BB0562 is a nutritional virulence determinant with lipase activity important for Borrelia burgdorferi infection and survival in fatty acid deficient environments

被引:7
作者
Kuhn, Hunter W. [1 ,5 ]
Lasseter, Amanda G. [1 ]
Adams, Philip P. [1 ,2 ,3 ]
Avile, Carlos Flores [1 ,6 ]
Stone, Brandee L. [4 ,7 ]
Akins, Darrin R. [4 ]
Jewett, Travis J. [1 ]
Jewett, Mollie W. [1 ]
机构
[1] Univ Cent Florida, Burnett Sch Biomed Sci, Div Immun & Pathogenesis, Coll Med, Orlando, FL 32816 USA
[2] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Div Mol & Cellular Biol, Bethesda, MD USA
[3] NIGMS, Postdoctoral Res Associate Program, NIH, Bethesda, MD USA
[4] Univ Oklahoma, Hlth Sci Ctr, Dept Microbiol & Immunol, Oklahoma City, OK 73190 USA
[5] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[6] Genesis Res, Hoboken, NJ USA
[7] Texas A&M Univ, Hlth Sci Ctr, Dept Microbial Pathogenesis & Immunol, Bryan, TX USA
基金
美国国家卫生研究院;
关键词
LYME-DISEASE SPIROCHETE; OUTER-MEMBRANE; MYCOBACTERIUM-TUBERCULOSIS; GENE-EXPRESSION; PROTEIN; PLASMID; GENOME; ANTIBODY; MICE; TRANSFORMATION;
D O I
10.1371/journal.ppat.1009869
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Lyme disease spirochete Borrelia burgdorferi relies on uptake of essential nutrients from its host environments for survival and infection. Therefore, nutrient acquisition mechanisms constitute key virulence properties of the pathogen, yet these mechanisms remain largely unknown. In vivo expression technology applied to B. burgdorferi (BbIVET) during mammalian infection identified gene bb0562, which encodes a hypothetical protein compromised of a conserved domain of unknown function, DUF3996. DUF3996 is also found across adjacent encoded hypothetical proteins BB0563 and BB0564, suggesting the possibility that the three proteins could be functionally related. Deletion of bb0562, bb0563 and bb0564 individually and together demonstrated that bb0562 alone was important for optimal disseminated infection in immunocompetent and immunocompromised mice by needle inoculation and tick bite transmission. Moreover, bb0562 promoted spirochete survival during the blood dissemination phase of infection. Gene bb0562 was also found to be important for spirochete growth in low serum media and the growth defect of Delta bb0562 B. burgdorferi was rescued with the addition of various long chain fatty acids, particularly oleic acid. In mammals, fatty acids are primarily stored in fat droplets in the form of triglycerides. Strikingly, addition of glyceryl trioleate, the triglyceride form of oleic acid, to the low serum media did not rescue the growth defect of the mutant, suggesting bb0562 may be important for the release of fatty acids from triglycerides. Therefore, we searched for and identified two canonical GXSXG lipase motifs within BB0562, despite the lack of homology to known bacterial lipases. Purified BB0562 demonstrated lipolytic activity dependent on the catalytic serine residues within the two motifs. In sum, we have established that bb0562 is a novel nutritional virulence determinant, encoding a lipase that contributes to fatty acid scavenge for spirochete survival in environments deficient in free fatty acids including the mammalian host. Author summary Borrelia burgdorferi, the causative agent of Lyme disease, has a small genome and lacks the ability to synthesize essential nutrients on its own as well as many of the virulence properties typical of bacterial pathogens that contribute to disease. The clinical manifestations of Lyme disease predominantly result from inflammation in response to the B. burgdorferi infection. Therefore, nutrient acquisition functions constitute key virulence factors for the pathogen. Fatty acids are critical components of B. burgdorferi membranes and lipoproteins, which the spirochete must scavenge from the host environment. Previously, through a genetic screen for B. burgdorferi genes that are expressed during mammalian infection we identified gene of unknown function, bb0562. Herein, we demonstrate that bb0562 encodes a lipase that plays a role in the release of free fatty acids from triglycerides. Furthermore, bb0562 contributes to B. burgdorferi survival and dissemination in the mammalian host. BB0562 is important for spirochete survival in environments low in free fatty acids thereby adding to B. burgdorferi's arsenal of nutritional virulence determinants necessary for the pathogen to be maintained in the tick-mouse enzootic cycle and to cause disseminated disease.
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页数:26
相关论文
共 94 条
  • [1] Microbial quest for food in vivo: "Nutritional virulence' as an emerging paradigm
    Abu Kwaik, Yousef
    Bumann, Dirk
    [J]. CELLULAR MICROBIOLOGY, 2013, 15 (06) : 882 - 890
  • [2] Regulatory roles of Escherichia coli 5′ UTR and ORF-internal RNAs detected by 3′ end mapping
    Adams, Philip P.
    Baniulyte, Gabriele
    Esnault, Caroline
    Chegireddy, Kavya
    Singh, Navjot
    Monge, Molly
    Dale, Ryan K.
    Storz, Gisela
    Wade, Joseph T.
    [J]. ELIFE, 2021, 10 : 1 - 33
  • [3] Adams PP, 2018, METHODS MOL BIOL, V1690, P137, DOI 10.1007/978-1-4939-7383-5_12
  • [4] A Dual Luciferase Reporter System for B-burgdorferi Measures Transcriptional Activity during Tick-Pathogen Interactions
    Adams, Philip P.
    Avile, Carlos Flores
    Jewett, Mollie W.
    [J]. FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2017, 7
  • [5] In vivo expression technology and 5′ end mapping of the Borrelia burgdorferi transcriptome identify novel RNAs expressed during mammalian infection
    Adams, Philip P.
    Avile, Carlos Flores
    Popitsch, Niko
    Bilusic, Ivana
    Schroeder, Renee
    Lybecker, Meghan
    Jewett, Mollie W.
    [J]. NUCLEIC ACIDS RESEARCH, 2017, 45 (02) : 775 - 792
  • [6] Mycoplasma bovis Membrane Protein MilA Is a Multifunctional Lipase with Novel Lipid and Glycosaminoglycan Binding Activity
    Adamu, James Yazah
    Wawegama, Nadeeka Kumari
    Condello, Anna Kanci
    Marenda, Marc Serge
    Markham, Philip Francis
    Browning, Glenn Francis
    Tivendale, Kelly Anne
    [J]. INFECTION AND IMMUNITY, 2020, 88 (06)
  • [7] GDSL family of serine esterases/lipases
    Akoh, CC
    Lee, GC
    Liaw, YC
    Huang, TH
    Shaw, JF
    [J]. PROGRESS IN LIPID RESEARCH, 2004, 43 (06) : 534 - 552
  • [8] [Anonymous], 1993, Biol. Chem. Hoppe Seyler
  • [9] Aranjuez GF, 2019, INFECT IMMUN, V87, DOI [10.1128/IAI.00887-18, 10.1128/iai.00887-18]
  • [10] Bandana K., 2018, Advances in Biotechnology and Microbiology, V10, P106, DOI DOI 10.19080/AIBM.2018.10.555798