Skip to main content
Download PDF

In vitro activity of ivermectin against Staphylococcus aureus clinical isolates

Antimicrobial Resistance & Infection Control volume 7, Article number: 27 (2018) Cite this article

Abstract

Background

Ivermectin is an endectocide against many parasites. Though being a macrocyclic lactone, its activity against bacteria has been less known, possibly due to the fact that micromolar concentrations at tissue levels are required to achieve a therapeutic effect. Among pathogenic bacteria of major medical significance, Staphylococcus aureus cause a number of diseases in a wide variety of hosts including humans and animals. It has been attributed as one of the most pathogenic organisms. The emergence of methicillin resistance has made the treatment of S. aureus even more difficult as it is now resistant to most of the available antibiotics. Thus, search for alternate anti-staphylococcal agents requires immediate attention.

Methods

Twenty-one clinical isolates of S. aureus were isolated from bovine milk collected from Lahore and Faisalabad Pakistan. Different anthelmintics including levamisole, albendazole and ivermectin were tested against S. aureus to determine their minimum inhibitory concentrations. This was followed-up by growth curve analysis, spot assay and time-kill kinetics.

Results

The results showed that ivermectin but not levamisole or albendazole exhibited a potent anti-staphylococcal activity at the concentrations of 6.25 and 12.5 μg/ml against two isolates. Interestingly, one of the isolate was sensitive while the other was resistant to methicillin/cefoxitin.

Conclusions

Our novel findings indicate that ivermectin has an anti-bacterial effect against certain S. aureus isolates. However, to comprehend why ivermectin did not inhibit the growth of all Staphylococci needs further investigation. Nevertheless, we have extended the broad range of known pharmacological effects of ivermectin. As pharmacology and toxicology of ivermectin are well known, its further development as an anti-staphylococcal agent is potentially appealing.

Background

Anthelmintics are drugs used for controlling helminthes. The major classes of broad spectrum anthelmintics include benzimidazoles (BZ) (e.g. albendazole (ALB)), imidathiozoles (e.g. levamisole (LEV)), tetrahydropyrimidines (e.g. pyrantel), and macrocyclic lactones (MLs) (e.g. ivermectin (IVM)). These four classes of anthelmintics have different modes of action. BZs act by binding to the growing ends of microtubules and thus prevent addition of new β-tubulin dimers. As a result, the microtubules shorten and ultimately disappear thus disrupting essential functions which leads to death of the parasite [1]. Imidathiozoles and tetrahydropyrimidines target the nicotinic receptors i.e. they bind to acetylcholine-gated cation channels as agonists at the neuromuscular receptor and cause spastic paralysis of the parasite leading to its death [2, 3]. MLs act on the ligand-gated-chloride channels (glutamate-gated chloride channels) and cause the channels to irreversibly open by binding to the site other than the glutamate binding site and this leads to a permanent hyperpolarization and paralysis of the cells and results in death of the parasite [4].

Due to limited numbers of drugs entering the market and emergence of drug resistance to major classes of anti-bacteria, scientists have been investigating known drugs with previous unknown anti-bacterial activities. Some groups have recently reported anti-bacterial activity of various anthelmintics against different bacteria. For example, Imperi et al. [5] have proposed that niclosamide which is an anthelmintic used against tapeworms could reduce the pathogenicity of Pseudomonas aeruginosa. Similarly, Rajamuthiah et al. [6] have reported an anti-staphylococcal activity of closantel which belongs to the salicylanilide group of anthelmintics. Furthermore, the activity of niclosamide and oxycolzanide (a flukicidal) against S. aureus has also been reported [7]. Finally, Gooyit and Janda [8] have reported that the salicylanilide anthelmintics (closantel, rafoxinide, niclosamide, oxyclozanide) were also effective against Clostridium difficile.

IVM has shown activities against a broad range of host species and thus it has earned the title of a wonder drug [9, 10]. This enigmatic multifaceted drug continues to surprise and exceed expectations. For example, IVM at sub-lethal concentrations has been reported to have an anti-plasmodial activity by inhibiting sporogony of Plasmodium falciparum [11]. IVM also acts as an anti-viral agent against flavivirus by inhibiting its replication through targeting the N3 helicase activity [12]. In addition, an anti-mycobacterial activity of IVM has also been identified against Mycobacterium tuberculosis and Mycobacterium ulcerans [13, 14]. Sharmeen et al. [15] found that IVM killed leukemic cells by a chloride dependent membrane hyperpolarization. Recently, anti-mitotic activities of IVM have also been reported i.e. by binding to the tubulins and consequently altering the polymerization equilibrium and leading the cells into mitotic arrest [16, 17]. However, despite being a macrocyclic lactone, its activity against bacteria has been less known, possibly because micromolar concentrations are required at tissue levels to achieve a therapeutic effect.

