Transcriptional response of OmpC and OmpF in Escherichia coli against differential gradient of carbapenem stress
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This study was designed to investigate the transcriptional response of OmpF and OmpC along with an antisense RNA, MicF under concentration gradient carbapenem exposure.
An elevation in the expression of OmpF gene under concentration gradient imipenem stress from a particular concentration was observed. For OmpC gene a significant decrease in the expression was noticed under concentration gradient imipenem and meropenem stress. The study showed reduction in the expression of OmpC gene against imipenem and meropenem possibly preventing the entry of carbapenem antibiotic inside the cell indicating a possible role in carbapenem resistance.
KeywordsOmpF OmpC micF Carbapenem Escherichia coli Real time PCR
outer membrane protein F
outer membrane protein C
carbonyl cyanide m-chlorophenylhydrazone
OmpC and OmpF are two major outer membrane proteins in E. coli which serve as a barrier for antibiotics and other toxic agents entering inside the cell . It is reported that sub lethal dose of antibiotics has protective role in bacterial cell against wide range of antimicrobials  and down regulation of porin genes are responsible in nonspecific resistance. OmpC and OmpF are known to be involved in non-specific solute transport and also it was reported that multidrug resistant E. coli had lower level of OmpC expression . Also, previous reports suggest that OmpC and OmpF share reciprocal relationship .
A total of 96 consecutive, non-duplicates, Escherichia coli clinical isolates resistant to at least one of the carbapenem antibiotic were collected from patients attended the clinic or admitted between August 2016 and July 2017 in Silchar Medical College and Hospital, Silchar, India.
Antibiotic susceptibility testing
A preliminary antibiotic susceptibility testing was performed to select the study isolates. Susceptibility was performed by Kirby Bauer method against different antibiotics viz, ciprofloxacin (5 μg),amikacin (30 μg),cefepime (30 μg), aztreonam (30 μg), ceftriaxone (30 μg), co-trimoxazole (25 μg), ceftazidime (30 μg), levofloxacin (5 μg) gentamicin (10 μg), carbenicillin (10 μg), ceftazidime (30 μg) and piperacillin-tazobactam (100/10 μg) (Hi-media, Mumbai, India) and results were interpreted as per Clinical and laboratory standards institute guidelines . E. coli ATCC 25922 was used as control.
Minimal inhibitory concentration (MIC) assay
As the study intends to investigate the OmpC and OmpF transcriptional expression under carbapenem stress, the minimum inhibitory concentration of the test isolates was determined against imipenem, meropenem and ertapenem by agar broth dilution method at varied concentration ranging from 0.125 to 512 µg/ml and the results were interpreted as per CLSI guidelines .
Detection of efflux pump mediated carbapenem resistance using an inhibitor
Porin loss/mutation and increased efflux pump activity are major contributor of innate resistance mechanism. Therefore, the efflux pump mediated carbapenem resistance was assessed using an inhibitor. This test was carried out for all the test isolates with meropenem (10 µg, Himedia, Mumbai) with and without an efflux pump inhibitor carbonyl cyanide m-chlorophenylhyrazone (12.5 µM), [Himedia, Mumbai, India]. A difference between zone of inhibition of ≥ 5 mm with the inhibitor and the carbapenems alone confirms to be having efflux pump activity. Ethidium bromide was taken as control substrate for the efflux pump activity . Disc with only CCCP was used to rule out any activity of the agent alone.
Detection of carbapenemases
To investigate the presence of carbapenemase activity among the selected isolates Modified Hodge test was performed. Further, polymerase chain reaction (PCR) assay was carried out in a 96 well thermal cycler (Applied Biosystems) in order to detect various carbapenemase-encoding genes which included blaKPC, blaIMP, blaVIM, blaNDM, blaOXA-23, blaOXA-48 and blaOXA-58 [7, 8, 9, 10]. This experiment was performed to rule out the role of any acquired mechanism in carbapenem resistance among study isolates.
Analysis of efflux pump component acrA gene expression
To detect the presence of any isolates with overexpressed acrAB-tolC system, the non carbapenemase producers were further selected and subjected to quantitative Real Time PCR to examine the expressional level of the efflux pump gene acrA under normal condition. The total RNA was isolated using QIAGEN Rneasy Mini Kit (QIAGEN, Germany) following manufacturer’s instructions. Estimation of the isolated RNA was performed using Picodrop (Pico200, Cambridge, UK) and further cDNA was synthesized using prepared mRNA as template via Qiagen Reverse Transcription Kit (QIAGEN, Germany). Quantitative Real-time PCR of the cDNA prepared was done using power Sybrgreen PCR master mix reagents kit (Applied Biosystems, Austin, USA) in StepOnePlus quantitative Real Time-PCR (Applied Biosystems, USA) in triplicates using specific primers-acrA (F): 5′CTCTCAGGCAGCTTAGCCCTAA3′, acrA (R): 5′TGCAGAGGTTCAGTTTTGACTGTT3′ . E. coli ATCC 25922 and RpslE was used as quality control and endogenous control.
