Volume 24, Number 6—June 2018
Urban Wild Boars and Risk for Zoonotic Streptococcus suis, Spain
Urban wild boars (Sus scrofa) from Barcelona, Spain, harbor great diversity of Streptococcus suis strains, including strains with the cps2 gene and with the same molecular profile as local human cases. The increasing trend of potential effective contacts for S. suis transmission is of public health concern.
Populations of the European wild boar (Sus scrofa) have been increasing (1). The wild boar’s high adaptability to human-dominated landscapes and its increase in human tolerance have also prompted its presence in urban areas, leading to conflicts with local humans (2,3). Health risk assessment should therefore be performed in this new scenario, in which wild boars and their interactions with humans are becoming common in heavily populated areas (3).
Streptococcus suis is an emerging zoonotic pathogen (4). Among the bacterium’s 35 described serotypes, serotypes 2, 5, and 14 are those most related to human disease (4,5). Several risk factors have been associated with S. suis infection in humans, such as consumption of undercooked pig meat or work in pig-related occupations (5). The wild boar has also been identified as a source of human infection in relation to hunting activities (6). However, the increasing presence of synanthropic wild boars may also pose a novel public health risk for nonhunters. The objective of this study was to investigate the presence of S. suis strains with zoonotic potential in wild boars from the metropolitan area of Barcelona, Spain, and assess the risk of transmission to humans.
The metropolitan area of Barcelona is heavily populated (>3.2 million) and includes Collserola Natural Park, 8,000 hectares of Mediterranean forest (Figure 1). The wild boar population in this forest is ≈1,200, and habituation to humans has become common (2). A total of 108 apparently healthy wild boars were sampled in the Barcelona area for the presence of S. suis during April–November 2015; the animals had been hunted in regular campaigns, captured by box traps and euthanized for population control, or captured with the aid of anesthetic darts and euthanized because of public risk. All procedures were performed under the regulation of the competent public administrations and in compliance with current guidelines for ethical use of animals in research, following European (2010/63/EU) and Spanish (R.D. 53/2013) legislation.
At postmortem examination, we collected tonsil and nasal swab specimens from each wild boar and cultured them on chocolate agar. For each sample, a maximum of 4 presumptive S. suis colonies were subcultured and subsequently identified with a S. suis–specific gene recN PCR (7). We molecularly serotyped Streptococcus suis isolates (8) and further serotyped positive isolates for cps2 gene by coagglutination (9). We also included 2 local S. suis serotype 2 strains of human origin for molecular characterization (Table 1). The source of the infection was not identified in 1 of these 2 patients (10), but the second patient acquired the infection through an accidental cut on his hand with a tusk while manipulating a wild boar hunted 50 km from Barcelona. In the days immediately following his injury, this patient developed pain in his hand; 5 days after the injury, he sought care at an emergency department. He had fever (body temperature 39.5°C), leukocytosis (35 × 109 cells/L; reference range 3.9–10 × 109 cells/L), limited arm mobility, headache, and lethargic mental status. At this stage, the patient received diagnoses of arthritis and meningitis.
We isolated S. suis from 91 (84.3%; 95% CI 76.2%–89.9%) wild boars, identifying 332 isolates from tonsil (n = 141) and nasal (n = 191) swab specimens. We found 17 different serotypes and nontypeable strains in the wild boar population (Table 2). Three of the colonies were serotype 2, isolated from 2 wild boars, and were confirmed along with the human strains as serotype 2 by coagglutination test. We further characterized serotype 2 strains (both wild boar and human origin) using multilocus sequence typing (11) and by assessing the presence of the genes muramidase-released protein (mrp), extracellular factor (ef), and hemolysin suilysin (sly), associated with invasiveness and zoonotic potential (12). These serotype 2 strains belonged to clonal complex 1 and had the same molecular characterization (sequence type [ST] 1; cps2/mrp+/ef+/sly+), with the exception of 1 human isolate that was ST3 (a single-locus variant of ST1) (Table 1). Results from enterobacterial repetitive intergenic consensus (ERIC) PCR (13) showed a unique fingerprint profile for all serotype 2 strains and 32 different fingerprints for 36 other isolates (originating from 10 wild boars). In addition, 4 of 94 wild boars (4.3%; 95% CI 1.7%–10.4%) tested positive for detection of the cps2 gene directly in nasal swab specimens.
