SciELO - Scientific Electronic Library Online

 
vol.36 número3Sistema de gestión de la calidad en laboratorios de diagnóstico veterinarioReporte de Aethina tumida Murray (Coleoptera, Nitidulidae) en colonias de la abeja sin aguijón Melipona beecheii Bennett de Matanzas y Mayabeque índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

  • No hay articulos citadosCitado por SciELO

Links relacionados

  • No hay articulos similaresSimilares en SciELO

Compartir


Revista de Salud Animal

versión impresa ISSN 0253-570X

Rev Salud Anim. vol.36 no.3 La Habana sep.-dic. 2014

 

SHORT COMMUNICATION

 

Serotyping of porcine Streptococcus suis recovered from diseased pigs in the western region of Cuba

 

Serotipificación de Streptococcus suis porcinos recobrados de cerdos enfermos en la región occidental de Cuba

 

 

Ivette EspinosaI, Michel ÁreasI, María Irian PercedoI, Evelyn LoboI, Siomara MartínezI, Marcelo GottschalkII

IDepartment of Microbiology, National Centre for Animal and Plant Health (CENSA), San José de las Lajas, Mayabeque, Cuba.
II
Groupe de Recherche sur les Maladies Infectieuses du Porc and Centre de Recherche en Infectiologie Porcine, Faculte de Medecine Veterinaire, Université de Montreal, St-Hyacinthe, Qc, J2S 2M2, Canada.

 

 


ABSTRACT

Streptococcus suis is an important swine pathogen in most countries with intensive swine production. S. suis has also been isolated in humans and other animal species. Data regarding serotyping of S. suis isolates from diseased pigs in Cuba using a reference antiserum are not available. S. suis isolates from pigs of four farms located in the western region of Cuba were characterized by serotyping. Most of the isolates was collected from pigs with pneumonia, followed by arthritis cases. Serotypes 2, 4, 8, 15, 16 and 34 were found in isolates from diseased pigs during the period 2002-2008, while serotypes 1, ½, 2, 3, 9, 13, 23, 24 and 31were found from samples collected during 2009-2014. Serotype 2 recovered from systemic (arthritis) and localized (pneumonia) infections was the most frequent. This research sets the basis for more complete studies on the infection status of S. suis in Cuba.

Key words: swine, Streptococcus suis, serotype.


RESUMEN

Streptococcus suis es uno de los patógenos de mayor importancia que afecta la crianza porcina en los países que se basan en sistemas de producción intensiva. S. suis se ha aislado en humanos y en otras especies de animales. En Cuba no existen datos con respecto a los serotipos existentes de S. suis. En este trabajo se realizó la serotipificación de aislados de S. suis procedentes de cerdos de cuatro granjas localizadas en la región occidental de Cuba. La mayor cantidad de aislados se obtuvo de animales con neumonía, seguidos por casos de artritis. Los serotipos 2, 4, 8, 15, 16 y 34 se encontraron en muestras procedentes de animales enfermos en el periodo 2002-2008, mientras que los serotipos 1, ½, 2, 3, 9, 13, 23, 24, 31 se encontraron en muestras colectadas en el período 2009 -2014. El serotipo 2 fue el más frecuente y se recobró de la infección localizada (neumonía) y de la sistémica (artritis). Esta investigación establece las bases para los estudios sobre el estado de la infección por S. suis en Cuba.

Palabras clave: cerdos, Streptococcus suis, serotipo.


 

 

Streptococcal diseases are a worldwide problem for the swine industry. In most parts of the world, S. suis is the predominant agent of streptococcal infections, and it is associated with a variety of diseases including meningitis, septicemia, arthritis, endocarditis, and pneumonia (1). In addition to swine, S. suis has also been isolated from humans and other mammalian (wild boars, horses, dogs, cats) and avian species (2, 3). Thirty-five serotypes of S. suis have been characterized, and serotype 2 has been the most virulent type to swine and humans (4,5).

Serotype specificity of S. suis is determined by the capsular polysaccharide present on its surface (6). The cps loci of all the serotypes have been sequenced (7). Based on serotype-specific genes in the cps locus, rapid, sensitive and specific PCR assays have been described (8, 9, 10, 11). A recent study at our laboratory identified two capsular types by using specific primers to cps2 and cps9 (12). However, due to the fact that the serotypes 1/2 and 2 share gene sequences, the reported PCR assays described to date are unable to distinguish between them (9). For that reason, it is necessary a serological assay to corroborate the detection of isolates belonging to serotype 2.The purpose of the present work was to provide data on the presence of different serotypes of S. suis recovered from diseased pigs in Cuba.

