Skip to main content
Journal of Biomedical Physics & Engineering logoLink to Journal of Biomedical Physics & Engineering
. 2019 Dec 1;9(6):637–646. doi: 10.31661/jbpe.v0i0.1107

Antibacterial Susceptibility Pattern of the Pseudomonas aeruginosa and Staphylococcus aureus after Exposure to Electromagnetic Waves Emitted from Mobile Phone Simulator

M M Movahedi 1,2, F Nouri 3, A Tavakoli Golpaygani 4, L Ataee 5, S Amani 5, M Taheri 6*
PMCID: PMC6943849  PMID: 32039094

Abstract

Background:

The increasing use of telecommunication devices such as Wi-Fi modems and mobile phones in the recent years can change the cellular structure of microorganisms so the generation of electromagnetic waves has led to concern in the community whenever be exposed to these fields and may have harmful effects on human health.

Material and Methods:

In this experimental study, standard strains of bacteria were prepared on Mueller-Hinton agar for bacterial growth to obtain 0.5 McFarland turbidity (1.5 × 108 CFU) of bacteria. Antibiotic susceptibility test using the Kirby-Bauer disk diffusion method was done. For Staphylococcus aureus and Pseudomonas aeruginosa, antibiotics susceptibility test was conducted. The test group was exposed to electromagnetic waves emitted by mobile phone simulator with a frequency of 900 MHz and the control group were not exposed.

Results:

The results revealed that increasing duration of exposure to electromagnetic waves emitted by the mobile simulators with a frequency of 900 MHz especially after 24 h of exposure, can increase bacterial resistance in S. aureus, and P. aeruginosa.

Conclusion:

Several factors can cause bacterial resistance against antibiotics. One of these factors is the electromagnetic waves emitted from mobile simulator with a frequency of 900 MHz, which can increase the permeability of the cell wall of bacteria.

Keywords: Microbial Sensitivity Tests , Electromagnetic waves , Mobile simulator , Pseudomonas aeruginosa, Staphylococcus aureus

Introduction

Antibiotic resistance is considered to be a major problem in the treatment and control of the infection. In recent years, bacterial resistance has become widespread to common antibiotics worldwide, so that the use of antimicrobials with this resistance pattern has been considered as a major problem in the medical community. In addition, since the detection of this resistance pattern due to their rapid spreads, an abundance of the antibiotic resistance across the universe has been observed. This can often occur due to the unnecessary consumption of antibiotics. On the other hand, patients’ specific conditions, long-term hospitalization, immunodeficiency and extensive use of immunosuppressive drugs and aggressive therapies (such as a catheter, intravascular shunt, and endotracheal tube), and other factors increase the drug resistance in different parts of the hospitals [ 1 ]. Therefore, the optimal applying and appropriate therapeutic strategies in order to control the infection and reducing the prevalence of antibiotic-resistant organisms is necessary [ 2 ]. P. aeruginosa is a hospital pathogen that causes infectious wounds and burns, and opportunistic diseases such as meningitis, urinary tract infection [ 3 ], respiratory system involvement [ 4 ], otitis media in swimmers [ 5 ], eye infections , and sepsis in infants or people with disabilities [ 6 ], especially in people with immune system deficiencies [ 7 ]. Also, S. aureus is a major pathogen, which is found everywhere, especially in infant ward, ICUs, surgery rooms and chemotherapy departments [ 8 , 9 ], and will lead to various types of infections such as food poisoning or life-threatening infections [ 10 ] caused by direct infection of the wound, such as Staphylococcus wound infection [ 11 ] after surgery or infection following trauma [ 10 , 12 ].

On the other hand, in recent years, the use of electromagnetic sources and telecommunication devices such as mobile phones have increased, and concerns have been raised for people in the community who are exposed to these fields, whose effects on the human health are under investigation [ 13 - 15 ]. Various classifications regarding the types of effects of waves on the human body have been made. In one classification, the effects of waves are divided into two categories. The first group has a reversible effect, such as the heat that increases its temperature, but after cooling, the nature of it remains preserved [ 16 ]. The second group, the irreversible effect, such as heat on the egg, increases the temperature and changes its nature, and does not return to the first state after cooling down [ 17 ].

