Plasmid composition in Aeromonas salmonicida subsp. salmonicida 01-B526 unravels unsuspected type three secretion system loss patterns.

Abstract:

BACKGROUND:Aeromonas salmonicida subsp. salmonicida is a ubiquitous psychrophilic waterborne bacterium and a fish pathogen. The numerous mobile elements, especially insertion sequences (IS), in its genome promote rearrangements that impact its phenotype. One of the main virulence factors of this bacterium, its type three secretion system (TTSS), is affected by these rearrangements. In Aeromonas salmonicida subsp. salmonicida most of the TTSS genes are encoded in a single locus on a large plasmid called pAsa5, and may be lost when the bacterium is cultivated at a higher temperature (25 °C), producing non-virulent mutants. In a previous study, pAsa5-rearranged strains that lacked the TTSS locus on pAsa5 were produced using parental strains, including 01-B526. Some of the generated deletions were explained by homologous recombination between ISs found on pAsa5, whereas the others remained unresolved. To investigate those rearrangements, short- and long-read high-throughput sequencing technologies were used on the A. salmonicida subsp. salmonicida 01-B526 whole genome. RESULTS:Whole genome sequencing of the 01-B526 strain revealed that its pAsa5 has an additional IS copy, an ISAS5, compared to the reference strain (A449) sequence, which allowed for a previously unknown rearrangement to occur. It also appeared that 01-B526 bears a second large plasmid, named pAsa9, which shares 40 kbp of highly similar sequences with pAsa5. Following these discoveries, previously unexplained deletions were elucidated by genotyping. Furthermore, in one of the derived strains a fusion of pAsa5 and pAsa9, involving the newly discovered ISAS5 copy, was observed. CONCLUSION:The loss of TTSS and hence virulence is explained by one consistent mechanism: IS-driven homologous recombination. The similarities between pAsa9 and pAsa5 also provide another example of genetic diversity driven by ISs.

journal_name

BMC Genomics

journal_title

BMC genomics

authors

Tanaka KH,Vincent AT,Emond-Rheault JG,Adamczuk M,Frenette M,Charette SJ

doi

10.1186/s12864-017-3921-1

subject

Has Abstract

pub_date

2017-07-12 00:00:00

pages

528

issue

1

issn

1471-2164

pii

10.1186/s12864-017-3921-1

journal_volume

18

pub_type

杂志文章
  • Whole genome sequencing analysis of Plasmodium vivax using whole genome capture.

    abstract:BACKGROUND:Malaria caused by Plasmodium vivax is an experimentally neglected severe disease with a substantial burden on human health. Because of technical limitations, little is known about the biology of this important human pathogen. Whole genome analysis methods on patient-derived material are thus likely to have a...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-13-262

    authors: Bright AT,Tewhey R,Abeles S,Chuquiyauri R,Llanos-Cuentas A,Ferreira MU,Schork NJ,Vinetz JM,Winzeler EA

    更新日期:2012-06-21 00:00:00

  • Functional elucidation of the non-coding RNAs of Kluyveromyces marxianus in the exponential growth phase.

    abstract:BACKGROUND:Non-coding RNAs (ncRNAs), which perform diverse regulatory roles, have been found in organisms from all superkingdoms of life. However, there have been limited numbers of studies on the functions of ncRNAs, especially in nonmodel organisms such as Kluyveromyces marxianus that is widely used in the field of i...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-016-2474-z

    authors: Cho YB,Lee EJ,Cho S,Kim TY,Park JH,Cho BK

    更新日期:2016-02-29 00:00:00

  • Developing the anemone Aiptasia as a tractable model for cnidarian-dinoflagellate symbiosis: the transcriptome of aposymbiotic A. pallida.

