National Clinical Bacteriology and Mycology Reference Laboratory, Ethiopian Public Health Institute, Addis Ababa, Ethiopia.
Department of Medical Laboratory Sciences, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
PLoS One. 2021 Dec 2;16(12):e0256556. doi: 10.1371/journal.pone.0256556. eCollection 2021.
Multidrug resistant, extremely drug-resistant, pan-drug resistant, carbapenem-resistant, and carbapenemase-producing gram-negative bacteria are becoming more common in health care settings and are posing a growing threat to public health.
The study was aimed to detect and phenotypically characterize carbapenem no- susceptible gram-negative bacilli at the Ethiopian Public Health Institute.
A prospective cross-sectional study was conducted from June 30, 2019, to May 30, 2020, at the national reference laboratory of the Ethiopian Public Health Institute. Clinical samples were collected, inoculated, and incubated for each sample in accordance with standard protocol. Antimicrobial susceptibility testing was conducted using Kirby-Bauer disk diffusion method. Identification was done using the traditional biochemical method. Multidrug-resistant and extensively drug-resistant isolates were classified using a standardized definition established by the European Centre for Disease Prevention and Control and the United States Centers for Disease Prevention and Control. Gram-negative organisms with reduced susceptibility to carbapenem antibiotics were considered candidate carbapenemase producers and subjected to modified carbapenem inactivation and simplified carbapenem inactivation methods. Meropenem with EDTA was used to differentiate metallo-β-lactamase (MBL) from serine carbapenemase. Meropenem (MRP)/meropenem + phenylboronic acid (MBO) were used to differentiate Klebsiella pneumoniae carbapenemase (KPC) from other serine carbapenemase producing gram-negative organisms.
A total of 1,337 clinical specimens were analyzed, of which 429 gram-negative bacterial isolates were recovered. Out of 429 isolates, 319, 74, and 36 were Enterobacterales, Acinetobacter species, and Pseudomonas aeruginosa respectively. In our study, the prevalence of multidrug-resistant, extensively drug-resistant, carbapenemase-producing, and carbapenem nonsusceptible gram-negative bacilli were 45.2%, 7.7%, 5.4%, and 15.4% respectively. Out of 429 isolates, 66 demonstrated reduced susceptibility to the antibiotics meropenem and imipenem. These isolates were tested for carbapenemase production of which 34.8% (23/66) were carbapenemase producers. Out of 23 carbapenemase positive gram-negative bacteria, ten (10) and thirteen (13) were metallo-beta-lactamase and serine carbapenemase respectively. Three of 13 serine carbapenemase positive organisms were Klebsiella pneumoniae carbapenemase.
This study revealed an alarming level of antimicrobial resistance (AMR), with a high prevalence of multidrug-resistant (MDR) and extremely drug-resistant, carbapenemase-producing gram-negative bacteria, particularly among intensive care unit patients at the health facility level. These findings point to a scenario in which clinical management of infected patients becomes increasingly difficult and necessitates the use of "last-resort" antimicrobials likely exacerbating the magnitude of the global AMR crisis. This mandates robust AMR monitoring and an infection prevention and control program.
在医疗机构中,耐多药、广泛耐药、泛耐药、碳青霉烯耐药和产碳青霉烯酶的革兰氏阴性菌越来越常见,对公共卫生构成日益严重的威胁。
本研究旨在埃塞俄比亚公共卫生研究所检测并表型鉴定耐碳青霉烯类的革兰氏阴性杆菌。
2019 年 6 月 30 日至 2020 年 5 月 30 日,在埃塞俄比亚公共卫生研究所的国家参考实验室进行了一项前瞻性横断面研究。按照标准方案采集临床样本、接种和孵育每个样本。使用 Kirby-Bauer 纸片扩散法进行抗生素敏感性测试。使用传统生化方法进行鉴定。使用欧洲疾病预防控制中心和美国疾病预防控制中心制定的标准化定义对多药耐药和广泛耐药的分离株进行分类。对碳青霉烯类抗生素敏感性降低的革兰氏阴性菌被认为是候选碳青霉烯酶产生菌,并采用改良碳青霉烯失活和简化碳青霉烯失活方法进行检测。使用亚乙基二胺四乙酸(EDTA)的美罗培南用于区分金属β-内酰胺酶(MBL)和丝氨酸碳青霉烯酶。使用美罗培南(MRP)/美罗培南+苯硼酸(MBO)区分肺炎克雷伯菌碳青霉烯酶(KPC)和其他产丝氨酸碳青霉烯酶的革兰氏阴性菌。
共分析了 1337 份临床标本,其中回收了 429 株革兰氏阴性细菌分离株。在 429 株分离株中,肠杆菌科、不动杆菌属和铜绿假单胞菌分别为 319、74 和 36 株。在我们的研究中,多药耐药、广泛耐药、产碳青霉烯酶和耐碳青霉烯类革兰氏阴性杆菌的流行率分别为 45.2%、7.7%、5.4%和 15.4%。在 429 株分离株中,有 66 株对美罗培南和亚胺培南的抗生素敏感性降低。对这些分离株进行了碳青霉烯酶产生的检测,其中 34.8%(23/66)为碳青霉烯酶产生菌。在 23 株碳青霉烯酶阳性革兰氏阴性菌中,10 株(10)和 13 株(13)分别为金属β-内酰胺酶和丝氨酸碳青霉烯酶。在 13 株产丝氨酸碳青霉烯酶的阳性菌中,有 3 株为肺炎克雷伯菌碳青霉烯酶。
本研究揭示了令人震惊的抗生素耐药水平,多药耐药(MDR)和广泛耐药、产碳青霉烯酶的革兰氏阴性菌的流行率很高,尤其是在医疗机构的重症监护病房患者中。这些发现表明,感染患者的临床管理变得越来越困难,需要使用“最后手段”的抗生素,这可能会加剧全球抗生素耐药性危机的严重程度。这需要进行强有力的抗生素耐药性监测和感染预防与控制计划。