In another classification, these damages are divided into thermal and non-thermal [ 18 ]. thermal damage means raising the temperature of cells and tissues without triggering temperature-sensitive receptors on the skin surface. Due to increased temperature in the tissues, chemical changes occur in the cells, which may lead to various disorders and illnesses. For example, due to increased body temperature, changes in enzymatic processes and cytokine levels [ 19 ], disturbances in calcium metabolism, and changes in growth and cell proliferation will occur [ 18 ]. Until recently, only thermal damages were considered and unhealthy electromagnetic waves were unaware [ 20 ]. Unhealthy damage causes permanent changes in the structure of the cell. Because of unhealthy damage due to the heat and the intensity of the wave, these damages may also be caused by the weakest wave. Some of these damages including altering blood chemistry such as reducing red blood cells, affecting the reproductive system, causing cancer, nervous disorders, increased irritability, headache, dizziness, nausea, eye irritation, and feeling of a foreign body in the eye. Mobile waves, with similar effects on the body, can cause discomfort and diseases such as cataracts [ 21 ]. The third-generation 3G (a new version of mobile phone technology) is an important wireless communication device that meets the needs of modern societies and is rapidly increasing worldwide. 3G mobile phones run on radiofrequency of 900-1800 MHz [ 22 , 23 ].

Nowadays, exposure to electromagnetic waves is unavoidable; as a result, many home appliances such as a hairdryer and washing machine produce harmful electromagnetic waves whose intensity can be as strong as waves of the electromagnetic emissions released below the high-pressure electric shock welder [ 24 ]. According to the reports, every healthy person is exposed to 361 million roentgen radiation [ 25 ]. Therefore, we should be aware of the safety and protection issues against the undesirable effects of electromagnetic waves [ 26 ]. In order to obtain a more accurate understanding of the effects of electromagnetic waves, the present study examined the effect of short-term exposure to electromagnetic waves emitted from mobile phone simulator with a frequency of 900 MHz as a mechanism of stress, on the sensitivity of pathogenic microorganisms’ P. aeruginosa and S. aureus against multiple antibiotics.

Material and Methods

Materials

Materials used in this experimental study, include Muller Hinton Agar and nutrient broth culture media, P. aeroginosa (ATCC No. 27853), S. aureus bacteria (ATCC No. 25923), antimicrobial discs (ROSCO, Denmark) (Table 1). The equipment used in this research include Digital balance A & D Model 120, (Japan), 37 ºC incubator (Behdad, Iran), UV/Vis Spectrophotometer 2100 (UNICO, America), RF Simulator (simulated mobile source with wave production of 900 MHz).

Table1.

Antimicrobial agents used in the present study.

Antimicrobials Abbreviation Potency (µg)
Piperacillin PIPRA 100
Cefotaxime CTX 30
Ceftriaxone CTR 30
Amikacin AMI 40
Imipenem IMI 10
Aztreonam AZT 30
Trimethoprim-Sulfamethoxazole SXT 25
Tetracycline TET 10
Vancomycin VANCO 5
Ciprofloxacin CIPR 5
Levofloxacin LEVO 5

Preparation of culture media

At the first step, a specific amount of each medium powder was dissolved in distilled water according to Manufacturer's instructions. After that, sterile Muller Hinton Agar media was dispersed in the microbiological plates.

