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Streptococcus agalactiae serotype IV in humans and cattle, northern Europe.

Streptococcus agalactiae (group B Streptococcus) is a major cause of neonatal infectious disease in humans in many countries and is carried asymptomatically by a large proportion of adults. It is also recognized as an emerging pathogen in human adults worldwide and as a reemerging mammary pathogen of cattle in northern Europe (1-3). In adults, S. agalactiae is primarily associated with bacteremia, skin and soft tissue infections (SSTI), and urinary tract infections (UTI) and occasionally with necrotizing fasciitis, arthritis, toxic shock syndrome, endocarditis, or meningitis (4-6). Host and pathogen factors contribute to the emergence of S. agalactiae among adults (3). Among hosts, at greater risk are elderly patients and persons with chronic underlying conditions such as alcohol abuse, diabetes mellitus, or immunosuppression (2,4,6). Within the pathogen, new strains such as serotype IV may contribute to disease emergence (7,8). Considering the risk factors for S. agalactiae in nonpregnant adults and demographic changes in many countries, the incidence of group B streptococcal disease can be anticipated to increase (4).

In the 1950s, S. agalactiae was the most common mastitis-causing bacterium among dairy cattle in Europe, severely reducing milk quality and quantity. In the 1960s, development of disease control programs and introduction of legislation resulted in near eradication of S. agalactiae from several northern European countries, a situation that continued until the end of the 20th century (9). In the 21st century, farm management in northern Europe changed (e.g., fewer herds, increased average herd size, and introduction of automated milking systems). Concomitantly, the prevalence of S. agalactiae in bovine milk increased. In Denmark, in the first years of the 21st century, the proportion of S. agalactiae--positive herds tripled (1,9). Similar phenomena have been described for Sweden and Norway (1).

The presence of S. agalactiae in humans and cattle raises the question of whether interspecies transmission occurs. This question is particularly pertinent in light of the emergence of S. agalactiae disease in adult humans and its reemergence in cattle. Several comparisons of S. agalactiae in humans and cattle have been published, and most authors conclude that isolates from these species form largely distinct populations with regard to the core genome and the accessory genome (10-12). Ideally, assessment of the potential for interspecies transmission is based on the analysis of contemporaneous, sympatric isolates. With 1 exception (13), however, most comparative studies were not based on isolates from the same geographic region and the same period, or, if they were, they covered a very limited number of S. agalactiae-positive farms or animals (14,15). Our aim with this study was to provide insight into the hazard of interspecies transmission of S. agalactiae by comparing contemporaneous populations of S. agalactiae from humans and dairy cattle in Finland and Sweden.

Materials and Methods


A total of 81 isolates were collected at the Seinajoki Central Hospital in the rural South Ostrobothnia district of Finland (2011, 2012) and from epidemiologically unrelated persons by the Department of Clinical Microbiology, University Hospital, Uppsala, in an urban area of Sweden (2012, 2013). Isolates originated from 12 patients with invasive disease (sepsis or meningitis), 37 with UTI, and 15 with SSTI and from 17 healthy carriers who were screened during pregnancy by use of vaginal swab or cervical fluid samples. Isolates represented a convenience sample that covered both sexes and all age classes (online Technical Appendix Figure 1, Data were not collected with regard to farm or animal contact or dietary exposure.

During 2010-2012, a total of 108 isolates from cattle were collected by the laboratory of Valio Ltd, Helsinki, Finland (63 isolates from 29 herds) and by the National Veterinary Institute, Uppsala, Sweden (45 isolates from 45 herds). Isolates were cultured from individual cow or quarter milk samples from animals with suspected intramammary infection with or without clinical signs. In both countries, samples originated from most of the major dairy regions (online Technical Appendix Figure 2). For 9 herds in Finland, isolates from multiple cows were available and 2-14 isolates/herd were used to assess within-herd strain heterogeneity (online Technical Appendix Table 1). For the remaining herds, 1 isolate was used.