    abstract:BACKGROUND:Coral reefs are hotspots of oceanic biodiversity, forming the foundation of ecosystems that are important both ecologically and for their direct practical impacts on humans. Corals are declining globally due to a number of stressors, including rising sea-surface temperatures and pollution; such stresses can ...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-13-271

    authors: Lehnert EM,Burriesci MS,Pringle JR

    更新日期:2012-06-22 00:00:00

  • The comparison of four mitochondrial genomes reveals cytoplasmic male sterility candidate genes in cotton.

    abstract:BACKGROUND:The mitochondrial genomes of higher plants vary remarkably in size, structure and sequence content, as demonstrated by the accumulation and activity of repetitive DNA sequences. Incompatibility between mitochondrial genome and nuclear genome leads to non-functional male reproductive organs and results in cyt...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-018-5122-y

    authors: Li S,Chen Z,Zhao N,Wang Y,Nie H,Hua J

    更新日期:2018-10-26 00:00:00

  • Glutamine rapidly induces the expression of key transcription factor genes involved in nitrogen and stress responses in rice roots.

    abstract:BACKGROUND:Glutamine is a major amino donor for the synthesis of amino acids, nucleotides, and other nitrogen-containing compounds in all organisms. In addition to its role in nutrition and metabolism, glutamine can also function as a signaling molecule in bacteria, yeast, and humans. By contrast, the functions of glut...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-015-1892-7

    authors: Kan CC,Chung TY,Juo YA,Hsieh MH

    更新日期:2015-09-25 00:00:00

  • Loss of WSTF results in spontaneous fluctuations of heterochromatin formation and resolution, combined with substantial changes to gene expression.

    abstract:BACKGROUND:Williams syndrome transcription factor (WSTF) is a multifaceted protein that is involved in several nuclear processes, including replication, transcription, and the DNA damage response. WSTF participates in a chromatin-remodeling complex with the ISWI ATPase, SNF2H, and is thought to contribute to the mainte...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-14-740

    authors: Culver-Cochran AE,Chadwick BP

    更新日期:2013-10-29 00:00:00

  • RBM6-RBM5 transcription-induced chimeras are differentially expressed in tumours.

    abstract:UNLABELLED:Transcription-induced chimerism, a mechanism involving the transcription and intergenic splicing of two consecutive genes, has recently been estimated to account for approximately 5% of the human transcriptome. Despite this prevalence, the regulation and function of these fused transcripts remains largely un...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-8-348

    authors: Wang K,Ubriaco G,Sutherland LC

    更新日期:2007-10-01 00:00:00

  • Gene2vec: distributed representation of genes based on co-expression.

    abstract:BACKGROUND:Existing functional description of genes are categorical, discrete, and mostly through manual process. In this work, we explore the idea of gene embedding, distributed representation of genes, in the spirit of word embedding. RESULTS:From a pure data-driven fashion, we trained a 200-dimension vector represe...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-018-5370-x

    authors: Du J,Jia P,Dai Y,Tao C,Zhao Z,Zhi D

    更新日期:2019-02-04 00:00:00

  • Genome-wide classification and expression analysis of MYB transcription factor families in rice and Arabidopsis.

    abstract:BACKGROUND:The MYB gene family comprises one of the richest groups of transcription factors in plants. Plant MYB proteins are characterized by a highly conserved MYB DNA-binding domain. MYB proteins are classified into four major groups namely, 1R-MYB, 2R-MYB, 3R-MYB and 4R-MYB based on the number and position of MYB r...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-13-544

    authors: Katiyar A,Smita S,Lenka SK,Rajwanshi R,Chinnusamy V,Bansal KC

    更新日期:2012-10-10 00:00:00

  • Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.

    abstract:BACKGROUND:Osteoporosis is a common and debilitating bone disease that is characterised by a low bone mineral density (BMD), a highly heritable trait. Genome-wide association studies (GWAS) have proven to be very successful in identifying common genetic variants associated with BMD adjusted for age, gender and weight, ...

    journal_title:BMC genomics

    pub_type: 杂志文章,meta分析

    doi:10.1186/s12864-016-2481-0

    authors: Mullin BH,Walsh JP,Zheng HF,Brown SJ,Surdulescu GL,Curtis C,Breen G,Dudbridge F,Richards JB,Spector TD,Wilson SG

