1.Occurrence and characterization of livestock-associated methicillin-resistant Staphylococcus aureus in pig industries of northern Thailand.
Prapas PATCHANEE ; Pakpoom TADEE ; Orapun ARJKUMPA ; David LOVE ; Karoon CHANACHAI ; Thomas ALTER ; Soawapak HINJOY ; Prasit THARAVICHITKUL
Journal of Veterinary Science 2014;15(4):529-536
This study was conducted to determine the prevalence of livestock-associated methicillin-resistant Staphylococcus aureus (LA-MRSA) in pigs, farm workers, and the environment in northern Thailand, and to assess LA-MRSA isolate phenotypic characteristics. One hundred and four pig farms were randomly selected from the 21,152 in Chiang Mai and Lamphun provinces in 2012. Nasal and skin swab samples were collected from pigs and farm workers. Environmental swabs (pig stable floor, faucet, and feeder) were also collected. MRSA was identified by conventional bacterial culture technique, with results confirmed by multiplex PCR and multi locus sequence typing (MLST). Herd prevalence of MRSA was 9.61% (10 of 104 farms). Among pigs, workers, and farm environments, prevalence was 0.68% (two of 292 samples), 2.53% (seven of 276 samples), and 1.28% (four of 312 samples), respectively. Thirteen MRSA isolates (seven from workers, four from environmental samples, and two from pigs) were identified as Staphylococcal chromosomal cassette mec IV sequences type 9. Antimicrobial sensitivity tests found 100% of the MRSA isolates resistant to clindamycin, oxytetracycline, and tetracycline, while 100% were susceptible to cloxacillin and vancomycin. All possessed a multidrug-resistant phenotype. This is the first evidence of an LA-MRSA interrelationship among pigs, workers, and the farm environment in Thailand.
*Animal Husbandry
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Animals
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Cross-Sectional Studies
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Genotype
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Humans
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Methicillin-Resistant Staphylococcus aureus/classification/*genetics/*isolation & purification
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Microbial Sensitivity Tests/veterinary
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Molecular Sequence Data
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Multilocus Sequence Typing/veterinary
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Multiplex Polymerase Chain Reaction/veterinary
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Occupational Diseases/*epidemiology/microbiology
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Phylogeny
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Prevalence
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Sequence Analysis, DNA/veterinary
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Staphylococcal Infections/*epidemiology/microbiology
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Swine
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Swine Diseases/*epidemiology/microbiology
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Thailand/epidemiology
2.Dissimilarity of ccrAB gene sequences between methicillin-resistant Staphylococcus epidermidis and methicillin-resistant Staphylococcus aureus among bovine isolates in Korea.
Young Kyung PARK ; Young Hwan PAIK ; Jang Won YOON ; Lawrence K FOX ; Sun Young HWANG ; Yong Ho PARK
Journal of Veterinary Science 2013;14(3):299-305
The sequences of the ccrAB genes from bovine-, canine- and chicken-originating methicillin-resistant Staphylococcus (S.) epidermidis (MRSE) and bovine methicillin-resistant Staphylococcus (S.) aureus (MRSA) were compared to investigate the frequency of intra-species horizontal transfer of the staphylococcal cassette chromosome mec (SCCmec) complex. Nineteen MRSE strains were isolated from bovine milk, chickens, and dogs, and their genetic characteristics were investigated by multilocus sequence typing and SCCmec typing. Among the animal MRSE strains, the most frequent SCCmec type was type IV, which consisted of the type B mec complex and ccrAB type 2. The ccrA2 and ccrB2 genes were sequenced from the bovine, chicken and canine MRSE strains and compared with those of the bovine MRSA strains. The sequences generally clustered as MRSA and MRSE groups, regardless of the animal source. Additionally, no bovine MRSE sequence was associated with the bovine MRSA groups. Although most of the bovine MRSE and MRSA isolates possessed SCCmec type IV sequences, our results suggest that the intra-species gene transfer of the SCCmec complex between bovine S. aureus and bovine S. epidermidis strains is not a frequent event.
Animals
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Anti-Bacterial Agents/*pharmacology
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Bacterial Proteins/*genetics/metabolism
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Bacterial Typing Techniques/veterinary
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Cattle
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Cattle Diseases/epidemiology/metabolism
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Chickens
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Dog Diseases/epidemiology/metabolism
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Dogs
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*Drug Resistance, Bacterial
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*Gene Transfer, Horizontal
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Methicillin/*pharmacology
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Methicillin-Resistant Staphylococcus aureus/genetics/isolation & purification
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Milk/microbiology
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Multilocus Sequence Typing/veterinary
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Poultry Diseases/epidemiology/metabolism
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Prevalence
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Republic of Korea/epidemiology
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Staphylococcal Infections/epidemiology/microbiology/*veterinary
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Staphylococcus epidermidis/genetics/isolation & purification
3.Prevalence and characteristics of Shiga toxin-producing Escherichia coli (STEC) from cattle in Korea between 2010 and 2011.