Phenotypic identification was based on colony morphology on blood agar, CAMP (Christie, Atkins, Munch-Peterson) reaction, and Lancefield grouping (15). Before use, isolates were stored at -80[degrees]C in brain-heart infusion broth (Oxoid, Basingstoke, UK) with 15% glycerol. After culture on blood agar, purity was checked and 1 colony was used to confirm species identity by PCR with primers STRA-AgI (5'-AAGGAAACCTGCCATTTG-3') and 5'-STRA-AgII (TTAACCTAGTTTCTTTAAAACTAGAA-3'). DNA extracts for molecular typing were prepared from overnight cultures in brain-heart infusion broth by using a DNeasy Blood & Tissue Kit (QIAGEN, Manchester, UK). Species confirmation, multilocus sequence typing (MLST), and serotyping were conducted for all isolates. Pilus island (PI) typing and lactose typing were conducted for all isolates from humans and 1 isolate from a bovid per sequence type (ST) per herd.


MLST was performed by using standard primers and HiMLST or Sanger sequencing of purified PCR amplicons (16,17). Alleles and STs were assigned by using the S. agalactiae database ( (18). New alleles were submitted to the database curator for quality control and allocation of allele numbers and STs. Novel allele combinations were also submitted for ST assignment.

Molecular Serotyping

For detection of molecular serotype (MS) II and MS IV, duplex PCR was used, and for detection of MS V, VI, VII, and VIII, multiplex PCR was used (19). PCR reactions for MS Ia, Ib, and III were run individually by using primers for MS Ia and Ib (19) and primers IIIcpsHS and IIIcpsHA for MS III (20). For all reactions, cycling conditions were 94[degrees]C (5 min), followed by 40 cycles of 94[degrees]C (60 s), 55[degrees]C (60 s), and 72[degrees]C (60 s) with final extension at 72[degrees]C (5 min). Each isolate was submitted to all molecular serotyping reactions to identify potential cross-reactivity.

PI Typing

Multiplex PCR was used to screen for presence of sag647 (PI-1), sag1406 (PI-2a), and san1517 (PI-2b); the housekeeping gene adhP was used as amplification control (11). Isolates that were negative for PI-1 were tested for presence of an intact integration site. Detection of a 684-bp amplicon indicates presence of an intact site, and absence of the amplicon indicates occupation by an alternative, uncharacterized genetic element. Isolates that were positive for PI-2a or PI-2b were further characterized by Pi-specific PCR-based restriction fragment length polymorphism analysis to detect allelic variation in the PI-2a adhesin gene (gbs59) and the PI-2b backbone protein (san1519) (11).

Lactose Typing

To detect lactose fermentation, we inoculated a single colony into phenol red broth (neutralized soya peptone with beef extract; Oxoid), supplemented with phenol red and [alpha] lactose (L2643; Sigma-Aldrich, Gillingham, UK). Broth was incubated at 37[degrees]C without shaking and was checked for change from red to yellow at 24 h, 48 h, and 7 days after inoculation. PCR was used to screen for presence of an [approximately equal to] 2.5-kbp region of lacEFG, which is part of the Lac.2 operon that encodes lactose fermentation (21).

Data Analysis

Comparisons of categorical variables were conducted in Statistix 10 (Analytical Software, Tallahassee, FL, USA) with use of the Fisher exact or Pearson [chi square] test, as appropriate. Global eBURST analysis was performed by using PHYLOViZ (22); double-locus variants were included in eBURST groups.



All isolates were confirmed as S. agalactiae and 33 STs were identified. Isolates from humans belonged to 16 allelic profiles, including 2 new profiles derived from isolates from patients with invasive disease in Sweden. Both profiles were single-locus variants (SLVs) of known STs, with ST751 based on a new combination of known alleles, whereas the second profile was based on a new atr allele with an internal deletion (ST not assigned). ST1 was most common, followed by ST19 and ST12 (21, 14, and 10 isolates, respectively). All STs were found in isolates from patients in at least 2 age groups and from 2 clinical sample types (online Technical Appendix Figure 3).

