Streptococcus suis Isolates-Serotypes and Susceptibility to Antimicrobials in Terms of Their Use on Selected Repopulated Czech Pig Farms

. 2021 Oct 13 ; 10 (10) : . [epub] 20211013

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid34684263

Grantová podpora
MZE-RO0518 Ministry of Agriculture
QK1920413 Ministry of Agriculture
QK1810193 Ministry of Agriculture

Streptococcus suis represents a primary health problem (such as meningitis, septicemia and arthritis in piglets and fatteners) in the swine industry worldwide and also an emerging zoonotic pathogen. In the Czech Republic, many pig farms repopulated their herds over the past decades to reduce morbidity and minimize treatment. The study analysed serotypes, sequence types and antimicrobial susceptibility in 39 S. suis isolates obtained from organs of diseased pigs from selected 16 repopulated farms with a history of S. suis-associated diseases and routine antimicrobial treatment with tulathromycin and/or amoxicillin. The analysis revealed diversity of collected isolates with regular occurrence of more than three serotypes per farm. The serotypes identified were 1/2 and 7, each in six isolates, followed by serotype 2 and 3 found in five isolates each, other serotypes were less frequent. Seven isolates were not typable by multiplex PCR and we also found sequence type of unknown type in thirteen isolates. The majority of S. suis isolates were resistant to clindamycin (n = 31), tetracycline (n = 29) and tilmicosin and tulathromycin (n = 28). On the other hand, with the exception of two isolates that were intermediately susceptible to penicillin and ampicillin, all isolates were susceptible to all three tested subgroups of beta-lactam antibiotics.

Zobrazit více v PubMed

Power S.B. Streptococcus suis type 2 infection in pigs. Vet. Res. 1978;102:215–216. doi: 10.1136/vr.102.10.215. PubMed DOI

Gottschalk M. Streptococcus suis infection. Merck manuals 2014. [(accessed on 21 August 2021)]. Available online: www.merckmanuals.com.

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. Microb. Infect. 2014;3:e45. doi: 10.1038/emi.2014.45. PubMed DOI PMC

de Briyne N., Iatridou D. Antimicrobial use in food-producing animals, FVE input to RONAFA report. EFSA J. 2016;15 doi: 10.2903/j.efsa.2017.4666. DOI

Perch B., Pedersen K.B., Heinrichsen J. Serology of capsulated streptococci pathogenic for pigs: Six new serotypes of Streptococcus suis. J. Clin. Microbiol. 1983;17:993–996. doi: 10.1128/jcm.17.6.993-996.1983. PubMed DOI PMC

Gottschalk M., Higgins R., Jacques M., Mittal K.R., Henrichsen J. Description of 14 new capsular types of Streptococcus suis. J. Clin. Microbiol. 1989;27:2633–2635. doi: 10.1128/jcm.27.12.2633-2636.1989. PubMed DOI PMC

Gottschalk M., Higgins R., Jacques M., Beaudoin M., Henrichsen J. Characterization of six new capsular types (23 through 28) of Streptococcus suis. J. Clin. Microbiol. 1991;29:2590–2594. doi: 10.1128/jcm.29.11.2590-2594.1991. PubMed DOI PMC

Higgins R., Gottschalk M., Boudreau M., Lebrun A., Henrichsen J. Description of six new capsular types (29-34) of Streptococcus suis. J. Vet. Diagn. Invest. 1995;7:405–406. doi: 10.1177/104063879500700322. PubMed DOI

Hill J.E., Gottschalk M., Brousseau R., Harel J., Hemmingsen S.M., Goh S.H. Biochemical analysis, cpn60 and 16S rDNA sequence data indicate that Streptococcus suis serotypes 32 and 34, isolated from pigs, are Streptococcus orisratti. Vet. Microbiol. 2005;107:63–69. doi: 10.1016/j.vetmic.2005.01.003. PubMed DOI

Tien H.T., Nishibori T., Nishitani Y., Nomoto R., Osawa R. Reappraisal of the taxonomy of Streptococcus suis serotypes 20, 22, 26, and 33 based on DNA-DNA homology and sodA and recN phylogenies. Vet. Microbiol. 2013;162:842–849. doi: 10.1016/j.vetmic.2012.11.001. PubMed DOI

Okura M., Lachance C., Osaki M., Sekizaki T., Maruyama F., Nozawa T., Nakagawa I., Hamada S., Rossignol C., Gottschalk M., 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;52:1714–1719. doi: 10.1128/JCM.03411-13. PubMed DOI PMC

