Jul 2026· Journal of the Association of Medical Microbiology and Infectious Disease Canada· Vol 11, pp. 294-301· 0 citations· 12 references
TL;DR
A remarkable extent of dissemination is demonstrated and the known clinical spectrum for hypervirulent K. pneumoniae infection in a middle-aged male presented with profound refractory septic shock leading to progressive multiorgan system failure.
Abstract
Emerging strains of hypervirulent
Klebsiella pneumoniae
are increasingly recognized to cause life-threatening, community-acquired infections in persons without significant immunocompromise. Beyond the association with pyogenic liver abscesses and bacteremia, additional sites of involvement include skin and soft tissue, bone, eyes, and the central nervous system. Individuals with diabetes mellitus and originating from the Asian Pacific Rim appear to be at higher risk for colonization and infection. Genetic testing for defining virulence factors was recently proposed as a standard for differentiating hypervirulent from classical
K. pneumoniae
strains.
Retrospective review of a
K. pneumoniae
infection in a middle-aged male.
The patient had untreated type 2 diabetes, hypertension, and obesity, and immigrated from a southeast Asian country to Canada over one decade prior. He presented with profound refractory septic shock leading to progressive multiorgan system failure. In totality, the infection involved necrotizing fasciitis of bilateral legs, bilateral emphysematous pyelonephritis, emphysematous cholecystitis, multifocal necrotizing pneumonia, and bacteremia notably without liver abscess.
K. pneumoniae
was later isolated from blood and sputum. Whole-genome sequencing identified
K. pneumoniae sensu stricto
with K1 capsule belonging to sequence type 23 and harbouring the characteristic virulence genes
iucA
,
iroB
,
peg-344
,
rmpA
, and
rmpA2
.
This case demonstrates a remarkable extent of dissemination and expands the known clinical spectrum for hypervirulent
K. pneumoniae
infection. Genetic testing has the potential to proactively identify hypervirulent strains and inform clinical management. Heightened clinical vigilance, development of accessible rapid diagnostic tools, and further research into treatment strategies are needed for this emerging pathogen.
A 77-year-old woman who presented with fever and right upper quadrant abdominal pain was diagnosed with a second episode of PLA within 3 months, caused by hypervirulent Kp, and whole-genome sequencing identified the isolate as hypervirulent Kp (hvKp) sequence type 23 (ST23).
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