Among 108 isolates from cattle, 22 STs were identified, including 12 new STs (5 from Finland, 7 from Sweden). The proportion of new STs was higher among isolates from cattle than from humans (54.5% vs. 12.5%, respectively; Pearson [chi square] = 4.7, df = 1, p = 0.03). A total of 3 new STs (ST632, ST633, ST726) were detected in multiple herds, whereas the remaining new STs (ST634-636, ST722-725, ST727, ST728) were each obtained from 1 herd. All were SLVs of known STs with 1 new allele. For 9 herds, >1 isolate was available and isolates within a herd belonged to a single ST, with 1 exception in which ST1 and its SLV ST635 were detected (online Technical Appendix Table 1). Both isolates from this herd were included in herd-level analysis and comparison between host species. In herd-level analysis of 74 isolates, ST1 was most common, followed by ST103 and ST196 (20, 10, and 8 herds, respectively; online Technical Appendix Table 2). We found no significant association between ST and country of origin.

Of 33 STs in this study, 5 were detected in both host species (Figure 1). ST1 was the most common shared ST, followed by ST23, ST196, ST12, and ST8 (41, 12, 12, 11, and 7 isolates, respectively). More than half (84) of the 155 isolates (54.2%) belonged to shared STs. Of 5 shared STs, 4 were represented by >10 isolates compared with 2 of 28 host-specific STs (p<0.001 by Fisher exact test). Using global eBURST, we identified 6 clusters, 2 of which were host specific (i.e., ST17 from humans and a cluster around ST103 from cattle). Both host-specific clusters included isolates from both countries (Figure 1).

Molecular Serotyping

Among isolates from humans, MS Ia, Ib, and II-VI were identified. Among isolates from cattle, 2 did not yield conclusive molecular serotyping results. Among the remaining isolates from cattle, MS Ia, Ib, II-V, and VII were identified. We found strong correlation between MS and ST (Table; online Technical Appendix Figure 4). For STs found in both host species, MS did not differ between isolates from humans or cattle, with the exception of ST23: isolates from humans belonged to MS Ia and those from cattle to MS Ia or III (Table).

PI Typing

We identified 5 PI profiles (Figure 2; online Technical Appendix Figure 5). Among PI-1-negative isolates, the integration site was intact in 14 of 19 isolates from humans and in 8 of 23 isolates from cattle (74% vs. 35%, [chi square] = 6.31, df = 1, p = 0.01). Within host-ST combinations, results for PI-1 and occupation of the integration site were consistent across isolates (online Technical Appendix Table 2). Across both host species, 1 PI-2a allele was identified in ST1, ST8, and ST196, respectively. ST12 included 2 PI2a alleles among isolates from humans (Figure 2). Within ST23, PI-2a alleles were MS specific. One combination was identified in both host species, and 1 was limited to cattle (Figure 2). PI-2b and PI-1 were present in all ST17 isolates (from humans) and 1 ST724 isolate (from cattle), and PI-2b alone was present in isolates with cattle-specific STs (online Technical Appendix Figure 5). One PI-2b allele was found in ST632, and a second allele was found across the entire bovine-specific eBURST cluster.

Lactose Typing

Of 81 isolates from humans and 73 isolates from cattle, lactose was fermented by 3 (3.7%) and 73 (100%), respectively ([chi square] = 142, df = 1, p<0.001). One isolate from cattle was nonviable and hence not tested. Of 81 isolates from humans, 2 (2.5%) were positive for lacEFG compared with 69 (94.5%) of 73 isolates from cattle ([chi square] = 131, df = 1, p<0.0001). Discrepancies between phenotype and genotype were confirmed by repeating culture, DNA extraction, and phenotypic and genotypic testing. Genotypic results that were atypical for the host species were observed only in STs that were found in both host species (i.e., in ST1, ST23, and ST196) (Figure 3).


In contrast to results of previous studies (11,12), our results showed no clear distinction between subpopulations of S. agalactiae from humans or cattle according to MLST, molecular serotyping, or PI typing. With few exceptions (13,14), previous comparative studies were not based on contemporaneous, sympatric isolates across host species. Our study showed that [approximately equal to] 54% of isolates belonged to a population that affects both host species. The convenience sample used may not be fully representative of the distribution of STs across the human population in those countries, and invasive isolates were obtained only from Sweden, but no significant clustering by country or clinical manifestation was observed, suggesting that the observed ST distribution is broadly indicative of the most common types.

