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Salmonellabacterial infections have become a major public health issue, causing a wide range of clinical manifestations, including acute gastroenteritis and bacteremia. Antibiotics are commonly used to treat and control salmonellosis in food animals, contributing to the increasing prevalence of antibiotic-resistantSalmonellathat has been attracting worldwide attention (1). Thus, investigating the prevalence of resistance-related genes inSalmonellacould enhance the understanding of drug impacts on epidemiology. The study mainly followed the 2019 National Surveillance Program of Antibiotic Resistance in Bacteria of Food Animal Origins to conduct animal-food sampling in 6 provincial-level administrative divisions (PLADs) in China: Hebei, Shanxi, Shandong, Sichuan, Inner Mongolia, and Beijing. In addition to a minor decline in prevalence ofSalmonellain chicken, results showed an increase in prevalence ofSalmonella in pigs, ducks, and milk.Salmonella contamination of food animals has become a serious public health threat in China. Through antimicrobial susceptibility testing,Salmonellaof animal origin was found to have multiple drug resistance and a high rate to ampicillin (59.6%). Therefore, in the animal breeding environment, public health practitioners should pay attention to the disinfection of the breeding farm environment and reduce the overuse of therapeutic drugs, promote the scientific use of drugs in the breeding process, and ensure the safety of public health.
In this study, a total of 1,493 non-duplicate samples were collected and stored in ESwabs (a swab-based collection kit) from animal farms and 85 from milk storage tanks on dairy farms. The sample collection method strictly complies with 2019 National Surveillance Program of Antibiotic Resistance in Bacteria of Food Animal Origins.Salmonellaisolates were identified by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS).Salmonellaserotyping was performed using the White-Kauffmann-Le Minor scheme. Minimum inhibitory concentrations (MICs) were determined by the broth microdilution method according to the recommendations in the Clinical and Laboratory Standards Institute guidelines (CLSI, 2015: M100-S25). Whole genome sequencing was conducted using an Illumina HiSeq2500 platform (Bionova Biotech Co. Beijing, China). Multilocus sequence typing (MLST) results were analyzed using MLST Version 2 (Seemann T, mlst Github
http://github.com/tseemann/mlst ), and plasmid replicon typing was conducted using online tools (Center for Genomic Epidemiology, Technical University of Denmark,http://www.genomicepidemiology.org/ ). Resistance genes were identified using SRST2 Toolkit (version 0.2.0, The University of Melbourne,http://katholt.github.io/srst2/ ).A total of 198Salmonellaisolates (198/1,578, 12.6%) were obtained from food animal samples from Hebei, Shanxi, Shandong, Sichuan, Inner Mongolia, and Beijing in 2019. Samples were collected from the feces, cecum, and milk of food animals. The highest rates ofSalmonellaisolates were obtained with the samples from cows. Beijing displayed the highestSalmonellaisolation rate among the examined PLADs (23.3%), while Hebei displayed the lowest isolation rate (8.8%) (Table 1).
PLAD Sample Source No. of samples No. of isolates Isolating rate (%) 95% CI Shanxi Cow Milk 85 25 29.4 (20.0, 40.3) Chicken Cecum 121 10 8.3 (4.0, 14.7) Sichuan Chicken Cecum 144 14 9.7 (5.4, 15.8) Fecal 60 14 23.3 (13.4, 36.0) Pig Fecal 90 22 24.4 (16.0, 34.6) Beijing Duck Fecal 30 7 23.3 (9.9, 42.3) Shandong Chicken Cecum 247 26 10.5 (7.0, 15.0) Fecal 712 72 10.1 (8.0, 12.6) Inner Mongolia Chicken Cecum 39 4 10.3 (2.9, 24.2) Hebei Chicken Fecal 50 4 8.0 (2.2, 19.2) Total Chicken Cecum/fecal 1,373 144 10.5 (8.9, 12.2) Pig Fecal 90 22 24.4 (16.0, 34.6) Duck Fecal 30 7 23.3 (9.9, 42.3) Cow Milk 85 25 29.4 (20.0, 40.3) Note: The six PLADs inculdes Hebei, Shanxi, Shandong, Sichuan, Inner Mongolia, and Beijing. The primary objective of the present study was to investigate the Isolating Rate and corresponding 95% CIs of prevalence ofSalmonellaisolates from the 6 PLADs, China, in 2019.
Abbreviations: PLADs=provincial-level administrative divisions; CI=confidence interval.Table 1.Characteristics and prevalence ofSalmonellaisolates from the 6 PLADs, China, 2019.
Salmonellaserotyping divided 133 isolates into 35 serotypes, with 65 isolates being incapable of being typed (Table 2).SalmonellaEnteritidis (S.Enteritidis; 37.6%, 50/133) was the predominant species, followed byS. Tympanum (9.0%, 12/133) andS. Kentucky (9.0%, 12/133). Notably, multidrug resistant (MDR) strains were widely distributed among the variousSalmonellaserotypes. Among all the serotypes,S. Agona (77.8%) showed the highest rates of antimicrobial resistance and MDR in the present study.
