TY - JOUR
T1 - Production of inactivated gram-positive and gram-negative species with preserved cellular morphology and integrity
AU - Taddese, Rahwa
AU - Belzer, Clara
AU - Aalvink, Steven
AU - de Jonge, Marien I.
AU - Nagtegaal, Iris D.
AU - Dutilh, Bas E.
AU - Boleij, Annemarie
PY - 2021
Y1 - 2021
N2 - There are many approaches available to produce inactive bacteria by termination of growth, each with a different efficacy, impact on cell integrity, and potential for application in standardized inactivation protocols. The aim of this study was to compare these approaches and develop a standardized protocol for generation of inactivated Gram-positive and Gram-negative bacteria, yielding cells that are metabolically dead with retained cellular integrity i.e., preserving the surface and limited leakage of intracellular proteins and DNA. These inactivated bacteria are required for various applications, for instance, when investigating receptor-triggered signaling or bacterial contact-dependent analysis of cell lines requiring long incubation times. We inactivated eight different bacterial strains of different species by treatment with beta-propiolactone, ethanol, formalin, sodium hydroxide, and pasteurization. Inactivation efficacy was determined by culturing, and cell wall integrity assessed by quantifying released DNA, bacterial membrane and intracellular DNA staining, and visualization by scanning electron microscopy. Based on these results, we discuss the bacterial inactivation methods, and their advantages and disadvantages to study host-microbe interactions with inactivated bacteria.
AB - There are many approaches available to produce inactive bacteria by termination of growth, each with a different efficacy, impact on cell integrity, and potential for application in standardized inactivation protocols. The aim of this study was to compare these approaches and develop a standardized protocol for generation of inactivated Gram-positive and Gram-negative bacteria, yielding cells that are metabolically dead with retained cellular integrity i.e., preserving the surface and limited leakage of intracellular proteins and DNA. These inactivated bacteria are required for various applications, for instance, when investigating receptor-triggered signaling or bacterial contact-dependent analysis of cell lines requiring long incubation times. We inactivated eight different bacterial strains of different species by treatment with beta-propiolactone, ethanol, formalin, sodium hydroxide, and pasteurization. Inactivation efficacy was determined by culturing, and cell wall integrity assessed by quantifying released DNA, bacterial membrane and intracellular DNA staining, and visualization by scanning electron microscopy. Based on these results, we discuss the bacterial inactivation methods, and their advantages and disadvantages to study host-microbe interactions with inactivated bacteria.
KW - Bacterial ghosts
KW - Bacterial inactivation
KW - Beta-propiolactone
KW - Heat-treatment
KW - Pasteurization
KW - Scanning electron microscopy
KW - Standardized protocol
U2 - 10.1016/j.mimet.2021.106208
DO - 10.1016/j.mimet.2021.106208
M3 - Article
AN - SCOPUS:85103118776
SN - 0167-7012
VL - 184
JO - Journal of Microbiological Methods
JF - Journal of Microbiological Methods
M1 - 106208
ER -