Staphylococci are gram-positive spherical bacteria that contain many species. It has been suggested that 30% of the world population are silent carriers of S. aureus without any symptoms [18]. However, S. aureus can cause a wide range of diseases from skin and soft-tissue infection to life-threatening diseases in humans and is also the leading cause of bacteremia [19]. In the dairy industry, S. aureus is also one of the most common bacteria causing mastitis [20]. β-lactams have been widely used for the treatment of S. aureus infections. Due to emergence of resistance to β-lactams, methicillin, a semi-synthetic penicillinase resistant β-lactam, was produced and introduced into the market in 1959. Unfortunately, it became resistant just two-years after its introduction [21]. Currently, many S. aureus clinical isolates are resistant to almost all the available antibiotics and the term methicillin resistant Staphylococcus aureus (MRSA) and vancomycin resistant S. aureus are heard all around the globe [22]. The challenges related to the MRSA type alone can be visualized as the mortality associated with invasiveness of MRSA has gone up to 20% [23]. Hence, in 2017, the World Health Organization has put S. aureus in the list of microorganisms which immediately need new antibiotics for its treatment. The main problem with MRSA phenotype is that the organisms that are methicillin resistant are often resistant to most of the known antibiotics.

In an effort to search for alternative treatment of S. aureus infections, in the present study, we screened three known anthelmintics (IVM, ALB, and LEV) and found that IVM but not ALB or LEV had a potent anti-bacterial activity against S. aureus species.

Methods

Bacterial isolates

Twenty-one S. aureus isolates were used in this study. The isolates were isolated from clinical mastitis cases from Lahore and Faisalabad, Pakistan. Among them 11 isolates were methicillin sensitive whereas 10 were methicillin resistant. The S. aureus isolates were grown in the Mueller Hinton (MH) broth or tryptic soya broth (TSB) (Sigma Aldrich, Canada) at 37 °C.

Determination of minimum inhibitory concentrations (MICs)

To determine the minimum inhibitory concentrations (MICs) for the S. aureus isolates, 5 X 105 CFU/ml cells were inoculated into the Mueller Hinton (MH) broth (Sigma Aldrich, Canada). One hundred fifty μl of the bacterial solution was dispensed into each well of 96-well round bottom microtiter plates (Sarstedt, Canada). The test compounds IVM, ALB, LEV, cefoxitin (FOX) and dimethyl sulfoxide (DMSO) (as a solvent control) (Sigma Aldrich) were serially diluted 2-fold in the MH broth. IVM and LEV dilutions were from 100 to 1.56 μg/ml, while ALB was from 50 to 0.78 μg/ml and FOX was from 128 to 2 μg/ml. The MH broth with the bacterial suspension and test compounds were incubated for 18 h at 35 °C. The MICs were determined by examining visible bacterial growth with naked eyes.

Effects of IVM on growth curves

To determine the effects of IVM on growth curves, glycerol stocks of MSSA (O9) and MRSA (P22) isolates were grown overnight in the tryptic soya broth (TSB) (Sigma Aldrich) at 35 °C. A loop full of overnight cultures were streaked on the MH agar and the plates were further incubated for 24 h at 35 °C. After 24 h, a 0.5 McFarland culture was prepared in the MH broth. The bacteria were diluted to a final concentration of 5 X 105 CFU/ml. Different test compounds including IVM, ALB, LEV, and FOX were then added at a concentration of 50, 50, 50 or 16 μg/ml, respectively. In addition,, FOX was also added at a concentration of 32 μg/ml. DMSO was used as a solvent control. The bacteria were then grown up to 14 h at 35 °C and 1 ml sample was taken every 2 h. The optical density (O.D) was measured at 600 nm. Among the 20 isolates tested, the two S. aureus isolates against which IVM had a more potent activity were used in further studies. For two specific S. aureus isolates (P22 (MRSA) and O9 (MSSA)), IVM was then serially titrated at concentrations of 100, 50, 25, 12.5, 6.25, 3.125 and 1.56 μg/ml and O.D values were taken at 2 h intervals for a total of 14 h. All the bacteria were grown at 200 rpm at 35 °C.