The most prevalent shared ST was ST1. Its presence in cattle from several countries has been described, but high prevalence among cattle has been reported in Denmark only (11,12,23). Serotype V and PI type 1/2a were predominant in ST1 from both host species, a finding that agrees with findings from previous studies (11,24). Surprisingly, ST196 was the second most common shared ST (equally with ST23), and all carried MS IV. Reports of ST196 and serotype IV used to be rare; only 1 of 158 isolates collected in Sweden over a 10-year period (1988-1997) belonged to ST196, but they are now recognized as emerging human pathogens (7,8,25). Furthermore, emergence of new STs with MS IV in humans, such as ST459, has been described (7,8). We describe the emergence of a new MS IV strain in cattle, ST723, in multiple dairy herds in Sweden. The relatively common occurrence of ST196 and its SLVs in cattle in the Nordic countries (this study; 26) suggests that cattle may serve as a reservoir for MS IV strains, although our study does not provide evidence for the direction or likelihood of potential transmission between host species.

ST23 affects many host species (12,27). In humans, it is more commonly associated with carriage than with infection (16,24), although all ST23 in our study originated from infections. Most ST23 from humans have serotype Ia, and it has been suggested that serotype III originated in cattle, but the association between host and serotype is not absolute (16,23,24). In our collection, ST23 from humans was associated with MS Ia, whereas isolates from cattle were associated with MS Ia or MS III. PI profiles for ST23 matched those described for other countries (11). ST8, which was found across countries and species, and ST12, which was limited to Finland but isolated from both host species, have also been associated with carriage and invasive disease in humans, albeit at lower frequency than ST1 or ST23 (16,24,25). ST8 from both hosts had MS 1b and carried PI-1/2a, as previously described for isolates from humans (11,28). ST12 isolates from our study were associated with MS II, regardless of host species, and mostly carried PI-1/2a. This pattern matches reports of isolates from humans, although ST12 from humans may occasionally have serotype Ib (11,28).

The shared pathogen population may result from transmission between host species or shared exposure to an external source. Potential routes of transmission from cattle to humans include direct contact, exposure to cattle feces, and consumption of cows' milk. Potential routes of transmission from humans to cattle include direct contact and indirect exposure to excreta from humans. In one prospective study, increased frequency of cattle exposure was associated with human colonization with S. agalactiae, although fecal colonization was detected in 1 cow only (14). The prevalence of fecal colonization on individual farms can be high (26), but gastrointestinal carriage is much more widespread among humans (16,29), which argues against exposure to cattle feces as a dominant reservoir for human colonization. Case reports and phenotyping of isolates show that raw milk consumption may lead to colonization of the human throat (30). This route may be of public health relevance in countries where milk is frequently consumed raw (e.g., Colombia) but not in countries where milk is routinely pasteurized (e.g., Europe and most of North America). In studies conducted in the United States, no significant association has been detected between consumption of milk and colonization of humans (29,31).

Several lines of evidence suggest that humans may be a source of infection for cattle. Experimental intramammary challenge of cattle with isolates of S. agalactiae from humans resulted in mastitis, although the duration of intramammary infection and hence the window of opportunity for transmission was less than that for infection with isolates from cattle (32). Similar observations have been made for naturally occurring bovine mastitis, whereby incidental cases in dairy herds were caused by strains that were otherwise predominantly found in humans (33). Epidemiologic studies also support the role of S. agalactiae sources other than cattle because introduction of the pathogen into dairy herds can often not be attributed to purchase of cattle, implying that alternative sources must exist (9). Some onfarm studies suggest that treatment of human oropharyngeal S. agalactiae carriers is a crucial step for eliminating S. agalactiae from dairy herds (34). Considering the frequent colonization of the human throat, gut, and urogenital tract with the shared STs observed in this study and the direct contact between human hands and the bovine mammary gland during milking, with or without use of gloves, a plausible mechanism for human-to-cattle transmission exists. The main difficulty in determining directionality of transmission between host species is establishing the order of events (i.e., which host species was positive first). Furthermore, efforts to detect alternative, potentially shared sources of S. agalactiae are limited by the preconceived but mistaken notion that S. agalactiae is an obligate intramammary pathogen in dairy cattle. Potentially shared sources include wastewater and surface water, including effluent from sewage treatment plants (27,35,36). Potential routes of within- and between-host species transmission, including horizontal and vertical transmission among humans (12,31,37) and contagious transmission among cattle via milking machines (12,26), are summarized in online Technical Appendix Figure 6.

