Genomic analysis provides insights into the transmission and pathogenicity of Talaromyces marneffei.
Animals
Antifungal Agents
DNA, Fungal
Fungal Proteins
/ genetics
Genes, Essential
/ genetics
Genome, Fungal
/ genetics
Genomics
Genotype
Humans
Multilocus Sequence Typing
Peptide Synthases
/ genetics
Phylogeny
Polyketide Synthases
/ genetics
Rats
Secondary Metabolism
/ genetics
Talaromyces
/ drug effects
Virulence
Virulence Factors
/ genetics
Whole Genome Sequencing
Drug target
Multilocus sequence typing
Talaromyces marneffei
Virulence factor
Whole genome sequencing
Journal
Fungal genetics and biology : FG & B
ISSN: 1096-0937
Titre abrégé: Fungal Genet Biol
Pays: United States
ID NLM: 9607601
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
27
04
2018
revised:
05
05
2019
accepted:
06
05
2019
pubmed:
11
5
2019
medline:
27
5
2020
entrez:
11
5
2019
Statut:
ppublish
Résumé
Talaromyces marneffei (T. marneffei) is a medically important opportunistic dimorphic fungus that infects both humans and bamboo rats. However, the mechanisms of transmission and pathogenicity of T. marneffei are poorly understood. In our study, we combined Illumina and PacBio sequencing technologies to sequence and assemble a complete genome of T. marneffei. To elucidate the transmission route and source, we sequenced three additional T. marneffei isolates using Illumina sequencing technology. Variations among isolates were used to develop a multilocus sequence typing (MLST) system comprising five housekeeping genes that can be used to discriminate between isolates derived from different sources. Our analysis revealed that human and bamboo rat share identical genotypes in these five loci. Thus, we hypothesized that T. marneffei is transmitted to humans through inhalation of spores in the surrounding environment into the lungs and that the bamboo rat can serve as an important natural reservoir for pathogens. Furthermore, we also identified temperature-dependent polyketide synthases, non-ribosomal peptide synthetases and secreted proteins as putative pathogenicity-related factors. In addition, we identified antifungal drug targets that can be investigated in future studies to elucidate the mechanisms underlying drug resistance. In summary, our study presents the basic features of the T. marneffei genome and provides insights into the transmission and pathogenicity of T. marneffei, which warrant fundamental experimental research.
Identifiants
pubmed: 31075360
pii: S1087-1845(19)30149-5
doi: 10.1016/j.fgb.2019.05.002
pii:
doi:
Substances chimiques
Antifungal Agents
0
DNA, Fungal
0
Fungal Proteins
0
Virulence Factors
0
Polyketide Synthases
79956-01-7
Peptide Synthases
EC 6.3.2.-
non-ribosomal peptide synthase
EC 6.3.2.-
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
54-61Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.