Bacterial culture and antimicrobial susceptibility test

P. aeruginosa and S. aureus bacteria inoculated in the nutrient broth medium separately and incubated at 37 ºC. Bacterial density was measured every 20 min using UV/Vis spectrophotometer at an optical density of 625 nm. When the bacterial concentration reached up to standard 0.5 McFarland, the fresh culture of each suspension was taken on, by the Muller Hinton Agar plates using sterile swabs. In order to examine the antibacterial susceptibility of the used microorganism, the antimicrobial discs were put on the Muller Hinton agar plates containing bacteria. Then these plates were classified as control (unexposed) and test or exposed group which were exposed to 900 MHz radiofrequency radiation emitted by mobile phone simulator for 2, 4, 6, 8, 10 and 24 h and incubated for 18 h at 37 ºC. Finally, the average inhibition zone of each antimicrobial disc was recorded and compared with the control group.

Statistical Analysis

Each experiment was carried out in triplicate to minimize the variations. Data reported as mean ± SD and data comparison was done using non-parametric Mann-Whitney test.

Results

The results of electromagnetic radiation from mobile simulator on P. aeruginosa

Inhibition zone diameter of P. aeruginosa bacteria after 2, 4, 6, 8, 10 and 24 h exposure to 900 MHz for each antibiotic was examined. As shown in Figure 1, for CTX after 2 and 4 h, for CTX and LEVO after 6 h, for CIPR, LEVO and IMI after 8 h, for CIPR and IMI after 10 h and finally for AMI, CIPR, CTX, PIPRA and LEVO after 24 h (Figure 2) bacterial exposure to 900 MHz radiofrequency radiation, antimicrobial susceptibility against P. aeruginosa decreased, hence the antibacterial resistance enhanced. In all measurements, statistical analysis revealed that all aforementioned changes were significant (p-value ≤ 0.05).

Figure1.

Figure1

Mean inhibition zone diameter in Pseudomonas aeruginosa against various antibiotics during 24 hours.

Figure2.

Figure2

Mean inhibition zone diameter in Pseudomonas aeruginosa against various antibiotics in 24 hr exposure.

The results of electromagnetic radiation from mobile simulator on S. aureus

Inhibition zone diameter in S. aureus bacteria after 2, 4, 6, 8, 10 and 24 h exposure to 900 MHz emitted from a mobile simulator for each antibiotic was examined. After 2 h for CTR and VANCO, after 4 and 6 h for CTR, AMI, and TET, after 8 h for CTR, LEVO, AMI, TET, SXT and AMP, and after 10 h for CTR, LEVO, AMI, TET, SXT and after 24 h exposure for LEVO, AMI, TET, SXT, AMP, and PIPRA were decreased in comparison with the non-exposed group. All of these differences were statistically significant (p<0.05). The results of the mean inhibition zone measurements in S. aureus were plotted in Figure 3. According to this chart, S. aureus bacteria had different changes in the response to antimicrobial discs at different times.

Figure3.

Figure3

Mean inhibition zone diameter in Staphylococcus aureus against various antibiotics during 24 hours.

The effect of mobile simulator radiation with a frequency of 900 MHz on S. aureus bacteria, revealed that after 8 h exposure bacteria tend to be resistant against used antimicrobial agents. This change is more remarkable in amikacin and tetracycline, although all agents in the bacteria encountered a mobile simulator after 8 h exhibit resistance (Figure 4).

Figure4.

Figure4

Mean inhibition zone diameter in Staphylococcus aureus against various antibiotics in 8 hr exposure.

In addition, the effect of the mobile simulator on the S. aureus bacteria was the most resistant to the group of sham after 24 h of radiation in the antibiotic of levofloxacin and increased sensitivity in the antibiotics of piperacillin and ampicillin. However, significant changes were observed in all antibiotics (Figure 5).

Figure5.

Figure5

Mean inhibition zone diameter in Staphylococcus aureus against various antibiotics in 24 hr exposure.

Discussion

The purpose of this study was to investigate the effect of short-term exposure to radiofrequency radiation from mobile phone simulator on the susceptibility of pathogenic microorganisms P. aeruginosa and S. aureus against multiple antibiotics. The results of this study showed that exposure to 900 MHz emitted from the mobile simulator for bacterial strains of S. aureus and P. aeruginosa during 24 h caused significant changes in structural properties and resistance to the antibiotics studied. So that P. aeruginosa bacteria were resistant to all antibiotics after 24 h of irradiation compared to the non-exposed (control) group, and S. aureus bacteria were resistant to some antibiotics such as LEVO, TET, and SXT, after 24 h of radiation compared with the control group and to the antibiotics of PIPRA, AMPI, and CTR were susceptible.

