Traglia German Matias, Pasteran Fernando, Escalante Jenny, Nishimura Brent, Tuttobene Marisel R, Subils Tomás, Nuñez Maria Rosa, Rivollier María Gabriela, Corso Alejandra, Tolmasky Marcelo E, Ramirez Maria Soledad
Departamento de Desarrollo Biotecnológico, Instituto de Higiene, Facultad de Medicina, Universidad de la Republica, Montevideo 11200, Uruguay.
National Regional Reference Laboratory for Antimicrobial Resistance (NRL), Servicio Antimicrobianos, Instituto Nacional de Enfermedades Infecciosas, ANLIS Dr. Carlos G. Malbrán, Buenos Aires 1282, Argentina.
Biology (Basel). 2023 Feb 24;12(3):358. doi: 10.3390/biology12030358.
After the emergence of COVID-19, numerous cases of /SARS-CoV-2 co-infection were reported. Whether the co-infecting strains have distinctive characteristics remains unknown.
AMA_NO was isolated in 2021 from a patient with COVID-19. AMA166 was isolated from a mini-BAL used on a patient with pneumonia in 2016. Both genomes were similar, but they possessed 337 (AMA_NO) and 93 (AMA166) unique genes that were associated with biofilm formation, flagellar assembly, antibiotic resistance, secretion systems, and other functions. The antibiotic resistance genes were found within mobile genetic elements. While both strains harbored the carbapenemase-coding gene , only the strain AMA_NO carried . Representative functions coded for by virulence genes are the synthesis of the outer core of lipooligosaccharide (OCL5), biosynthesis and export of the capsular polysaccharide (KL2 cluster), high-efficiency iron uptake systems (acinetobactin and baumannoferrin), adherence, and quorum sensing. A comparative phylogenetic analysis including 239 additional sequence type (ST) 2 representative genomes showed high similarity to ABBL141. Since the degree of similarity that was observed between AMA_NO and AMA166 is higher than that found among other ST2 strains, we propose that they derive from a unique background based on core-genome phylogeny and comparative genome analysis.
Acquisition or shedding of specific genes could increase the ability of to infect patients with COVID-19.
新型冠状病毒肺炎(COVID-19)出现后,有大量关于/SARS-CoV-2合并感染病例的报道。合并感染的毒株是否具有独特特征仍不清楚。
AMA_NO于2021年从一名COVID-19患者中分离得到。AMA166于2016年从一名肺炎患者使用的小型支气管肺泡灌洗样本中分离得到。两种菌株的基因组相似,但它们分别拥有337个(AMA_NO)和93个(AMA166)与生物膜形成、鞭毛组装、抗生素耐药性、分泌系统及其他功能相关的独特基因。抗生素耐药基因存在于可移动遗传元件中。虽然两种菌株都含有碳青霉烯酶编码基因,但只有AMA_NO菌株携带。毒力基因编码的代表性功能包括脂寡糖外核心的合成(OCL5)、荚膜多糖的生物合成与输出(KL2簇)、高效铁摄取系统(不动杆菌铁载体和鲍氏铁载体)、黏附及群体感应。一项纳入另外239个序列型(ST)2代表性基因组的比较系统发育分析显示,它们与ABBL141高度相似。由于AMA_NO和AMA166之间观察到的相似程度高于其他ST2菌株,基于核心基因组系统发育和比较基因组分析,我们认为它们源自独特的背景。
特定基因的获得或丢失可能会增加感染COVID-19患者的能力。