Spot assay

The 0.5 McFarland culture of both isolates was prepared and further diluted (as described above) to get final concentrations of 5 X 105 CFU/ml. IVM was added at concentrations of 0, 1.56, 3.125, 6.25, 12.5, 25, 50, and 100 μg/ml. After 12 h incubation at 35 °C, 5 μl bacteria from both isolates were spotted on the MH agar. The plates were then incubated at 35 °C for 24 h. Pictures were then taken using a transilluminator FBTIV-816, Kodak EDAS 290 (Fischer Scientific, Canada).

Time kill-kinetics

For further confirmation of the above results, bacterial suspension of 0.5 McFarland was prepared for both isolates from freshly prepared overnight cultures as described above. 0.5 McFarland culture for both S. aureus (MSSA and MRSA) isolates was transferred to the MH broth to attain a final concentration of 5 X 105 CFU/ml. Then IVM was added at concentrations of 1/4X(MIC), 1/2X(MIC), 0X(MIC), 1X(MIC), 2X(MIC), 4X(MIC), 8X(MIC) and 12X(MIC) for both isolates. The tubes were then incubated at 35 °C and 100 μl samples were taken at 0, 2, 4, 8 and 12 h. The aliquots were then plated onto MH agar plates to assess viable bacteria by CFU counting. After 24 h of incubation at 35 °C, plates were examined for growth.

Results

Minimum inhibitory concentrations of different drugs against S. aureus

As shown in Table 1, MICs for IVM were 6.25 μg/ml and 12.5 μg/ml for O9 (MSSA) and P22 (MRSA), respectively. The bacterial growth was not inhibited by ALB up to 50 μg/ml or by LEV up to 100 μg/ml. The limited solubility of ALB and LEV did not allow us to go beyond 50 and 100 μg/ml, respectively. The MIC of FOX was 4 μg/ml for O9 and 16 μg/ml for P22.

Table 1 Minimum inhibitory concentration (MIC)
Full size table

Inhibition of S. aureus growth by IVM as evidenced by growth curves

The growth curve analysis demonstrated that ALB, LEV, and DMSO did not have any effect on the growth of both S. aureus isolates (Fig. 1a, b), whereas IVM reduced the growth of both isolates. For FOX, O9 showed no growth at both concentrations tested whereas P22 showed growth at 16 μg/ml but no growth was observed at 32 μg/ml. The 2-fold IVM titration from 100 to 1.56 μg/ml demonstrated that IVM inhibited bacterial growth at concentrations above 3.125 μg/ml for O9 and 6.25 μg/ml for the P22 isolates (Fig. 1c, d).

Fig. 1
figure 1

Growth curves of the P22 (MRSA) (a, c) and O9 (MSSA) (b, d) isolates in the presence of different drugs. Ivermectin (IVM), levamisole (LEV), albendazole (ALB), dimethyl-sulphoxide (DMSO) and cefoxitin (FOX) were used as test compounds at fixed concentrations

Full size image
Fig. 2
figure 2

Time-kill kinetics and the spot assay results for P22 (MRSA) (a, d) and O9 (MSSA) (b, c) respectively. The error bars were standard error of the means for three independent experiments for the time-kill kinetics. The spots are representative of three independent experiments

Full size image

Inhibition of S. aureus growth by IVM as shown in the spot assay and time-kill kinetics

The spot assay showed no growth in both isolates beyond their MICs representing absence of any bacterial spots at concentration of 12.5 μg/ml for the O9 (MSSA) and 25 μg/ml for the P22 (MRSA) isolates (Fig. 2c, d). The results of time-kill kinetics were similar to those of the spot assay and IVM showed reduction in CFU/ml as compared to the control (DMSO) which suggested that bacterial growth was completely inhibited by IVM at concentrations of 1X(MIC) and above for both isolates (Fig. 2a, b).

Discussion

IVM is a drug used against helminthes of human and veterinary importance. To our knowledge, this study is a maiden attempt reporting the activity of IVM against S. aureus clinical isolates. Interestingly, one of the isolates had a methicillin sensitive and the other had a methicillin resistant phenotype. The MICs for IVM against the MSSA (O9) and MRSA (P22) isolates were 6.25 and 12.5 μg/ml, respectively. The findings of growth curve experiments were in correlation with the MICs as there was no increase in the O.D values beyond 3.125 μg/ml and 6.25 μg/ml for both isolates. The spot assay also showed similar results to the MIC, and growth curve experiments as there was complete inhibition of growth on the bacterial spots beyond the MICs. Time-kill kinetics was also in complete agreement with the other data and showed complete inhibition of bacterial growth beyond 1X(MIC) which means the CFU did not go above 5 X 105 CFU/ml. However, the isolates were not killed even when the concentration of IVM was increased up to 12X (MIC). In contrast, the number of bacteria increased when IVM concentrations were tested below the MICs.