In a study, Mortazavi et al. showed antimicrobial susceptibility of Klebsiella spp., S. aureus and streptococci (group A), were investigated bacteria after exposure to 7 - 13.5 MHz diagnostic ultrasound probes for 5 minutes. For S. aureus bacteria, vancomycin, erythomycin and amoxicillin antibiotics and for streptococci and Klebsiella spp. nitrofurantoin, nalidixic acid, and gentamicin antibiotics were used. The results showed that S. aureus was resistant to erythomycin and sensitive to vancomycin [ 27 ]. In this study, ultrasound waves altered the antimicrobial susceptibility in staphylococcus bacteria that is inconsistent with the present study findings.

In 2017, Taheri et al. reported the Escherichia coli and Listeria monocytogenes after 3, 6, 9, 18 and 24 h of radiation emitted by Wi-Fi modems with the frequency of 2.4 GHz and mobile simulator with a frequency of 900 MHz showed different responses. In this study, the antibiotics of piperacillin, levofloxacin, aztreonam, ciprofloxacin, and cefotaxime were used. After 9 h exposure to Wi-Fi frequencies, the bacteria were resistant to ciprofloxacin antibiotic and were susceptible to ceftriaxone, cefotaxime and levofloxacin antibiotics [ 28 ]. However, in our study S. aureus bacteria were resistant to the antibiotics of levofloxacin and TET after 24 h of radiation with 900 MHz radiation made by the mobile simulator. This difference in response to antibiotic sensitivity can result in the difference in the radiation frequency, the duration of radiation, the type of antibiotic and the structure of the bacteria. Adebayo et al. (2014) investigated the effect of radiofrequency radiations emitted from telecommunication base stations on the resistance of Bacillus bacteria, which increased the resistance of this bacterium [ 29 ]. This study, with our results, increased the resistance of both S. aureus and P. aeruginosa bacteria after 24 h exposure to 900 MHz emitted waves from the mobile simulator.

Several studies have highlighted the causes of antimicrobial susceptibility changes of bacteria under the influence of electromagnetic fields [ 29 - 31 ]. A study showed that antimicrobial susceptibility depends on the physical properties of the magnetic field, such as frequency, duration of radiation, and the type of bacteria [ 32 ]. Another factor that can affect the antimicrobial susceptibility is the structure of the bacterial cell wall and the nature of the peptidoglycan properties in the cell wall of the gram-positive and negative bacteria [ 33 ].

Torgomyan et al. showed that changes in proteins in the bacterial cell wall could be the most important membrane mechanism for low-intensity electromagnetic field radiation [ 34 ]. Overall, studies in this area have described the following effective mechanisms: first, due to the importance of the membrane potential of the bacterial cell wall, these waves can have an effect on the antibiotic susceptibility [ 32 ]. Secondly, increased antibiotic susceptibility may be due to the interaction of electromagnetic fields on the water molecules in the cell. Other suggested mechanisms include increase in the permeability of the bacteria and making the ion channels to be kept open in the bacterial wall, efflux pumps and ion channels in the cell wall, play an important role in the absorption of antibiotics, and finally, another factor that can affect bacterial sensitivity in magnetic conditions is the antibiotic structure [ 28 , 35 ]. Hydrophilicity or hydrophobicity of the antibiotic, antibiotic activity and antibiotic molecule size are other factors [ 36 ].

Conclusion

In the present study, it has been shown that the waves emitted from the mobile simulator with a frequency of 900 MHz can change the antimicrobial susceptibility of S. aureus and P. aeruginosa as a physical method. According to the obtained results, it can be concluded that the bacterial species used in this study were influenced by the electromagnetic field and responded differently.