Werinder A., Aspan A., Backhans A., Sjolund M., Guss B., Jacobson M. Streptococcus suis in Swedish grower pigs: Occurence, serotypes, and antimicrobial susceptibility. A. Vet. Scand. 2020;62:36. doi: 10.1186/s13028-020-00533-3. PubMed DOI PMC

Liu Z., Zheng H., Gottschalk M., Bai X., Lan R., Ji S., Liu H., Xu J. Development of multiplex PCR assays for the identification of the 33 serotypes of Streptococcus suis. PLoS ONE. 2013;8:e72070. doi: 10.1371/journal.pone.0072070. PubMed DOI PMC

Gottschalk M., Higgins R., Boudreau M. Use of polyvalent coagglutination reagents for serotyping of Streptococcus suis. J. Clin. Microbiol. 1993;31:2192–2194. doi: 10.1128/jcm.31.8.2192-2194.1993. PubMed DOI PMC

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. doi: 10.1017/S1466252307001247. PubMed DOI

Athey T.B., Teatero S., Lacouture S., Takamatsu D., Gottschalk M., Fittipaldi N. Determining Streptococcus suis serotype from short-read whole-genome sequencing data. BMC Microbiol. 2016;16:162. doi: 10.1186/s12866-016-0782-8. PubMed DOI PMC

Roy D., Athey T.B.T., Auger J.P., Goyette-Desjardins G., Van Calsteren M.R., Takamatsu D., Okura M., Teatero S., Alcorlo M., Hermoso J.A., et al. A single amino acid polymorphism in the glycosyltransferase CpsK defines four Streptococcus suis serotypes. Sci. Rep. 2017;7:4066. doi: 10.1038/s41598-017-04403-3. PubMed DOI PMC

Scherrer S., Rademacher F., Spoerry Serrano N., Schrenzel J., Gottschalk M., Stephan R., Landolt P. Rapid high resolution melting assay to differentiate Streptococcus suis serotypes 2, 1/2, 1, and 14. Microbiol. open. 2020;9:e995. doi: 10.1002/mbo3.995. PubMed DOI PMC

Matiasovic J., Zouharova M., Nedbalcova K., Kralova N., Matiaskova K., Simek B., Kucharovicova I., Gottschalk M. Resolution of Streptococcus suis serotypes 1/2 versus 2 and 1 versus 14 by PCR-Restriction Fragment Lenght Polymorphism Method. J. Clin. Microbiol. 2020;58:e00480-20. doi: 10.1128/JCM.00480-20. PubMed DOI PMC

Lopez A., Martinson S. Streptococcal pneumonia. In: Zachary J.F., editor. Pathologic Basis of Veterinary Disease. 6th ed. Elsevier; Amsterdam, The Netherlands: 2017. pp. v–vi. DOI

Segura M., Aragon V., Brockmeier S.L., Gebhart C., de Greeff A., Kerdsin A., O’Dea M.A., Okura M., Saléry M., Schultsz C., et al. Update on Streptococcus suis Research and Prevention in the Era of Antimicrobial Restriction: 4th International Workshop on S. suis. Pathogens. 2020;9:374. doi: 10.3390/pathogens9050374. PubMed DOI PMC

Varela N.P., Gadbois P., Tibault C., Gottschalk M., Dick P., Wilson J. Antimicrobial resistance and prudent drug use for Streptococcus suis. Anim. Health Res. Rev. 2013;14:68–77. doi: 10.1017/S1466252313000029. PubMed DOI

SVS ČR (State Veterinary Administration CZ), SVÚ (State Veterinary Institute) Jihlava (2019) National Programme of Monitoring Antimicrobial Resistance of Pathogens with Veterinary Importance for 2017-Part I (Národní Program Sledování Rezistencí k Antimikrobikům u Veterinárně Významných patogenů za rok 2017 -část I) in Czech. 24 p. [(accessed on 1 October 2021)]. Available online: https://www.svscr.cz/wp-content/files/dokumenty-a-publikace/Narodni-program-sledovani-rezistenci-k-antimikrobikum-u-veterinarne-vyznamnych-patogenu-2017-cast-I.pdf.

