 25 A allele bovine isolates appear closely related to human restriction digest pattern type III-1 strains because the isolates lack inserted sequences at any of the three loci examined and had a sequence type (ST) identical to those of previously studied III-1 strains (ST-23) or that was different by only one allele (ST-90, ST-92, or ST-94) (Table 3). Thus, a substantial proportion of the serotype III bovine GBS in this sample appear to come from a lineage that is associated with invasive neonatal disease, albeit rarely (9,17,18). Bovine III-1 strains appear to be genetically heterogeneous since they are found in RAPD groups III, IV-A, and IV-C, but no human III-1 strains were found in this sample; thus, the bovine III-1 strains most closely related to human III-1 strains could not be identified in this sample. Nineteen of the III-1 bovine isolates appear to lack the scpb-lmb locus because PCR with primers flanking the intergenic locus of lmb and scpB did not produce an amplicon.

Seven of the A allele strains appear to be restriction digest pattern type III-2 strains on the basis of an analysis of inserted sequences and MLST (Table 3). Only one of these seven isolates, NI-96-2836, is of bovine origin, however, and is found in RAPD group III, whereas the six human A allele isolates are found in RAPD groups IV-A and IV-C. These data suggest that the bovine NI-96-2836 strain is genetically divergent from human III-2 strains, despite sharing the same infB allele, inserted sequences, and ST with human III-2 strains. These data also suggest that restriction digest pattern type III-2 strains, a major cause of human neonatal infections, are rarely, if ever, isolated from bovine milk.

One of the two remaining A allele strains, SH-96-4807, appears indistinguishable from III-3 strains on the basis of MLST because it has ST-17, which is characteristic of III-3 strains. Unlike III-3 strains, however, SH-96-4807 has no inserted sequences in any of the three sites and contains an infB A allele instead of the C allele typical of III-3 strains. The remaining A allele isolate, SH-96-3696, appears to be most closely related to H allele strains, on the basis of its RAPD group, inserted sequences, and ST. No bovine isolate related to restriction digest pattern type III-4 was found in this sample.

The four C allele isolates have the typical inserted sequences and ST (ST-17) found in restriction digest pattern type III-3 strains, with the exception of human isolate 1004A, which has a truncated form of IS1548 in the scpb-lmb intergenic region (Table 4). These strains, which cluster together in RAPD Group IV-C, were isolated from both human and bovine sources. These data indicate that strains from the restriction digest pattern type III-3 lineage infect both humans and bovine udders but that bovine III-3 strains are rare. The only D allele strain has ST-93, an ST which differs by at least three alleles from all the STs previously described for human GBS, which again indicates that D allele serotype III GBS rarely or never colonize humans.

Analysis of H Allele Isolates

Ten H allele isolates were selected to represent strains from RAPD Group II, Group III, and the ungrouped isolates and analyzed in the same fashion. As shown in Table 5, all of the isolates studied have large inserts in the AW-10 site. The 1,700-bp inserts would be the correct size for the GBSi1 insert found in III-3 strains, and sequencing demonstrated an intact copy of GBSi1 in a 1,700-bp amplicon from one of the strains. A 3,000-bp insert from one strain was amplified and sequenced and found to comprise GBSi1, interrupted by an IS3-like insertion sequence identical to sequences found in both the genome M1 strain of S. pyogenes and the genome serotype V strain of S. agalactiae (19,20).

A 3,400-bp insert was sequenced and found to consist of an inserted sequence that has identical direct and inverted repeat sequences to the insertion sequence IS1563, but it has a predicted amino acid sequence that is 75% identical to that of IS1563. This IS1563-like insertion sequence is located upstream of GBSi1 exactly as IS1563 is found upstream of GBSi1 in this locus in restriction digest pattern type II-2 strains (11).

The AW-10, hylB, and scpb-lmb loci were studied in the remaining H allele strains not shown in Table 5. No inserted sequences were found in the AW-10 site in seven isolates, while the remaining strains have either the 1,700-bp, 3,000-bp, or 3,400-bp inserts at AW-10. No inserted sequences were found in the hylB and scpb-lmb sites in any of the H allele strains. Two of the H allele strains, both of which are in RAPD group IV-B, appear to lack the scpb-lmb locus.