Alternatively, the co-occurrence of STs in both host species may not be the result of ongoing interspecies transmission but rather that of incidental spillover, with subsequent adaptation and dissemination within the new host, leading to parallel circulation of populations that have the same ST but encode host-specific adaptations elsewhere in the genome. This chain of events has been described for Staphylococcus aureus (38). Among S. agalactiae isolates from cattle, >90% are lactose fermenters, whereas the reverse is true among isolates from humans, providing an example of a host adaptation mechanism (10,23). The genes targeted by our PCR, lacEFG, form part of the Lac.2 operon, which is located on an integrative conjugative element and forms part of the S. agalactiae mobilome (10). Regulation of the S. agalactiae mobilome is a relatively new area of study (39); little is known about its contribution to host adaptation or interspecies transmission. Atypical combinations (i.e., lacEFG-positive isolates from humans and lacEFG-negative isolates from cattle) belonged to STs that are shared across host species, potentially indicating recent transmission events.

In our study, 2 STs occurred frequently but in only 1 host species. ST19 was commonly detected in humans but not in cattle. ST19 is generally rare in cattle, although its association with humans is not absolute (11,12). Conversely, ST103 was commonly found in cattle in our study and in Denmark, Norway, and China (12,26,40) but not in isolates from humans in our study or those mentioned in any of the references cited. ST103 and its SLVs were invariably associated with serotype Ia (40) and PI-2b (online Technical Appendix Figure 5). We detected 4 new STs in the eBURST cluster around ST103, indicating ongoing evolution of this cattle-specific subpopulation. Those STs, and all other new STs detected in this study, were SLVs of known STs. The fact that all new STs were limited to 1 country and that they were SLVs of existing STs indicates that we still observe local microevolution but that we are starting to exhaust the variability in the S. agalactiae population.

In summary, according to MLST, molecular serotyping, and PI typing of contemporaneous S. agalactiae isolates from humans and cattle in Finland and Sweden, we identified 3 subpopulations: 1 from humans, 1 from cattle, and 1 from both hosts. The latter subpopulation accounted for more than half of the isolates, implying that the host species barrier separating S. agalactiae from both species may be more porous than previously thought. For STs commonly carried by humans (e.g., ST1 and ST23), the direction of transmission, if any, may be from humans to cattle. ST196/MS IV was relatively common among cattle, which may potentially constitute a reservoir of this recently recognized emerging pathogen of humans. The only characteristic that differentiated most isolates from the 2 species in this study was the ability to ferment lactose, which is encoded in the mobilome. Considering the new evidence for potential interspecies transmission of S. agalactiae, its emergence in adult humans and its reemergence in cattle, further studies into the mechanisms and frequency of transmission and host adaptation seem warranted.


We thank Charlotta Fasth and Asa Melhus for providing the bacterial isolates from Sweden, Vince Richards for help with lactose typing, Shannon Manning for help with PI typing, and Ann-Kristin Nyman for production of the map.

This study was financially supported by the Ministry of Agriculture and Forestry, Finland, through project no. 2500/31/2009, "S. agalactiae-an increasing risk for dairy herds in loose housing systems."

Ms. Lyhs is head of the Section for Bacteriology and Pathology at the National Veterinary Institute of the Technical University of Denmark. Her research interests include microbiology, food hygiene and safety, the health of production animals, and zoonotic bacterial diseases.


(1.) Katholm J, Bennedsgaard TW, Koskinen MT, Rattenborg E. Quality of bulk tank milk samples from Danish dairy herds based on real-time polymerase chain reaction identification of mastitis pathogens. J Dairy Sci. 2012; 95:5702-8. jds.2011-5307

(2.) Lambertsen L, Ekelund K, Skovsted IC, Liboriussen A, Slotved HC. Characterisation of invasive group B Streptococci from adults in Denmark 1999 to 2004. Eur J Clin Microbiol Infect Dis. 2010; 29:1071-7.

