LAPSE:2023.2229
Published Article

LAPSE:2023.2229
Untargeted Metabolomics of Streptomyces Species Isolated from Soils of Nepal
February 21, 2023
Abstract
Actinomycetes are natural architects of numerous secondary metabolites including antibiotics. With increased multidrug-resistant (MDR) pathogens, antibiotics that can combat such pathogens are urgently required to improve the health care system globally. The characterization of actinomycetes available in Nepal is still very much untouched which is the reason why this paper showcases the characterization of actinomycetes from Nepal based on their morphology, 16S rRNA gene sequencing, and metabolic profiling. Additionally, antimicrobial assays and liquid chromatography-high resolution mass spectrometry (LC-HRMS) of ethyl acetate extracts were performed. In this study, we employed a computational-based dereplication strategy for annotating molecules which is also time-efficient. Molecular annotation was performed through the GNPS server, the SIRIUS platform, and the available databases to predict the secondary metabolites. The sequencing of the 16S rRNA gene revealed that the isolates BN6 and BN14 are closely related to Streptomyces species. BN14 showed broad-spectrum antibacterial activity with the zone of inhibition up to 30 mm against Staphylococcus aureus (MIC: 0.3051 µg/mL and MBC: 9.7656 µg/mL) and Shigella sonnei (MIC: 0.3051 µg/mL and MBC: 4.882 µg/mL). Likewise, BN14 also displayed significant inhibition to Acinetobacter baumannii, Klebsiella pneumoniae, and Salmonella typhi. GNPS approach suggested that the extracts of BN6 and BN14 consisted of diketopiperazines ((cyclo(D-Trp-L-Pro), cyclo(L-Leu-L-4-hydroxy-Pro), cyclo(L-Phe-D-Pro), cyclo(L-Trp-L-Pro), cyclo(L-Val-L-Pro)), and polypeptide antibiotics (actinomycin D and X2). Additional chemical scaffolds such as bacterial alkaloids (bohemamine, venezueline B, and G), anthramycin-type antibiotics (abbeymycin), lipase inhibitor (ebelactone B), cytocidal (oxopropaline D), antifungal and antitumor antibiotics (reductiomycin, streptimidone, deoxynybomycin), alaremycin, fumaramidmycin, anisomycin, and others were also annotated, which were further confirmed by using the SIRIUS platform, and literature survey. Thus, the bioprospecting of natural products from Streptomyces species from Nepal could be a potential source for the discovery of clinically significant and new antimicrobial agents in the future.
Actinomycetes are natural architects of numerous secondary metabolites including antibiotics. With increased multidrug-resistant (MDR) pathogens, antibiotics that can combat such pathogens are urgently required to improve the health care system globally. The characterization of actinomycetes available in Nepal is still very much untouched which is the reason why this paper showcases the characterization of actinomycetes from Nepal based on their morphology, 16S rRNA gene sequencing, and metabolic profiling. Additionally, antimicrobial assays and liquid chromatography-high resolution mass spectrometry (LC-HRMS) of ethyl acetate extracts were performed. In this study, we employed a computational-based dereplication strategy for annotating molecules which is also time-efficient. Molecular annotation was performed through the GNPS server, the SIRIUS platform, and the available databases to predict the secondary metabolites. The sequencing of the 16S rRNA gene revealed that the isolates BN6 and BN14 are closely related to Streptomyces species. BN14 showed broad-spectrum antibacterial activity with the zone of inhibition up to 30 mm against Staphylococcus aureus (MIC: 0.3051 µg/mL and MBC: 9.7656 µg/mL) and Shigella sonnei (MIC: 0.3051 µg/mL and MBC: 4.882 µg/mL). Likewise, BN14 also displayed significant inhibition to Acinetobacter baumannii, Klebsiella pneumoniae, and Salmonella typhi. GNPS approach suggested that the extracts of BN6 and BN14 consisted of diketopiperazines ((cyclo(D-Trp-L-Pro), cyclo(L-Leu-L-4-hydroxy-Pro), cyclo(L-Phe-D-Pro), cyclo(L-Trp-L-Pro), cyclo(L-Val-L-Pro)), and polypeptide antibiotics (actinomycin D and X2). Additional chemical scaffolds such as bacterial alkaloids (bohemamine, venezueline B, and G), anthramycin-type antibiotics (abbeymycin), lipase inhibitor (ebelactone B), cytocidal (oxopropaline D), antifungal and antitumor antibiotics (reductiomycin, streptimidone, deoxynybomycin), alaremycin, fumaramidmycin, anisomycin, and others were also annotated, which were further confirmed by using the SIRIUS platform, and literature survey. Thus, the bioprospecting of natural products from Streptomyces species from Nepal could be a potential source for the discovery of clinically significant and new antimicrobial agents in the future.
Record ID
Keywords
antibiotics, metabolomics, molecular annotation, Streptomyces
Subject
Suggested Citation
Bhattarai BR, Khadayat K, Aryal N, Aryal B, Lamichhane U, Bhattarai K, Rana N, Regmi BP, Adhikari A, Thapa S, Parajuli N. Untargeted Metabolomics of Streptomyces Species Isolated from Soils of Nepal. (2023). LAPSE:2023.2229
Author Affiliations
Bhattarai BR: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Khadayat K: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Aryal N: Department of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI 53706-1521, USA
Aryal B: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Lamichhane U: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Bhattarai K: Department of Pharmaceutical Biology, University of Tübingen, 72076 Tübingen, Germany
Rana N: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Regmi BP: Department of Chemistry, Florida Agricultural and Mechanical University, Tallahassee, FL 32307, USA [ORCID]
Adhikari A: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal
Thapa S: Kathmandu Center for Genomics and Research Laboratory, Lalitpur 44600, Nepal [ORCID]
Parajuli N: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Khadayat K: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Aryal N: Department of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI 53706-1521, USA
Aryal B: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Lamichhane U: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Bhattarai K: Department of Pharmaceutical Biology, University of Tübingen, 72076 Tübingen, Germany
Rana N: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Regmi BP: Department of Chemistry, Florida Agricultural and Mechanical University, Tallahassee, FL 32307, USA [ORCID]
Adhikari A: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal
Thapa S: Kathmandu Center for Genomics and Research Laboratory, Lalitpur 44600, Nepal [ORCID]
Parajuli N: Biological Chemistry Laboratory, Central Department of Chemistry, Tribhuvan University, Kirtipur 44618, Nepal [ORCID]
Journal Name
Processes
Volume
10
Issue
6
First Page
1173
Year
2022
Publication Date
2022-06-10
ISSN
2227-9717
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Original Submission
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PII: pr10061173, Publication Type: Journal Article
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LAPSE:2023.2229
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