The distinct transcriptome of virulence-associated phylogenetic group B2 Escherichia coli

被引:4
|
作者
Hogins, Jacob [1 ]
Xuan, Zhenyu [1 ]
Zimmern, Philippe E. [2 ]
Reitzer, Larry [1 ]
机构
[1] Univ Texas Dallas, Dept Biol Sci, Richardson, TX 75083 USA
[2] Univ Texas Southwestern, Dept Urol, Dallas, TX USA
来源
MICROBIOLOGY SPECTRUM | 2023年 / 11卷 / 05期
关键词
Escherichia coli; pathogens; urinary tract infection; transcriptional regulation; transcription factors; phylogenetic analysis; metabolism; URINARY-TRACT-INFECTIONS; DIFFERENTIAL EXPRESSION ANALYSIS; ALTERNATIVE SIGMA-FACTOR; STRAINS; CLUSTERPROFILER; EPIDEMIOLOGY; RESISTANCE; RESPONSES; PACKAGE; GROWTH;
D O I
10.1128/spectrum.02085-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Escherichia coli strains of phylogenetic group B2 are often associated with urinary tract infections (UTIs) and several other diseases. Recent genomic and transcriptomic analyses have not suggested or identified specific genes required for virulence, but have instead suggested multiple virulence strategies and complex host-pathogen interactions. Previous analyses have not compared core gene expression between phylogenetic groups or between pathogens and nonpathogens within phylogenetic groups. We compared the core gene expression of 35 strains from three phylogenetic groups that included both pathogens and nonpathogens after growth in a medium that allowed comparable growth of both types of strains. K-means clustering suggested a B2 cluster with 17 group B2 strains and two group A strains; an AD cluster with six group A strains, five group D strains and one B2 strain; and four outliers which included the highly studied model uropathogenic E. coli strains UTI89 and CFT073. Half of the core genes were differentially expressed between B2 and AD cluster strains, including transcripts of genes for all aspects of macromolecular synthesis-replication, transcription, translation, and peptidoglycan synthesis-energy metabolism, and environmental-sensing transcriptional regulators. Notably, core gene expression between nonpathogenic and uropathogenic transcriptomes within phylogenetic groups did not differ. If differences between pathogens and nonpathogens exist, then the differences do not require transcriptional reprogramming. In summary, B2 cluster strains have a distinct transcription pattern that involves hundreds of genes. We propose that this transcription pattern is one factor that contributes to virulence. IMPORTANCE Escherichia coli is a diverse species and an opportunistic pathogen that is associated with various diseases, such as urinary tract infections. When examined, phylogenetic group B2 strains are more often associated with these diseases, but the specific properties that contribute to their virulence are not known. From a comparative transcriptomic analysis, we found that group B2 strains grown in a nutrient-rich medium had a distinct transcription pattern, which is the first evidence that core gene expression differs between phylogenetic groups. Understanding the consequences of group B2 transcription pattern will provide important information on basic E. coli biology, the basis for E. coli virulence, and possibly for developing therapies for a majority of urinary tract infections and other group B2-associated diseases.
引用
收藏
页数:22
相关论文
共 50 条
  • [31] Virulence-associated genes analysis of carbapenemase-producing Escherichia coli isolates
    Jomehzadeh, Nabi
    Jahangirimehr, Fateme
    Chegeni, Sina Ahmadi
    PLOS ONE, 2022, 17 (05):
  • [32] Escherichia colistrains of phylogenetic group B2 and D and bacteriocin production are associated with advanced colorectal neoplasia
    Darina Kohoutova
    David Smajs
    Paula Moravkova
    Jiri Cyrany
    Monika Moravkova
    Miroslava Forstlova
    Michal Cihak
    Stanislav Rejchrt
    Jan Bures
    BMC Infectious Diseases, 14
  • [33] Virulence-associated genes in Escherichia coli isolates from poultry with colibacillosis:: correction
    Vidotto, MC
    Gaziri, LCJ
    Delicato, ER
    VETERINARY MICROBIOLOGY, 2004, 102 (1-2) : 95 - 96
  • [35] Detection of virulence-associated genes in pathogenic and commensal avian Escherichia coli isolates
    Paixao, A. C.
    Ferreira, A. C.
    Fontes, M.
    Themudo, P.
    Albuquerque, T.
    Soares, M. C.
    Fevereiro, M.
    Martins, L.
    Correa de Sa, M. I.
    POULTRY SCIENCE, 2016, 95 (07) : 1646 - 1652
  • [36] Virulence-associated factors of uropathogenic Escherichia coli strains isolated from pigs
    de Brito, BG
    Leite, DD
    Linhares, REC
    Vidotto, MC
    VETERINARY MICROBIOLOGY, 1999, 65 (02) : 123 - 132
  • [37] Characterization of avian pathogenic Escherichia coli isolates based on biofilm formation, ESBL production, virulence-associated genes, and phylogenetic groups
    Karen Apellanis Borges
    Thales Quedi Furian
    Benito Guimarães de Brito
    Kelly Cristina Tagliari de Brito
    Daniela Tonini da Rocha
    Carlos Tadeu Pippi Salle
    Hamilton Luiz de Souza Moraes
    Vladimir Pinheiro do Nascimento
    Brazilian Journal of Microbiology, 2023, 54 : 2413 - 2425
  • [38] Characterization of avian pathogenic Escherichia coli isolates based on biofilm formation, ESBL production, virulence-associated genes, and phylogenetic groups
    Borges, Karen Apellanis
    Furian, Thales Quedi
    de Brito, Benito Guimaraes
    de Brito, Kelly Cristina Tagliari
    da Rocha, Daniela Tonini
    Salle, Carlos Tadeu Pippi
    Moraes, Hamilton Luiz de Souza
    do Nascimento, Vladimir Pinheiro
    BRAZILIAN JOURNAL OF MICROBIOLOGY, 2023, 54 (03) : 2413 - 2425
  • [39] Escherichia coli strains belonging to phylogenetic group B2 have superior capacity to persist in the intestinal microflora of infants
    Nowrouzian, FL
    Wold, AE
    Adlerberth, I
    JOURNAL OF INFECTIOUS DISEASES, 2005, 191 (07): : 1078 - 1083
  • [40] Sex-dependent competitive dominance of phylogenetic group B2 Escherichia coli strains within human hosts
    Blyton, Michaela D. J.
    Cornall, Samantha J.
    Kennedy, Karina
    Colligon, Peter
    Gordon, David M.
    ENVIRONMENTAL MICROBIOLOGY REPORTS, 2014, 6 (06): : 605 - 610