We investigated Salmonella contamination in a slaughterhouse in Jiangsu province (China) by analysing
prevalences, loads, and serotypes of Salmonella isolates. In total, 480 samples were collected, with total
prevalence of 25.4%. High Salmonella prevalence and load were observed at exsanguination and splitting
stages (40.6% and 75.0%; 2.50 ± 0.94 and 2.24 ± 0.72 logMPN/m2
, respectively), with low prevalence and
load at dehairing, flaming, and chilling stages (2.5%, 5.0%, and 15.0%; 1.39 ± 0.42, 1.36 ± 0.31, and
1.38 ± 0.30 logMPN/m2
, respectively). The Salmonella prevalence and load increased substantially from
flaming to splitting stage. Six serovars were represented among 122 Salmonella isolates; S. De... More
We investigated Salmonella contamination in a slaughterhouse in Jiangsu province (China) by analysing
prevalences, loads, and serotypes of Salmonella isolates. In total, 480 samples were collected, with total
prevalence of 25.4%. High Salmonella prevalence and load were observed at exsanguination and splitting
stages (40.6% and 75.0%; 2.50 ± 0.94 and 2.24 ± 0.72 logMPN/m2
, respectively), with low prevalence and
load at dehairing, flaming, and chilling stages (2.5%, 5.0%, and 15.0%; 1.39 ± 0.42, 1.36 ± 0.31, and
1.38 ± 0.30 logMPN/m2
, respectively). The Salmonella prevalence and load increased substantially from
flaming to splitting stage. Six serovars were represented among 122 Salmonella isolates; S. Derby and S.
Typhimurium were predominant and were subtyped using PFGE and CRISPR typing approaches. Fourteen
PFGE clusters were identified, with discrimination indices (DI) of 0.929 and 0.976 for S. Derby and S.
Typhimurium, respectively. Clusters A1, A2, B, C1, C3, C4, D1, F, I, J, L1, M2, and N2 indicated the isolates
from same sampling visit were distributed in same cluster. Cluster D1 and K showed that the strains
isolated from splitter and carcass swab-samples were highly resemble. Salmonella serovars with the
same CRISPR type were mostly isolated after splitting (represented by Dercr 1, Dercr 2, Dercr 3, Tycr 1,
Tycr 2, Tycr 3, Tycr 4, and Tycr 6). Our findings revealed that introduced Salmonella was the major source
of swine carcass contamination; three slaughtering steps (polishing, rectal drilling, and evisceration)
between flaming and splitting were important risk points for Salmonella release, post-splitting slaughtering
processes were major contamination risk points, and the splitter was a contamination factor. Our
data suggest routes for controlling Salmonella contamination in a swine slaughterhouse.