Updated genome assembly and annotation of Paenibacillus larvae, the agent of American foulbrood disease of honey bees

被引:30
作者
Chan, Queenie W. T. [1 ]
Cornman, R. Scott [2 ]
Birol, Inanc [3 ]
Liao, Nancy Y. [3 ]
Chan, Simon K. [3 ]
Docking, T. Roderick [3 ]
Jackman, Shaun D. [3 ]
Taylor, Greg A. [3 ]
Jones, Steven J. M. [3 ]
de Graaf, Dirk C. [4 ,5 ]
Evans, Jay D. [2 ]
Foster, Leonard J. [1 ]
机构
[1] Univ British Columbia, Ctr Highthroughput Biol, Dept Biochem Z Mol Biol, Vancouver, BC V6T 1Z4, Canada
[2] ARS, Bee Res Lab, USDA, Beltsville, MD 20705 USA
[3] British Columbia Canc Agcy, Michael Smith Genome Sci Ctr, Vancouver, BC V5Z 4S6, Canada
[4] Univ Ghent, Lab Zoophysiol, B-9000 Ghent, Belgium
[5] Inst Marine Sci Kiel, D-24105 Kiel, Germany
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
IN-VITRO; STAPHYLOCOCCUS-AUREUS; BACILLUS-SUBTILIS; APIS-MELLIFERA; BACTERIA; BIOSYNTHESIS; SURFACTIN; PROTEASES; PATHWAYS; PATHOGEN;
D O I
10.1186/1471-2164-12-450
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: As scientists continue to pursue various 'omics-based research, there is a need for high quality data for the most fundamental 'omics of all: genomics. The bacterium Paenibacillus larvae is the causative agent of the honey bee disease American foulbrood. If untreated, it can lead to the demise of an entire hive; the highly social nature of bees also leads to easy disease spread, between both individuals and colonies. Biologists have studied this organism since the early 1900s, and a century later, the molecular mechanism of infection remains elusive. Transcriptomics and proteomics, because of their ability to analyze multiple genes and proteins in a high-throughput manner, may be very helpful to its study. However, the power of these methodologies is severely limited without a complete genome; we undertake to address that deficiency here. Results: We used the Illumina GAIIx platform and conventional Sanger sequencing to generate a 182-fold sequence coverage of the P. larvae genome, and assembled the data using ABySS into a total of 388 contigs spanning 4.5 Mbp. Comparative genomics analysis against fully-sequenced soil bacteria P. JDR2 and P. vortex showed that regions of poor conservation may contain putative virulence factors. We used GLIMMER to predict 3568 gene models, and named them based on homology revealed by BLAST searches; proteases, hemolytic factors, toxins, and antibiotic resistance enzymes were identified in this way. Finally, mass spectrometry was used to provide experimental evidence that at least 35% of the genes are expressed at the protein level. Conclusions: This update on the genome of P. larvae and annotation represents an immense advancement from what we had previously known about this species. We provide here a reliable resource that can be used to elucidate the mechanism of infection, and by extension, more effective methods to control and cure this widespread honey bee disease.
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页数:15
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