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Genetic relatedness of ceftriaxone-resistant and high-level azithromycin resistant Neisseria gonorrhoeae cases, United Kingdom and Australia, February to April 2018

机译:头孢曲松耐药和阿奇霉素耐药的淋病奈瑟菌病例的遗传相关性,英国和澳大利亚,2018年2月至4月

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Between February and April 2018, three ceftriaxone-resistant and high-level azithromycin-resistant Neisseria gonorrhoeae cases were identified; one in the United Kingdom and two in Australia. Whole genome sequencing was used to show that the isolates from these cases belong to a single gonococcal clone, which we name the A2543 clone. Keywords: Neisseria gonorrhoeae, microbial drug resistance, whole genome sequencing, PCR, United Kingdom, Australia, XDR, antimicrobial resistance, AMRBetween February and April 2018, Neisseria gonorrhoeae (NG) isolates displaying ceftriaxone resistance and high-level azithromycin resistance were independently reported from both the United Kingdom (UK) (one case) and Australia (two cases) [1,2]. Here, genomic analysis is used to demonstrate that these cases were caused by a single clone of extensively drug-resistant (XDR) NG. This study has demonstrated that a single XDR clone, with epidemiological links to Asia, has been successfully transmitted on least three independent occasions and may be still circulating, which is of global public health significance.Case descriptionOf three XDR NG cases, the first was identified in February 2018, in a heterosexual male in the UK, presenting with urethral discharge, who reported sexual contact with a female resident in Thailand in January 2018 [1]. NG was cultured from both a urethral swab taken at the first clinical presentation ({"type":"entrez-nucleotide","attrs":{"text":"G97687","term_id":"22750764","term_text":"G97687"}}G97687) and a pharyngeal swab taken during follow-up (G7944). The two Australian cases were identified in March and April 2018. One case was a male experiencing urethral discharge, who reported sexual contact with a female in south-east Asia, the other case was female, who presented with cervicitis, with no travel history outside of Australia [2].Extensive drug resistanceFirst line treatment for NG typically involves a dual treatment regime of ceftriaxone (500mg intramuscularly) and azithromycin (1 or 2g orally). While in the past 10 years, there have been numerous reports of sustained transmission of high-level azithromycin resistant NG, there has only been several different gonococcal strains observed exhibiting ceftriaxone resistance and these have been sporadic (i.e. limited or no further reports of transmission). Prior to the three cases reported here, no ceftriaxone resistant isolates have additionally exhibited high-level resistance to azithromycin (minimum inhibitory concentration (MIC)?≥?256 mg/L) [3-8]. Isolates from the three cases exhibited both resistance to ceftriaxone (0.25–0.5 mg/L) and high-level resistance to azithromycin according to European Committee on Antimicrobial Susceptibility Testing (EUCAST) resistance breakpoints, requiring the patients to undergo extensive follow-up and treatments including days of hospitalisation and intravenous therapies [1,2]. All three patients were subsequently followed up for test of cure and confirmed to have cleared their infection.Genomic analysisThe pharyngeal isolate from the UK case has been recently assigned as the World Health Organization (WHO) reference strain Q (WHO-Q; NCTC 14208), while the two isolates from the Australian cases represent a cluster referred to