Abstract

Pork meat is estimated to be responsible for 10–20% of human salmonellosis cases in Europe. Control strategies at the farm could reduce contamination at the slaughterhouse. One of the targeted sectors of production is maternity, where sows could be Salmonella reservoirs. The aim of this study was to assess the dynamics of shedding of Salmonella in terms of variation in both shedding prevalence and strains excreted during gestation in Quebec’s maternity sector. The evolution of the fecal microbiota of these sows during gestation was also assessed to detect bacterial populations associated with these variations. A total of 73 sows both at the beginning and the end of the gestation were randomly selected and their fecal matter was analyzed. Salmonella detection was conducted using a method that includes two selective enrichment media (MSRV and TBG). Nine isolates per positive samples were collected. Among the 73 sows tested, 27 were shedding Salmonella. Sows in the first third of their gestation shed Salmonella significantly more frequently (21/27) than those in the last third (6/46) (χ2 P < 0.05). The shedding status of 19 of the sows that were previously sampled in the first third of their gestation was followed, this time in the last third of their gestation, which confirmed reduction of shedding. Using 16S rRNA gene sequencing and qPCR, significant differences between the fecal flora of sows at the beginning and the end of the gestation, shedding Salmonella or not and with different parity number were detected. Using MaAsLin, multiple OTUs were found to be associated with the time of gestation, the status of Salmonella excretion and parity number. Some of the identified taxa could be linked to the reduction of the shedding of Salmonella at the end of gestation. In this study, we showed that the level of Salmonella shedding was variable during gestation with significantly higher shedding at the beginning rather than at the end of gestation. We also observed for the first time a significant change in the microbiota during sow gestation and identified interesting taxa which could be linked to a reduced Salmonella shedding.

Highlights

  • In Canada, Salmonella enterica is estimated to cause 269.26 infections per 100,000 inhabitants each year, confirming this pathogen as a public health priority (Thomas et al, 2013)

  • Since it has been shown that the entrance of contaminated pigs into slaughterhouses is linked with an increased risk for the contamination of carcasses, a reduction at the first stages of the production could be an important step in the reduction of the contamination of the meat (Letellier et al, 2009; EFSA Panel on Biological Hazards [BIOHAZ], 2010)

  • Similar results were obtained when sampling for a second time at the end of gestation the 19 sows that had already been sampled at the beginning of their gestation, with a statistically (McNemar’s, p < 0.05) lower proportion of positive samples at the end of the gestation (2 of 19, 11%) than at the beginning (13 of 19, 68%)

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Summary

Introduction

In Canada, Salmonella enterica is estimated to cause 269.26 infections per 100,000 inhabitants each year, confirming this pathogen as a public health priority (Thomas et al, 2013). In Canada, the part of salmonellosis that are caused by consumption of pork products is not known. In Europe, it has been estimated that between 10 and 20% of all salmonellosis cases are due to the consumption of contaminated pork meat (EFSA Panel on Biological Hazards [BIOHAZ], 2010). Salmonella can contaminate swine on the farm and most of the serotypes can be carried asymptomatically in their intestinal tract, gut-associated lymphoid tissue and tonsils, and enter slaughterhouses with the animals where it can contaminate the meat (Boyen et al, 2008). Since it has been shown that the entrance of contaminated pigs into slaughterhouses is linked with an increased risk for the contamination of carcasses, a reduction at the first stages of the production could be an important step in the reduction of the contamination of the meat (Letellier et al, 2009; EFSA Panel on Biological Hazards [BIOHAZ], 2010)

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