Maghembe Reuben S, Magulye Maximilian A K, Makaranga Abdalah, Bahati Samweli, Mark Deogratius, Sekyanzi Simon, Agbaje AbdulGaniy B, Eilu Emmanuel, Mwesigwa Savannah, Katagirya Eric
Department of Microbiology and Parasitology, Faculty of Medicine, St. Francis University College of Health and Allied Sciences (SFUCHAS), Ifakara, Tanzania.
Omics and Bioinformatics Section, DABA Biotech Ltd, Plot No.46; Kijitonyama; Nzasa Street; P.O. Box 55082; Mwenge; Dar es Salaam-Tanzania.
Gene Rep. 2025 Jun;39. doi: 10.1016/j.genrep.2025.102198. Epub 2025 Mar 14.
Gastrointestinal and bloodstream infections account for a major cause of medical emergency and mortality among pediatric populations. Although is implicated in multiple infections, its virulence and antimicrobial resistance are elusive. Here we aimed to uncover the pathogen associated with diarrhea and sepsis from a 3-year-old patient under ICU in Kampala. We isolated an strain, challenged it with a panel of 16 antibiotics and whole-genome sequenced it to delve into the virulome and resistome underlying the pathogenicity and relevance to the patient's disease. Antibiotic susceptibility test (AST) results revealed that the isolate was resistant to 12 antibiotics. Combining PathogenFinder with multilocus sequence typing (MLST), we found a high-risk human pathogen (p = 99.9%), ST648/*a194 (serotype O8:H4), which possesses autotransporters and enteroaggregative immunoglobulin repeat protein among other virulence factors. This strain has acquired plasmids harboring multidrug resistance genes of the beta lactamase family (, , and aminoglycoside resistance genes including , and , and fluroquinolone resistance gene . Using the comprehensive antibiotic resistance database (CARD), we identified multiple nonsynonymous mutations for the genes (D87N, S83L, (S80I), conferring fluroquinolone resistance along with the multidrug resistance gene with mutations (Y137H, G103S). Overall, we infer a hybrid pathotype of enteroaggregative-hemorrhagic (EAHEC) with the potential for gastrointestinal tract, systemic infection and multidrug resistance covering third-generation cephalosporins. Comprehensive genomic surveillance is urgently required to enhance our therapeutic intervention of these high-risk clones in low-resource settings.
胃肠道和血流感染是儿科人群医疗紧急情况和死亡的主要原因。虽然[具体细菌名称未给出]与多种感染有关,但其毒力和抗菌耐药性尚不清楚。在此,我们旨在从坎帕拉一家重症监护病房的一名3岁患者中找出与腹泻和败血症相关的病原体。我们分离出一株[具体细菌名称未给出]菌株,用一组16种抗生素对其进行挑战,并对其进行全基因组测序,以深入研究其致病性和与患者疾病相关性的毒力组和耐药组。抗生素敏感性试验(AST)结果显示,该分离株对12种抗生素耐药。将PathogenFinder与多位点序列分型(MLST)相结合,我们发现了一种高风险的人类病原体(p = 99.9%),ST648/*a194(血清型O8:H4),它除了其他毒力因子外,还拥有自转运蛋白和肠聚集性免疫球蛋白重复蛋白。该菌株获得了携带β-内酰胺酶家族多药耐药基因([具体基因名称未给出])的质粒,以及氨基糖苷类耐药基因,包括[具体基因名称未给出]和[具体基因名称未给出],还有氟喹诺酮耐药基因[具体基因名称未给出]。使用综合抗生素耐药性数据库(CARD),我们鉴定出基因[具体基因名称未给出](D87N、S83L、[具体基因名称未给出](S80I)的多个非同义突变,这些突变与多药耐药基因[具体基因名称未给出]的突变(Y137H、G103S)一起赋予氟喹诺酮耐药性。总体而言,我们推断出一种具有胃肠道、全身感染和对第三代头孢菌素耐药潜力的肠聚集性出血性[具体细菌名称未给出](EAHEC)混合致病型。迫切需要进行全面的基因组监测,以加强我们在资源匮乏地区对这些高风险[具体细菌名称未给出]克隆的治疗干预。