DOI: 10.1128/iai.00335-26 ISSN: 0019-9567
Comparison of
Galleria mellonella
, epithelial cell cytotoxicity, and mouse model of bacteremia to measure
Pseudomonas aeruginosa
virulence
Aliki Valdes, Christopher Axline, Travis J. Kochan, Sophia Nozick, Timothy Ward, Issay Niki, Ethan VanGosen, David Hynes, Julia Nelson, Preeti Garai, Tania Afzal, Daniel Amusin, Sumitra D. Mitra, Timothy L. Turner, William Cheng, Joanne J. Lee, Prarthana Prashanth, Nathan B. Pincus, Jonathan P. Allen, Jake Hauser, Egon A. Ozer, Kelly E. R. Bachta, Cheng-Hsun Chiu, Antonio Oliver, Alan R. Hauser ABSTRACT
Considerable effort has focused on identifying alternatives to mouse models in research studies. In the field of bacterial pathogenesis,
Galleria mellonella
and epithelial cell lines have been widely used for this purpose, but the concordance of these models with mice remains unclear. To begin to address this knowledge gap, we used 105 clinical isolates of
Pseudomonas aeruginosa
for which virulence had previously been determined in a mouse bacteremia model. A semistrong correlation was observed between
G. mellonella
median time to 50% mortality and mouse 50% pre-lethal dose (LD
50
) values (Spearman’s rank correlation coefficient [ρ] = 0.75), whereas percent A549 epithelial-like cell lysis during co-culture showed a weak correlation to mouse LD
50
values (ρ=−0.47). Given the stronger correlation between
G. mellonella
and mouse virulence, we next examined whether
G. mellonella
could substitute for mice when asking questions about the virulence of large numbers of
P. aeruginosa
isolates. Results from mice indicated that isolates with resistance to more antibiotics were significantly less virulent, and the use of
G. mellonella
identified the same inverse correlation. Furthermore, both models found no evidence for the existence of hypervirulent clonal lineages. In particular, isolates belonging to sequence types defined as high-risk clones were not consistently more virulent than other isolates, despite the known association of high-risk clones with poor clinical outcomes. These findings suggest that
G. mellonella
can serve as an adequate substitute for mice when addressing specific population-based virulence questions, although conclusions should be confirmed in mice.