TY - JOUR
T1 - Systematic discovery of antibacterial and antifungal bacterial toxins
AU - Nachmias, Nimrod
AU - Dotan, Noam
AU - Rocha, Marina Campos
AU - Fraenkel, Rina
AU - Detert, Katharina
AU - Kluzek, Monika
AU - Shalom, Maor
AU - Cheskis, Shani
AU - Peedikayil-Kurien, Sonu
AU - Meitav, Gilad
AU - Rivitz, Arbel
AU - Shamash-Halevy, Naama
AU - Cahana, Inbar
AU - Deouell, Noam
AU - Klein, Jacob
AU - Oren-Suissa, Meital
AU - Schmidt, Herbert
AU - Schlezinger, Neta
AU - Tzarum, Netanel
AU - Oppenheimer-Shaanan, Yaara
AU - Levy, Asaf
N1 - Publisher Copyright: © The Author(s), under exclusive licence to Springer Nature Limited 2024.
PY - 2024/11
Y1 - 2024/11
N2 - Microorganisms use toxins to kill competing microorganisms or eukaryotic cells. Polymorphic toxins are proteins that encode carboxy-terminal toxin domains. Here we developed a computational approach to identify previously undiscovered, conserved toxin domains of polymorphic toxins within 105,438 microbial genomes. We validated nine short toxins, showing that they cause cell death upon heterologous expression in either Escherichia coli or Saccharomyces cerevisiae. Five cognate immunity genes that neutralize the toxins were also discovered. The toxins are encoded by 2.2% of sequenced bacteria. A subset of the toxins exhibited potent antifungal activity against various pathogenic fungi but not against two invertebrate model organisms or macrophages. Experimental validation suggested that these toxins probably target the cell membrane or DNA or inhibit cell division. Further characterization and structural analysis of two toxin–immunity protein complexes confirmed DNase activity. These findings expand our knowledge of microbial toxins involved in inter-microbial competition that may have the potential for clinical and biotechnological applications.
AB - Microorganisms use toxins to kill competing microorganisms or eukaryotic cells. Polymorphic toxins are proteins that encode carboxy-terminal toxin domains. Here we developed a computational approach to identify previously undiscovered, conserved toxin domains of polymorphic toxins within 105,438 microbial genomes. We validated nine short toxins, showing that they cause cell death upon heterologous expression in either Escherichia coli or Saccharomyces cerevisiae. Five cognate immunity genes that neutralize the toxins were also discovered. The toxins are encoded by 2.2% of sequenced bacteria. A subset of the toxins exhibited potent antifungal activity against various pathogenic fungi but not against two invertebrate model organisms or macrophages. Experimental validation suggested that these toxins probably target the cell membrane or DNA or inhibit cell division. Further characterization and structural analysis of two toxin–immunity protein complexes confirmed DNase activity. These findings expand our knowledge of microbial toxins involved in inter-microbial competition that may have the potential for clinical and biotechnological applications.
UR - http://www.scopus.com/inward/record.url?scp=85207228155&partnerID=8YFLogxK
U2 - https://doi.org/10.1038/s41564-024-01820-9
DO - https://doi.org/10.1038/s41564-024-01820-9
M3 - مقالة
C2 - 39438720
SN - 2058-5276
VL - 9
SP - 3041
EP - 3058
JO - Nature Microbiology
JF - Nature Microbiology
IS - 11
ER -