Transcriptional expression of OmpF and OmpC and an antisense RNA gene micF gene
The overnight cultures of E. coli isolates on Luria Broth (Hi-media, Mumbai, India) were centrifuged and subjected to total RNA isolation using QIAGEN Rneasy Mini Kit (QIAGEN, Germany) according to manufacturer’s guidelines. The isolated RNA was then estimated with the use of Picodrop (Pico200, Cambridge, UK) and further synthesis of cDNA was done using Qiagen Reverse Transcription Kit (QIAGEN, Germany). Quantitative Real-time PCR of the cDNA prepared was performed by using power Sybrgreen PCR master mix reagents kit (Applied Biosystems, Austin, USA). Analysis of the synthesized cDNA levels was carried out in triplicate in StepOnePlus quantitative Real Time-PCR (Applied Biosystems, USA) using specific primers (Additional file 1: Table S1). E. coli ATCC 25922 was used as a reference for the analysis of relative fold changes in gene expression.
Transcriptional expression of OmpF and OmpC porin genes and MicF gene under concentration gradient carbapenem stress
To investigate the role of porin genes OmpF and OmpC during carbapenem stress the isolates were grown on LB broth containing 0.25 µg/ml, 0.5 µg/ml, 1 µg/ml, 2 µg/ml and 4 µg/ml of imipenem, meropenem and ertapenem individually. The culture was incubated for 16 h till late log phase. The mRNA was isolated immediately and reverse transcribed into cDNA. Quantitative Real Time PCR was performed to assess the transcriptional response of OmpF, OmpC and MicF against concentration gradient carbapenem stress. All the protocols were followed as described earlier in the text.
The relative expression differences of porin genes OmpF and OmpC along with an antisense RNA gene, MicF was compared with their respective wild type strain under concentration gradient carbapenem stress between samples were determined with the help of one-way ANOVA followed by Tukey–Kramer (Tukey’s W) multiple comparison test. Differences were considered statistically significant at both 5% and 1% level when p < 0.05. SPSS version 17.0 was used for statistical analysis.
This study deals with the outer-membrane porin genes OmpF, OmpC and MicF gene which perhaps has a role in developing resistance towards carbapenems. As reported by Nikaido and Vaara, the expression of OmpF gene is reduced in high osmolarity condition whereas, for OmpC the same environment was found to be favorable . However, efflux pump gene AcrB has also been reported to repress the expression of the porin OmpF gene [13, 14]. In this study carbapenem resistant E. coli isolates were studied of which decrease in the expression of OmpF and OmpC genes were observed in AcrAB overexpressed isolates which is in agreement with previous studies [15, 16, 17]. In a study done by Yigit et al., in Enterobacter strain 810, alteration in the porin genes OmpF and OmpC resulted in imipenem resistance along with reduced susceptibility towards meropenem and cefepime . After, exposure to sub inhibitory concentration of imipenem down regulation of OmpC gene was also observed which is in support of the present study. However, it was observed under imipenem stress an increase in the expression of OmpF gene was observed which has not been reported earlier. The expression level of OmpF is also affected by a small antisense RNA, MicF which inhibits the expression of OmpF gene . However, in the present study meropenem stress reduced the expression of OmpF and micF as well, indicating that there may be other factors responsible for the down regulation of OmpF against carbapenem exposure. Therefore, it is probably the major porin that prevents entry of carbapenem inside the cell which calls for further investigation.
This study warrants a proteomic approach to analyze the expression of porin genes at translational level.
SC performed the experimental work, data collection and analysis and prepared the manuscript. MS, DB and KN analyzed the data. DDC and AC have designed work plan and corrected manuscript. AB has conceived the plan and supervised the whole study. All authors ensured that this is the case. All authors read and approved the final manuscript.
The authors would like to acknowledge Assam University Biotech Hub for providing infrastructure facility.
The authors declare that they have no competing interests.
Availability of data and materials
All the data generated in this research work are presented in this research article. In case of any additional information requirement corresponding author will be providing the necessary information as per ethical guidelines.
Consent for publication
Ethics approval and consent to participate
The work was approved by Institutional Ethical committee of Assam University, Silchar. The authors confirm that participants provided their written informed consent to participate in this study.
The study was supported by Indian Council of Medical Research (Letter No: 2018-3430/CMB-BMS), dated: 12.07.2018 by awarding Senior Research Fellowship to Shiela Chetri. The study design and protocol was approved by the funding agency. However, the funding body has no role in analysis and interpretation of data and in writing the manuscript.
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