Kindu Mizan, Moges Feleke, Alemu Ashenafi, Hailu Dawit, Joseph Rafael, Besufikad Esmael, Tsehay Dareskedar, Bashah Daniel, Tigabu Zemene, Mihret Adane, Gelaw Baye
Department of Medical Microbiology, University of Gondar, Gondar, Ethiopia.
Department of Medical Laboratory Science, School of Medicine, MaddaWalabu University, Bale Goba, Ethiopia.
PLoS One. 2025 Sep 4;20(9):e0330613. doi: 10.1371/journal.pone.0330613. eCollection 2025.
Effective infection control requires identifying and eliminating carbapenemase-producing (CP) Gram-negative bacteria (GNB) in high-risk groups like intensive care unit (ICU) patients and from contaminated environmental surfaces. This study aimed to describe the diversity of carbapenemase-encoding genes among critical GNB isolates from ICU patients with infection and/or gastrointestinal (GI) colonization, as well as from ICU environmental surfaces in the Amhara National Regional state, Ethiopia.A total of 169 carbapenem-resistant isolates were identified, including 26 from infections, 82 from GI colonization, and 61 from environmental samples. These comprised Klebsiellapneumoniae (n = 107), Escherichia coli (n = 16), Pseudomonas aeruginosa (n = 9), and Acinetobacter species (n = 37), of which 147 were analyzed.Singleplex and multiplex PCR were performed to detect predominant carbapenemase-encoding genes, including KPC (blaKPC), MBLs (blaIMP, blaVIM, and blaNDM), and OXA (blaOXA-48, blaOXA-23, and blaOXA-58). PCR analysis revealed that at least one carbapenemase-encoding gene was detected in 133 (78.7%) of the 169 carbapenem-resistant isolates from patients and environmental surfaces. They were detected in 22/133(16.5%), 70/133(52.6%), and 41/133(30.8%) isolates obtained from infection, GI colonization, and environmental samples, respectively. The most prevalent carbapenemase-encoding gene, blaNDM, was found in 101 (75.9%) of the 133 CP isolates. Other detected carbapenemase-encoding genes included blaOXA-23 in 5 (3.8%) isolates, blaVIM in 4 (3.0%), blaOXA-48 in 1 (0.8%), and blaOXA-58 in 1 (0.8%). K. pneumoniae and Acinetobacter spp. harbored all the gene types detected in this study. Co-harboring of two or more carbapenemase-encoding genes, in combination with blaNDM, was observed in 21 of 133 (15.8%) isolates, including 7 K. pneumoniae and 14 Acinetobacter spp. isolates. However, blaKPC and blaIMP were not identified in any of the tested isolates. This study highlights the presence of carbapenemase-encoding genes among critical GNB across all sample source types in the study area. Moreover, the detection of isolates harboring multiple carbapenemase-encoding genes underscores the need for enhanced infection control measures in ICU settings.
有效的感染控制需要识别并清除重症监护病房(ICU)患者等高风险人群以及受污染环境表面中产碳青霉烯酶(CP)的革兰氏阴性菌(GNB)。本研究旨在描述来自埃塞俄比亚阿姆哈拉民族州ICU感染和/或胃肠道(GI)定植患者以及ICU环境表面的关键GNB分离株中碳青霉烯酶编码基因的多样性。共鉴定出169株耐碳青霉烯类分离株,其中26株来自感染患者,82株来自胃肠道定植患者,61株来自环境样本。这些分离株包括肺炎克雷伯菌(n = 107)、大肠杆菌(n = 16)、铜绿假单胞菌(n = 9)和不动杆菌属(n = 37),对其中147株进行了分析。采用单重和多重PCR检测主要的碳青霉烯酶编码基因,包括KPC(blaKPC)、金属β-内酰胺酶(MBLs,blaIMP、blaVIM和blaNDM)以及OXA(blaOXA - 48、blaOXA - 23和blaOXA - 58)。PCR分析显示,在169株来自患者和环境表面的耐碳青霉烯类分离株中,有133株(78.7%)检测到至少一种碳青霉烯酶编码基因。分别在22/133(16.5%)、70/133(52.6%)和41/133(30.8%)的感染、胃肠道定植和环境样本分离株中检测到这些基因。在133株CP分离株中,最常见的碳青霉烯酶编码基因blaNDM在101株(75.9%)中被发现。其他检测到的碳青霉烯酶编码基因包括5株(3.8%)中的blaOXA - 23、4株(3.0%)中的blaVIM、1株(0.8%)中的blaOXA - 48和1株(0.8%)中的blaOXA - 58。肺炎克雷伯菌和不动杆菌属含有本研究中检测到的所有基因类型。在133株分离株中有21株(15.8%)观察到两种或更多种碳青霉烯酶编码基因与blaNDM共同存在,包括7株肺炎克雷伯菌和14株不动杆菌属分离株。然而,在任何测试分离株中均未鉴定出blaKPC和blaIMP。本研究强调了研究区域内所有样本来源类型的关键GNB中碳青霉烯酶编码基因的存在。此外,对携带多种碳青霉烯酶编码基因的分离株的检测突出了在ICU环境中加强感染控制措施的必要性。