To evaluate the occurrence and trend of potential effective contacts between urban wild boars and humans, we examined 174 veterinary field interventions related to wild boar incidents in Barcelona during 2013–2016. We found that both the number of interventions and the percentage of interventions motivated by violent physical contacts or aggressive interactions with humans (charges, bites, or injuries) showed an increasing trend (Figure 2).
The isolation of S. suis in apparently healthy wild boars from the metropolitan area of Barcelona highlights its reservoir role and identifies this species as a potential source for human infections in urban areas. The high number of wild boars carrying S. suis confirms results obtained in a previous study, in which S. suis and S. suis–like strains were detected together through the use of a PCR for the gdh gene (14). Our results show a high diversity of S. suis serotypes, with and without pathogenic relevance for humans (4). A high percentage of isolates was nontypeable, as previously found in both domestic pig and wild boar carriers (4). These results further suggest that S. suis and serotype 2 strains are widely distributed in European wild boar populations (14).
Most human disease cases reported worldwide are associated with invasive serotype 2 strains that typically cause meningitis and, ultimately, neurologic sequelae or death (4,5). ST1, belonging to clonal complex 1, is one of the most frequent sequence types found in human and pig disease cases from Europe and other regions; it often involves the encoding virulence genes mrp, ef, and sly found in cps2-positive wild boar strains (15). Despite the high diversity of genomic fingerprints found in wild boar isolates, a unique fingerprint included all serotype 2 strains, suggesting no consistent differences between human and wild boar isolates. However, wild boars harboring cps2-positive strains were apparently healthy carriers. Other serotypes found in apparently healthy wild boars, such as 5, 9, 14, 16, and 21, have also been occasionally associated with severe human disease (4,5).
At least 7 human cases of wild boar bites were treated at the emergency department of a main local hospital (2012–2015, Communication Unit of Vall d’Hebron, Barcelona), yet small wounds not attended in health centers can be enough to acquire systemic infections (4). Human S. suis infections are associated mainly with pig farming and the food industry, being considered an occupational disease or foodborne disease in developing countries (5). The increasing trend of potential effective contacts for S. suis transmission between urban wild boars and humans in Barcelona suggests that S. suis can be acquired by humans who belong to apparently low-risk collectives.
Wild boars from the metropolitan area of Barcelona harbor S. suis strains with the same enterobacterial repetitive intergenic consensus PCR fingerprints and virulence gene profiles as invasive strains of local human origin; thus, they have zoonotic and invasive potential. The increasing interactions of wild boars with humans in urban areas pose risks for S. suis or other directly or indirectly transmitted zoonoses, making the presence of urban wild boars a public health concern.
Dr. Fernández-Aguilar is a researcher in the Wildlife Ecology and Health Group and the Servei d’Ecopatologia de Fauna Salvatge, Departament de Medicina i Cirurgia Animals, Universitat Autònoma de Barcelona, Spain. His main research interests are the ecology of infectious diseases at the wildlife–livestock interface and disease dynamics in wild animal populations.
The authors are indebted to the Generalitat de Catalunya (Serveis Territorials d’Agricultura, Ramaderia, Pesca i Alimentació a Barcelona) and the Parc Natural de Collserola for their collaboration. The authors are also grateful for the technical contribution of Sonia Lacouture from the Diagnostic Service of the University of Montreal and to the colleagues from Servei d’Ecopatologia de Fauna Salvatge who contributed to the wild boar sample collection.
This research benefited from contracts 13/051 and 15/0174 between the Universitat Autònoma de Barcelona and the Ajuntament de Barcelona. This study was also supported by Centro de Investigación Biomédica en Red (CIBER) de Enfermedades Respiratorias (CIBERES CB06/06/0037), an initiative of the Instituto de Salud Carlos III, Madrid, Spain. Xavier Fernández-Aguilar, Andreu Colom-Cadena, and Raquel Castillo-Contreras were supported by a PhD grant FI-DGR co-financed by Generalitat de Catalunya and European Social Fund (ESF).