    更新日期:2016-02-25 00:00:00

  • Visualizing spatiotemporal dynamics of apoptosis after G1 arrest by human T cell leukemia virus type 1 Tax and insights into gene expression changes using microarray-based gene expression analysis.

    abstract:BACKGROUND:Human T cell leukemia virus type 1 (HTLV-1) Tax is a potent activator of viral and cellular gene expression that interacts with a number of cellular proteins. Many reports show that Tax is capable of regulating cell cycle progression and apoptosis both positively and negatively. However, it still remains to ...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-13-275

    authors: Arainga M,Murakami H,Aida Y

    更新日期:2012-06-22 00:00:00

  • Assisted clustering of gene expression data using ANCut.

    abstract:BACKGROUND:In biomedical research, gene expression profiling studies have been extensively conducted. The analysis of gene expression data has led to a deeper understanding of human genetics as well as practically useful models. Clustering analysis has been a critical component of gene expression data analysis and can ...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-017-3990-1

    authors: Teran Hidalgo SJ,Wu M,Ma S

    更新日期:2017-08-16 00:00:00

  • Differences in DNA curvature-related sequence periodicity between prokaryotic chromosomes and phages, and relationship to chromosomal prophage content.

    abstract:BACKGROUND:Periodic spacing of A-tracts (short runs of A or T) with the DNA helical period of ~10-11 bp is characteristic of intrinsically bent DNA. In eukaryotes, the DNA bending is related to chromatin structure and nucleosome positioning. However, the physiological role of strong sequence periodicity detected in man...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-13-188

    authors: Abel J,Mrázek J

    更新日期:2012-05-15 00:00:00

  • Integrated "omics" profiling indicates that miRNAs are modulators of the ontogenetic venom composition shift in the Central American rattlesnake, Crotalus simus simus.

    abstract:BACKGROUND:Understanding the processes that drive the evolution of snake venom is a topic of great research interest in molecular and evolutionary toxinology. Recent studies suggest that ontogenetic changes in venom composition are genetically controlled rather than environmentally induced. However, the molecular mecha...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-14-234

    authors: Durban J,Pérez A,Sanz L,Gómez A,Bonilla F,Rodríguez S,Chacón D,Sasa M,Angulo Y,Gutiérrez JM,Calvete JJ

    更新日期:2013-04-10 00:00:00

  • Expression profiles of urbilaterian genes uniquely shared between honey bee and vertebrates.

    abstract:BACKGROUND:Large-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria (Urbilateria) is lost in each animal lineage. This event could be one of the underlying mechanisms involved in generating metazoan diversity. However, the present functions of...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-10-17

    authors: Matsui T,Yamamoto T,Wyder S,Zdobnov EM,Kadowaki T

    更新日期:2009-01-12 00:00:00

  • Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies.

    abstract:BACKGROUND:By assaying hundreds of thousands of single nucleotide polymorphisms, genome wide association studies (GWAS) allow for a powerful, unbiased review of the entire genome to localize common genetic variants that influence health and disease. Although it is widely recognized that some correction for multiple tes...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-9-516

    authors: Duggal P,Gillanders EM,Holmes TN,Bailey-Wilson JE

    更新日期:2008-10-31 00:00:00

  • Effects of Alu elements on global nucleosome positioning in the human genome.

    abstract:BACKGROUND:Understanding the genome sequence-specific positioning of nucleosomes is essential to understand various cellular processes, such as transcriptional regulation and replication. As a typical example, the 10-bp periodicity of AA/TT and GC dinucleotides has been reported in several species, but it is still uncl...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-11-309

    authors: Tanaka Y,Yamashita R,Suzuki Y,Nakai K

    更新日期:2010-05-17 00:00:00

  • Dual transcriptional profiling of mice and Toxoplasma gondii during acute and chronic infection.

