[2]单相肠沙门氏菌亚种的发生与鉴定。具有抗原式1,4,[5],12:i:-的肠球菌[2007-2012年在波兰分离]。

Grzegorz Madajczak, Tomasz Wołkowicz, Bozena Dera-Tomaszewska, Monika Wasiak, Anna Chróst, Jolanta Szych
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引用次数: 0

摘要

简介:沙门氏菌是波兰和其他欧盟国家细菌肠道感染的重要病原体。自20世纪90年代以来,观察到单相沙门氏菌抗原式1,4,[5],12:i:-的发病率不断上升,其分为两个谱系:西班牙和欧洲。更常见的欧洲谱系以抗微生物药物耐药性ASSuT和DT193噬菌体型为特征。在许多欧洲国家,这些生物已成为最常见的分离血清型之一。本研究的目的是分析肠道沙门氏菌亚种的菌株。2007-2012年在波兰分离到具有抗原式1,4,[5],12:i:-的肠杆菌菌株。材料与方法:本研究的材料为2007-2012年从临床、食品和动物样本中分离的146株沙门氏菌,初步鉴定为沙门氏菌抗原式1,4,[5],12:i,-。所有菌株已根据实验室常规使用的方法重新鉴定。血清型的鉴定采用经典的方法——体细胞和鞭毛抗原的玻片凝集和Check&Trace沙门氏菌微阵列。采用PCR技术检测了沙门氏菌fljB基因、fliB-fliA基因间区、选定的沙门氏菌致病岛(SPIs)基因和spvC。用HindIII酶对所有菌株进行了PFGE分型和噬菌体分型。此外,根据EUCAST的建议,通过建立MIC来评估抗生素耐药性。结果:肠道沙门氏菌1、4、[5]、12:i、- 110株(75%)。该组对17株沙门菌进行了“鼠伤寒沙门菌”的微阵列鉴定。110株鼠伤寒沙门氏菌均具有1000 bp大小的IS200序列DNA片段。仅在4株中检测到fljB基因。所有菌株均含有avrA、ssaQ、mgtC和siiD基因。6株未检出spvC基因。92株(83.6%)被分型为DT193,另有40株与18号噬菌体发生附加反应。104株(94.5%)已检出对至少一种抗菌素耐药。最常见的耐药模式为ASSuT(44株- 40%)。所有菌株中有11个脉冲型,其中2个或2个以上的菌株已被识别,其中有37个菌株。其余菌株具有独特的REA-PFGE模式。结论:目前尚未确认波兰从人间病例中分离出的肠链球菌1,4,[5],12:i:-的流行病学情况。目前的研究结果表明,所研究的菌株属于欧洲非西班牙的单相鼠伤寒沙门氏菌谱系,这些菌株引起的感染问题尚未得到认识,并可能增加。
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[Occurrence and characterization of monophasic Salmonella enterica subsp. enterica with antigenic formula 1,4, [5], 12: i:-isolated in Poland in 2007-2012].

Introduction: Salmonella is significant etiological agent of bacterial intestinal infections in Poland and other European Union countries. Since the 90's increasing incidence of monophasic Salmonella antigenic formula 1,4,[5],12:i:-has been observed, which are divided into two lineages: Spanish and European. More common European lineage are characterized by antimicrobial resistance ASSuT and DT193 phagetype. In many European countries, these organisms have become one of the most commonly isolated serovars. The aim of this study was to analyze strains of Salmonella enterica subsp. enterica strains with antigenic formula 1,4,[5],12: i:-, isolated in Poland in 2007-2012 years.

Material and methods: The material for the study was 146 Salmonella strains initially identified as Salmonella antigenic formula 1,4,[5],12:i,-, isolated in 2007-2012 from clinical, food and animal samples. All strains has been reidentified according to the methodology routinely used in the laboratory. Serovar has been identified using classical method--slide agglutination for somatic and flagellar antigens and using Check&Trace Salmonella microarray. The fljB gene,fliB-fliA intergenic region, selected Salmonella Pathogenicity Islands' (SPIs) genes and spvC has been detected using PCR. For all strains PFGE typing with HindIII enzyme has been performed and phagetyping also. Moreover antimicrobial resistance has been evaluated by establishing of MIC according EUCAST recommendation.

Results: 110 (75%) strains were S. enterica 1,4,[5],12:i,-. In this group for 17 strains in Check&Trace Salmonella microarray result of identification "Salmonella Typhimurium" have been obtained. All 110 strains have 1000 bp size DNA fragment with IS200 sequence, characteristic for S. Typhimurium. Only in case of 4 strains fljB gene has been detected. All strains harbor avrA, ssaQ, mgtC and siiD genes. For 6 strains spvC gene has been not detected. 92 strains (83.6%) have been typed as DT193, but in case of 40 strains additional reaction with phage no 18 has been observed. For 104 (94.5%) strains resistance for at least one antimicrobial have been detected. Most frequent (44 strains - 40%) resistance pattern was ASSuT. Among all strains 11 pulsotypes, which group two or more strains have been recognized, which contain 37 strains. The rest of strains have unique REA-PFGE patterns.

Conclusions: To this time epidemiological situation of S. enterisa 1,4,[5],12:i:- isolated from human cases in Poland has been not recognized. Results of current studies show, that studied strains belong to european non-spanish lineage of monophasic S. Typhimurium and problem of infection caused by those strains is unrecognized and probably increase.

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