Background
The current conventional serotyping based on antigen-antisera agglutination could not provide a better understanding of the potential pathogenicity of
Salmonella enterica
subsp.
enterica
serovar Brancaster. Surveillance data from Malaysian poultry farms indicated an increase in its presence over the years.
Objective
This study aims to investigate the virulence determinants and antimicrobial resistance in
S.
Brancaster isolated from chickens in Malaysia.
Methods
One hundred strains of archived
S.
Brancaster isolated from chicken cloacal swabs and raw chicken meat from 2017 to 2022 were studied. Two sets of multiplex polymerase chain reaction (PCR) were conducted to identify eight virulence genes associated with pathogenicity in
Salmonella
(invasion protein gene [
invA
],
Salmonella
invasion protein gene [
sipB
],
Salmonella-
induced filament gene [
sifA
], cytolethal-distending toxin B gene [
cdtB
],
Salmonella
iron transporter gene [
sitC
],
Salmonella
pathogenicity islands gene [
spiA
],
Salmonella
plasmid virulence gene [
spvB
], and inositol phosphate phosphatase gene [
sopB
]). Antimicrobial susceptibility assessment was conducted by disc diffusion method on nine selected antibiotics for the
S.
Brancaster isolates.
S.
Brancaster, with the phenotypic ACSSuT-resistance pattern (ampicillin, chloramphenicol, streptomycin, sulphonamides, and tetracycline), was subjected to PCR to detect the corresponding resistance gene(s).
Results
Virulence genes detected in
S
. Brancaster in this study were
invA
,
sitC
,
spiA
,
sipB
,
sopB
,
sifA
,
cdtB
, and
spvB
. A total of 36 antibiogram patterns of
S
. Brancaster with a high level of multidrug resistance were observed, with ampicillin exhibiting the highest resistance. Over a third of the isolates displayed ACSSuT-resistance, and seven resistance genes (β-lactamase temoneira [
bla
TEM
], florfenicol/chloramphenicol resistance gene [
floR
], streptomycin resistance gene [
strA
], aminoglycoside nucleotidyltransferase gene [
ant(3″)-Ia
], sulfo...