A collection of 41 S. suis isolates was investigated in this study. The samples were obtained from four farms located in different regions of Cuba. Isolation and identification of S. suis was performed at laboratories of the National Centre for Animal and Plant Health (CENSA) over a 12 year period (2002-2014). Isolates were recovered in pure culture or as predominant bacteria from lungs with gross abnormalities (n=34), from animals with abscess in joints (n=3) and spleen (n=1), from different organs of an aborted fetus (n=1), and vagina discharge (n =2). Origin, type of production, and the number of isolate of each year are shown in Table 1. Each isolate was chosen according to the following criteria: the isolates originated from different site of isolation as well as the same farm and date of collection were considered as one isolate and conserved when at least three out of 10 animals were positive.

Appropriate amounts of materials from infected organs or swabs were aseptically transferred to the surface of a Columbia agar plate (Oxoid, LTD, Basingstone, Hampshire, UK) supplemented with 5% bovine blood. The plates were incubated aerobically at 37oC and inspected for growth after 24 and 48h. Colonies 1-2 mm in diameter showing alpha-hemolysis were suspected of being potentially S. suis. If Gram staining showed Gram positive cocci in pairs or chains, isolates were biochemically typed using the API 20 STREP test kit (Bio Mérieux, L´etoile,France) and further confirmed as S. suis by a species-specific PCR assay (13).

For the coagglutination test used for serotyping, S. suis isolates were grown overnight in 5 ml of Todd Hewitt broth (Sigma-Aldrich, NichtDirektem, Sonnenlicht). The culture was centrifuged at 3000 rpm for 15 min and resuspended in saline solution (0.9%). The coagglutination test using rabbit hyperimmune sera and a reference panel of all 35 S. suis serotypes was performed as previously described (6, 14). Based on capsular typing, we confirmed that different serotypes of S. suis are circulating among swine herds located in different region of Cuba. From this small scale survey, fourteen serotypes (1, ½, 2, 3, 4, 8, 9, 13, 15, 16, 19, 23, 31, 34) were identified among the 41clinical isolates of S. suis. Results showed that serotype 2 (n=16) was the most frequently isolated, followed by serotype 9 (n=2), serotype 3 (n=3) and serotype 34 (n=2) (Table 2). These four serotypes together accounted for 60% of the isolates.

The 37 isolates of S. suis recovered from lungs were included in this study because they were isolated in pure culture from organs presenting compatible lesions. Respiratory diseases are one of the most important problems in intensive swine production in most countries (15), including Cuba. Important economic losses are observed due to reduced daily gain, prolonged time of fattening and enlarged costs of treatment (16). The interpretation of bacteriologic examination results of lung samples has been questioned, mainly due to the fact that, under some conditions, bacteria can be found in both healthy and diseased lungs with little or no clinical significance (17). However, reports about the isolation of this bacterium from pigs suffering from pneumonia are frequent, especially when isolated in pure cultures (18, 19).

The isolate recovered from abscess in joints, aborted fetus, and vaginal discharge from one farrow-to-finish farm was confirmed as one isolate belonging to the serotype 2; this serotype has been significantly associated with systemic infections worldwide (20). Serotype 2 was the only type found in each of the four farms. Serotype 3 associated with pneumonia has been also found highly prevalent in China, although it is rare in other countries, except in Canada (20, 21). Serotypes 4, 8, 13, 15, 16, 19, 23 and 31 comprised only one isolates. From them, serotypes 13, 19, 23 and 31 were detected during the period 2009-2011.

The distribution of different serotypes varies depending on the geographical origins of the strains. S. suis serotype 2 has been considered the most pathogenic and the most prevalent capsular type among diseased pigs in North America and China, followed by serotypes 3 and 1/2 (20, 23). The serotype 9 was also frequently isolated in the samples examined in this study. The serotype 9 is prevalent in several European countries (8, 9, 24).

A total of seven strains were nontypable and they were confirmed to belong to the S. suis species by using a previously described specific PCR test targeting the r16S DNA gene (13). Two strains reacted with more than one antiserum, for example with antiserum 13-23 and 15-16. Nontypeable strains are frequently isolated from diseased pigs in other countries. Recently, it has been reported that most of them are non encapsulated (20).

