Skip to main content
Download PDF

Antibiotic delivery evaluation against Mycobacterium fortuitum using nanofluids containing carbon nanotubes

BMC Microbiology volume 22, Article number: 96 (2022) Cite this article

Abstract

Background

Mycobacterium fortuitum (M. fortuitum) is a bacterium, which can cause infections in many anatomical regions of the body, including the skin, lymph nodes, and joints. This bacterium, which belongs to a group of bacteria known as nontuberculous mycobacteria, is regarded as an important nosocomial pathogen worldwide owing to its increasing antibiotic resistance. Recently, the antimicrobial effects of carbon nanotubes have been reported in numerous studies. These nanotubes can be very useful in drug delivery; besides, they exhibit unique properties against multidrug-resistant bacterial infections. This study aimed to investigate the antimicrobial effects of carboxyl-functionalized multi-walled carbon nanotubes (MWCNT-COOH) to reduce antibiotic resistance.

Methods

In this study, antibacterial effects of nanofluids containing functionalized MWCNTs at initial concentration of 2 mg/mL and serial dilutions of 54, 28.5, 14.25, 7.12, 3.5 µg/mL, antibiotics alone and combination of nanofluids with antibiotics were investigated.

Standard and resistant strains of M. fortuitum were obtained from the microbial bank of the Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran.

Results

It was observed that nanofluid containing MWCNT-COOH can exert antimicrobial effects on M. fortuitum and significantly reduce bacterial resistance to antibiotics including kanamycin and streptomycin. In the presence of antibiotics and nanofluids containing MWCNT-COOH at a dose of 28.5 µg/mL, no growth was observed.

Conclusion

One of the main antimicrobial mechanisms of MWCNT-COOH is penetration into the bacterial cell wall. In this study, by using the nanofluid containing MWCNT-COOH with increased stability, the antibiotic resistance of M. fortuitum was significantly reduced at lower dilutions compared to the antibiotic alone.

Peer Review reports

Introduction

Non-tuberculous mycobacterial (NTM) is a challenging infection that has spread for a number of reasons, including antibiotic resistance. They are organisms found everywhere in the environment around the world and are resistant to extreme heat and pH and many disinfectants and antibiotics due to their thick fat cell wall [1]. Mycobacterium fortuitum was first described in 1938 by Costa Cruz who isolated it from the pus of an abscess in a woman who had received injections of a vitamin preparation This pathogen is widely distributed in soil and water worldwide [2]. Generally, the NTM can be classified depending on their growth rate. Accordingly, M. fortuitum is known as a rapidly growing mycobacterium (RGM) [3].

M. fortuitum infection is recognized as a nosocomial infection, which can affect many areas of the body, including the skin [4], lymph nodes [5], lungs [6], and bones (osteomyelitis), especially after a catheterization surgery [7, 8]. The M. fortuitum group consists of about 15 fast-growing NTM species. These globally distributed microorganisms can cause disease in humans and animals [9]. The presence of M. fortuitum in the respiratory tract has been reported mainly as a simple or transient infection. However, M. fortuitum-induced lung infection remains rare and generally occurs in patients with gastroesophageal reflux disease or in elderly patients with chronic cough [10, 11]. The antibacterial resistance of nosocomial infections has become a global health concern [12]. Due to differences in susceptibility between Mycobacterium species with rapid growth and even within species, susceptibility testing should be performed on all clinically important isolates as well as isolates that have improved after treatment failure or recurrence. Mycobacterium fast-growing antimicrobial susceptibility testing differs from other NTMs. Most drugs are different, although the methods are similar to those used to test for other bacteria [13, 14]. Infections caused by M. fortuitum isolates also require long-term antibiotic treatment due to their high resistance to a variety of antibiotics and disinfectants [15]. Previous studies have shown that M. fortuitum strains are susceptible to fluoroquinolones and amikacins, while they are resistant to macrolides; therefore, understanding the mechanisms of drug resistance and effective treatments for M. fortuitum infections are essential [16, 17]. Currently, the use of the combination of antibiotics has been able to control infections caused by M. fortuitum to some extent [18].