Acknowledgement

We would like to acknowledge Shiraz University of Medical Sciences, for the generous funding of this work through grant No 94-01-75-10643.

Conflict of Interest: None

References

  • 1.Andersson D I. Persistence of antibiotic resistant bacteria. Curr Opin Microbiol. 2003;6:452–6. doi: 10.1016/j.mib.2003.09.001. [DOI] [PubMed] [Google Scholar]
  • 2.Meyer E, Jonas D, Schwab F, Rueden H, Gastmeier P, Daschner F D. Design of a surveillance system of antibiotic use and bacterial resistance in German intensive care units (SARI) Infection. 2003;31:208–15. doi: 10.1007/s15010-003-3201-7. [DOI] [PubMed] [Google Scholar]
  • 3.Huang C R, Lu C H, Chuang Y C, Tsai N W, Chang C C, Chen S F, et al. Adult Pseudomonas aeruginosa meningitis: high incidence of underlying medical and/or postneurosurgical conditions and high mortality rate. Jpn J Infect Dis. 2007;60:397–9. [PubMed] [Google Scholar]
  • 4.Jensen T, Pedersen S S, Garne S, Heilmann C, Hoiby N, Koch C. Colistin inhalation therapy in cystic fibrosis patients with chronic Pseudomonas aeruginosa lung infection. J Antimicrob Chemother. 1987;19:831–8. doi: 10.1093/jac/19.6.831. [DOI] [PubMed] [Google Scholar]
  • 5.Mena K D, Gerba C P. Risk assessment of Pseudomonas aeruginosa in water. Rev Environ Contam Toxicol. 2009;201:71–115. doi: 10.1007/978-1-4419-0032-6_3. [DOI] [PubMed] [Google Scholar]
  • 6.Bodey G P, Bolivar R, Fainstein V, Jadeja L. Infections caused by Pseudomonas aeruginosa. Rev Infect Dis. 1983;5:279–313. doi: 10.1093/clinids/5.2.279. [DOI] [PubMed] [Google Scholar]
  • 7.Lang A B, Furer E, Senyk G, Larrick J W, Cryz Jr S J. Systematic generation of antigen specific human monoclonal antibodies with therapeutical activities using active immunization. Hum Antibodies Hybridomas. 1990;1:96–103. doi: 10.3233/hab-1990-1204. [DOI] [PubMed] [Google Scholar]
  • 8.Merrer J, Santoli F, Appere De Vecchi C, Tran B, De Jonghe B, Outin H. “Colonization pressure” and risk of acquisition of methicillin-resistant Staphylococcus aureus in a medical intensive care unit. Infect Control Hosp Epidemiol. 2000;21:718–23. doi: 10.1086/501721. [DOI] [PubMed] [Google Scholar]
  • 9.Haddadin A S, Fappiano S A, Lipsett P A. Methicillin resistant Staphylococcus aureus (MRSA) in the intensive care unit. Postgrad Med J. 2002;78:385–92. doi: 10.1136/pmj.78.921.385. [ PMC Free Article ] [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Le Loir Y, Baron F, Gautier M. Staphylococcus aureus and food poisoning. Genet Mol Res. 2003;2:63–76. [PubMed] [Google Scholar]
  • 11.Roy S, Santra S, Das A, Dixith S, Sinha M, Ghatak S, et al. Staphylococcus aureus Biofilm Infection Compromises Wound Healing by Causing Deficiencies in Granulation Tissue Collagen. Ann Surg. 2019 doi: 10.1097/SLA.0000000000003053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Centers for Disease Control and Prevention (CDC) Staphylococcus aureus resistant to vancomycin--United States, 2002. MMWR Morb Mortal Wkly Rep. 2002;51:565–7. [PubMed] [Google Scholar]
  • 13.Tang J, Zhang Y, Yang L, Chen Q, Tan L, Zuo S, et al. Exposure to 900 MHz electromagnetic fields activates the mkp-1/ERK pathway and causes blood-brain barrier damage and cognitive impairment in rats. Brain Res. 2015;1601:92–101. doi: 10.1016/j.brainres.2015.01.019. [DOI] [PubMed] [Google Scholar]
