Tierarztl Prax Ausg G Grosstiere Nutztiere 2016; 44(01): 13-18
DOI: 10.15653/TPG-150674
Original Article
Schattauer GmbH

Occurrence of Brachyspira hyodysenteriae in multiplier pig herds in Switzerland

Vorkommen von Brachyspira hyodysenteriae in Schweizer Vermehrungsbetrieben für Schweine
S. Löbert
1   Chamber for Agriculture North Rhine-Westphalia, Animal Health Services, Bad Sassendorf, Germany
2   Clinic for Swine, Vetsuisse Faculty, University of Bern, Bern, Switzerland
,
W. Zimmermann
2   Clinic for Swine, Vetsuisse Faculty, University of Bern, Bern, Switzerland
,
S. Bürki
3   Institute of Veterinary Bacteriology, Vetsuisse Faculty, University of Bern, Bern, Switzerland
,
J. Frey
3   Institute of Veterinary Bacteriology, Vetsuisse Faculty, University of Bern, Bern, Switzerland
,
H. Nathues
2   Clinic for Swine, Vetsuisse Faculty, University of Bern, Bern, Switzerland
,
P. Scheer
4   SUISAG, Pig Health Service, Sempach, Switzerland
,
M. G. Doherr
5   Institute for Veterinary Epidemiology and Biostatistics, Department of Veterinary Medicine, Berlin, Germany
,
U. Stalder
6   Veterinary practice Bleumatt, Büron, Switzerland
,
F. Zeeh
2   Clinic for Swine, Vetsuisse Faculty, University of Bern, Bern, Switzerland
› Author Affiliations
Further Information

Publication History

Received: 24 August 2015

Accepted after major revision: 23 January 2015

Publication Date:
20 December 2017 (online)

Summary

Objective: This research was aimed to determine the occurrence of Brachyspira (B.) hyodysenteriae in Swiss multiplier pig herds. Materials and methods: In a pilot study a direct real-time polymerase chain reaction (PCR) method for B. hyodysenteriae was compared to culture followed by PCR on 106 samples from three herds. Subsequently 40 multiplier herds were epidemiologically characterized and analysed for the presence of B. hyodysenteriae using direct PCR on 1412 rectal swabs. For external validation 20 swabs obtained from two positive conventional herds were analysed. Results: The comparison of direct PCR with culture followed by PCR resulted in a moderate agreement (kappa index: 0.58). In the two conventional herds, 35% of the samples (7/20) tested positive. Samples from 39 multipliers tested negative. In one multiplier herd, 25% (9/36) of the samples tested PCR positive. Risk factors in the multiplier herd may have been rodents or birds, but not pig purchase. Conclusion and clinical relevance: B. hyodysenteriae have been detected in a Swiss multiplier herd, which underlines the threat of potential spread by replacement pigs. Consequently, a Brachyspira monitoring programme was established for Swiss multiplier herds.

Zusammenfassung

Gegenstand und Ziel: Die Studie untersuchte das Vorkommen von Brachyspira (B.) hyodysenteriae in Schweizer Vermehrungsbetrieben für Schweine. Material und Methoden: In einer Pilotstudie wurden anhand von 106 Proben aus drei Herden Ergebnisse einer direkten Real-Time-Polymerasekettenreaktion mit einer kulturellen Untersu - chung gefolgt von einer Polymerasekettenreaktion (PCR) verglichen. Anschließend wurden 40 Vermehrungsbetriebe epidemiologisch charakterisiert und 1412 Kottupfer dieser Bestände mit der direkten PCR untersucht. Für eine externe Validierung wurden 20 Proben von zwei positiven konventionellen Herden untersucht. Ergebnisse: Der Vergleich der direkten PCR mit der Kultur und der nachfolgenden PCR ergab eine moderate Übereinstimmung (Kappa-Index: 0,58). In den zwei konventionellen Herden waren 35% (7/20) der Proben positiv. Kottupfer aus 39 Vermehrungsbetrieben erwiesen sich als negativ. In einem Vermehrungsbestand waren 25% (9/36) der Proben positiv. Risikofaktoren könnten im positiven Vermehrungsbetrieb Nager oder Vögel, nicht aber Tierzukauf gewesen sein. Schlussfolgerung und klinische Relevanz: Der Nachweis von B. hyodysenteriae in einem Vermehrungsbetrieb betont die Gefahr einer möglichen Verbreitung durch Zuchttiere. Daher wurde in Schweizer Vermehrungsbetrieben ein Brachyspiren-Monitoringprogramm eingeführt.