(3.) Skoff TH, Farley MM, Petit S, Craig AS, Schaffner W, Gershman K, et al. Increasing burden of invasive group B streptococcal disease in nonpregnant adults, 1990-2007. Clin Infect Dis. 2009; 49:85-92.

(4.) Sendi P, Johansson L, Norrby-Teglund A. Invasive group B streptococcal disease in non-pregnant adults: a review with emphasis on skin and soft-tissue infections. Infection. 2008; 36:100-11.

(5.) Sendi P, Christensson B, Ujkay I, Trampuz A, Achermann Y, Boggian K, et al.; GBS PJI Study Group. Group B Streptococcus in prosthetic hip and knee joint-associated infections. J Hosp Infect. 2011; 79:64-9.

(6.) Sunkara B, Bheemreddy S, Lorber B, Lephart PR, Hayakawa K, Sobel JD, et al. Group B Streptococcus infections in non-pregnant adults: the role of immunosuppression. Int J Infect Dis. 2012; 16:e182-6.

(7.) Diedrick MJ, Flores AE, Hillier SL, Creti R, Ferrieri P. Clonal analysis of colonizing group B Streptococcus, serotype IV, an emerging pathogen in the United States. J Clin Microbiol. 2010; 48:3100-4.

(8.) Teatero S, McGeer A, Li A, Gomes J, Seah C, Demczuk W, et al. Population structure and antimicrobial resistance of invasive serotype IV group B Streptococcus, Toronto, Ontario, Canada. Emerg Infect Dis. 2015; 21:585-91. eid2014.140759

(9.) Mweu MM, Nielsen SS, Halasa T, Toft N. Annual incidence, prevalence and transmission characteristics of Streptococcus agalactiae in Danish dairy herds. Prev Vet Med. 2012; 106:244-50.

(10.) Richards VP, Lang P, Bitar PD, Lefebure T, Schukken YH, Zadoks RN, et al. Comparative genomics and the role of lateral gene transfer in the evolution of bovine adapted Streptococcus agalactiae. Infect Genet Evol. 2011; 11:1263-75.

(11.) Springman AC, Lacher DW, Waymire EA, Wengert SL, Singh P, Zadoks RN, et al. Pilus distribution among lineages of group B Streptococcus: an evolutionary and clinical perspective. BMC Microbiol. 2014; 14:159.

(12.) Zadoks RN, Middleton JR, McDougall S, Katholm J, Schukken YH. Molecular epidemiology of mastitis pathogens of dairy cattle and comparative relevance to humans. J Mammary Gland Biol Neoplasia. 2011; 16:357-72.

(13.) Sukhnanand S, Dogan B, Ayodele MO, Zadoks RN, Craver MP, Dumas NB, et al. Molecular subtyping and characterization of bovine and human Streptococcus agalactiae isolates. J Clin Microbiol. 2005; 43:1177-86. JCM.43.3.1177-1186.2005

(14.) Manning SD, Springman AC, Million AD, Milton NR, McNamara SE, Somsel PA, et al. Association of group B Streptococcus colonization and bovine exposure: a prospective cross-sectional cohort study. PLoS One. 2010; 5:e8795.

(15.) Oliveira IC, de Mattos MC, Pinto TA, Ferreira-Carvalho BT, Benchetrit LC, Whiting AA, et al. Genetic relatedness between group B streptococci originating from bovine mastitis and a human group B Streptococcus type V cluster displaying an identical pulsed-field gel electrophoresis pattern. Clin Microbiol Infect. 2006; 12:887-93.

(16.) Jones N, Bohnsack JF, Takahashi S, Oliver KA, Chan MS, Kunst F, et al. Multilocus sequence typing system for group B Streptococcus. J Clin Microbiol. 2003; 41:2530-6.

(17.) Boers SA, van der Reijden WA, Jansen R. High-throughput multilocus sequence typing: bringing molecular typing to the next level. PLoS One. 2012; 7:e39630. journal.pone.0039630

(18.) Jolley KA, Chan MS, Maiden MC. mlstdbNet-distributed multi-locus sequence typing (MLST) databases. BMC Bioinformatics. 2004; 5:86.