MLST shows that 8 of these 10 H allele isolates are ST-61. ST-61 isolates are found in RAPD groups II, IV, and in ungrouped isolates, which indicates genetic divergence among H allele strains that is detected by RAPD but not by MLST. ST-61 differs from ST-67 by one allele, which confirms that SH-96-3696, the A allele strain found in RAPD II that has ST-67, is in the same clonal complex as the H allele serotype III strains. SH-96-3696 also has a 3,400-bp insert at AW-10, and no insert at the other two sites, which provides further evidence that this isolate is related to H allele strains. The other two STs found in the H allele strains, ST-91 and ST-105, differ from ST-61 by two alleles. Thus, the H allele strains are clonally related.

III-3–specific Sequence Tags in H Allele Serotype III GBS

ST-61, the most common ST of the H allele strains, differs by two alleles from ST-17, the most common ST of III-3 strains. This two-allele difference in ST and the observation that isolates from these two lineages both have GBSi1 in the AW-10 site led us to search for other evidence that the two lineages are related.

We previously described 10 short sequence tags that are found in all III-3 strains but not in III-1 or III-2 strains (16). We therefore performed dot-blot hybridization with eight of these probes on a selection of A, H, and C allele strains from this sample to determine the distribution of the III-3–specific sequences among these various lineages. As expected, all of the III-3–specific probes hybridized with every C allele strain tested, whereas the III-3 probes hybridized rarely or never with the A allele strains. In contrast, seven of the eight III-3 probes hybridized with almost all the H allele strains (Table 6).


A key finding of this investigation is that the serotype III GBS strains isolated from bovine milk in this sample are largely genetically distinct from the serotype III GBS strains that commonly infect humans. The two most common lineages of serotype III GBS that colonize women and infect infants in the United States and Japan are restriction digest pattern types III-2 and III-3, whereas III-1 and III-4 strains are rarely isolated from the genitourinary tract of women and are rarely associated with invasive disease (11,16).

Only one bovine strain that resembled RDP type III-2 GBS was identified in the 67 isolates, and RAPD analysis indicates that this isolate is distinct from the 7 human III-2 strains in the sample. Thus, III-2 strains that infect humans are unlikely to infect bovine udders. Only two bovine strains were identified that had the genotypic characteristics of restriction digest pattern type III-3 strains. These two strains appear closely related to two human III-3 isolates by RAPD analysis, which makes it likely that III-3 strains can infect bovine udders, but they appear to do so infrequently.

We also found that the vast majority of bovine serotype III GBS in this sample belong to one of two major phylogenetic lineages. A separate study of bovine GBS isolates collected in the United Kingdom used MLST to identify two clonal complexes that are similar, if not identical, to the two lineages identified here; this finding suggests that two clones of GBS may predominate among bovine mastitis caused by GBS in North America and England (21).

The data presented here show that the first bovine lineage is closely related to restriction digest pattern type III-1 GBS (Table 7). The lack of human III-1 strains in this sample makes it difficult to use the RAPD analysis to determine how closely these III-1–like bovine strains resemble human III-1 strains. That no III-1 human isolates were found in this small sample is not surprising because human III-1 isolates rarely colonize the female genitourinary tract (although they occasionally cause neonatal infections) (9,17,18). Most III-1 bovine isolates in the sample studied here appear to lack the scpb-lmb locus, a finding consistent with that reported by Francken et al., who showed that absence of a putative composite transposon that contains the scpB and lmb genes is a feature of bovine GBS (22). Possibly only a few of the III-1 bovine GBS are capable of infecting both humans and cows, since all human GBS appear to have the scpb-lmb locus.

The other major bovine serotype III GBS lineage in this sample is composed of strains that possess an infB H allele, with the exception of a single A allele strain that, on the basis of RAPD and MLST, appears closely related to the H allele strains. The H allele strains have STs that differ from each other by no more than two alleles, which indicates that these strains are likely to have a recent common ancestor.

We believe that strains in this lineage are unlikely to colonize or infect humans since we have not identified an infB H allele strain in >160 human serotype III GBS isolates, and since the STs of the bacteria in this lineage were not found in a large sample of human GBS obtained from diverse geographic areas (9). However, the major ST (ST-61) found in this lineage differs from the major ST of III-3 strains by only two alleles, which suggests that strains from this group may share a relatively recent common ancestor. H allele strains were found to contain previously identified III-3–specific sequence tags, which supports this hypothesis.