Previous studies reported the presence of genotype cps2j in Cuba by using PCR assays (12). However, the primers used in the PCR assay are unable to discriminate between serotype 2 and 1/2. To the best of our knowledge, this study is the first report of S. suis serotyping from pigs in Cuba using reference rabbit hyperimmune sera that confirms the presence of isolates of S. suis serotype 2 and other serotypes from diseased pigs with pneumonia and invasive diseases. Although the current use of molecular assays like PCR for the characterization of microorganisms is based on its advantages such as sensitivity and fast performing, serological confirmation is needed, at least for serotype 2.

Although S. suis serotype 2 is considered to be the most virulent type to swine and humans (25), it is well known that strains within serotype 2 may differ substantially in virulence. S. suis as a zoonotic pathogen has received only limited attention with respect to epidemiology in humans, except for the outbreak in Sichuan, People's Republic of China, in 2005 (26, 28, 29 and 30). Other serotypes like 5, 16, 14, and 21 have been identified in human isolates (27). No human S. suis cases attributable to S. suis strains have been reported so far in Cuba. But in this country, the swine production has significantly increased. It is speculated that factors associated with modern swine production, such as early weaning, high concentrations of animals, and corrosive gases, all of them led to the selection of highly virulent S. suis strains (31). Among others, causes for disease emergence in swine, particularly for zoonotic agents, may be the rapid expansion and intensification of swine industries in the developing countries without incorporating the stringent biosecurity measures and a veterinary oversight (32). Based on these observations and the results obtained in this study, and aware of the zoonotic risk, we recommend caution when dealing with S. suis infected pigs and the implementation of a biosecurity manual for the farm as a way to prevent all risk though a health education program addressing food safety, in addition to encourage the proper handling of pork.

 

REFERENCES

1. Chanter N, Jones PW, Alexander TJ. Meningitis in pigs caused by Streptococcus suis a speculative review. Vet Microbiol. 1999;36:39-55.

2. Gottschalk M, Segura M, Xu J. Streptococcus suis infections in humans: the Chinese experience and the situation in North America. Anim Health J. 2007;8:29-45.

3. Lun ZR, Wang QP, Chen XG, Li AX, Zhu XQ. Streptococcus suis: an emerging zoonotic pathogen. Lancet Infect Dis. 2007;7:201-209.

4. Staats JJ, Feder I, Okwumabua O, Chengappa MM. Streptococcus suis: past and present. Vet Res Commun. 1997;2:381-407.

5. Gottschalk M, Higgins R, Gottschalk M. An update on Streptococcus suis identification. J Vet Diagn Invest. 1990;2:249-252.

6. Okura M, Takamatsu D, Maruyama F, Nozawa T, Nakagawa I, Osaki M, et al. Genetic Analysis of Capsular Polysaccharide Synthesis Gene Clusters from All Serotypes of Streptococcus suis: Potential Mechanisms for Generation of Capsular Variation. Appl Environ Microbiol. 2013;79(8):2796-2806.

7. Smith HE, Damman M, Van der Velde F, Wagenaar J, Wisselink HJ, et al. Identification and characterization of the cps locus of Streptococcus suis serotype 2: the capsule protects against phagocytosis and is an important virulence factor. Infect Immun. 1999;67:1750-1756.

8. Smith HE, Veenbergen V, Van der Velde J, Damman M, Wisselink HJ, Smits MA. The cps genes of Streptococcus suis serotypes 1, 2, and 9: development of rapid serotype-specific PCR assays. J Clin Microbiol. 1999;37(10):3146-3152.

9. Smith HE, Van Bruijnsvoort L, Buijs H, Wisselink HJ, Smits MA. Rapid PCR test for Streptococcus suis serotype 7. FEMS Microbiol Lett. 1999;178(2):265-270.

10.Wang K, Fan W, Cai L, Huang B, Lu C. Genetic analysis of the capsular polysaccharide synthesis locus in 15 Streptococcus suis serotypes. FEMS Microbiol Lett. 2011;324:117-124.

11.Espinosa I, Báez M, Corona B, Chong D, Lobo E, Martínez S. Molecular typing of Streptococcus suis from pigs in Cuba. Biotecnología Aplic. 2013;30(1):39-34.