The findings from the time-kill kinetics data indicated that the effects of IVM was probably bacteriostatic rather than bactericidal. When IVM acts as a bacteriostatic agent, it would be beneficial as the bacteriostatic antibiotics could circumvent some problems related to bactericidal drugs. For example, when the bactericidal drugs kill the bacteria, endotoxins are released which may be toxic to the host, whereas, in the case of bacteriostatic drugs, the bacterial growth is inhibited enabling the host to elicit protective immunity and thus results in immunological clearance of the bacteria [24]. Torres et al. [25] reported that IVM was effective against biofilm formation by S. aureus. Our results extend these previous findings about antibacterial efficacy of IVM against S. aureus.

S. aureus infections have been reported all over the world. The treatment of infections associated to S. aureus infections has become difficult because of the emergence of antibiotic resistance. Hence, new drugs other than conventional antibiotics should be immediately introduced to tackle the problem and minimize the selection pressure on resistant isolates. To that end, we tested antibacterial activities of anthelmintics on S. aureus and found that IVM showed antibacterial activities against 2 isolates of 20 S aureus isolates. It would be of interest to further investigate the reason why other isolates were not sensitive to this drug. It is known that IVM is a good substrate of P-glycoprotein (efflux pumps) in helminthes [26, 27]. The evidence of involvement of drug efflux pumps clearly requires further investigations. IVM is used at a dose rate of 200 μg/kg body weight in humans and animals. At this dosage, the maximum plasma concentration of IVM goes up to 52 ng/ml [28]. The concentration at which the anti-staphylococcal activity of IVM was evident in this study is higher than the concentration of its current therapeutic use and perhaps this might be the reason why this mechanism has not been reported previously. However, the lethal dose 50 (LD50) of IVM has been reported up to 50 mg/kg [29], which suggests that IVM has a wide therapeutic index. At this dosage, IVM concentration at tissue levels is at the low micromolar range. Hence, we report anti-staphylococcal activity of IVM against MRSA and MSSA isolates at pharmacologically relevant concentrations. Given that IVM is already approved for treatment against various parasites in humans and animals, its development as a potential antimicrobial agent to kill S. aureus, especially MRSA, is an appealing option.

Conclusions

The present study investigated the antibacterial effects of IVM, ALB and LEV against methicillin sensitive and methicillin resistant S. aureus. Among these anthelmintics, only IVM showed a potent anti-staphylococcal activity. The MICs for IVM against MSSA and MRSA isolates were 6.25 and 12.5 μg/ml, respectively. The growth curves corresponded to the MICs. The spot assay and time kill kinetics also showed similar results to the MIC, and growth curve experiments. In summary, this study is the first attempt to indicate that IVMs also has anti-bacterial efficacy against S. aureus. Further development of IVM as an anti-microbial agent is potentially appealing, as its pharmacokinetics and pharmacodynamics have already been studied in mammals.

Abbreviations

ALB:

Albendazole

BZ:

Benzimidazole

CFU:

Colony Forming Unit

DMSO:

Dimethy-Sulphoxide

FOX:

Cefoxitin

IVM:

Ivermectin

LEV:

Levamisole

MIC:

Minimum Inhibitory Concentration

MRSA:

Methicillin Resistant Staphylococcus aureus

MSSA:

Methicillin Sensitive Staphylococcus aureus

References

  1. Lacey E. The role of the cytoskeletal protein, tubulin, in the mode of action and mechanism of drug resistance to benzimidazoles. Int J Parasitol. 1988;18(7):885–936.

    Article  CAS  PubMed  Google Scholar 

  2. Fleming JT, Squire MD, Barnes TM, Tornoe C, Matsuda K, Ahnn J, Fire A, Sulston JE, Barnard EA, Sattelle DB, Lewis JA. Caenorhabditis elegans levamisole resistance genes lev-1, unc-29, and unc-38 encode functional nicotinic acetylcholine receptor subunits. J Neurosci. 1997;17(15):5843–57.

    CAS  PubMed  Google Scholar 

  3. Robertson AP, Bjorn HE, Martin RJ. Pyrantel resistance alters nematode nicotinic acetylcholine receptor single-channel properties. Eur J Pharmacol. 2000;394(1):1–8.