as the A2543 clone [1,2]. Isolates from each of the three cases were independently whole genome sequenced in the UK and Australia (European Nucleotide Archive (ENA) PRJEB26560 for UK urethral ({"type":"entrez-nucleotide","attrs":{"text":"G97687","term_id":"22750764","term_text":"G97687"}}G97687) and pharyngeal (G7944) isolates, and PRJEB29480 for Australian male (A2735) and female (A2543) case isolates). All four isolates shared the same NG-multi-antigen sequence type (NG-MAST) (ST 16848), multilocus sequence type (MLST) (ST 12039) and NG-Sequence Typing for Antimicrobial Resistance type (NG-STAR 996) [5]. The isolates harboured a mosaic penA allele, type 60.001, conferring ceftriaxone resistance as well as four copies of the 23S rRNA A2059G mutation responsible for high-level azithromycin resistance [9,10]. These findings suggest the UK and Australian isolates are all closely related, however the exact phylogenetic relationship between them has not yet been determined.Phylogenetic investigationWe mapped UK and Australian sequence reads against a hybrid assembly reference generated from one of the UK isolates, {"type":"entrez-nucleotide","attrs":{"text":"G97687","term_id":"22750764","term_text":"G97687"}}G97687, and compared the sequences as described previously [1]. The Figure shows a recombination-corrected maximum likelihood phylogeny of the four sequences from the three XDR NG cases and the six most closely related publicly available sequences in the ENA and National Center for Biotechnology Information (NCBI) short read archives. Sequences from the two isolates from the UK case and the isolate from female Australian case were indistinguishable; there was only one single nucleotide polymorphi
机译:在2018年2月至2018年4月期间,确定了三例耐头孢曲松和高水平耐阿奇霉素的淋病奈瑟菌病例;一台在英国,两台在澳大利亚。使用全基因组测序显示来自这些病例的分离物属于单个淋球菌克隆,我们将其命名为A2543克隆。关键字:淋病奈瑟菌,微生物耐药性,全基因组测序,PCR,英国,澳大利亚,XDR,抗菌素耐药性,AMB在2018年2月至4月之间,分别从头孢曲松耐药性和高水平阿奇霉素耐药性报告了淋病奈瑟氏菌(NG)分离株英国(UK)(1例)和澳大利亚(2例)[1,2]。在这里,基因组分析用于证明这些病例是由单一的广泛耐药(XDR)NG克隆引起的。这项研究表明,具有与亚洲流行病学联系的单个XDR克隆已成功在至少三个独立的场合成功传播,并且可能仍在传播,这具有全球公共卫生意义。 2018年2月,在英国的一名异性恋男性中,尿道排出物,他于2018年1月报告与泰国一名女性居民发生性接触[1]。从第一次临床表现中取出的两个尿道拭子中培养NG({“ type”:“ entrez-nucleotide”,“ attrs”:{“ text”:“ G97687”,“ term_id”:“ 22750764”,“ term_text” :“ G97687”}} G97687)和在随访期间服用的咽拭子(G7944)。澳大利亚在2018年3月和2018年4月发现了两例。一例是男性尿道排出物,报告与东南亚的一名女性发生性接触,另一例是女性,患有宫颈炎,没有外游史(2)。广泛的耐药性NG的一线治疗通常涉及头孢曲松(肌注500mg)和阿奇霉素(口服1或2g)的双重治疗方案。尽管在过去的十年中,有许多关于高水平对阿奇霉素耐药的NG持续传播的报道,但仅观察到几种表现出对头孢曲松耐药的不同的淋球菌菌株,并且这些菌株是零星的(即有限或没有进一步的传播报道) 。在这里报道的三例之前,没有头孢曲松抗药性菌株对阿奇霉素具有更高的抗药性(最低抑菌浓度(MIC)≥≥256mg / L)[3-8]。根据欧洲抗菌药物敏感性试验(EUCAST)耐药性断点,这三例病例的分离株均显示出对头孢曲松(0.25-0.5 mg / L)的耐药性和对阿奇霉素的高水平耐药性,要求患者进行广泛的随访和治疗包括住院天数和静脉治疗[1,2]。这三名患者随后均接受了随访以进行治愈测试,并确认已清除感染。基因组分析英国病例的咽部分离株最近已被指定为世界卫生组织(WHO)参考菌株Q(WHO-Q; NCTC 14208) ,而来自澳大利亚病例的两个分离株代表一个称为A2543克隆的簇[1,2]。在英国和澳大利亚,分别对这三例病例的分离株进行了全基因组测序(针对英国尿道的欧洲核苷酸档案库(ENA)PRJEB26560({“ type”:“ entrez-nucleotide”,“ attrs”:{“ text”:“ G97687”,“ term_id”:“ 22750764”,“ term_text”:“ G97687”}} G97687)和咽部(G7944)分离株,PRJEB29480用于澳大利亚男性(A2735)和女性(A2543)病例分离株)。这四个分离株均具有相同的NG-多抗原序列类型(NG-MAST)(ST 16848),多基因座序列类型(MLST)(ST 12039)和NG序列分型的抗菌素耐药性类型(NG-STAR 996)[5 ]。这些分离株具有60.001型的花叶penA等位基因,赋予头孢曲松抗性以及负责高水平阿奇霉素抗性的23S rRNA A2059G突变的四个拷贝[9,10]。这些发现表明英国和澳大利亚分离株都密切相关,但是尚未确定它们之间的确切系统发育关系。系统发育研究我们将英国和澳大利亚分离的序列读数与从英国分离株之一产生的杂交装配参照图进行了映射“:” entrez-nucleotide“,” attrs“:{” text“:” G97687“,” term_id“:” 22750764“,” term_text“:” G97687“}}} G97687,并比较了先前描述的序列[1] 。该图显示了ENA和国家生物技术信息中心(NCBI)短读档案中来自三个XDR NG病例和四个最密切相关的公开可用序列的四个序列的重组校正最大似然系统发育。来自英国病例的两个分离株和澳大利亚女性病例的分离株的序列是难以区分的。只有一个单核苷酸多态性

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