The identification of two III-3 strains of bovine origin and a third bovine strain (SH-96-4807) that is genetically distinct from III-3 strains but with the ST typical of III-3 strains (ST-17) supports the concept that III-3 strains share a recent common ancestor with H allele strains and retain some genetic traits necessary for bovine udder colonization. No bovine III-2 strains were identified, but a single bovine strain (NI-96-2836) appears to be related to strains in the III-2 lineage by all molecular markers (although RAPD analysis found it to be clearly distinct from human III-2 isolates). These III-3–like and III-2–like bovine strains are both in RAPD group III (Table 3) and thus appear by RAPD analysis to be more related to each other than to other major bovine lineages or to human isolates. RAPD analysis also suggests that human III-3 strains are more related to human III-2 strains than to the H allele strains, despite the observation that MLST puts human III-3 strains at a greater phylogenetic distance from III-2 strains than from the H allele strains.

The clustering together of human III-2 and III-3 isolates by RAPD analysis, despite their clear distinction by MLST, leads us to hypothesize that common genetic determinants that account for host tropism (human versus bovine) have been acquired by both the III-2 and III-3 lineages and strongly influence the clustering of isolates, as shown by RAPD analysis. If so, the two bovine isolates that closely resemble III-3 and III-2 strains by MLST, but which resemble each other more closely by RAPD analysis, may represent intermediate genotypes between GBS lineages that have a more clear-cut tropism for either humans or bovines. The exact relationship between these human and bovine lineages, and genes important for host tropism, could be clarified by comparative genomics. Such studies, along with further studies of bovine GBS lineages of other serotypes, could also provide insight into the exact relationship between human and bovine strains and help determine whether these hosts act as reservoirs for each other’s pathogenetic lineages and for the emergence of new pathogenic clones.

Dr. Bohnsack received research training at the University of Washington, in the National Institute for Allergy and Infectious Diseases Intramural Program at National Institutes of Health, Bethesda, Maryland, and at Scripps Research Institute. He began his studies of group B streptococcus shortly after joining the faculty of the University of Utah in 1988.



This study was supported by the following grants: USPHS NIH RO1 AI 40918 (J.F.B., E.E.A.); Thrasher Research Fund (J.F.B.); Cancer Center Support CORE Grant P30 CA 21765 (E.E.A.); and the American Lebanese Syrian Associated Charities (E.E.A.).



