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Molecular Signatures Related to the Virulence of Bacillus cereus Sensu Lato, a Leading Cause of Devastating Endophthalmitis

Bacillus endophthalmitis is a devastating eye infection that causes rapid blindness through extracellular tissue-destructive exotoxins. Despite its importance, knowledge of the phylogenetic relationships and population structure of intraocular Bacillus spp. is lacking. In this study, we sequenced th...

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Autores principales: Yuan, Jian, Li, Yu-Yu, Xu, Yi, Sun, Bian-Jin, Shao, Jiao, Zhang, Die, Li, Kai, Fan, Dan-Dan, Xue, Zheng-Bo, Chen, Wei-Hua, Pak, Clara, Lou, Yong-Liang, Su, Jian-Zhong, Zheng, Mei-Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890933/
https://www.ncbi.nlm.nih.gov/pubmed/31796569
http://dx.doi.org/10.1128/mSystems.00745-19
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author Yuan, Jian
Li, Yu-Yu
Xu, Yi
Sun, Bian-Jin
Shao, Jiao
Zhang, Die
Li, Kai
Fan, Dan-Dan
Xue, Zheng-Bo
Chen, Wei-Hua
Pak, Clara
Lou, Yong-Liang
Su, Jian-Zhong
Zheng, Mei-Qin
author_facet Yuan, Jian
Li, Yu-Yu
Xu, Yi
Sun, Bian-Jin
Shao, Jiao
Zhang, Die
Li, Kai
Fan, Dan-Dan
Xue, Zheng-Bo
Chen, Wei-Hua
Pak, Clara
Lou, Yong-Liang
Su, Jian-Zhong
Zheng, Mei-Qin
author_sort Yuan, Jian
collection PubMed
description Bacillus endophthalmitis is a devastating eye infection that causes rapid blindness through extracellular tissue-destructive exotoxins. Despite its importance, knowledge of the phylogenetic relationships and population structure of intraocular Bacillus spp. is lacking. In this study, we sequenced the whole genomes of eight Bacillus intraocular pathogens independently isolated from 8/52 patients with posttraumatic Bacillus endophthalmitis infections in the Eye Hospital of Wenzhou Medical University between January 2010 and December 2018. Phylogenetic analysis revealed that the pathogenic intraocular isolates belonged to Bacillus cereus, Bacillus thuringiensis and Bacillus toyonensis. To determine the virulence of the ocular isolates, three representative strains were injected into mouse models, and severe endophthalmitis leading to blindness was observed. Through incorporating publicly available genomes for Bacillus spp., we found that the intraocular pathogens could be isolated independently but displayed a similar genetic context. In addition, our data provide genome-wide support for intraocular and gastrointestinal sources of Bacillus spp. belonging to different lineages. Importantly, we identified five molecular signatures of virulence and motility genes associated with intraocular infection, namely, plcA-2, InhA-3, InhA-4, hblA-5, and fliD using pangenome-wide association studies. The characterization of overrepresented genes in the intraocular isolates holds value to predict bacterial evolution and for the design of future intervention strategies in patients with endophthalmitis. IMPORTANCE In this study, we provided a detailed and comprehensive clinicopathological and pathogenic report of Bacillus endophthalmitis over the 8 years of the study period. We first reported the whole-genome sequence of Bacillus spp. causing devastating endophthalmitis and found that Bacillus toyonensis is able to cause endophthalmitis. Finally, we revealed significant endophthalmitis-associated virulence genes involved in hemolysis, immunity inhibition, and pathogenesis. Overall, as more sequencing data sets become available, these data will facilitate comparative research and will reveal the emergence of pathogenic “ocular bacteria.”