12.Marois C, Devendec L, Gottschalk M, Kobisch M. Detection and molecular typing of Streptococcus suis in tonsils from live pigs in France. Can J Vet Res. 2007;71(1):14-22.

13.Gottschalk M, Higgins R, Boudreau M. Use of polyvalent coagglutination reagents for serotyping of Streptococcus suis. J Clin Microbiol. 1993;31:2192-2194.

14.Christensen G, Sorensen V, Mousing J. Diseases of swine. In: Straw BE, D'Allaire S, Mengeling WL, Taylor DJ, eds. Diseases in Swine, 8th edn. Oxford: Blackwell Science. 1999; 913-940.

15.Portis E, Lindeman C, Johansen K. Antimicrobial susceptibility of porcine Pasteurella multocida, Streptococcus suis, Actinobacillus pleuroneumoniae from the United States and Canada, 2001 to 2010. J Swine Health Prod. 2013;21(1):30-41.

16.Straw B, Dewey E, Erickson ED. Interpreting culture reports from swine lungs. Notes diagnostic in Swine Health Prod. 1996;4:200-201.

17.Macinnes JI, Desrosiers R. Agents of the «suis-ide diseases» of swine: Actinobacillus suis, Haemophiluspara suis, and Streptococcus suis. Can J Vet Res. 1999;63(2):83-89.

18.Liu M, Fang L, Tan Long T, Chenand H, Xiao Sh. Understanding Streptococcus suis serotype 2 infection in pigs through a transcriptional approach. BMC Genomics. 2011;12:253.

19.Goyette-Desjardins G, Jean-Philippe A, Jianguo X, 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 Microb Infect. 2014;3(45):1-20.

20.Zigong Wei, Li R, Zhang A, He H, Hua JY, Cai X, et al. Characterization of Streptococcus suis isolates from the diseased pigs in China between 2003 and 2007. Vet Microbiol. 2009;137:196-201.

21.Higgins R, Gottschalk M. Streptococcocal diseases. In: Straw BE, D'Allaire S, Mengeling WL, Taylor DJ (Eds.). Diseases of Swine. Blackwell Publishing. 2006;769-783.

22.Wei Z, Li R, Zhang A, He H, Hua Y, Xia J, et al. Characterization of Streptococcus suis isolates from the diseased pigs in China between 2003 and 2007. Vet Microbiol. 2009;137(1-2):196-201.

23.Tarradas C, Perea A, Vela AI, Goyache J, Dominguez L. Distribution of serotypes of Streptococcus suis isolated from diseased pigs in Spain. Vet Rec. 2004;154:665-666.

24.Gottschalk M, Segura M, Xu J. Streptococcus suis infections in humans: the Chinese experience and the situation in North America. Anim Health Res Rev. 2007;8:29-45.

25.Yu H, Jing H, Chen Z, Zheng H, Zhu X. Human Streptococcus suis outbreak, Sichuan, China. Emerg Infect Dis. 2006;12:914-920.

26.Poggenborg R, Gaini S, Kjaeldgaard P, Christensen J. Streptococcus suis: meningitis, spondylodiscitis and bacteraemia with a serotype 14 strain. Scand J Infect Dis. 2008;40(4):346-349.

27.Haleis A, Alfa M, Gottschalk M, Bernard K, Ronald A, Manickam K. Meningitis caused by Streptococcus suis serotype 14, North America. Emerg Infect Dis. 2009;15(2):350-352.

28.Kerdsin A, Dejsirilert S, Akeda Y, Sekizaki T, Hamada S, et al. Clonal dissemination of human isolates of Streptococcus suis serotype 14 in Thailand. J Med Microbiol. 2009;58(Pt 11):1508-1513.

29.Kerdsin A, Dejsirilert S, Akeda Y, Sekizaki T, Hamada S, et al. Fifteen Streptococcus suis serotypes identified by multiplex PCR. J Med Microbiol. 2012;61(Pt 12):1669-1672.

30.Baums CG, Verku¨hlen GJ, Rehm T, Silva LMG, Beyerbach M, et al. Prevalence of Streptococcus suis Genotypes in Wild Boars of Northwestern Germany. Appl Environ Microbiol. 2007;73(3):117-117.

31.Davies PR. One World, One Health: The Threat of Emerging Swine Diseases. A North American Perspective Transbound Emerg Dis. 2012;59(Suppl. 1):18-26.

 

 

Recibido: 18-9-2014.
Aceptado: 15-11-2014.