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Cytotoxicity of the effector protein BteA was attenuated in Bordetella pertussis by insertion of an alanine residue

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F20%3A00533321" target="_blank" >RIV/61388971:_____/20:00533321 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378050:_____/20:00533321

  • Result on the web

    <a href="https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1008512" target="_blank" >https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1008512</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1371/journal.ppat.1008512" target="_blank" >10.1371/journal.ppat.1008512</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Cytotoxicity of the effector protein BteA was attenuated in Bordetella pertussis by insertion of an alanine residue

  • Original language description

    Bordetella bronchisepticaandBordetella pertussisare closely related respiratory pathogens that evolved from a common bacterial ancestor. WhileB.bronchisepticahas an environmental reservoir and mostly establishes chronic infections in a broad range of mammals,B.pertussisis a human-specific pathogen causing acute pulmonary pertussis in infants and whooping cough illness in older humans. Both species employ a type III secretion system (T3SS) to inject a cytotoxic BteA effector protein into host cells. However, compared to the high BteA-mediated cytotoxicity ofB.bronchiseptica, the cytotoxicity induced byB.pertussisBteA (BpBteA) appears to be quite low and this has been attributed to the reduced T3SS gene expression inB.pertussis. We show that the presence of an alanine residue inserted at position 503 (A503) ofBpBteA accounts for its strongly attenuated cytotoxic potency. The deletion of A503 fromBpBteA greatly enhanced the cytotoxic activity ofB.pertussisB1917 on mammalian HeLa cells and expression ofBpBteA Delta A503 was highly toxic toSaccharomyces cerevisiaecells.Vice versa, insertion of A503 intoB.bronchisepticaBteA (BbBteA) strongly decreased its cytotoxicity to yeast and HeLa cells. Moreover, the production ofBpBteA Delta A503 increased virulence ofB.pertussisB1917 in the mouse model of intranasal infection (reduced LD50) but yielded less inflammatory pathology in infected mouse lungs at sublethal infectious doses. This suggests that A503 insertion in the T3SS effectorBpBteA may represent an evolutionary adaptation that fine-tunesB.pertussisvirulence and host immune response.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10606 - Microbiology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    PLoS Pathogens

  • ISSN

    1553-7366

  • e-ISSN

  • Volume of the periodical

    16

  • Issue of the periodical within the volume

    8

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    20

  • Pages from-to

    e1008512

  • UT code for WoS article

    000561392400003

  • EID of the result in the Scopus database

    2-s2.0-85089787575