 
  • Literatur

  • 1 Alvarez-Ordóñez A, Martínez-Lobo FJ, Arguello H, Carvajal A, Rubio P. Swine dysentery: Aetiology, pathogenicity, determinants of transmission and the fight against the disease. Int J Environ Res Public Health 2013; 10: 1927-1947.
  • 2 Backhans A, Jacobson M, Hansson I, Lebbad M, Lambertz ST, Gammelgård E, Saager M, Akande O, Fellström C. Occurrence of pathogens in wild rodents caught on Swedish pig and chicken farms. Epidemiol Infect 2013; 141: 1885-1891.
  • 3 Barcellos DESN, de Uzeda M, Mathiesen MR, Duhamel GE, Kader IITA. Prevalence of Brachyspira species isolated from diarrhoeic pigs in Brazil. Vet Rec 2000; 146: 398-403.
  • 4 Biksi I, Lorincz M, Molnár B, Kecskés T, Takács N, Mirt D, Cizek A, Pejsak Z, Martineau GP, Sevin JL, Szenci O. Prevalence of selected enteropathogenic bacteria in Hungarian finishing pigs. Acta Vet Hung 2007; 55: 219-227.
  • 5 Bürki S, Vilei EM, Frey J, Wittenbrink MM. Allelic variations of the nox gene of Brachyspira pilosicoli impair its detection by qPCR. Vet Microbiol 2011; 149: 291-292.
  • 6 Carvajal A, de Arriba ML, Rodríguez H, Vidal AB, Duhamel GE, Rubio P. Prevalence of Brachyspira species in pigs with diarrhoea in Spain. Vet Rec 2006; 158: 700-701.
  • 7 Dünser M, Schweighardt H, Awad-Masalmeh M, Schuh M. Schweinedysenteriae und Spirochaetendiarrhoe – vergleichende Untersuchungen serpulinenbedingter Enteritiden. Wien Tierärztl Monatsschr 1997; 84: 151-161.
  • 8 Fellström C, Landén A, Gunnarsson A, Holmgren N. Mice as a reservoir of Brachyspira hyodysenteriae in repeated outbreaks of swine dysentery in a Swedish fattening herd. Proceedings of the 18th International Pig Veterinary Society Congress. Hamburg: 2004: 280.
  • 9 Fellström C, Pettersson B, Johansson K, Lundeheim N, Gunnarson A. Prevalence of Serpulina species in relation to diarrhea and feed medication in pig-rearing herds in Sweden. Am J Vet Res 1996; 57: 807-811.
  • 10 Hampson DJ. Brachyspiral Colitis. Diseases of Swine.. Zimmermann JJ, Karriker LA, Ramirez A, Schwartz KJ, Stevenson GW. Hrsg. Chichester, West Sussex: John Wiley and Sons; 2012: 680-696.
  • 11 Heinonen M, Fossi M, Jall J-P, Saloniemi H, Tuovinen V. Detectability and prevalence of Brachyspira species in herds rearing health class feeder pigs in Finland. Vet Rec 2000; 146: 343-347.
  • 12 Herbst W, Willems H, Baljer G. Verbreitung von Brachyspira hyodysenteriae und Lawsonia intracellularis bei gesunden und durchfallkranken Schweinen. Berl Münch Tierärztl Wochenschr 2004; 117: 493-498.
  • 13 Hillen S, Willems H, Herbst W, Rohde J, Reiner G. Mutations in the 50S ribosomal subunit of Brachyspira hyodysenteriae associated with altered minimum inhibitory concentrations of pleuromutilins. Vet Microbiol 2014; 172: 223-229.
  • 14 Jacobson M, Gerth Löfstedt M, Holmgren N, Lundeheim N, Fellström C. The prevalences of Brachyspira spp. and Lawsonia intracellularis in Swedish piglet producing herds and wild boar population. J Vet Med B 2005; 52: 386-391.
  • 15 Janetschke P, Kielstein P. Möglichkeiten zur Diagnostik und Bekämpfung der Schweinedysenterie. Mh Vet Med 1976; 31: 721-726.
  • 16 Joens LA. Experimental transmission of Treponema hyodysenteriae from mice to pigs. Am J Vet Res 1980; 41: 1225-1226.
  • 17 La T, Phillips ND, Hampson DJ. Development of a duplex PCR assay for detection of Brachyspira hyodysenteriae and Brachyspira pilosicoli in pig feces. J Clin Microbiol 2003; 41: 3372-3375.
  • 18 Møller K, Jensen TK, Jorsal SE, Leser TD, Carstensen BE, Jorsal S, Leser TD, Carstensen B. Detection of Lawsonia intracellularis Serpulina hyodysenteriae, weakly beta-haemolytic intestinal spirochaetes, Salmonella enterica, and haemolytic Escherichia coli from swine herds with and without diarrhoea among growing pigs. Vet Microbiol 1998; 62: 59-72.