SVS ČR (State Veterinary Administration CZ), SVÚ (State Veterinary Institute) Jihlava (2019) National Programme of Monitoring Antimicrobial Resistance of Pathogens with Veterinary Importance for 2018 (Národní Program Sledování Rezistencí k Antimikrobikům u Veterinárně Významných Patogenů za rok 2018) in Czech. 36 p. [(accessed on 21 August 2021)]. Available online: https://www.svscr.cz/wp-content/files/dokumenty-a-publikace/Zprava-RL-antibioticke-centrum-pro-veterinarni-klinickou-praxi-za-rok-2018.pdf.

SVS ČR (State Veterinary Administration CZ), SVÚ (State Veterinary Institute) Jihlava (2020) National Programme of Monitoring Antimicrobial Resistance of Pathogens with Veterinary Importance for 2019 (Národní Program Sledování Rezistencí k Antimikrobikům u Veterinárně Významných Patogenů za rok 2019) in Czech. 36 p. [(accessed on 21 August 2021)]. Available online: https://www.svscr.cz/wp-content/files/dokumenty-a-publikace/Zprava-RL-2019.pdf.

SVÚ (State Veterinary Institute) Jihlava, SVS ČR (State Veterinary Administration CZ) (2021) National Programme of Monitoring Antimicrobial Resistance of Pathogens with Veterinary Importance for 2020 (Národní Program Sledování Rezistencí k Antimikrobikům u Veterinárně Významných Patogenů za rok 2020) in Czech. 36 p. [(accessed on 21 August 2021)]. Available online: https://www.svscr.cz/wp-content/files/dokumenty-a-publikace/Narodni-program-sledovani-rezistenci-k-antimikrobikum-u-veterinarne-vyznamnych-patogenu-2020.pdf.

Helke K.L., Ezell P.C., Duran-Struuck R., Swindle M.M. Chapter 16—Biology and Diseases of Swine. In: Fox J.G., Anderson L.C., Otto G.M., Pritchett-Corning K.R., Whary M.T., editors. Laboratory Animal Medicine. 3rd ed. Elsevier; Amsterdam, The Netherlands: 2015. pp. 695–769.

Okura M., Osaki M., Nomoto R., Arai S., Osawa R., Sekizaki T., Takamatsu D. Current taxonomical situation of Streptococcus suis. Pathogens. 2016;5:45. doi: 10.3390/pathogens5030045. PubMed DOI PMC

Mai N.T.H., Hoa N.T., Nga T.V.T., Linh L.D., Chau T.T.H., Sinh D.X., Phu N.H., Chuong L.V., Diep T.S., Campbell J., et al. Streptococcus suis meningitis in adults in Vietnam. Clin. Infect. Dis. 2008;46:659–667. doi: 10.1086/527385. PubMed DOI

Schultsz C., Jansen E., Keijzers W., Rothkamp A., Duim B., Wagenaar J.A., van der Ende A. Differences in the population structure of invasive Streptococcus suis strains isolated from pigs and from humans in The Netherlands. PLoS ONE. 2012;7:e33854. doi: 10.1371/journal.pone.0033854. PubMed DOI PMC

Fittipaldi N., Xu J., Lacouture S., Tharavichitkul P., Osaki M., Sekizaki T., Takamatsu D., Gottschalk M. Lineage and virulence of Streptococcus suis serotype 2 isolates from North America. Emerg. Infect. Dis. 2011;17:2239–2244. doi: 10.3201/eid1712.110609. PubMed DOI PMC

Vötsch D., Willenborg M., Weldearegay Y.B., Valentin-Weigand P. Streptococcus suis—The “Two Faces” of a Pathobiont in the Porcine Respiratory Tract. Front. Microbiol. 2018;9:480. doi: 10.3389/fmicb.2018.00480. PubMed DOI PMC

Zhu Y., Dong W., Ma J., Zhang Y., Zhong X., Pan Z., Liu G., Wu Z., Yao H. Comparative genetic analyses provide clues about capsule switching in Streptococcus suis 2 strains with different virulence levels and genetic backgrounds. Microbiol. Res. 2021;250:126814. doi: 10.1016/j.micres.2021.126814. PubMed DOI

ÚSKVBL (Institute for State Control of Veterinary Biologicals and Medicines) 2020 Consumption of Antimicrobials in Veterinary Medicine in CZ: Comparison of Trends in Consumption of Antimicrobials 2010-2018 Commented in Details (Spotřeba Antimikrobik ve Veterinární Medicíně v ČR: Detailní Komentované Srovnání Trendů ve Spotřebách Antimikrobik 2010-2018) in Czech. 48 p. [(accessed on 31 August 2021)]. Available online: http://www.uskvbl.cz/cs/informace/tiskove-centrum/tiskprohl.

