Human neutrophils release extracellular RNA that modulates Aspergillus fumigatus gene expression across kingdoms

Abstract

Extracellular RNAs (exRNAs) are emerging as potent bidirectional interkingdom effectors of host-pathogen interactions, particularly in plant and insect systems. Here, using small RNA-sequencing and genetic manipulation, we provide evidence consistent with a function of the human neutrophil exRNA-ome in modulating gene expression across kingdoms in the fungal pathogen Aspergillus fumigatus. The neutrophil extracellular space contains a diverse repertoire of RNA, which was corroborated using a droplet-digital stem-loop RT-PCR protocol to measure differential abundance of several tRNA-derived RNAs between two extracellular fractions. A closer inspection of the extracellular miRNA pool revealed enrichment of antimicrobial Let-7 family sRNAs and immunomodulatory miR-223, among others. Secretion of these sRNAs was largely impervious to infection status, suggesting that neutrophils produce and maintain an antimicrobial exRNA environment against A. fumigatus that requires further targeting. Cross-kingdom miRNA target prediction and exRNA delivery experiments revealed that putative fungal targets are modulated independently of the fungal argonaute proteins and in a donor-dependent manner. Although heterogeneous, for donors that exhibited a silencing effect, mutated target sequences in the fungus did reverse silencing. We hypothesize that the exRNA landscape produced by neutrophils contributes to their multifaceted role in antifungal defense.

Alexander Bruch
Postdoctoral Fellow
Lukas Schrettenbrunner
Doctoral Researcher
Bhawana Israni
Bhawana Israni
Postdoctoral Fellow
Erik Böhm
Erik Böhm
Doctoral Researcher
Xiaoqing Pan
Doctoral Researcher
Matthew G. Blango
Matthew G. Blango
Independent Junior Group Leader

Matt leads the RNA Biology of Fungal Infections Junior Research Group.