| Literature DB >> 31160365 |
Mafeng Liu1,2,3, Mi Huang4,2,3, Li Huang4,2,3, Francis Biville5, Dekang Zhu2,3, Mingshu Wang4,2,3, Renyong Jia4,2,3, Shun Chen4,2,3, Xinxin Zhao4,2,3, Qiao Yang4,2,3, Ying Wu4,2,3, Shaqiu Zhang4,2,3, Juan Huang4,2,3, Bin Tian4,2,3, Xiaoyue Chen2,3, Yunya Liu4,2,3, Ling Zhang2,3, Yanling Yu2,3, Leichang Pan4,2,3, Mujeeb Ur Rehman4,2,3, Anchun Cheng1,2,3.
Abstract
Galleria mellonella larvae have been used as a host model to study interactions between pathogens and hosts for several years. However, whether the model is useful to interrogate Riemerella anatipestifer infection biology remained unknown. This study aimed to exploit the potential of G. mellonella larvae and reveal their limitations as a host model for R. anatipestifer infection. G. mellonella larvae were shown to be effective for virulence evaluations of different R. anatipestifer strains. Furthermore, the virulent strain R. anatipestifer CH-1 had a stronger ability to proliferate than the attenuated strain R. anatipestifer ATCC 11845 in both G. mellonella larvae and ducklings. Unconventionally it was shown that G. mellonella larvae cannot be used to evaluate the efficacy of antimicrobials and their combinations. Additionally, it was shown that certain virulence factors, such as OmpA (B739_0861), B739_1208, B739_1343, and Wza (B739_1124), were specific only for ducklings, suggesting that G. mellonella larvae must be cautiously used to identify virulence factors of R. anatipestifer Evaluation of heme uptake-related virulence genes, such as tonB1 and tonB2, required preincubating the strains with hemoglobin before infection of G. mellonella larvae since R. anatipestifer cannot obtain a heme source from G. mellonella larvae. In conclusion, this study revealed the applicability and limitations of G. mellonella as a model with which to study the pathogen-host interaction, particularly in the context of R. anatipestifer infection.Entities:
Keywords: Galleria mellonellazzm321990; R. anatipestiferzzm321990; virulence
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Year: 2019 PMID: 31160365 PMCID: PMC6652747 DOI: 10.1128/IAI.00072-19
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441