Eun KANG ; Sun Young HWANG ; Ka Hee KWON ; Ki Yeon KIM ; Jae Hong KIM ; Yong Ho PARK
Journal of Veterinary Science 2014;15(3):369-379
A total of 156 Shiga-like toxin producing Escherichia coli (STEC) were isolated from fecal samples of Korean native (100/568, 18%) and Holstein dairy cattle (56/524, 11%) in Korea between September 2010 and July 2011. Fifty-two STEC isolates (33%) harbored both of shiga toxin1 (stx1) and shiga toxin2 (stx2) genes encoding enterohemolysin (EhxA) and autoagglutinating adhesion (Saa) were detected by PCR in 83 (53%) and 65 (42%) isolates, respectively. By serotyping, six STEC from native cattle and four STEC from dairy cattle were identified as O-serotypes (O26, O111, O104, and O157) that can cause human disease. Multilocus sequence typing and pulsed-field gel electrophoresis patterns highlighted the genetic diversity of the STEC strains and difference between strains collected during different years. Antimicrobial susceptibility tests showed that the multidrug resistance rate increased from 12% in 2010 to 42% in 2011. Differences between isolates collected in 2010 and 2011 may have resulted from seasonal variations or large-scale slaughtering in Korea performed to control a foot and mouth disease outbreak that occurred in early 2011. However, continuous epidemiologic studies will be needed to understand mechanisms. More public health efforts are required to minimize STEC infection transmitted via dairy products and the prevalence of these bacteria in dairy cattle.
Animals
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Anti-Bacterial Agents/pharmacology
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Cattle/microbiology
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Drug Resistance, Multiple, Bacterial
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Electrophoresis, Gel, Pulsed-Field/veterinary
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Escherichia coli Infections/epidemiology/microbiology/*veterinary
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Female
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Genes, Bacterial/genetics
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Latex Fixation Tests/veterinary
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Microbial Sensitivity Tests/veterinary
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Multilocus Sequence Typing/veterinary
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Prevalence
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Republic of Korea/epidemiology
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Shiga Toxin 1/genetics
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Shiga Toxin 2/genetics
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*Shiga-Toxigenic Escherichia coli/drug effects/genetics
4.Genotyping of Giardia duodenalis Isolates from Dogs in Guangdong, China Based on Multi-Locus Sequence.
Guochao ZHENG ; Muhamd ALSARAKIBI ; Yuanjia LIU ; Wei HU ; Qin LUO ; Liping TAN ; Guoqing LI
The Korean Journal of Parasitology 2014;52(3):299-304
This study aimed to identify the assemblages (or subassemblages) of Giardia duodenalis by using normal or nested PCR based on 4 genetic loci: glutamate dehydrogenase (gdh), triose phosphate isomerase (tpi), beta-giardin (bg), and small subunit ribosomal DNA (18S rRNA) genes. For this work, a total of 216 dogs' fecal samples were collected in Guangdong, China. The phylogenetic trees were constructed with MEGA5.2 by using the neighbor-joining method. Results showed that 9.7% (21/216) samples were found to be positive; moreover, 10 samples were single infection (7 isolates assemblage A, 2 isolates assemblage C, and 1 isolate assemblage D) and 11 samples were mixed infections where assemblage A was predominant, which was potentially zoonotic. These findings showed that most of the dogs in Guangdong were infected or mixed-infected with assemblage A, and multi-locus sequence typing could be the best selection for the genotype analysis of dog-derived Giardia isolates.
Animals
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China
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Cluster Analysis
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Coinfection/parasitology/veterinary
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Cytoskeletal Proteins/genetics
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DNA, Protozoan/chemistry/genetics
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Dog Diseases/parasitology
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Dogs
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Genotype
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Giardia lamblia/*classification/*genetics/isolation & purification
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Giardiasis/parasitology/*veterinary
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Glutamate Dehydrogenase/genetics
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Molecular Sequence Data
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*Multilocus Sequence Typing
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Phylogeny
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Polymerase Chain Reaction
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RNA, Ribosomal, 18S/genetics
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Triose-Phosphate Isomerase/genetics