Over the past few years, there has been a growing interest in using nanoparticles in various biomedical applications such as targeted drug delivery, bioimaging, and biosensors [19]. Various nanoparticles such as carbon nanotubes (CNTs) have been used for antibiotic resistance. CNTs discovered by Iijima in 1991 have enhanced technological advances in nanotechnology [20]. Due to their high surface-to-volume ratio and unique physical and chemical properties, particular attention has been paid to the antibacterial properties of nanoparticles [21]. CNTs are one of the most important types of nanoparticles.

Recently, cancer diagnosis and treatment, as well as antibiotic resistance, have become important research topics [22, 23]. The CNTs can exist into two categories depending upon the number of layers: single-walled carbon nanotubes (SWCNTs) and multi-walled carbon nanotubes (MWCNTs). The antibiotic properties of MWCNTs have been reported in previous studies [24, 25]. It seems that the functionalization of MWCNTs with a carboxyl agent (MWCNT-COOH) can improve their antimicrobial properties [26]. The present study aimed to investigate the antimicrobial effects of nanofluid containing MWCNTs-COOH and to examine their simultaneous use with antibiotics, including kanamycin and streptomycin, against M. fortuitum to reduce its antibiotic resistance.

Materials and methods

Preparation of multi-wall carbon nanotube (MWCNTs) based aqueous nanofluid

The MWCNTs (US Research Nanomaterials, Inc., USA) were used in the present study. For this purpose, 0.2 g of MWCNT-COOH powder, 6 mL of 96% ethanol, and 0.06 g of Arabic gum were added to 100 mL of deionized water, and the mixture was stirred for 20 min [27]. Next, the solution was placed in an ice bucket. The suspension was placed in an ice bucket to the ultrasonic device (Ultrasonic Homogenizer 400 w, 200 kHz), with the power of 200 W for 20 min.

Bacterial strains and culture conditions

Two M. fortuitum strains (resistant and ATCC 6841) were provided by the microbial bank of the Department of Mycobacteriology and Pulmonary Research of Pasteur Institute of Iran. Resistant strains were isolated from clinical specimens. The ATCC and resistant strains were cultured in a Lowenstein-Jensen (LJ) medium and incubated at 37 °C [28]; bacterial growth was monitored at 4 weeks. Antibiotic susceptibility of bacterial strains was determined by antibiogram method according to CLSI guidelines. Ofloxacin (35 µg/mL), streptomycin (32 µg/mL), kanamycin 30 (µg/mL), ethambutol (256 µg/mL), rifampicin (32 µg/mL), and isoniazid (16 µg/mL) were used in this study to treat pulmonary diseases and control M. fortuitum [29]. At this stage, a 0.5-McFarland microbial suspension was prepared from bacterial strains, and then, antibiotics were added to the LJ medium. After a week, the final results were observed.

Microbial testing

First, a 0.5-McFarland microbial suspension was purified from bacteria, and then, different dilutions (54, 28.5, 14.25, 7.12, 3.5 µg/mL) of the nanofluid at a concentration of 2 mg/mL were prepared and added to each strain; the tests were performed twice for each sample. The LJ medium was incubated at 37 °C during the first week of bacterial growth. Besides, the simultaneous effects of the nanofluid and antibiotics on the ATCC and resistant strains were examined. Different concentrations of the nanofluid were used in this study, with an initial concentration of 2 mg/mL. The LJ culture media, containing streptomycin and kanamycin, were prepared for both ATCC strains and pathogens.

Molecular detection

The M. fortuitum RNAs were extracted using Triazole (GeneAll RiboEx) and then, stored at -70 °C until further cDNA synthesis. Following RNA extraction, cDNA synthesis was carried out using a Takara cDNA synthesis kit (Takara Bio Inc., Japan). Each cDNA sample was amplified using specific primers, Gene expression level was comparable to 16S rRNA of housekeeping [30] (Table 1).