- Massei G, Kindberg J, Licoppe A, Gačić D, Šprem N, Kamler J, et al. Wild boar populations up, numbers of hunters down? A review of trends and implications for Europe. Pest Manag Sci. 2015;71:492–500. DOIPubMedGoogle Scholar
- Castillo-Contreras R, Carvalho J, Serrano E, Mentaberre G, Fernández-Aguilar X, Colom A, et al. Urban wild boars prefer fragmented areas with food resources near natural corridors. Sci Total Environ. 2018;615:282–8. DOIPubMedGoogle Scholar
- Jansen A, Luge E, Guerra B, Wittschen P, Gruber AD, Loddenkemper C, et al. Leptospirosis in urban wild boars, Berlin, Germany. Emerg Infect Dis. 2007;13:739–42. DOIPubMedGoogle Scholar
- Goyette-Desjardins G, Auger J-P, Xu J, Segura M, Gottschalk M. Streptococcus suis, an important pig pathogen and emerging zoonotic agent-an update on the worldwide distribution based on serotyping and sequence typing. Emerg Microbes Infect. 2014;3:e45. DOIPubMedGoogle Scholar
- Huong VTL, Ha N, Huy NT, Horby P, Nghia HDT, Thiem VD, et al. Epidemiology, clinical manifestations, and outcomes of Streptococcus suis infection in humans. Emerg Infect Dis. 2014;20:1105–14. DOIPubMedGoogle Scholar
- Rosenkranz M, Elsner H-A, Stürenburg HJ, Weiller C, Röther J, Sobottka I. Streptococcus suis meningitis and septicemia contracted from a wild boar in Germany. J Neurol. 2003;250:869–70. DOIPubMedGoogle Scholar
- Ishida S, Tien HT, Osawa R, Tohya M, Nomoto R, Kawamura Y, et al. Development of an appropriate PCR system for the reclassification of Streptococcus suis. J Microbiol Methods. 2014;107:66–70. DOIPubMedGoogle Scholar
- Okura M, Lachance C, Osaki M, Sekizaki T, Maruyama F, Nozawa T, et al. Development of a two-step multiplex PCR assay for typing of capsular polysaccharide synthesis gene clusters of Streptococcus suis. J Clin Microbiol. 2014;52:1714–9. DOIPubMedGoogle Scholar
- Gottschalk M, Higgins R, Boudreau M. Use of polyvalent coagglutination reagents for serotyping of Streptococcus suis. J Clin Microbiol. 1993;31:2192–4.PubMedGoogle Scholar
- Gómez-Zorrilla S, Ardanuy C, Lora-Tamayo J, Cámara J, García-Somoza D, Peña C, et al. Streptococcus suis infection and malignancy in man, Spain. Emerg Infect Dis. 2014;20:1067–8. DOIPubMedGoogle Scholar
- King SJ, Leigh JA, Heath PJ, Luque I, Tarradas C, Dowson CG, et al. Development of a multilocus sequence typing scheme for the pig pathogen Streptococcus suis: identification of virulent clones and potential capsular serotype exchange. J Clin Microbiol. 2002;40:3671–80. DOIPubMedGoogle Scholar
- Silva LMG, Baums CG, Rehm T, Wisselink HJ, Goethe R, Valentin-Weigand P. Virulence-associated gene profiling of Streptococcus suis isolates by PCR. Vet Microbiol. 2006;115:117–27. DOIPubMedGoogle Scholar
- Versalovic J, Koeuth T, Lupski JR. Distribution of repetitive DNA sequences in eubacteria and application to fingerprinting of bacterial genomes. Nucleic Acids Res. 1991;19:6823–31. DOIPubMedGoogle Scholar
- Baums CG, Verkühlen GJ, Rehm T, Silva LMG, Beyerbach M, Pohlmeyer K, et al. Prevalence of Streptococcus suis genotypes in wild boars of Northwestern Germany. Appl Environ Microbiol. 2007;73:711–7. DOIPubMedGoogle Scholar
- Fittipaldi N, Segura M, Grenier D, Gottschalk M. Virulence factors involved in the pathogenesis of the infection caused by the swine pathogen and zoonotic agent Streptococcus suis. Future Microbiol. 2012;7:259–79. DOIPubMedGoogle Scholar
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Original Publication Date: May 03, 2018
Table of Contents – Volume 24, Number 6—June 2018
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Xavier Fernández-Aguilar, Universitat Autònoma de Barcelona, Medicina i Cirurgia Animals, Faculty of Veterinary Medicine, Edifici V, Bellaterra, 08193 Spain