(19.) Poyart C, Tazi A, Reglier-Poupet H, Billoet A, Tavares N, Raymond J, et al. Multiplex PCR assay for rapid and accurate capsular typing of group B streptococci. J Clin Microbiol. 2007; 45:1985-8.

(20.) Kong F, Ma L, Gilbert GL. Simultaneous detection and serotype identification of Streptococcus agalactiae using multiplex PCR and reverse line blot hybridization. J Med Microbiol. 2005; 54:1133-8.

(21.) Richards VP, Choi SC, Pavinski Bitar PD, Gurjar AA, Stanhope MJ. Transcriptomic and genomic evidence for Streptococcus agalactiae adaptation to the bovine environment. BMC Genomics. 2013; 14:920.

(22.) Francisco AP, Vaz C, Monteiro PT, Melo-Cristino J, Ramirez M, Carrico JA. PHYLOViZ: phylogenetic inference and data visualization for sequence based typing methods. BMC Bioinformatics. 2012; 13:87.

(23.) Sorensen UB, Poulsen K, Ghezzo C, Margarit I, Kilian M. Emergence and global dissemination of host-specific Streptococcus agalactiae clones. MBio. 2010; 1:e00178-10.

(24.) Manning SD, Springman AC, Lehotzky E, Lewis MA, Whittam TS, Davies HD. Multilocus sequence types associated with neonatal group B streptococcal sepsis and meningitis in Canada. J Clin Microbiol. 2009; 47:1143-8. JCM.01424-08

(25.) Luan SL, Granlund M, Sellin M, Lagergard T, Spratt BG, Norgren M. Multilocus sequence typing of Swedish invasive group B Streptococcus isolates indicates a neonatally associated genetic lineage and capsule switching. J Clin Microbiol. 2005; 43:3727-33.

(26.) Jorgensen HJ, Nordstoga AB, Sviland S, Zadoks RN, Solverod L, Kvitle B, et al. Streptococcus agalactiae in the environment of bovine dairy herds-rewriting the textbooks? Vet Microbiol. 2016; 184:64-72. vetmic.2015.12.014

(27.) Delannoy CM, Crumlish M, Fontaine MC, Pollock J, Foster G, Dagleish MP, et al. Human Streptococcus agalactiae strains in aquatic mammals and fish. BMC Microbiol. 2013; 13:41.

(28.) Manning SD, Lewis MA, Springman AC, Lehotzky E, Whittam TS, Davies HD. Genotypic diversity and serotype distribution of group B Streptococcus isolated from women before and after delivery. Clin Infect Dis. 2008; 46:1829-37.

(29.) Bliss SJ, Manning SD, Tallman P, Baker CJ, Pearlman MD, Marrs CF, et al. Group B Streptococcus colonization in male and nonpregnant female university students: a cross-sectional prevalence study. Clin Infect Dis. 2002; 34:184-90.

(30.) Brglez I. A contribution to the research of infection of cows and humans with Streptococcus agalactiae. Zentralbl Bakteriol Mikrobiol Hyg B. 1981; 172:434-9.

(31.) Foxman B, Gillespie BW, Manning SD, Marrs CF. Risk factors for group B streptococcal colonization: potential for different transmission systems by capsular type. Ann Epidemiol. 2007; 17:854-62.

(32.) Jensen NE. Experimental bovine group-B streptococcal mastitis induced by strains of human and bovine origin. Nord Vet Med. 1982; 34:441-50.

(33.) Dogan B, Schukken YH, Santisteban C, Boor KJ. Distribution of serotypes and antimicrobial resistance genes among Streptococcus agalactiae isolates from bovine and human hosts. J Clin Microbiol. 2005; 43:5899-906.

(34.) Nielsen AL. Group B streptococci in humans as a cause of bovine mastitis [in Danish]. Danish Vet J. 1987; 70:154-7.

(35.) Jensen AN, Berg B. Wastewater and aquatic biotopes are potential reservoirs of group B streptococci. [in Danish]. Danish Veterinary Journal. 1982; 65:197-200.