Table 1 Primer sequences used in the study
Full size table

In this study, expression level of aph(3'')-Ic and Blaf genes involved in a aminoglycoside O-phosphotransferase and beta-lactamase pathways were examined. Moreover, real-time polymerase chain reaction (PCR) was performed using a QIAGEN apparatus under the following conditions in 40 cycles: at 95 °C for five seconds; at 60 °C for 20 s; and at 72 °C for 30 s. Amplification was also performed using an SYBR Premix Ex Taq™ II PCR Master Mix (Takara Bio Inc., Japan). The gene expression data were analyzed using the 2−ΔCT and 2−ΔΔCT methods after normalization.

Results

Microbial testing results

The antibiograms showed that the ATCC strain of M. fortuitum was susceptible to ofloxacin and streptomycin (Fig. 1), while the resistant strain was susceptible to ofloxacin and kanamycin (Fig. 2).

Fig. 1
figure 1

Results of antibiogram testing in ATCC strain. ATCC strains show sensitivity to antibiotics ofloxacin and streptomycin

Full size image
Fig. 2
figure 2

Results of antibiogram testing in pathogen strain. Resistance strains show sensitivity to antibiotics ofloxacin and kanamycin

Full size image

The bacterial culture results were studied, and the antibacterial efficacy of the nanofluid was examined after two weeks. The examination of the effects of the nanofluid on the ATCC strain showed no bacterial growth at a dilution of (28.5 µg/mL). In the resistant strain, no growth was observed at a dilution of (54 µg/mL). Moreover, analysis of the simultaneous effects of the nanofluid and antibiotics on bacteria showed no bacterial growth in the ATCC strain at a dilution of (14.25 µg/mL) with kanamycin, while in the resistant strain, no growth was observed at a dilution of (28.5 µg/mL) using streptomycin (Table 2), (Figures S1 and S2).

Table 2 Summary of the effects of drugs and carbon nanotubes in this study
Full size table

Results of statistical analysis

Statistical analysis of aph(3'')-Ic gene expression and blaF was performed using one-way ANOVA to compare the results of the group by GraphPad Prism 8 (San Diego, California, USA).A P value less than 0.05 was considered significant. The analysis of gene expression showed that the expression of aph(3'')-Ic and blaF genes decreased more significantly following exposure to a combination of the nanofluid and antibiotics, compared to the nanofluid or antibiotic alone; the expression levels of the genes were comparable to that of 16S rRNA housekeeping gene (Fig. 3).

Fig. 3
figure 3

A Bla gene expression level in ATCC strain. B Bla gene expression level in resistance strain. C Aph(3″) gene expression level in ATCC strain. D Aph(3″) gene expression level in resistance strain

Full size image

Conclusions and implications for future research

M. fortuitum is one of the most well-known NTMs that can cause various infections, including lung and wound infections [11]. Results of this study showed that nanofluids containing functionalized (carboxyl), carbon nanotubes have significant antibacterial effects and their effects were examined alone or in combination with common antibiotics, such as kanamycin and streptomycin. This nanofluid contained carbon nanotubes with superior characteristics, such as increased penetration into bacterial membranes, increased efficiency at lower concentrations compared to common therapeutic doses, and reduced bacterial resistance to common antibiotics.

In a study, the antibacterial performance of silver-functionalized and non-functionalized carbon nanotubes was compared. It was found that silver-functionalized carbon nanotubes exerted antibacterial effects on Escherichia coli [31]. Another study in 2020 evaluated the effects of isoniazid-functionalized MWCNTs on M. tuberculosis. Their results showed that isoniazid-functionalized MWCNTs exerted antimicrobial effects at lower concentrations compared to the usual doses of antibiotics [32]. In a recent study. The antimicrobial effects of nanofluid containing functional carbon nanotubes on Acinetobacter baumannii were studied. This study showed that nanofluids containing nanotubes with carbon results could have significant antibacterial effects on Acinetobacter baumannii [33]. In another study, the molecular effects of combination therapy with antibiotics and carbon nanotubes containing nanofluids on Klebsiella pneumoniae were performed. The results of this study showed that the combination of antibiotics with carbon nanotubes could significantly inhibit bacterial growth [34]. Using a variety of antibiotics to treat infections caused by Mycobacterium fortitum can have side effects. Nowadays, it is possible to reduce the side effects of antibiotics such as the metabolic side effects by using nano drug delivery systems.