  • 14.Urbinello D, Joseph W, Verloock L, Martens L, Roosli M. Temporal trends of radio-frequency electromagnetic field (RF-EMF) exposure in everyday environments across European cities. Environ Res. 2014;134:134–42. doi: 10.1016/j.envres.2014.07.003. [DOI] [PubMed] [Google Scholar]
  • 15.Urbinello D, Joseph W, Huss A, Verloock L, Beekhuizen J, Vermeulen R, et al. Radio-frequency electromagnetic field (RF-EMF) exposure levels in different European outdoor urban environments in comparison with regulatory limits. Environ Int. 2014;68:49–54. doi: 10.1016/j.envint.2014.03.007. [DOI] [PubMed] [Google Scholar]
  • 16.Repacholi M H. Low-level exposure to radiofrequency electromagnetic fields: health effects and research needs. Bioelectromagnetics. 1998;19:1–19. doi: 10.1002/(sici)1521-186x(1998)19:1<1:aid-bem1>3.3.co;2-8. [DOI] [PubMed] [Google Scholar]
  • 17.Agarwal A, Desai N R, Makker K, Varghese A, Mouradi R, Sabanegh E, et al. Effects of radiofrequency electromagnetic waves (RF-EMW) from cellular phones on human ejaculated semen: an in vitro pilot study. Fertil Steril. 2009;92:1318–25. doi: 10.1016/j.fertnstert.2008.08.022. [DOI] [PubMed] [Google Scholar]
  • 18.McNamee J P, Chauhan V. Radiofrequency radiation and gene/protein expression: a review. Radiat Res. 2009;172:265–87. doi: 10.1667/RR1726.1. [DOI] [PubMed] [Google Scholar]
  • 19.Salehi I, Sani K G, Zamani A. Exposure of rats to extremely low-frequency electromagnetic fields (ELF-EMF) alters cytokines production. Electromagn Biol Med. 2013;32:1–8. doi: 10.3109/15368378.2012.692343. [DOI] [PubMed] [Google Scholar]
  • 20.Moreau E. Airflow control by non-thermal plasma actuators. Journal of physics D: applied physics. 2007;40:605. doi: 10.1088/0022-3727/40/3/s01. [DOI] [Google Scholar]
  • 21.Preece A. Effect of a 915-MHz simulated mobile phone signal on cognitive function in man. Int J Radiat Biol. 1999;75:447–56. doi: 10.1080/095530099140375. [DOI] [PubMed] [Google Scholar]
  • 22.Dogan M, Turtay M G, Oguzturk H, Samdanci E, Turkoz Y, Tasdemir S, et al. Effects of electromagnetic radiation produced by 3G mobile phones on rat brains: magnetic resonance spectroscopy, biochemical, and histopathological evaluation. Hum Exp Toxicol. 2012;31:557–64. doi: 10.1177/0960327111412092. [DOI] [PubMed] [Google Scholar]
  • 23.Fu T C. A Dual Communication and Imaging Underwater Acoustic System. University of California: Santa Barbara; 2011. [Google Scholar]
  • 24.Lerner E J. Biological effect of electromagnetic fields: New findings linking changes in organisms to irradiation by weak fields encourage researchers to posit theories, although research is incomplete. IEEE spectrum. 1984;21:57–69. doi: 10.1109/mspec.1984.6370269. [DOI] [Google Scholar]
  • 25.Krewski D, Glickman B W, Habash R W, Habbick B, Lotz W G, Mandeville R, et al. Recent advances in research on radiofrequency fields and health: 2001-2003. J Toxicol Environ Health B Crit Rev. 2007;10:287–318. doi: 10.1080/15287390600974973. [DOI] [PubMed] [Google Scholar]
