Gómez Paula, Lozano Carmen, Camacho Mari Cruz, Lima-Barbero José-Francisco, Hernández José-Manuel, Zarazaga Myriam, Höfle Úrsula, 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.
J Antimicrob Chemother. 2016 Jan;71(1):53-7. doi: 10.1093/jac/dkv314. Epub 2015 Oct 21.
The objective of this study was to analyse the prevalence of tracheal carriage of Staphylococcus aureus/MRSA in storks and to study the resistance and virulence genes in the obtained isolates.
Tracheal samples from 92 stork nestlings of two landfill-associated and two natural-habitat colonies were inoculated in specific media for S. aureus and MRSA recovery. Antimicrobial susceptibility was tested, and the presence of resistance, virulence and immune evasion cluster (IEC) genes was analysed by PCR. S. aureus isolates were characterized by spa and agr typing. Staphylococcal cassette chromosome (SCC) mec type was determined for mecC-positive isolates, and MLST was performed for 17 selected S. aureus isolates.
S. aureus isolates were identified in 32/92 samples (34.8%), and 38 isolates were recovered. The prevalence of S. aureus was higher in nestlings from landfills (24/43, 55.8%) than in those from natural habitats (8/49, 16.3%). Three birds from landfill-associated colonies carried MRSA, two with mecA-positive strains [clonal complex (CC) 5-spa-t002 and CC398-spa-t011] and one with a mecC-positive strain [sequence type (ST) 3061-CC130-spa-t843-agr-III-SCCmecXI). None of the MRSA isolates presented IEC genes. Thirty-five MSSA isolates, which showed 18 different spa types (ascribed to CC5, CC7, CC22, CC30, CC45, CC59, CC133 and CC398), were obtained. The agr types detected were I (63%), II (29%) and III (8%). Resistance and virulence genes identified in MSSA were blaZ (n = 25), erm(T) (n = 9), erm(A) (n = 1), tet(M) (n = 2), fexA (n = 3), str (n = 2), tst (n = 2), eta (n = 1) and cna (n = 15). The IEC types B, C, D and G were found in MSSA isolates, and two new STs were identified (ST3060 and ST3061).
White storks are frequently tracheal carriers of S. aureus, including ST398 isolates. MRSA isolates of lineages CC398-mecA and CC130-mecC were detected in storks from landfill-associated colonies exposed to human residues.
本研究的目的是分析鹳中金黄色葡萄球菌/耐甲氧西林金黄色葡萄球菌(MRSA)的气管携带率,并研究分离株中的耐药基因和毒力基因。
从两个与垃圾填埋场相关的和两个自然栖息地群落的92只鹳雏鸟中采集气管样本,接种于用于金黄色葡萄球菌和MRSA分离的特定培养基中。检测抗菌药物敏感性,并通过聚合酶链反应(PCR)分析耐药、毒力和免疫逃避簇(IEC)基因的存在情况。金黄色葡萄球菌分离株通过spa和agr分型进行鉴定。对mecC阳性分离株测定葡萄球菌盒式染色体(SCC)mec类型,并对17株选定的金黄色葡萄球菌分离株进行多位点序列分型(MLST)。
在32/92份样本(34.8%)中鉴定出金黄色葡萄球菌分离株,共分离出38株。来自垃圾填埋场的雏鸟中金黄色葡萄球菌的携带率(24/43,55.8%)高于来自自然栖息地的雏鸟(8/49,16.3%)。来自与垃圾填埋场相关群落的三只鸟携带MRSA,两只携带mecA阳性菌株[克隆复合体(CC)5-spa-t002和CC398-spa-t011],一只携带mecC阳性菌株[序列类型(ST)3061-CC130-spa-t843-agr-III-SCCmecXI]。所有MRSA分离株均未呈现IEC基因。获得了35株甲氧西林敏感金黄色葡萄球菌(MSSA)分离株,它们显示出18种不同的spa类型(归属于CC5、CC7、CC22、CC30、CC45、CC59、CC133和CC398)。检测到的agr类型为I(63%)、II(29%)和III(8%)。在MSSA中鉴定出的耐药和毒力基因有blaZ(n = 25)、erm(T)(n = 9)、erm(A)(n = 1)、tet(M)(n = 2)、fexA(n = 3)、str(n = 2)、tst(n = 2)、eta(n = 1)和cna(n = 15)。在MSSA分离株中发现了IEC类型B、C、D和G,并鉴定出两个新的STs(ST3060和ST3061)。
白鹳经常是金黄色葡萄球菌的气管携带者,包括ST398分离株。在接触人类残留物的与垃圾填埋场相关群落的鹳中检测到CC398-mecA和CC130-mecC谱系的MRSA分离株。