Gómez Paula, Lozano Carmen, González-Barrio David, Zarazaga Myriam, Ruiz-Fons Francisco, Torres Carmen
Area of Biochemistry and Molecular Biology, University of La Rioja, Logroño, Spain.
SaBio, Spanish Wildlife Research Institute IREC (CSIC-UCLM-JCCM), Ciudad Real, Spain.
Vet Microbiol. 2015 Jun 12;177(3-4):326-31. doi: 10.1016/j.vetmic.2015.03.029. Epub 2015 Apr 14.
The objective was to determine the prevalence of Staphylococcus aureus nasal carriage in red deer of a semi-extensive farm and in humans in contact with the estate animals, and to characterize obtained isolates. Nasal swabs of 65 deer and 15 humans were seeded on mannitol-salt-agar and oxacillin-resistance-screening-agar-base. Isolates were identified by microbiological and molecular methods. Antimicrobial susceptibility profile was determined for 16 antibiotics by disk-diffusion and the presence of eight antibiotic resistance genes, seven virulence genes and genes of immune-evasion-cluster (IEC) was analyzed by PCR. S. aureus was typed by PFGE-SmaI, spa, agr, SCCmec and MLST. Isolates were detected in 16 deer (24.6%). Eleven S. aureus isolates were methicillin-resistant (MRSA), and five were methicillin-susceptible (MSSA). All MRSA harbored mecC gene and were agr-III/SCCmecXI/ST1945 (four spa-t843 and seven spa-t1535). All mecC-MRSA carried blaZ-SCCmecXI and etd2, were IEC-type-E, and belonged to the same PFGE pattern. The five MSSA were typed as spa-t2420/agr-I/ST133. Regarding humans, S. aureus was recovered from six samples (40%). The isolates were MSSA and were typed as spa-t002/agr-II, spa-t012/agr-III or spa-t822/agr-III and showed different IEC types (A, B, D and F). blaZ and erm(A) genes were detected, as well as cna and tst genes. As conclusion, red deer analyzed in this study are frequent carriers of mecC-MRSA CC130 (16.9%), they are characterized by few resistance and virulence determinants, and by the presence of IEC type-E. Deer could be a source of mecC-MRSA which could potentially be transmitted to other animals, or even to humans.
目的是确定半粗放式农场的马鹿以及与家畜接触的人群中金黄色葡萄球菌鼻腔携带情况,并对分离株进行特征分析。采集了65只鹿和15人的鼻拭子,接种于甘露醇盐琼脂和苯唑西林耐药筛选琼脂基础培养基上。通过微生物学和分子方法鉴定分离株。采用纸片扩散法测定16种抗生素的抗菌药敏谱,并通过聚合酶链反应分析8种抗生素耐药基因、7种毒力基因和免疫逃避簇(IEC)基因的存在情况。通过脉冲场凝胶电泳-SmaI、spa、agr、SCCmec和多位点序列分型(MLST)对金黄色葡萄球菌进行分型。在16只鹿(24.6%)中检测到分离株。11株金黄色葡萄球菌分离株对甲氧西林耐药(MRSA),5株对甲氧西林敏感(MSSA)。所有MRSA均携带mecC基因,属于agr-III/SCCmecXI/ST1945(4株spa-t843和7株spa-t1535)。所有mecC-MRSA均携带blaZ-SCCmecXI和etd2,为IEC-E型,且属于相同的脉冲场凝胶电泳图谱。5株MSSA分型为spa-t2420/agr-I/ST133。在人类方面,从6份样本(40%)中分离出金黄色葡萄球菌。分离株为MSSA,分型为spa-t002/agr-II、spa-t012/agr-III或spa-t822/agr-III,并表现出不同的IEC类型(A、B、D和F)。检测到blaZ和erm(A)基因,以及cna和tst基因。作为结论,本研究分析的马鹿是mecC-MRSA CC130的常见携带者(16.9%),其特征为耐药和毒力决定因素较少,且存在IEC-E型。鹿可能是mecC-MRSA的来源,有可能传播给其他动物,甚至人类。