  1. Baker  CJ. Group B streptococcal infections. In: Stevens DL, Kaplan EL, editors. Streptococcal infections. Clinical aspects, microbiology, and molecular pathogenesis. New York: Oxford University Press; 2000. p. 222–37.
  2. Schuchat  A. Epidemiology of group B streptococcal disease in the United States: shifting paradigms. Clin Microbiol Rev. 1998;11:497513.PubMedGoogle Scholar
  3. Henning  KJ, Hall  EL, Dwyer  DM, Billmann  L, Schuchat  A, Johnson  JA, Invasive group B streptococcal disease in Maryland nursing home residents. J Infect Dis. 2001;183:113842. DOIPubMedGoogle Scholar
  4. Anthony  BF, Okada  DM. The emergence of group B streptococci in infections of the newborn infant. Annu Rev Med. 1977;28:35569. DOIPubMedGoogle Scholar
  5. Pattison  IH, Matthews  PRJ, Howell  DG. The type classification of group-B streptococci, with special reference to bovine strains apparently lacking in type polysaccharide. J Pathol Bacteriol. 1955;69:5160. DOIPubMedGoogle Scholar
  6. Finch  LA, Martin  DR. Human and bovine group B streptococci: two distinct populations. J Appl Bacteriol. 1984;57:2738.PubMedGoogle Scholar
  7. Martinez  G, Harel  J, Higgins  R, Lacouture  S, Daignault  D, Gottschalk  M. Characterization of Streptococcus agalactiae isolates of bovine and human origin by randomly amplified polymorphic DNA analysis. J Clin Microbiol. 2000;38:718.PubMedGoogle Scholar
  8. Wibawan  IW, Lammler  C. Properties of group B streptococci with protein surface antigens X and R. J Clin Microbiol. 1990;28:28346.PubMedGoogle Scholar
  9. Jones  N, Bohnsack  JF, Takahashi  S, Oliver  KA, Chan  MS, Kunst  F, Multilocus sequence typing system for group B streptococcus. J Clin Microbiol. 2003;41:25306. DOIPubMedGoogle Scholar
  10. Musser  JM, Mattingly  SJ, Quentin  R, Goudeau  A, Selander  RK. Identification of a high-virulence clone of type III Streptococcus agalactiae (group B Streptococcus) causing invasive neonatal disease. Proc Natl Acad Sci U S A. 1989;86:47315. DOIPubMedGoogle Scholar
  11. Takahashi  S, Detrick  S, Whiting  AA, Blaschke-Bonkowksy  AJ, Aoyagi  Y, Adderson  EE, Correlation of phylogenetic lineages of group B streptococci, identified by analysis of restriction-digestion patterns of genomic DNA, with infB alleles and mobile genetic elements. J Infect Dis. 2002;186:10348. DOIPubMedGoogle Scholar
  12. Rolland  K, Marois  C, Siquier  V, Cattier  B, Quentin  R. Genetic features of Streptococcus agalactiae strains causing severe neonatal infections, as revealed by pulsed-field gel electrophoresis and hylB gene analysis. J Clin Microbiol. 1999;37:18928.PubMedGoogle Scholar
  13. Hauge  M, Jespersgaard  C, Poulsen  K, Kilian  M. Population structure of Streptococcus agalactiae reveals an association between specific evolutionary lineages and putative virulence factors but not disease. Infect Immun. 1996;64:91925.PubMedGoogle Scholar
  14. Hedegaard  J, Hauge  M, Fage-Larsen  J, Mortenson  KK, Kilian  M, Sperling-Petersen  HU, Investigation of the translation-initiation factor IF2 gene, infB, as a tool to study the population structure of Streptococcus agalactiae. Microbiology. 2000;146:166170.PubMedGoogle Scholar
  15. Luan  SL, Granlund  M, Norgren  M. An inserted DNA fragment with plasmid features is uniquely associated with the presence of the GBSi1 group II intron in Streptococcus agalactiae. Gene. 2003;312:30512. DOIPubMedGoogle Scholar
  16. Bohnsack  JF, Takahashi  S, Detrick  SR, Pelinka  LR, Hammitt  LL, Aly  AA, Phylogenetic classification of serotype III group B streptococci on the basis of hylB gene analysis and DNA sequences specific to restriction digest pattern type III-3. J Infect Dis. 2001;183:16947. DOIPubMedGoogle Scholar
  17. Takahashi  S, Adderson  EE, Nagano  Y, Nagano  N, Briesacher  MR, Bohnsack  JF. Identification of a highly encapsulated, genetically related group of invasive type III GBS. J Infect Dis. 1998;177:11169. DOIPubMedGoogle Scholar
  18. Glaser  P, Rusniok  C, Buchrieser  C, Chevalier  F, Frangeul  L, Msadek  T, Genome sequence of Streptococcus agalactiae, a pathogen causing invasive neonatal disease. Mol Microbiol. 2002;45:1499513. DOIPubMedGoogle Scholar
  19. Ferretti  J, McShan  W, Ajdic  D, Savic  D, Savic  G, Lyon  K, Complete genome sequence of an M1 strain of Streptococcus pyogenes. Proc Natl Acad Sci U S A. 2001;98:465863. DOIPubMedGoogle Scholar
  20. Tettelin  H, Saunders  NJ, Heidelberg  J, Jeffries  AC, Nelson  KE, Eisen  JA, Complete genome sequence of Neisseria meningitidis serogroup B strain MC58. Science. 2000;287:180915. DOIPubMedGoogle Scholar
  21. Bisharat  N, Crook  DW, Leigh  J, Harding  RM, Ward  PN, Coffey  TJ, Hyperinvasive neonatal group B streptococcus has arisen from a bovine ancestor. J Clin Microbiol. 2004;42:21617. DOIPubMedGoogle Scholar
  22. Franken  C, Haase  G, Brandt  C, Weber-Heynemann  J, Martin  S, Lammler  C, Horizontal gene transfer and host specificity of beta-haemolytic streptococci: the role of a putative composite transposon containing scpB and lmb. Mol Microbiol. 2001;41:92535. DOIPubMedGoogle Scholar




Cite This Article

DOI: 10.3201/eid1008.030917

1Presented in part at the XVth Lancefield International Symposium on Streptococci and Streptococcal Diseases, October 6–11, 2002, Goa, India.

Table of Contents – Volume 10, Number 8—August 2004

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