Ben Chehida Faten, Gharsa Haythem, Tombari Wafa, Selmi Rachid, Khaldi Sana, Daaloul Monia, Ben Slama Karim, Messadi Lilia
Laboratory of Microbiology, Immunology and General Pathology, Institution of Agricultural Research and Higher Education, National School of Veterinary Medicine of Sidi Thabet, University of Manouba, Sidi Thabet 2020, Tunisia.
Laboratory of Microorganisms and Active Biomolecules, Higher Institute of Applied Biological Sciences of Tunis, University of Tunis El Manar, Tunis 2092, Tunisia.
Animals (Basel). 2021 Sep 21;11(9):2754. doi: 10.3390/ani11092754.
A total of 318 nasal and rectal swabs were collected from 159 apparently healthy camels () randomly selected from five regions in southern and central Tunisia and screened for carriage. spp. were recovered from 152 of 159 camels studied (95.6%) and in total 258 swabs (81%) were positive. Among these isolates, 16 were coagulase positive (CoPS) (6.2%) and were characterized by biochemical and molecular tests as . These were isolated from 14 camels (8.8%) with co-carriage in nasal and rectal mucosa by two camels. All isolates recovered were methicillin-susceptible Staphylococcus aureus (MSSA) and were characterized by typing and PFGE. Three different types were recovered: t729, t4013 and a type newly registered as t19687, which was the most common. PFGE analysis revealed seven different patterns and these were characterized by MLST, which revealed five different sequence types (ST6, ST88, ST3583 and two new sequences, ST6504 and ST6506). All isolates harbored different virulence genes, including , encoding delta hemolysin; E-D, encoding bicomponent leukotoxin LukE-LukD; the B gene, encoding clumping factor B; the gene, encoding laminin-binding protein; and 8, encoding capsule type 8. Fifteen isolates harbored hemolysin beta () and fourteen encoded hemolysin alpha () and hemolysin G2 (). Adhesin factors, including and , were detected in five and four isolates respectively. Binding proteins, including collagen () and elastin-binding protein (), were detected in two isolates while fibrinogen-binding protein () was identified in four isolates. This study provides the first set of genotyping data on the population structure and presence of toxin genes of strains in Tunisian camels.
从突尼斯南部和中部五个地区随机选取159头看似健康的骆驼,共采集了318份鼻拭子和直肠拭子,用于筛查 携带情况。在159头被研究的骆驼中,有152头(95.6%)检测出 属细菌,总共258份拭子(81%)呈阳性。在这些分离株中,16株为凝固酶阳性葡萄球菌(CoPS)(6.2%),通过生化和分子检测鉴定为 。这些菌株从14头骆驼(8.8%)的鼻黏膜和直肠黏膜中分离得到,有两头骆驼同时携带。所有分离得到的 菌株均为甲氧西林敏感金黄色葡萄球菌(MSSA),并通过 分型和脉冲场凝胶电泳(PFGE)进行鉴定。共鉴定出三种不同的 类型:t729、t4013和一种新注册的t19687型,其中t19687型最为常见。PFGE分析显示有七种不同的图谱,通过多位点序列分型(MLST)进行特征分析,结果显示有五种不同的序列类型(ST6、ST88、ST3583以及两个新序列ST6504和ST6506)。所有分离株都携带不同的毒力基因,包括编码δ溶血素的 ;编码双组分白细胞毒素LukE-LukD的E-D;编码聚集因子B的B基因;编码层粘连蛋白结合蛋白的 基因;以及编码8型荚膜的8。15株分离株携带β溶血素( ),14株编码α溶血素( )和G2溶血素( )。分别在5株和4株分离株中检测到黏附因子,包括 和 。在两株 分离株中检测到结合蛋白,包括胶原蛋白( )和弹性蛋白结合蛋白( ),同时在4株分离株中鉴定出纤维蛋白原结合蛋白( )。本研究提供了关于突尼斯骆驼中 菌株群体结构和毒素基因存在情况的第一组基因分型数据。