Serovar Chicken Pig Cow Duck Total Enteritidis 44 5 1 50 Tymphimurium 1 6 5 12 Kentucky 12 12 Agona 4 2 3 9 Djugu 6 6 Corvallis 4 4 Paratyphi B 4 4 Essen 2 1 3 Koenigstuhl 1 1 2 Norwich 1 1 2 Schwarzengrund 2 2 Trachau 2 2 Meleagridis 2 2 Kedougou 2 2 Kingston 1 1 Shannon 1 1 Stuttgart 1 1 Bovismorbificans 1 1 Mbandaka 1 1 Uppsale 1 1 Eschweiler 1 1 Braenderup 1 1 Derby 1 1 Havana 1 1 Anatum 1 1 Waycross 1 1 Bareilly 1 1 Azteca 1 1 Gueuletapee 1 1 Bloomsbury 1 1 Hato 1 1 Powel 2 1 1 Rissen 1 1 Menden 1 1 Nola 1 1 Total 93 27 10 3 133 Note: The six PLADs inculdes Hebei, Shanxi, Shandong, Sichuan, Inner Mongolia, and Beijing.
Abbreviation: PLADs=provincial-level administrative divisions.Table 2.Salmonellaserovar isolates obtained from chicken, pig, cow, and duck samples from the six PLADs, China, 2019.
The MDR rates amongSalmonellafrom animal sources were different in different PLADs. Beijing displayed the highest rate of MDR, reaching 100% (Figure 1A), followed by Shandong (52.0%), Inner Mongolia (50.0%), Sichuan (48.0%), Shanxi (45.7%), and Hebei (25.0%).Salmonellaisolates from six different PLADs were highly resistant to ampicillin (Figure 1Band1C). A total of 18 strains ofSalmonellawith unique drug-resistant phenotypes were selected for whole-genome sequencing. MostSalmonellastrains were resistant to multiple drugs. These strains were derived from chickens and pigs, and the MLST type was mainly ST11. The predominant serotype among these 18Salmonellastrains was enteritidis.
Figure 1.Multidrug resistance and distribution ofSalmonellafrom the six PLADs, China, 2019. (A) The proportion of different antibiotic resistant types. (B) Distribution ofSalmonellaresistance phenotypes from different PLADs and cities in China. (C) Resistant phenotypes ofSalmonellafrom different host sources.
Note: The six PLADs include Hebei, Shanxi, Shandong, Sichuan, Inner Mongolia, and Beijing. Abbreviations: PLADs=provincial-level administrative divisions; A/C=amoxicilin-clavulanic acid; AMP=ampicillin; CEF=ceftiofur; CAZ=ceftazidime; GEM=gentamicin; SPT=spectinomycin; APR=apramycin; ENR=enrofloxacin; OFL=ofloxacin; MEM=meropenem; SXT=trimethoprim-sulfamethoxazole; SF=sulfamethoxazole; FFC=florfenicol; TET=tetracycline; CL=colistin.
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In the present study, the prevalence ofSalmonellawas 10.5% in chicken samples, 24.4% in pig, 23.3% in duck, and 29.4% in milk. The high contamination rate ofSalmonellain milk samples indicated that milk is an important medium forSalmonellatransmission. These results indicated thatSalmonellacontamination of food animals in China was a serious public health problem. Better measures should thus be taken to controlSalmonellaon dairy farms. Antimicrobial susceptibility tests in this study revealed that all the 198Salmonellaisolates were highly resistant to at least one tested antibiotic class (penicillin, folate pathway antagonists, tetracyclines, quinolones, and fluoroquinolones). The highest rates of antimicrobial resistance were observed for ampicillin (59.6%). High prevalence of resistance to ampicillin is due to this antibiotic has been widely used in animal husbandry in China (2). At present, clinics have reported high resistance ofSalmonellato ampicillin (53%) (3) and high resistance in food animals (68.7%) in China (4). We should carry out regular disinfection and sterilization of the breeding environment and avoid eating meat, eggs, and other dairy products that have not been treated with high temperatures. This research provided important guidance and reference value for animal breeding drugs, and provided data reference value for the detection, diagnosis, and treatment ofSalmonellainfection in clinic.
Compared with other research reports in China, the prevalence ofSalmonellawas 43.3% for chickens (5), 17.4% for pigs (6), 2.1% for ducks (7), and 1.3% for milk (8). In addition to the reduction in the prevalence ofSalmonellafrom chickens, our results showed an increase in the prevalence ofSalmonellain pigs, ducks, and milk. In this study, the high rate ofSalmonellacontamination in cow milk samples. Other studies have reportedSalmonellainfection in raw milk and milk-related infant foods (9) as well, which might threaten the health of babies. Although the milk sample sources used in this study were limited, the findings suggested thatSalmonellaposes a threat to the milk supply. The highest rates of antimicrobial resistance were observed for ampicillin (59.6%), in agreement with the results of many previous studies onSalmonellaisolates from food animals (10).
This study was subject to several limitations. First, the geographically concentrated nature of the samples in the present study does not represent China as a whole. Second, the types of the samples collected from each of the six PLADs and cities were not uniform, leading to sample biases as the collected samples could not represent the overall circumstances.
This was a survey of the prevalence ofSalmonellain samples obtained from food animals from six PLADs in China. The isolates showed high antimicrobial resistance, with resistance to ampicillin being the most common. It is worth noting that in this study,S.Enteritidis displayed the most prevalent drug resistance and MDR. MDRSalmonellaisolates from humans have a common ancestor with the isolates from food animals, increasing the difficulty of curing human infections and increasing healthcare costs. A nationally coordinated intervention strategy for drug use in farmed animals is needed to limit the spread of MDRSalmonella. Better methods for monitoring the emergence and spread of MDRSalmonellawould facilitate disease control and treatment. To prevent these strains from becoming a worldwide pandemic, internationally coordinated intervention strategies to limit further dissemination of MDRSalmonellaare required.
Acknowledgement:Research staff at College of Veterinary Medicine, China Agricultural University.
Conflicts of interest:No conflicts of interest.
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