    Article  CAS  PubMed  Google Scholar 

  4. Wolstenholme AJ, Rogers AT. Glutamate-gated chloride channels and the mode of action of the avermectin/milbemycin anthelmintics. Parasitology. 2005;131(Suppl):S85–95.

    CAS  PubMed  Google Scholar 

  5. Imperi F, Massai F, Ramachandran Pillai C, Longo F, Zennaro E, Rampioni G, Visca P, Leoni L. New life for an old drug: the anthelmintic drug niclosamide inhibits Pseudomonas aeruginosa quorum sensing. Antimicrob Agents Chemother. 2013;57(2):996–1005.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Rajamuthiah R, Fuchs BB, Jayamani E, Kim Y, Larkins-Ford J, Conery A, Ausubel FM, Mylonakis E. Whole animal automated platform for drug discovery against multi-drug resistant Staphylococcus aureus. PLoS One. 2014;9(2):e89189.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Rajamuthiah R, Fuchs BB, Conery AL, Kim W, Jayamani E, Kwon B, Ausubel FM, Mylonakis E. Repurposing Salicylanilide anthelmintic drugs to combat drug resistant Staphylococcus aureus. PLoS One. 2015;10(4):e0124595.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Gooyit M, Janda KD. Reprofiled anthelmintics abate hypervirulent stationary-phase Clostridium difficile. Sci Reports. 2016;6:33642.

    Article  CAS  Google Scholar 

  9. Geary TG. Ivermectin 20 years on: maturation of a wonder drug. Trends Parasitol. 2005;21(11):530–2.

    Article  CAS  PubMed  Google Scholar 

  10. Crump A. Ivermectin: enigmatic multifaceted 'wonder' drug continues to surprise and exceed expectations. J Antibiot. 2017;70(5):495–505.

    Article  CAS  PubMed  Google Scholar 

  11. Kobylinski KC, Foy BD, Richardson JH. Ivermectin inhibits the sporogony of Plasmodium falciparum in Anopheles Gambiae. Malaria J. 2012;11(1):381.

    Article  CAS  Google Scholar 

  12. Mastrangelo E, Pezzullo M, De Burghgraeve T, Kaptein S, Pastorino B, Dallmeier K, de Lamballerie X, Neyts J, Hanson AM, Frick DN, Bolognesi M, Milani M. Ivermectin is a potent inhibitor of flavivirus replication specifically targeting NS3 helicase activity: new prospects for an old drug. J Antimicrob Chemother. 2012;67(8):1884–94.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Lim LE, Vilcheze C, Ng C, Jacobs WR, Jr., Ramon-Garcia S, Thompson CJ. Anthelmintic avermectins kill Mycobacterium tuberculosis, including multidrug-resistant clinical strains. Antimicrob Agents Chemother 2013. 57(2): p. 1040–1046.

  14. Omansen TF, Porter JL, Johnson PDR, van der Werf TS, Stienstra Y, Stinear TP. In-vitro activity of Avermectins against Mycobacterium ulcerans. PLOS Neg Trop Dis. 2015;9(3):e0003549.

    Article  Google Scholar 

  15. Sharmeen S, Skrtic M, Sukhai MA, Hurren R, Gronda M, Wang X, Fonseca SB, Sun H, Wood TE, Ward R, Minden MD, Batey RA, Datti A, Wrana J, Kelley SO, Schimmer AD. The antiparasitic agent ivermectin induces chloride-dependent membrane hyperpolarization and cell death in leukemia cells. Blood. 2010;116(18):3593–603.

    Article  CAS  PubMed  Google Scholar 

  16. Ashraf S, Mani T, Beech R, Prichard R. Macrocyclic lactones and their relationship to the SNPs related to benzimidazole resistance. Mol Biochem Parasitol. 2015;201(2):128–34.

    Article  CAS  PubMed  Google Scholar 

  17. Ashraf S, Prichard R. Ivermectin exhibits potent anti-mitotic activity. Vet Parasitol. 2016;226:1–4.

    Article  CAS  PubMed  Google Scholar 

  18. Chambers HF, Deleo FR. Waves of resistance: Staphylococcus aureus in the antibiotic era. Nat Rev Microbiol. 2009;7(9):629–41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Tong SY, Davis JS, Eichenberger E, Holland TL, Fowler VG, Jr. Staphylococcus aureus infections: epidemiology, pathophysiology, clinical manifestations, and management. Clin Microbiol Rev 2015. 28(3): p. 603–661.