Hernandez-Garcia J., Wang J., Restif O., Holmes M.A., Mather A.E., Weinert L.A., Wileman T.M., Thomson J.R., Langford P.R., Wren B.W., et al. Patterns of antimicrobial resistance in Streptococcus suis isolates from pigs with or without streptococcal disease in England between 2009 and 2014. Vet. Microbiol. 2017;207:117–124. doi: 10.1016/j.vetmic.2017.06.002. PubMed DOI PMC

Vela A.I., Moreno M.A., Cebolla J.A., González S., Latre M.V., Domínguez L., Fernández Garayzábala J.F. Antimicrobial susceptibility of clinical strains of Streptococcus suis isolated from pigs in Spain. Vet. Microbiol. 2004;105:143–147. doi: 10.1016/j.vetmic.2004.10.009. PubMed DOI

Soares T.C., Paes A.C., Megid J., Ribolla P.E., Paduan K., Gottschalk M. Antimicrobial susceptibility of Streptococcus suis isolated from clinically healthy swine in Brazil. Canadian, J. Vet. Res. 2014;78:145–149. PubMed PMC

Yongkiettrakul S., Maneerat K., Arechanajan B., Malila Y., Srimanote P., Gottschalk M., Visessanguan W. Antimicrobial susceptibility of Streptococcus suis isolated from diseased pigs, asymptomatic pigs, and human patients in Thailand. BMC Vet. Res. 2019;15:5. doi: 10.1186/s12917-018-1732-5. PubMed DOI PMC

EMA 2019: Categorisation of Antibiotics for Use in Animals for Prudent and Responsible Use. Available online: https://www.ema.europa.eu/en/documents/report/infographic-categorisation-antibiotics-use-animals-prudent-responsible-use_en.pdf.

Kerdsin A., Akeda Y., Hatrongjit R., Detchawna U., Sekizaki T., Hamada S., Gottschalk M., Oishi K. Streptococcus suis serotyping by a new multiplex PCR. J. Med. Microbiol. 2014;63:824–830. doi: 10.1099/jmm.0.069757-0. PubMed DOI

Van Hout J., Heuvelink A., Gonggrijp M. Monitoring of antimicrobial susceptibility of Streptococcus suis in the Netherlands, 2013–2015. Vet. Microbiol. 2016;194:5–10. doi: 10.1016/j.vetmic.2016.03.014. PubMed DOI

Ishida S., Tien le H.T., Osawa R., Tohya M., Nomoto R., Kawamura Y., Takahashi T., Kikuchi N., Kikuchi K., Sekizaki T. Development of an appropriate PCR system for the reclassification of Streptococcus suis. J. Microbiol. Methods. 2014;107:66–70. doi: 10.1016/j.mimet.2014.09.003. PubMed DOI

Mittal K.R., Higgins R., Larivière S. Identification and serotyping of Haemophilus pleuropneumoniae by coagglutination test. J. Clin. Microbiol. 1983;18:1351–1354. doi: 10.1128/jcm.18.6.1351-1354.1983. PubMed DOI PMC

King S.J., Leigh J.A., Heath P.J., Luque I., Tarradas C., Dowson C.G., Whatmore A.M. 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;40:3671–3680. doi: 10.1128/JCM.40.10.3671-3680.2002. PubMed DOI PMC

Saitou N., Nei M. The neighbor-joining method: A new method for reconstructing phylogenetic trees. Mol. Biol. Evol. 1987;4:406–425. PubMed

Felsenstein J. Confidence limits on phylogenies: An approach using the bootstrap. Evolution. 1985;39:783–791. doi: 10.1111/j.1558-5646.1985.tb00420.x. PubMed DOI

Tamura K., Nei M., Kumar S. Prospects for inferring very large phylogenies by using the neighbor-joining method. Proc. Natl. Acad. Sci. USA. 2004;101:11030–11035. doi: 10.1073/pnas.0404206101. PubMed DOI PMC

Kumar S., Stecher G., Li M., Knyaz C., Tamura K. MEGA X: Molecular Evolutionary Genetics Analysis across computing platforms. Mol. Biol. Evol. 2018;35:1547–1549. doi: 10.1093/molbev/msy096. PubMed DOI PMC

CLSI (Clinical and Laboratory Standards Institute) (2018) Performance Standards for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated from Animals. 4th ed. Clinical and Laboratory Standards Institute; Wayne, PA, USA: p. 170. CLSI supplement VET08.

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...