(36.) Jafar QA, Sameer AZ, Salwa AM, Samee AA, Ahmed AM, Al-Sharifi F. Molecular investigation of Streptococcus agalactiae isolates from environmental samples and fish specimens during a massive fish kill in Kuwait Bay. Pak J Biol Sci. 2008; 11:2500-4.

(37.) Phares CR, Lynfield R, Farley MM, Mohle-Boetani J, Harrison LH, Petit S, et al.; Active Bacterial Core surveillance/Emerging Infections Program Network. Epidemiology of invasive group B streptococcal disease in the United States, 1999-2005. JAMA. 2008; 299:2056-65.

(38.) Spoor LE, McAdam PR, Weinert LA, Rambaut A, Hasman H, Aarestrup FM, et al. Livestock origin for a human pandemic clone of community-associated methicillin-resistant Staphylococcus aureus. MBio. 2013; 4:e00356-13.

(39.) Lopez-Sanchez MJ, Sauvage E, Da Cunha V, Clermont D, Ratsima Hariniaina E, Gonzalez-Zorn B, et al. The highly dynamic CRISPR1 system of Streptococcus agalactiae controls the diversity of its mobilome. Mol Microbiol. 2012; 85:1057-71.

(40.) Yang Y, Liu Y, Ding Y, Yi L, Ma Z, Fan H, et al. Molecular characterization of Streptococcus agalactiae isolated from bovine mastitis in eastern China. PLoS One. 2013; 8:e67755.

Author affiliations: University of Helsinki, Seinajoki, Finland (U. Lyhs); Valio Ltd., Helsinki, Finland (L. Kulkas); SEGES (formerly Knowledge Centre for Agriculture), Aarhus, Denmark (J. Katholm); National Veterinary Institute, Uppsala, Sweden (K. Persson Waller); Central Hospital, Seinajoki (K. Saha); University of Glasgow, Glasgow, Scotland, UK (R.J. Tomusk, R.N. Zadoks); Moredun Research Institute, Penicuik, Scotland, UK (R.N. Zadoks)

DOI: 10.3201/eid2212.151447

Ulrike Lyhs, [2] Laura Kulkas, Jorgen Katholm, [3] Karin Persson Waller, Kerttu Saha, Richard J. Tomusk, Ruth N. Zadoks

[1] Preliminary results from this study were presented at the 25th European Congress of Clinical Microbiology and Infectious Diseases; April 24-28, 2015; Copenhagen, Denmark.

[2] Current affiliation: Danish Technical University, Copenhagen, Denmark.

[3] Current affiliation: DNA Diagnostic A/S, Risskov, Denmark.

Address for correspondence: Ruth N. Zadoks, Institute for Biodiversity, Animal Health and Comparative Medicine, College of Medical, Veterinary and Life Sciences, Jarrett Building, University of Glasgow, Glasgow G61 1QH, Scotland, UK; email:

Table. Streptococcus agalactiae isolates from humans and cattle,
Finland and Sweden, 2010-2013 *

Molecular           No. isolates from humans/cattle
             ST1    ST8   ST12   ST23   ST196   Other

Ia           1/0    --     --    7/2     --      1/3
Ib           --     4/3    --     --     --      1/0
II           1/0    --    10/1    --     --      2/1
III          --     --     --    0/2     --      1/4
IV           --     --     --     --     4/8     2/1
V           18/19   --     --     --     --      1/4
Other        1/1    --     --    0/1     --      --

Molecular   No. isolates from humans only
            ST17   ST19   ST28   ST144

Ia           --     --     --      6
Ib           --     --     --     --
II           --     1      3      --
III          4      13     --     --
IV           --     --     --     --
V            --     --     --     --
Other        --     --     --     --

Molecular          No. isolates from cattle only
            ST10   ST103   ST314   ST633   ST726

Ia           --     10       3       3      --
Ib           1      --      --      --      --
II           3      --      --      --      --
III          --     --      --      --      --
IV           --     --      --      --       3
V            --     --      --      --      --
Other        1      --      --      --      --

* ST, sequence type; --, no isolates.


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Author:Lyhs, Ulrike; Kulkas, Laura; Katholm, Jorgen; Waller, Karin Persson; Saha, Kerttu; Tomusk, Richard J
Publication:Emerging Infectious Diseases
Date:Dec 1, 2016
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