Department of Respiratory Medicine, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
Department of Respiratory Medicine, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University, No. 168 Litang Road, Changping District, Beijing, 102218, China.
Ann Clin Microbiol Antimicrob. 2019 Jan 21;18(1):4. doi: 10.1186/s12941-018-0302-9.
The definition of hypervirulent Klebsiella pneumoniae (hvKp), traditionally regarded as hypermucoviscosity, is controversial. However, data based on both phenotype (hypermucoviscous) and genetic (aerobactin) criteria are limited.
A retrospective study was conducted in 175 geriatric patients between January 2008 and January 2014. The clinical and molecular data, including antimicrobial susceptibility testing, extended-spectrum-β-lactamase (ESBL) production, virulence gene, and multilocus sequence typing of the hvKp-group (hypermucoviscosity and aerobactin positive) were compared with those of classic K. pneumoniae (cKp) isolates.
Of 175 Kp isolates, 45.7% were hvKp. In pathogenicity, K1, K2, magA, rmpA, and rmpA2 genes were strongly associated with hvKp (P < 0.01). In the hvKp group, invasive infections (P < 0.000), liver abscess (P = 0.008), abdominal infection (P = 0.002) and septic shock (P = 0.035) are significantly higher than cKp group. Patients with better nutritional status were frequently infected with hvKp. However, host inflammatory reaction is most severe in hvKp group. Patients with diabetes (odds ratio [OR] = 2.548) and digestive diseases (OR = 2.196) are more likely to be infected with hvKp. Importantly, the detection of hvKp isolates increased from January 2008 to January 2010, January 2010 to January 2012, and January 2010 to January 2014 (12, 30, and 48 isolates, respectively). Overall, 16.3% of hvKp isolates produced ESBLs and 20.0% were MDR-hvKp. Multivariate analysis implied that infection occurred in the ICU (OR = 5.826) and patients with indwelling stomach tubes (OR = 6.461) are independent risk factors for ESBL-hvKp infection.
HvKp, especially ESBL-hvKp and MDR-hvKp, is emerging in the elderly. It is essential to enhance clinical awareness and management of hvKp infections.
传统上认为高毒力肺炎克雷伯菌(hvKp)是高黏液性的,但这种定义存在争议。然而,基于表型(高黏液性)和遗传(aerobactin)标准的数据有限。
对 2008 年 1 月至 2014 年 1 月间的 175 例老年患者进行了回顾性研究。比较了 hvKp 组(高黏液性和 aerobactin 阳性)与经典肺炎克雷伯菌(cKp)分离株的临床和分子数据,包括药敏试验、产超广谱β-内酰胺酶(ESBL)、毒力基因和多位点序列分型。
在 175 株 Kp 分离株中,45.7%为 hvKp。在致病性方面,K1、K2、magA、rmpA 和 rmpA2 基因与 hvKp 密切相关(P<0.01)。在 hvKp 组中,侵袭性感染(P<0.000)、肝脓肿(P=0.008)、腹部感染(P=0.002)和感染性休克(P=0.035)的发生率明显高于 cKp 组。营养状况较好的患者常感染 hvKp,但 hvKp 组的宿主炎症反应更为严重。糖尿病(比值比[OR] = 2.548)和消化系统疾病(OR = 2.196)患者更易感染 hvKp。重要的是,从 2008 年 1 月到 2010 年 1 月、从 2010 年 1 月到 2012 年 1 月以及从 2010 年 1 月到 2014 年 1 月,hvKp 分离株的检出率分别增加了 12、30 和 48 株(分别为)。总的来说,16.3%的 hvKp 分离株产生 ESBLs,20.0%为 MDR-hvKp。多变量分析表明,重症监护病房(OR=5.826)和留置胃管(OR=6.461)感染是 ESBL-hvKp 感染的独立危险因素。
高毒力肺炎克雷伯菌(hvKp),特别是 ESBL-hvKp 和 MDR-hvKp,在老年人中正在出现。必须提高对 hvKp 感染的临床认识和管理。