Characterization of germinants and their receptors for spores of non-food-borne Clostridium perfringens strain F4969

Saeed Banawas, Daniel Paredes-Sabja, Peter Setlow, Mahfuzur R. Sarker

Resultado de la investigación: Article

4 Citas (Scopus)

Resumen

Clostridium perfringens type A can cause both food poisoning (FP) and non-food-borne (NFB) gastrointestinal diseases. Our previous study reported that a mixture of L-asparagine and KCl (AK)- germinated spores of FP and NFB isolates well, but KCl and, to a lesser extent, L-asparagine induced spore germination only in FP isolates. We now report that the germination response of FP and NFB spores differsignificantly in several defined germinants and rich media. Spores of NFB strain F4969 gerAA, gerKA-KC or gerKC mutants lacking specific germinant receptor proteins germinated more slowly than wild-type spores with rich media, did not germinate with AK and germinated poorly compared to wild-type spores with L-cysteine. The germination defects in the gerKA-KC spores were largely due to loss of GerKC as (i) gerKA spores germinated significantly with all tested germinants, while gerKC spores exhibited poor or no germination; and (ii) germination defects in gerKC spores were largely restored by expressing the wild-type gerKA-KC operon in trans. We also found that gerKA-KC, gerAA and gerKC spores, but not gerKA spores, released dipicolinic acid at a slower rate than wild-type spores with AK. The colony-forming efficiency of F4969 gerKC spores was also ~35-fold lower than that of wild-type spores, while gerAA and wild-type spores had similar viability. Collectively, these results suggest that the GerAA and GerKC proteins play roles in normal germination of C. perfringens NFB isolates and that GerKC, but not GerAA, is important in these spores’apparent viability.

Idioma originalEnglish
Número de artículo000378
Páginas (desde-hasta)1972-1983
Número de páginas12
PublicaciónMicrobiology (United Kingdom)
Volumen162
N.º11
DOI
EstadoPublished - 1 nov 2016

Huella dactilar

Clostridium perfringens
Spores
Germination
Foodborne Diseases
Asparagine
Gastrointestinal Diseases
Operon

ASJC Scopus subject areas

  • Microbiology

Citar esto

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title = "Characterization of germinants and their receptors for spores of non-food-borne Clostridium perfringens strain F4969",
abstract = "Clostridium perfringens type A can cause both food poisoning (FP) and non-food-borne (NFB) gastrointestinal diseases. Our previous study reported that a mixture of L-asparagine and KCl (AK)- germinated spores of FP and NFB isolates well, but KCl and, to a lesser extent, L-asparagine induced spore germination only in FP isolates. We now report that the germination response of FP and NFB spores differsignificantly in several defined germinants and rich media. Spores of NFB strain F4969 gerAA, gerKA-KC or gerKC mutants lacking specific germinant receptor proteins germinated more slowly than wild-type spores with rich media, did not germinate with AK and germinated poorly compared to wild-type spores with L-cysteine. The germination defects in the gerKA-KC spores were largely due to loss of GerKC as (i) gerKA spores germinated significantly with all tested germinants, while gerKC spores exhibited poor or no germination; and (ii) germination defects in gerKC spores were largely restored by expressing the wild-type gerKA-KC operon in trans. We also found that gerKA-KC, gerAA and gerKC spores, but not gerKA spores, released dipicolinic acid at a slower rate than wild-type spores with AK. The colony-forming efficiency of F4969 gerKC spores was also ~35-fold lower than that of wild-type spores, while gerAA and wild-type spores had similar viability. Collectively, these results suggest that the GerAA and GerKC proteins play roles in normal germination of C. perfringens NFB isolates and that GerKC, but not GerAA, is important in these spores’apparent viability.",
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Characterization of germinants and their receptors for spores of non-food-borne Clostridium perfringens strain F4969. / Banawas, Saeed; Paredes-Sabja, Daniel; Setlow, Peter; Sarker, Mahfuzur R.

En: Microbiology (United Kingdom), Vol. 162, N.º 11, 000378, 01.11.2016, p. 1972-1983.

Resultado de la investigación: Article

TY - JOUR

T1 - Characterization of germinants and their receptors for spores of non-food-borne Clostridium perfringens strain F4969

AU - Banawas, Saeed

AU - Paredes-Sabja, Daniel

AU - Setlow, Peter

AU - Sarker, Mahfuzur R.

PY - 2016/11/1

Y1 - 2016/11/1

N2 - Clostridium perfringens type A can cause both food poisoning (FP) and non-food-borne (NFB) gastrointestinal diseases. Our previous study reported that a mixture of L-asparagine and KCl (AK)- germinated spores of FP and NFB isolates well, but KCl and, to a lesser extent, L-asparagine induced spore germination only in FP isolates. We now report that the germination response of FP and NFB spores differsignificantly in several defined germinants and rich media. Spores of NFB strain F4969 gerAA, gerKA-KC or gerKC mutants lacking specific germinant receptor proteins germinated more slowly than wild-type spores with rich media, did not germinate with AK and germinated poorly compared to wild-type spores with L-cysteine. The germination defects in the gerKA-KC spores were largely due to loss of GerKC as (i) gerKA spores germinated significantly with all tested germinants, while gerKC spores exhibited poor or no germination; and (ii) germination defects in gerKC spores were largely restored by expressing the wild-type gerKA-KC operon in trans. We also found that gerKA-KC, gerAA and gerKC spores, but not gerKA spores, released dipicolinic acid at a slower rate than wild-type spores with AK. The colony-forming efficiency of F4969 gerKC spores was also ~35-fold lower than that of wild-type spores, while gerAA and wild-type spores had similar viability. Collectively, these results suggest that the GerAA and GerKC proteins play roles in normal germination of C. perfringens NFB isolates and that GerKC, but not GerAA, is important in these spores’apparent viability.

AB - Clostridium perfringens type A can cause both food poisoning (FP) and non-food-borne (NFB) gastrointestinal diseases. Our previous study reported that a mixture of L-asparagine and KCl (AK)- germinated spores of FP and NFB isolates well, but KCl and, to a lesser extent, L-asparagine induced spore germination only in FP isolates. We now report that the germination response of FP and NFB spores differsignificantly in several defined germinants and rich media. Spores of NFB strain F4969 gerAA, gerKA-KC or gerKC mutants lacking specific germinant receptor proteins germinated more slowly than wild-type spores with rich media, did not germinate with AK and germinated poorly compared to wild-type spores with L-cysteine. The germination defects in the gerKA-KC spores were largely due to loss of GerKC as (i) gerKA spores germinated significantly with all tested germinants, while gerKC spores exhibited poor or no germination; and (ii) germination defects in gerKC spores were largely restored by expressing the wild-type gerKA-KC operon in trans. We also found that gerKA-KC, gerAA and gerKC spores, but not gerKA spores, released dipicolinic acid at a slower rate than wild-type spores with AK. The colony-forming efficiency of F4969 gerKC spores was also ~35-fold lower than that of wild-type spores, while gerAA and wild-type spores had similar viability. Collectively, these results suggest that the GerAA and GerKC proteins play roles in normal germination of C. perfringens NFB isolates and that GerKC, but not GerAA, is important in these spores’apparent viability.

KW - C. perfringens

KW - Germinant receptors

KW - Germination

KW - Spores

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DO - 10.1099/mic.0.000378

M3 - Article

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SP - 1972

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JO - Microbiology (United Kingdom)

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