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spelling pubmed-68909332019-12-16 Molecular Signatures Related to the Virulence of Bacillus cereus Sensu Lato, a Leading Cause of Devastating Endophthalmitis Yuan, Jian Li, Yu-Yu Xu, Yi Sun, Bian-Jin Shao, Jiao Zhang, Die Li, Kai Fan, Dan-Dan Xue, Zheng-Bo Chen, Wei-Hua Pak, Clara Lou, Yong-Liang Su, Jian-Zhong Zheng, Mei-Qin mSystems Research Article Bacillus endophthalmitis is a devastating eye infection that causes rapid blindness through extracellular tissue-destructive exotoxins. Despite its importance, knowledge of the phylogenetic relationships and population structure of intraocular Bacillus spp. is lacking. In this study, we sequenced the whole genomes of eight Bacillus intraocular pathogens independently isolated from 8/52 patients with posttraumatic Bacillus endophthalmitis infections in the Eye Hospital of Wenzhou Medical University between January 2010 and December 2018. Phylogenetic analysis revealed that the pathogenic intraocular isolates belonged to Bacillus cereus, Bacillus thuringiensis and Bacillus toyonensis. To determine the virulence of the ocular isolates, three representative strains were injected into mouse models, and severe endophthalmitis leading to blindness was observed. Through incorporating publicly available genomes for Bacillus spp., we found that the intraocular pathogens could be isolated independently but displayed a similar genetic context. In addition, our data provide genome-wide support for intraocular and gastrointestinal sources of Bacillus spp. belonging to different lineages. Importantly, we identified five molecular signatures of virulence and motility genes associated with intraocular infection, namely, plcA-2, InhA-3, InhA-4, hblA-5, and fliD using pangenome-wide association studies. The characterization of overrepresented genes in the intraocular isolates holds value to predict bacterial evolution and for the design of future intervention strategies in patients with endophthalmitis. IMPORTANCE In this study, we provided a detailed and comprehensive clinicopathological and pathogenic report of Bacillus endophthalmitis over the 8 years of the study period. We first reported the whole-genome sequence of Bacillus spp. causing devastating endophthalmitis and found that Bacillus toyonensis is able to cause endophthalmitis. Finally, we revealed significant endophthalmitis-associated virulence genes involved in hemolysis, immunity inhibition, and pathogenesis. Overall, as more sequencing data sets become available, these data will facilitate comparative research and will reveal the emergence of pathogenic “ocular bacteria.” American Society for Microbiology 2019-12-03 /pmc/articles/PMC6890933/ /pubmed/31796569 http://dx.doi.org/10.1128/mSystems.00745-19 Text en Copyright © 2019 Yuan et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Yuan, Jian
Li, Yu-Yu
Xu, Yi
Sun, Bian-Jin
Shao, Jiao
Zhang, Die
Li, Kai
Fan, Dan-Dan
Xue, Zheng-Bo
Chen, Wei-Hua
Pak, Clara
Lou, Yong-Liang
Su, Jian-Zhong
Zheng, Mei-Qin
Molecular Signatures Related to the Virulence of Bacillus cereus Sensu Lato, a Leading Cause of Devastating Endophthalmitis
title Molecular Signatures Related to the Virulence of Bacillus cereus Sensu Lato, a Leading Cause of Devastating Endophthalmitis
title_full Molecular Signatures Related to the Virulence of Bacillus cereus Sensu Lato, a Leading Cause of Devastating Endophthalmitis
title_fullStr Molecular Signatures Related to the Virulence of Bacillus cereus Sensu Lato, a Leading Cause of Devastating Endophthalmitis
title_full_unstemmed Molecular Signatures Related to the Virulence of Bacillus cereus Sensu Lato, a Leading Cause of Devastating Endophthalmitis
title_short Molecular Signatures Related to the Virulence of Bacillus cereus Sensu Lato, a Leading Cause of Devastating Endophthalmitis
title_sort molecular signatures related to the virulence of bacillus cereus sensu lato, a leading cause of devastating endophthalmitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890933/
https://www.ncbi.nlm.nih.gov/pubmed/31796569
http://dx.doi.org/10.1128/mSystems.00745-19
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