  20. Olde Riekerink RG, Barkema HW, Kelton DF, Scholl DT. Incidence rate of clinical mastitis on Canadian dairy farms. J Dairy Sci. 2008;91(4):1366–77.

    Article  CAS  PubMed  Google Scholar 

  21. Jevons MP, Coe AW, Parker MT. Methicillin resistance in staphylococci. Lancet. 1963;281(7287):904–7.

    Article  Google Scholar 

  22. Grundmann H, Aanensen DM, van den Wijngaard CC, Spratt BG, Harmsen D, Friedrich AW. Geographic distribution of Staphylococcus aureus causing invasive infections in Europe: a molecular-epidemiological analysis. PLoS Med. 2010;7(1):e1000215.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Stefani S, Chung DR, Lindsay JA, Friedrich AW, Kearns AM, Westh H, Mackenzie FM. Meticillin-resistant Staphylococcus aureus (MRSA): global epidemiology and harmonisation of typing methods. Int J Antimicrob Agents. 2012;39(4):273–82.

    Article  CAS  PubMed  Google Scholar 

  24. Krachler AM, Orth K. Targeting the bacteria–host interface. Virulence. 2013;4(4):284–94.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Torres NS, Abercrombie JJ, Srinivasan A, Lopez-Ribot JL, Ramasubramanian AK, Leung KP. Screening a commercial library of pharmacologically active small molecules against Staphylococcus aureus biofilms. Antimicrob Agents Chemother. 2016;60(10):5663–72.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Mani T, Bourguinat C, Keller K, Ashraf S, Blagburn B, Prichard RK. Interaction of macrocyclic lactones with a Dirofilaria immitis P-glycoprotein. Int J Parasitol. 2016;46(10):631–40.

    Article  CAS  PubMed  Google Scholar 

  27. Raza A, Kopp SR, Bagnall NH, Jabbar A, Kotze AC. Effects of in vitro exposure to ivermectin and levamisole on the expression patterns of ABC transporters in Haemonchus contortus larvae. Int J Parasitol: Drugs and Drug Resist. 2016;6(2):103–15.

    Google Scholar 

  28. Baraka OZ, Mahmoud BM, Marschke CK, Geary TG, Homeida MM, Williams JF. Ivermectin distribution in the plasma and tissues of patients infected with Onchocerca volvulus. Eur J Clin Pharmacol. 1996;50(5):407–10.

    Article  CAS  PubMed  Google Scholar 

  29. Dadarkar SS, Deore MD, Gatne MM. Comparative evaluation of acute toxicity of ivermectin by two methods after single subcutaneous administration in rats. Regul Toxicol Pharmacol. 2007;47(3):257–60.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

The authors thank all the farms who provided samples for the study.

Funding

The study was supported financially in part by Natural Sciences and engineering Research Council (NSERC) of Canada.

Availability of data and materials

All data supporting the findings of the study are present in the manuscript.

Author information

Authors and Affiliations

  1. Department of Animal Science, McGill University, Sainte-Anne-de-Bellevue, Canada

    Shoaib Ashraf, Debasri Ghosh & Xin Zhao

  2. Department of Parasitology, University of Veterinary and Animal Sciences, Lahore, Pakistan

    Umer Chaudhry

  3. Department of Clinical Medicine and Surgery, University of Agriculture Faisalabad, Faisalabad, Pakistan

    Ali Raza

Authors
  1. Shoaib Ashraf
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Umer Chaudhry
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Ali Raza
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Debasri Ghosh
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Xin Zhao
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

SA, XZ designed the study. SA, DG and XZ analyzed and interpreted the data. SA, UC, AR, DG conducted experiments. SA and XZ wrote the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Xin Zhao.

Ethics declarations

Ethics approval and consent to participate

No permission was required to work in specific locations regarding sample collection for bacterial isolation from cattle. However, consent was taken from all participating farms and no endangered species were involved or harmed in the current study.

Consent for publication

All authors agreed on the publication of the paper.

Competing interests

The authors have no competing interests.

Publisher’s Note

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

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Ashraf, S., Chaudhry, U., Raza, A. et al. In vitro activity of ivermectin against Staphylococcus aureus clinical isolates. Antimicrob Resist Infect Control 7, 27 (2018). https://0-doi-org.brum.beds.ac.uk/10.1186/s13756-018-0314-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/s13756-018-0314-4

Keywords

  • Anthelmintics
  • Ivermectin
  • Staphylococcus aureus
  • Time-kill kinetics

Antimicrobial Resistance & Infection Control

ISSN: 2047-2994

Contact us