    abstract:BACKGROUND:The obligate intracellular parasite Toxoplasma gondii establishes a life-long chronic infection within any warm-blooded host. After ingestion of an encysted parasite, T. gondii disseminates throughout the body as a rapidly replicating form during acute infection. Over time and after stimulation of the host i...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-15-806

    authors: Pittman KJ,Aliota MT,Knoll LJ

    更新日期:2014-09-20 00:00:00

  • Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.

    abstract:BACKGROUND:The ability to identify regions of the genome inherited with a dominant trait in one or more families has become increasingly valuable with the wide availability of high throughput sequencing technology. While a number of methods exist for mapping of homozygous variants segregating with recessive traits in c...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-015-1360-4

    authors: Levine AP,Connor TM,Oygar DD,Neild GH,Segal AW,Maxwell PH,Gale DP

    更新日期:2015-03-10 00:00:00

  • Complete haplotype phasing of the MHC and KIR loci with targeted HaploSeq.

    abstract:BACKGROUND:The MHC and KIR loci are clinically relevant regions of the genome. Typing the sequence of these loci has a wide range of applications including organ transplantation, drug discovery, pharmacogenomics and furthering fundamental research in immune genetics. Rapid advances in biochemical and next-generation se...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-015-1949-7

    authors: Selvaraj S,Schmitt AD,Dixon JR,Ren B

    更新日期:2015-11-05 00:00:00

  • Deep sequencing for de novo construction of a marine fish (Sparus aurata) transcriptome database with a large coverage of protein-coding transcripts.

    abstract:BACKGROUND:The gilthead sea bream (Sparus aurata) is the main fish species cultured in the Mediterranean area and constitutes an interesting model of research. Nevertheless, transcriptomic and genomic data are still scarce for this highly valuable species. A transcriptome database was constructed by de novo assembly of...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-14-178

    authors: Calduch-Giner JA,Bermejo-Nogales A,Benedito-Palos L,Estensoro I,Ballester-Lozano G,Sitjà-Bobadilla A,Pérez-Sánchez J

    更新日期:2013-03-15 00:00:00

  • Structured RNAs and synteny regions in the pig genome.

    abstract:BACKGROUND:Annotating mammalian genomes for noncoding RNAs (ncRNAs) is nontrivial since far from all ncRNAs are known and the computational models are resource demanding. Currently, the human genome holds the best mammalian ncRNA annotation, a result of numerous efforts by several groups. However, a more direct strateg...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-15-459

    authors: Anthon C,Tafer H,Havgaard JH,Thomsen B,Hedegaard J,Seemann SE,Pundhir S,Kehr S,Bartschat S,Nielsen M,Nielsen RO,Fredholm M,Stadler PF,Gorodkin J

    更新日期:2014-06-10 00:00:00

  • Blood-based epigenetic estimators of chronological age in human adults using DNA methylation data from the Illumina MethylationEPIC array.

    abstract:BACKGROUND:Epigenetic clocks have been recognized for their precise prediction of chronological age, age-related diseases, and all-cause mortality. Existing epigenetic clocks are based on CpGs from the Illumina HumanMethylation450 BeadChip (450 K) which has now been replaced by the latest platform, Illumina Methylation...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-020-07168-8

    authors: Lee Y,Haftorn KL,Denault WRP,Nustad HE,Page CM,Lyle R,Lee-Ødegård S,Moen GH,Prasad RB,Groop LC,Sletner L,Sommer C,Magnus MC,Gjessing HK,Harris JR,Magnus P,Håberg SE,Jugessur A,Bohlin J

    更新日期:2020-10-27 00:00:00

  • Introduction to the proceedings of the Avian Genomics and Gene Ontology Annotation Workshop.

    abstract::The Avian Genomics Conference and Gene Ontology Annotation Workshop brought together researchers and students from around the world to present their latest research addressing the delivery of value from the billions of base-pairs of Archosaur sequence that have become available in the last few years. This editorial de...