The present study showed that the efficacy of nanofluids containing MWCNTs, functionalized with carboxylic acid, differed from that of nanofluids containing non-functionalized MWCNTs. This difference appears to have changed following bacterial exposure to the nanofluid, which might be related to decreased bacterial growth due to the binding of the nanofluid containing carbon nanotubes (functionalized with carboxylic acid) to the bacterial membrane, thereby eliminating the membrane integrity. On the other hand, based on molecular studies and analysis of bla and aph(3″)-IC gene expression, the number of bacteria significantly reduced in the presence of CNTs. However, further studies are needed to examine this method (i.e., the combination of carbon nanotubes with antibiotics in the form of nano-drugs) and obtain better results. Also, further cellular and molecular studies are recommended to identify the mechanisms of antibacterial effects.

Availability of data and materials

All data generated or analyzed during this study are included in this published article [and its supplementary information files].

References

  1. Cowman S, van Ingen J, Griffith DE, Loebinger MR. Non-tuberculous mycobacterial pulmonary disease. Eur Respir J. 2019;54(1).

  2. Jayasingam SD, Zin T, Ngeow YF. Antibiotic resistance in mycobacterium abscessus and mycobacterium fortuitum isolates from Malaysian patients. Intern J mycobacteriol. 2017;6(4):387.

    Article  CAS  Google Scholar 

  3. Porvaznik I, Solovic I, Mokry J. Non-tuberculous mycobacteria: classification, diagnostics, and therapy. Adv Exp Med Biol. 2017;944:19–25.

    Article  CAS  Google Scholar 

  4. Gonzalez-Diaz E, Morfin-Otero R, Perez-Gomez HR, Esparza-Ahumada S, Rodriguez-Noriega E. Rapidly growing mycobacterial infections of the skin and soft tissues caused by M. fortuitum and M. chelonae. Curr Trop Med Rep. 2018;5(3):162–9.

    Article  Google Scholar 

  5. Nguyen D-Q, Righini C, Darouassi Y, Schmerber S. Nasal infection due to mycobacterium fortuitum. Eur Ann Otorhinolaryngol Head Neck Dis. 2011;128(4):197–9.

    Article  Google Scholar 

  6. Prevots DR, Marras TK. Epidemiology of human pulmonary infection with nontuberculous mycobacteria: a review. Clin Chest Med. 2015;36(1):13–34.

    Article  Google Scholar 

  7. Smith BD, Liras IN, De Cicco IA, Aisenberg GM. Mycobacterium fortuitum infection of the scalp after a skin graft. BMJ Case Rep. 2016;2016:bcr2016216968.

    Article  Google Scholar 

  8. Aksu G, Trpan C, Çavusoglu C, Soydan S, Altare F, Casanova J-L, et al. Mycobacterium fortuitum-chelonae complex infection in a child with complete interleukin-12 receptor beta 1 deficiency. Pediatr Infect Dis J. 2001;20(5):551–3.

    Article  CAS  Google Scholar 

  9. Mugetti D, Tomasoni M, Pastorino P, Esposito G, Menconi V, Dondo A, et al. Gene sequencing and phylogenetic analysis: powerful tools for an improved diagnosis of fish mycobacteriosis caused by Mycobacterium fortuitum group members. Microorganisms. 2021;9(4):797.

    Article  CAS  Google Scholar 

  10. Gharbi R, Khanna V, Frigui W, Mhenni B, Brosch R, Mardassi H. Phenotypic and genomic hallmarks of a novel, potentially pathogenic rapidly growing Mycobacterium species related to the Mycobacterium fortuitum complex. Sci Rep. 2021;11(1):1–12.

    Article  Google Scholar 

  11. Cowman S, Burns K, Benson S, Wilson R, Loebinger MR. The antimicrobial susceptibility of non-tuberculous mycobacteria. J Infect. 2016;72(3):324–31.

