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. 2023 Jul 5;10:1220118. doi: 10.3389/fvets.2023.1220118

Table 2.

The developed multiplex PCR method was applied for the identification of S. Pullorum and S. Gallinarum isolates from one chicken farm.

Serovar (no. of isolates) Isolate no. PCR results (torT/I137_14430/stn) Dulcitol fermentation Ornithine decarboxylase
Pullorum (10) Ch4 −/+/+ +
Ch5 −/+/+ +
Ch9 −/+/+ +
Ch10 −/+/+ +
Ch11 −/+/+ +
Ch12 −/+/+ +
Ch16 −/+/+ +
Ch17 −/+/+ +
Ch18 −/+/+ +
Ch24 −/+/+ +
Gallinarum (2) Ch22 +/−/+ +
Ch23 +/−/+ +
Enteritidis (9) Ch1 +/+/+ / /
Ch2 +/+/+ / /
Ch3 +/+/+ / /
Ch6 +/+/+ / /
Ch7 +/+/+ / /
Ch8 +/+/+ / /
Ch13 +/+/+ / /
Ch14 +/+/+ / /
Ch15 +/+/+ / /
Indiana (3) Ch19 +/+/+ / /
Ch20 +/+/+ / /
Ch21 +/+/+ / /

The traditional serotyping of the Salmonella isolates was determined based on the White-Kauffmann-Le Minor scheme. The traditional differentiation of Salmonella biovars Pullorum and Gallinarum was conducted with the dulcitol fermentation and ornithine decarboxylation. +, positive; −, negative.