Evaluation of Mycoplasma hyopneumoniae bacterins for porcine torque teno virus DNAs

Steven Krakowka Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH 43210

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Susan S. Ringler Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH 43210

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Prakash Arumugam Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH 43210

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John McKillen Queens University Belfast and Agri-Food and Biosciences Institute, Belfast, BT4 3SD, Northern Ireland

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Kathy McIntosh Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK S7N 5B4, Canada

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Catherine Hartunian Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH 43210

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Alexander Hamberg Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH 43210

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Michael Rings Department of Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH 43210

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Gordon Allan Queens University Belfast and Agri-Food and Biosciences Institute, Belfast, BT4 3SD, Northern Ireland

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John A. Ellis Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK S7N 5B4, Canada

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Abstract

Objective—To determine whether commercial Mycoplasma hyopneumoniae bacterins sold for use in swine contain porcine torque teno virus (TTV).

Sample Population—22 commercially available M hyopneumoniae bacterins.

Procedures—Direct and nested PCR assays for genogroup-specific TTV DNAs were performed on serials of M hyopneumoniae bacterins by use of published and custom-designed primer pairs at 3 laboratories in North America and Europe.

Results—Of the 22 bacterins tested by use of direct and nested PCR assays, 7 of 9 from the United States, 2 of 5 from Canada, and 4 of 8 from Europe contained genogroup 1– and genogroup 2–TTV DNAs. In some bacterins, the TTV DNAs were readily detected by use of direct PCR assays.

Conclusions and Clinical Relevance—Analysis of these data indicated that many of the commercially available M hyopneumoniae bacterins were contaminated with TTV DNA. It is possible that some of these bacterins could inadvertently transmit porcine TTV infection to TTV-naïve swine.

Abstract

Objective—To determine whether commercial Mycoplasma hyopneumoniae bacterins sold for use in swine contain porcine torque teno virus (TTV).

Sample Population—22 commercially available M hyopneumoniae bacterins.

Procedures—Direct and nested PCR assays for genogroup-specific TTV DNAs were performed on serials of M hyopneumoniae bacterins by use of published and custom-designed primer pairs at 3 laboratories in North America and Europe.

Results—Of the 22 bacterins tested by use of direct and nested PCR assays, 7 of 9 from the United States, 2 of 5 from Canada, and 4 of 8 from Europe contained genogroup 1– and genogroup 2–TTV DNAs. In some bacterins, the TTV DNAs were readily detected by use of direct PCR assays.

Conclusions and Clinical Relevance—Analysis of these data indicated that many of the commercially available M hyopneumoniae bacterins were contaminated with TTV DNA. It is possible that some of these bacterins could inadvertently transmit porcine TTV infection to TTV-naïve swine.

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