  12. Bhagirath AY, Li Y, Patidar R, Yerex K, Ma X, Kumar A, et al. Two component regulatory systems and antibiotic resistance in gram-negative pathogens. Intern J Mol Sci. 2019;20(7):1781.

    Article  CAS  Google Scholar 

  13. Official T. Diagnosis and treatment of disease caused by nontuberculous mycobacteria. Am Rev Respir Dis. 1990;142:940–53.

    Article  Google Scholar 

  14. Griffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, Daley C, Gordin F, et al. An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases. Am J Respir Crit Care Med. 2007;175(4):367–416.

    Article  CAS  Google Scholar 

  15. Santos DRdS, Lourenço MCS, Coelho FS, Mello FCQ, Duarte RS. Resistance profile of strains of Mycobacterium fortuitum isolated from clinical specimens. J Bras Pneumol. 2016;42:299–301.

    Article  Google Scholar 

  16. Zheng HW, Pang Y, He GX, Song YY, Zhao YL. Antimicrobial susceptibility testing and molecular characterization of mycobacterium fortuitum isolates in China. Biomed Environ Sci. 2017;30(5):376–9.

    CAS  PubMed  Google Scholar 

  17. Huang C-W, Chen J-H, Hu S-T, Huang W-C, Lee Y-C, Huang C-C, et al. Synergistic activities of tigecycline with clarithromycin or amikacin against rapidly growing mycobacteria in Taiwan. Int J Antimicrob Agents. 2013;41(3):218–23.

    Article  CAS  Google Scholar 

  18. Saxena S, Spaink HP, Forn-Cuní G. Drug resistance in nontuberculous mycobacteria: mechanisms and models. Biology. 2021;10(2):96.

    Article  CAS  Google Scholar 

  19. McNamara K, Tofail SA. Nanoparticles in biomedical applications. Advances in Physics: X. 2017;2(1):54–88.

    CAS  Google Scholar 

  20. Iijima S. Helical microtubules of graphitic carbon. Nature. 1991;354(6348):56–8.

    Article  CAS  Google Scholar 

  21. Eleraky NE, Allam A, Hassan SB, Omar MMJP. Nanomedicine fight against antibacterial resistance: an overview of the recent pharmaceutical innovations. Pharmaceutics. 2020;12(2):142.

    Article  CAS  Google Scholar 

  22. Sheikhpour M, Golbabaie A, Kasaeian AJMS. Carbon nanotubes: a review of novel strategies for cancer diagnosis and treatment. Mater Sci Eng C Mater Biol Appl. 2017;76:1289–304.

    Article  CAS  Google Scholar 

  23. Mocan T, Matea CT, Pop T, Mosteanu O, Buzoianu AD, Suciu S, et al. Carbon nanotubes as anti-bacterial agents. Cell Mol Life Sci. 2017;74(19):3467–79.

    Article  CAS  Google Scholar 

  24. He H, Pham-Huy LA, Dramou P, Xiao D, Zuo P, Pham-Huy C. Carbon nanotubes: applications in pharmacy and medicine. Biomed Res Int. 2013;2013:578290.

    PubMed  PubMed Central  Google Scholar 

  25. Liu D, Luo J, Wang H, Ding L, Zeng X-AJJoN. Nanotechnology. synthesis of Dihydromyricetin Coated Multi-Walled Carbon Nanotubes (MWCNTs) and antibacterial activities. J Nanosci Nanotechnol. 2020;20(10):6148–54.

    Article  CAS  Google Scholar 

  26. Silva M, Felgueiras H, de Amorim MJC. Carbon based membranes with modified properties: thermal, morphological, mechanical and antimicrobial. Cellulose. 2020;27(3):1497–516.

    Article  CAS  Google Scholar 

  27. Stefanovic J, Jakovljevic D, Gojgic‐Cvijovic G, Lazic M, Vrvic MJJoaps. Synthesis, characterization, and antifungal activity of nystatin-gum arabic conjugates. J Appl Polym Sci. 2013;127(6):4736–43.