  • 19 Nathues H, Oliveira CJB, Wurm M, Grosse Beilage E, Givisiez PEN. Simultaneous detection of Brachyspira hyodysenteriae, Brachyspira pilosicoli and Lawsonia intracellularis in porcine faeces and tissue samples by multiplex-PCR. J Vet Med A 2007; 54: 532-538.
  • 20 Novotna M, Skardova O. Brachyspira hyodysenteriae: detection, identification and antibiotic susceptibility. Vet Med 2002; 47: 104-109.
  • 21 Pearce GP. Epidemiology of enteric disease in grower-finisher pigs: a postal survey of pig producers in England. Vet Rec 1999; 144: 338-342.
  • 22 Råsbäck T, Fellström C, Gunnarsson A, Aspán A. Comparison of culture and biochemical tests with PCR for detection of Brachyspira hyodysenteriae and Brachyspira pilosicoli . J Microbiol Methods 2006; 66: 347-353.
  • 23 Robertson I, Mhoma J, Hampson D. Risk factors associated with the occurrence of swine dysentery in Western Australia: results of a postal survey. Aust Vet J 1992; 69: 92-93.
  • 24 Rohde J, Habighorst-Blome K. An update on the differentiation of Brachyspira species from pigs with nox-PCR-based restriction fragment length polymorphism. Vet Microbiol 2012; 158: 211-215.
  • 25 Rohde J, Rothkamp A, Gerlach GF. Differentiation of Porcine Brachyspira Species by a Novel nox PCR-Based Restriction Fragment Length Polymorphism Analysis. J Clin Microbiol 2002; 40: 2598-2600.
  • 26 Rugna G, Bonilauri P, Carra E, Bergamini F, Luppi A, Gherpelli Y, Magistrali CFF, Nigrelli A, Alborali GLL, Martelli P, La T, Hampson DJ, Merialdi G. Sequence types and pleuromutilin susceptibility of Brachyspira hyodysenteriae isolates from Italian pigs with swine dysentery: 2003-2012. Vet J 2015; 203: 115-119.
  • 27 Song Y, Hampson DJ. Development of a multiplex qPCR for detection and quantitation of pathogenic intestinal spirochaetes in the faeces of pigs and chickens. Vet Microbiol 2009; 137: 129-136.
  • 28 Songer JG, Harris DL. Transmission of swine dysentery by carrier pigs. Am J Vet Res 1978; 39: 913-916.
  • 29 Speiser SA, Goy N, Albini S, Zimmermann W, Scheer P, Doherr MG, Zeeh F. Occurence of Brachyspira hyodysenteriae and Brachyspira pilosicoli and assessment of risk factors in Switzerland. Oral Proceedings of the 20th IPVS Congress. Durban, South Africa: 2008: 127.
  • 30 Stege H, Jensen T, Møller K, Bækbo P, Jorsal S. Prevalence of intestinal pathogens in Danish finishing pig herds. Prev Vet Med 2000; 46: 279-292.
  • 31 Thomson JR, Smith WJ, Murray BP. Investigations into field cases of porcine colitis with particular reference to infection with Serpulina pilosicoli. Vet Rec 1998; 142: 235-239.
  • 32 Thomson JR, Smith WJ, Murray BP, Murray D, Dic JE, Sumption KJ. Porcine enteric spirochete infections in the UK: surveillance data and preliminary investigation of atypical isolates. Anim Heal Res Rev 2001; 2: 31-36.
  • 33 Vilei EM, Frey J. Detection of Mycoplasma mycoides subsp. mycoides SC in bronchoalveolar lavage fluids of cows based on a TaqMan real-time PCR discriminating wild type strains from an lppQ(-) mutant vaccine strain used for DIVA-strategies. J Microbiol Methods 2010; 81: 211-218.
  • 34 Waldmann KH. Voraussetzungen und Maßnahmen zur Sanierung von Ferkelerzeugerbetrieben mit latenter Schweindysenterie. Tierärztl Prax 1992; 20: 159-163.
  • 35 Willems H, Reiner G. Eine Multiplex Realtime-PCR für den gleichzeitigen Nachweis und Quantifizierung von Brachyspira hyodysenteriae, Brachyspira pilosicoli und Lawsonia intracellularis in Schweinekot. Berl Münch Tierärztl Wochenschr 2010; 123 (56) 205-209.