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SRX26930830: GSM8658630: ATCC 8739, high pressure, 300 MPa, rep3; Escherichia coli; RNA-Seq
1 ILLUMINA (Illumina NovaSeq X Plus) run: 8.8M spots, 2.6G bases, 797.3Mb downloads

External Id: GSM8658630_r1
Submitted by: Food Microbiology, Department of Chemistry, Universität Hamburg
Study: Differential gene expression of Escherichia coli ATCC 8739 in strawberry nectar after thermal and non-thermal treatments
show Abstracthide Abstract
Red fruits are valued for their vitamin C and polyphenol content, but traditional heat preservation methods used in juice and nectar production can significantly reduce these components. Therefore, alternative non-thermal methods are explored to inactivate foodborne pathogens like Escherichia coli while maintaining the nutritional value. However, knowledge about the effects of these technologies on bacterial cells is limited. This study analyzed differentially expressed genes of E. coli ATCC 8739 inoculated in strawberry nectar after exposure to three treatments with two sets of parameters each, namely thermal treatment, high-pressure processing (HPP), and moderate-intensity pulsed electric field (MIPEF). The highest inactivation efficiency was achieved with HPP at 400 MPa, 1 min, reducing microbial counts by 5.0±0.3 log cfu/mL, and thermal treatment at 60°C, 200 s, achieving a reduction of 4.4±0.2 log cfu/mL, while no inactivation was observed with MIPEF at 6 kV/cm. Transcriptomic analysis showed that thermal and HPP treatments caused similar molecular stress responses in E. coli. In both cases, the most overexpressed genes encoded outer membrane proteins, which may lead to the activation of the envelope stress response. Despite no microbial inactivation was revealed after MIPEF treatment, strong transcriptomic responses were observed, particularly in genes related to membrane integrity and metabolic activity. Numerous overexpressed genes associated with ABC transporters, outer membrane proteins, and lipoproteins were identified, which could increase the strain's virulence. This study provides insights into the stress response mechanisms induced by conventional and novel treatments. Nevertheless, further research is needed to investigate the long-term effects on bacterial populations. Overall design: RNA-seq profiling of E. coli ATCC 8739 inoculated in strawberry nectar after exposure to six different treatments, including thermal treatment, high pressure processing, and pulsed electric field (3 replicates)
Sample: ATCC 8739, high pressure, 300 MPa, rep3
SAMN45122726 • SRS23404383 • All experiments • All runs
Library:
Name: GSM8658630
Instrument: Illumina NovaSeq X Plus
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA was harvested using Rneasy Mini Kit from Qiagen. Firstly, ribosomal RNA was removed from total RNA, followed by ethanol precipitation. After fragmentation, the first strand cDNA was synthesized using random hexamer primers. During the second strand cDNA synthesis, dUTPs were replaced with dTTPs in the reaction buffer. The directional library was ready after end repair, A-tailing, adapter ligation, size selection, USER enzyme digestion, amplification, and purification.
Runs: 1 run, 8.8M spots, 2.6G bases, 797.3Mb
Run# of Spots# of BasesSizePublished
SRR315649268,822,6842.6G797.3Mb2024-12-03

ID:
36377793

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