    Article  CAS  Google Scholar 

  28. Shah SR, Shenai S, Desai DC, Joshi A, Abraham P, Rodrigues C. Comparison of Mycobacterium tuberculosis culture using liquid culture medium and Lowenstein Jensen medium in abdominal tuberculosis. Indian J Gastroenterol. 2010;29(6):237–9.

    Article  Google Scholar 

  29. Shen Y, Wang X, Jin J, Wu J, Zhang X, Chen J, et al. In vitro susceptibility of Mycobacterium abscessus and Mycobacterium fortuitum isolates to 30 antibiotics. BioMed Res Intern. 2018;2018:4902941.

    Google Scholar 

  30. Nasr Esfahani B, Rezaei Yazdi H, Moghim S, Ghasemian Safaei H, Zarkesh EH. Rapid and accurate identification of Mycobacterium tuberculosis complex and common non-tuberculous mycobacteria by multiplex real-time PCR targeting different housekeeping genes. Curr Microbiol. 2012;65(5):493–9.

    Article  CAS  Google Scholar 

  31. Prodana M, Ionita D, Ungureanu C, Bojin D, Demetrescu IJM. Enhancing antibacterial effect of multiwalled carbon nanotubes using silver nanoparticles. Microscopy. 2011;6(2):549–56.

    Google Scholar 

  32. Zomorodbakhsh S, Abbasian Y, Naghinejad M, Sheikhpour MJIJoN. The Effects Study of Isoniazid Conjugated Multi-Wall Carbon Nanotubes Nanofluid on Mycobacterium tuberculosis. Int J Nanomedicine. 2020;15:5901–9.

    Article  CAS  Google Scholar 

  33. Yazdani MR, Sheikhpour M, Siadat SD, Safarian P. Overcoming the antibiotic resistance of Acinetobacter baumannii by using nanofluid containing functionalized carbon nanotubes. Nanomedicine Research Journal. 2021;6(2):179–87.

    CAS  Google Scholar 

  34. Mehdizadeh M, Sheikhpour M, Salahshourifar I, Siadat SD, Saffarian P. An In-vitro study of molecular effects of a combination treat-ment with antibiotics and nanofluid containing carbon nano-tubes on Klebsiella pneumoniae. Iran J Public Health. 2021;50(11):2292–301.

    PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We thank our colleagues from the Department of Mycobacteriology and Pulmonary Research, Microbiology Research Center, Pasteur Institute of Iran.

Methods and instructions

All methods and instructions in the article "Antibiotic delivery evaluation against Mycobacterium fortuitum using nanofluids containing carbon nanotubes" according to previous articles and also microbial methods were performed according to the CLSI guidelines and according to the instructions of the Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran.

Funding

The authors have no funding source.

Author information

Authors and Affiliations

  1. Department of Biology, Faculty of Life Sciences, Danesh Alborz University, Abyek, Iran

    Hamid Naderi Pargami

  2. Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran

    Hamid Naderi Pargami, Seyed Davar Siadat, Vahid Amiri & Mojgan Sheikhpour

  3. Microbiology Research Center, Pasteur Institute of Iran, Tehran, Iran

    Seyed Davar Siadat & Mojgan Sheikhpour

Authors
  1. Hamid Naderi Pargami
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Seyed Davar Siadat
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Vahid Amiri
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Mojgan Sheikhpour
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

H.N. performed the experiments; V.A. analyzed data, interpreted data, SD.S, read and approved the final manuscript, MSH, designed and supervised the study, interpreted data, read and approved the manuscript. All authors reviewed the manuscript. The author(s) read and approved the final manuscript.

Corresponding author

Correspondence to Mojgan Sheikhpour.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the research and ethics committee of the Faculty of Life Sciences, Danesh Alborz University of Iran.

Consent for publication

Not applicable.

Competing interests

The authors declare that there is no conflict of interest.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pargami, H.N., Siadat, S.D., Amiri, V. et al. Antibiotic delivery evaluation against Mycobacterium fortuitum using nanofluids containing carbon nanotubes. BMC Microbiol 22, 96 (2022). https://doi.org/10.1186/s12866-022-02523-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12866-022-02523-z

Keywords

BMC Microbiology

ISSN: 1471-2180

Contact us