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Predicting antimicrobial mechanism-of-action from transcriptomes: A generalizable explainable artificial intelligence approach.
Espinoza, Josh L; Dupont, Chris L; O'Rourke, Aubrie; Beyhan, Sinem; Morales, Pavel; Spoering, Amy; Meyer, Kirsten J; Chan, Agnes P; Choi, Yongwook; Nierman, William C; Lewis, Kim; Nelson, Karen E.
Afiliación
  • Espinoza JL; J. Craig Venter Institute, La Jolla, CA, United States of America.
  • Dupont CL; Department of Applied Sciences, Durban University of Technology, Durban, South Africa.
  • O'Rourke A; J. Craig Venter Institute, La Jolla, CA, United States of America.
  • Beyhan S; J. Craig Venter Institute, La Jolla, CA, United States of America.
  • Morales P; J. Craig Venter Institute, La Jolla, CA, United States of America.
  • Spoering A; J. Craig Venter Institute, La Jolla, CA, United States of America.
  • Meyer KJ; NovoBiotic Pharmaceuticals, Cambridge, MA, United States of America.
  • Chan AP; Department of Biology, Northeastern University, Boston, MA, United States of America.
  • Choi Y; J. Craig Venter Institute, Rockville, MD, United States of America.
  • Nierman WC; J. Craig Venter Institute, Rockville, MD, United States of America.
  • Lewis K; J. Craig Venter Institute, Rockville, MD, United States of America.
  • Nelson KE; Department of Biology, Northeastern University, Boston, MA, United States of America.
PLoS Comput Biol ; 17(3): e1008857, 2021 03.
Article en En | MEDLINE | ID: mdl-33780444
To better combat the expansion of antibiotic resistance in pathogens, new compounds, particularly those with novel mechanisms-of-action [MOA], represent a major research priority in biomedical science. However, rediscovery of known antibiotics demonstrates a need for approaches that accurately identify potential novelty with higher throughput and reduced labor. Here we describe an explainable artificial intelligence classification methodology that emphasizes prediction performance and human interpretability by using a Hierarchical Ensemble of Classifiers model optimized with a novel feature selection algorithm called Clairvoyance; collectively referred to as a CoHEC model. We evaluated our methods using whole transcriptome responses from Escherichia coli challenged with 41 known antibiotics and 9 crude extracts while depositing 122 transcriptomes unique to this study. Our CoHEC model can properly predict the primary MOA of previously unobserved compounds in both purified forms and crude extracts at an accuracy above 99%, while also correctly identifying darobactin, a newly discovered antibiotic, as having a novel MOA. In addition, we deploy our methods on a recent E. coli transcriptomics dataset from a different strain and a Mycobacterium smegmatis metabolomics timeseries dataset showcasing exceptionally high performance; improving upon the performance metrics of the original publications. We not only provide insight into the biological interpretation of our model but also that the concept of MOA is a non-discrete heuristic with diverse effects for different compounds within the same MOA, suggesting substantial antibiotic diversity awaiting discovery within existing MOA.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenilpropionatos / Inteligencia Artificial / Farmacorresistencia Bacteriana / Metaboloma / Transcriptoma / Antiinfecciosos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenilpropionatos / Inteligencia Artificial / Farmacorresistencia Bacteriana / Metaboloma / Transcriptoma / Antiinfecciosos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos