Hypervirulent Capsular Serotypes K1 and K2 Klebsiella pneumoniae Strains Demonstrate Resistance to Serum Bactericidal Activity and Galleria mellonella Lethality

被引:9
作者
AL-Busaidi, Basaier [1 ]
AL-Muzahmi, Muna [2 ]
AL-Shabibi, Zahra [3 ]
Rizvi, Meher [4 ]
AL-Rashdi, Azza [5 ]
AL-Jardani, Amina [5 ]
Farzand, Robeena [6 ]
AL-Jabri, Zaaima [3 ]
机构
[1] Sultan Qaboos Univ Hosp, Dept Microbiol & Immunol, Microbiol & Immunol Diagnost Lab, Muscat 123, Oman
[2] Diwan Hlth Ctr, Med Lab, Muscat 130, Oman
[3] Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Genet, Muscat 123, Oman
[4] Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Microbiol & Immunol, Muscat 123, Oman
[5] Minist Hlth, Dept Med Microbiol, Cent Publ Hlth Lab, Muscat 100, Oman
[6] Univ Leicester, Dept Genet & Genome Biol, Leicester LE1 7RH, England
关键词
hypermucoviscous; Klebsiella pneumoniae; hypervirulent; mobile genetic elements; capsule serotypes; virulence; whole genome sequencing; sequence types; ESCHERICHIA-COLI; SEQUENCE; PLASMID; ENTEROBACTERIACEAE; CARBAPENEMASES; ANTIGENS; IDENTIFICATION; VISUALIZATION; SURVEILLANCE; EXPRESSION;
D O I
10.3390/ijms25031944
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypervirulent Klebsiella pneumoniae (hvKp) is a variant that has been increasingly linked to severe, life-threatening infections including pyogenic liver abscess and bloodstream infections. HvKps belonging to the capsular serotypes K1 and K2 have been reported worldwide, however, very scarce studies are available on their genomics and virulence. In the current study, we report four hypermucoviscous extended-spectrum beta-lactamase-producing hvKp clinical strains of capsular serotype K1 and K2 isolated from pus and urine of critically ill patients in tertiary care hospitals in Oman. These strains belong to diverse sequence types (STs), namely ST-23(K1), ST-231(K2), ST-881(K2), and ST-14(K2). To study their virulence, a Galleria mellonella model and resistance to human serum killing were used. The G. mellonella model revealed that the K1/ST-23 isolate was the most virulent, as 50% of the larvae died in the first day, followed by isolate K2/ST-231 and K2/ST-14, for which 75% and 50% of the larvae died in the second day, respectively. Resistance to human serum killing showed there was complete inhibition of bacterial growth of all four isolates by the end of the first hour and up to the third hour. Whole genome sequencing (WGS) revealed that hvKp strains display a unique genetic arrangement of k-loci. Whole-genome single-nucleotide polymorphism-based phylogenetic analysis revealed that these hvKp isolates were phylogenetically distinct, belonging to diverse clades, and belonged to different STs in comparison to global isolates. For ST-23(K1), ST-231(K2), ST-881(K2), and ST-14(K2), there was a gradual decrease in the number of colonies up to the second to third hour, which indicates neutralization of bacterial cells by the serum components. However, this was followed by a sudden increase of bacterial growth, indicating possible resistance of bacteria against human serum bactericidal activity. This is the first report from Oman detailing the WGS of hvKp clinical isolates and assessing their resistance and virulence genomics, which reinforce our understanding of their epidemiology and dissemination in clinical settings.
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