    journal_title:BMC genomics

    pub_type:

    doi:10.1186/1471-2164-10-S2-I1

    authors: Bridges SM,Burgess SC,McCarthy FM

    更新日期:2009-07-14 00:00:00

  • Identification of functional regulatory elements in the human genome using pooled CRISPR screens.

    abstract:BACKGROUND:Genome-scale pooled CRISPR screens are powerful tools for identifying genetic dependencies across varied cellular processes. The vast majority of CRISPR screens reported to date have focused exclusively on the perturbation of protein-coding gene function. However, protein-coding genes comprise < 2% of the se...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-020-6497-0

    authors: Borys SM,Younger ST

    更新日期:2020-01-31 00:00:00

  • Contrasting genetic variation and positive selection followed the divergence of NBS-encoding genes in Asian and European pears.

    abstract:BACKGROUND:The NBS disease-related gene family coordinates the inherent immune system in plants in response to pathogen infections. Previous studies have identified NBS-encoding genes in Pyrus bretschneideri ('Dangshansuli', an Asian pear) and Pyrus communis ('Bartlett', a European pear) genomes, but the patterns of ge...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-020-07226-1

    authors: Sun M,Zhang M,Singh J,Song B,Tang Z,Liu Y,Wang R,Qin M,Li J,Khan A,Wu J

    更新日期:2020-11-19 00:00:00

  • Estimating the total genome length of a metagenomic sample using k-mers.

    abstract:BACKGROUND:Metagenomic sequencing is a powerful technology for studying the mixture of microbes or the microbiomes on human and in the environment. One basic task of analyzing metagenomic data is to identify the component genomes in the community. This task is challenging due to the complexity of microbiome composition...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-019-5467-x

    authors: Hua K,Zhang X

    更新日期:2019-04-04 00:00:00

  • Assessing genomic diversity and signatures of selection in Jiaxian Red cattle using whole-genome sequencing data.

    abstract:BACKGROUND:Native cattle breeds are an important source of genetic variation because they might carry alleles that enable them to adapt to local environment and tough feeding conditions. Jiaxian Red, a Chinese native cattle breed, is reported to have originated from crossbreeding between taurine and indicine cattle; th...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-020-07340-0

    authors: Xia X,Zhang S,Zhang H,Zhang Z,Chen N,Li Z,Sun H,Liu X,Lyu S,Wang X,Li Z,Yang P,Xu J,Ding X,Shi Q,Wang E,Ru B,Xu Z,Lei C,Chen H,Huang Y

    更新日期:2021-01-09 00:00:00

  • Recurrent miscalling of missense variation from short-read genome sequence data.

    abstract:BACKGROUND:Short-read resequencing of genomes produces abundant information of the genetic variation of individuals. Due to their numerous nature, these variants are rarely exhaustively validated. Furthermore, low levels of undetected variant miscalling will have a systematic and disproportionate impact on the interpre...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/s12864-019-5863-2

    authors: Field MA,Burgio G,Chuah A,Al Shekaili J,Hassan B,Al Sukaiti N,Foote SJ,Cook MC,Andrews TD

    更新日期:2019-07-16 00:00:00

  • Celiac disease T-cell epitopes from gamma-gliadins: immunoreactivity depends on the genome of origin, transcript frequency, and flanking protein variation.

    abstract:BACKGROUND:Celiac disease (CD) is caused by an uncontrolled immune response to gluten, a heterogeneous mixture of wheat storage proteins. The CD-toxicity of these proteins and their derived peptides is depending on the presence of specific T-cell epitopes (9-mer peptides; CD epitopes) that mediate the stimulation of HL...

    journal_title:BMC genomics

    pub_type: 杂志文章

    doi:10.1186/1471-2164-13-277

    authors: Salentijn EM,Mitea DC,Goryunova SV,van der Meer IM,Padioleau I,Gilissen LJ,Koning F,Smulders MJ

    更新日期:2012-06-22 00:00:00