Purpose
This study aimed to investigate the prevalence and genetic characterization of
Serratia marcescens
isolates from clinical bovine mastitis in Ningxia Hui Autonomous Region of China.
Methods
S. marcescens
was identified by the polymerase-chain reaction of 16S rRNA gene and sequencing. Antimicrobial susceptibility was tested by the disk diffusion method. Genes of resistance and virulence were determined by the PCR.
Results
Overall,
S. marcescens
were confirmed from 32 of 2897 (1.1%) mastitis milk samples. These isolates showed high resistance to cefazolin (30/32, 93.8%) and chloramphenicol (28/32, 87.5%). A 12.5% (4/32) of the isolates displayed multidrug resistance (MDR). The most prevalent resistant genes found in
S. marcescens
were
TEM
(32/32, 100%) and
CTX-M
(24/32, 75.0%;
CTX-M-15
, 14/32, 43.8%;
CTX-M-14
, 8/32, 25.0%;
CTX-M-65
, 2/32, 6.3%) for extended-spectrum beta-lactamase,
cmlA
(28/32, 87.5%) and
floR
(16/32, 50.0%) for chloramphenicol resistance,
SIM-1
(2/32, 6.3%) for carbapenemases, and
sdeB
(28/32, 87.5%),
sdeY
(26/32, 81.3%),
sdeR
(26/32, 81.3%) and
sdeD
(20/32, 62.5%) for efflux pumps. Moreover, all isolates carried virulence genes
flhD, entB
, and
kpn
, and most of them contained
mrkD
(30/32, 93.8%),
ycfM
(26/32, 81.3%),
bsmB
(26/32, 81.3%),
pigP
(26/32, 81.3%),
kfu
(24/32, 75.0%) and
shlB
(24/32, 75.0%).
Conclusion
To our knowledge, this is the first report of genetic determinants for antimicrobial resistance and virulence in
S. marcescens
isolated from bovine mastitis cases in China. These findings are useful for developing strategies for prevention and treatment of bovine mastitis caused by
S. marcescens
in China.