  • 26.Parajuli P, Panday J P, Koirala R P, Shah B R. Study of the Electromagnetic Field Radiated from the Cell Phone Towers Within Kathmandu Valley. International Journal of Applied Sciences and Biotechnology. 2015;3:179–87. doi: 10.3126/ijasbt.v3i2.12297. [DOI] [Google Scholar]
  • 27.Mortazavi S M J, Darvish L, Abounajmi M, Zarei S, Zare T, Taheri M, et al. Alteration of Bacterial Antibiotic Sensitivity After Short-Term Exposure to Diagnostic Ultrasound. Iran Red Crescent Med J. 2015;17:e26622. doi: 10.5812/ircmj.26622. [ PMC Free Article ] [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Taheri M, Mortazavi S M J, Moradi M, Mansouri S, Hatam G R, Nouri F. Evaluation of the Effect of Radiofrequency Radiation Emitted From Wi-Fi Router and Mobile Phone Simulator on the Antibacterial Susceptibility of Pathogenic Bacteria Listeria monocytogenes and Escherichia coli. Dose Response. 2017;15:1–8. doi: 10.1177/1559325816688527. [ PMC Free Article ] [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Adebayo E, Adeeyo A, Ayandele A, Omomowo I. Effect of radiofrequency radiation from telecommunication base stations on microbial diversity and antibiotic resistance. Journal of Applied Sciences and Environmental Management. 2014;18:669–74. [Google Scholar]
  • 30.Crabtree D P E, Herrera B J, Kang S. The response of human bacteria to static magnetic field and radiofrequency electromagnetic field. J Microbiol. 2017;55:809–15. doi: 10.1007/s12275-017-7208-7. [DOI] [PubMed] [Google Scholar]
  • 31.Salmen S H, Alharbi S A, Faden A A, Wainwright M. Evaluation of effect of high frequency electromagnetic field on growth and antibiotic sensitivity of bacteria. Saudi J Biol Sci. 2018;25:105–110. doi: 10.1016/j.sjbs.2017.07.006. [ PMC Free Article ] [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Nguyen T H, Shamis Y, Croft R J, Wood A, McIntosh R L, Crawford R J, et al. 18 GHz electromagnetic field induces permeability of Gram-positive cocci. Sci Rep. 2015;5:10980. doi: 10.1038/srep10980. [ PMC Free Article ] [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Belyaev I. Toxicity and SOS-response to ELF magnetic fields and nalidixic acid in E. coli cells. Mutat Res 2011;722:56–61. doi: 10.1016/j.mrgentox.2011.03.012. [DOI] [PubMed] [Google Scholar]
  • 34.Torgomyan H, Tadevosyan H, Trchounian A. Extremely high frequency electromagnetic irradiation in combination with antibiotics enhances antibacterial effects on Escherichia coli. Curr Microbiol. 2011;62:962–7. doi: 10.1007/s00284-010-9811-2. [DOI] [PubMed] [Google Scholar]
  • 35.Taheri M, Mortazavi S, Moradi M, Mansouri S, Nouri F, Mortazavi S, et al. Klebsiella pneumonia, a microorganism that approves the non-linear responses to antibiotics and window theory after exposure to Wi-Fi 2.4 GHz electromagnetic radiofrequency radiation. Journal of biomedical physics &amp engineering. 2015;5:115. [PMC free article] [PubMed] [Google Scholar]
  • 36.Taheri M, Moradi M, Mortazavi S, Mansouri S, Hatam G, Nouri F. Evaluation of the 900 MHz Radiofrequency Radiation Effects on the Antimicrobial Susceptibility and Growth Rate of Klebsiella pneumoniae. Shiraz E-Medical Journal. 2017;18(3): e44946. doi: 10.17795/semj44946. [DOI] [Google Scholar]

Articles from Journal of Biomedical Physics & Engineering are provided here courtesy of Shiraz University of Medical Sciences

RESOURCES