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Antimicrobial Agents and Chemotherapy, May 2009, p. 2209-2211, Vol. 53, No. 5
0066-4804/09/$08.00+0     doi:10.1128/AAC.00919-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Geraniol Restores Antibiotic Activities against Multidrug-Resistant Isolates from Gram-Negative Species ^,

Vannina Lorenzi,^1, Alain Muselli,² Antoine François Bernardini,² Liliane Berti,³ Jean-Marie Pagès,¹ Leonard Amaral,⁴ and Jean-Michel Bolla^1*

Université de la Méditerranée, UMR-MD1, IFR88, Faculté de Médecine, 13385 Marseille Cedex 05, France,¹ Université de Corse, Equipe Chimie des Produits Naturels, UMR-CNRS 6134, Quartier Grossetti, BP 52, 20250 Corte, France,² Université de Corse, Laboratoire de Biochimie et de Biologie Moléculaire du Végétal, UMR-CNRS 6134, Quartier Grossetti, BP 52, 20250 Corte, France,³ Unit of Mycobacteriology, Institute of Hygiene and Tropical Medicine, Universidade Nova de Lisboa, Lisbon, Portugal⁴

Received 11 July 2008/ Returned for modification 5 September 2008/ Accepted 16 February 2009

Top ABSTRACT INTRODUCTION REFERENCES

 
The essential oil of Helichrysum italicum significantly reduces the multidrug resistance of Enterobacter aerogenes, Escherichia coli, Pseudomonas aeruginosa, and Acinetobacter baumannii. Combinations of the two most active fractions of the essential oil with each other or with phenylalanine arginine β-naphthylamide yield synergistic activity. Geraniol, a component of one fraction, significantly increased the efficacy of β-lactams, quinolones, and chloramphenicol.

Top ABSTRACT INTRODUCTION REFERENCES

 
The constant use of antibiotics in the hospital environment has selected bacterial populations that are resistant to many antibiotics. This multidrug resistance (MDR) results in part because of the activation of efflux pumps (8). The vast majority of efflux pump inhibitors (EPIs) identified so far are active against gram-positive bacteria, particularly Staphylococcus aureus. The very few EPIs that are active against gram-negative bacteria are toxic, and gram-negative bacteria such as Pseudomonas, Acinetobacter, Escherichia, and Enterobacter spp. are rapidly becoming the most problematic bacteria to treat due to the expression of MDR phenotypes and nosocomial status (1, 3, 4). There is a dire need to search for EPIs that are effective in rendering MDR gram-negative bacteria susceptible to antibiotics to which they are initially resistant (6, 7, 10, 12). The aim of this study was to discover EPIs in essential oils obtained from Corsican plants that are effective against efflux systems of gram-negative bacteria.

Among the 15 plant extracts tested, the essential oil derived from Helichrysum italicum when used at a concentration of 2.5% reduces the MIC of chloramphenicol from 1,024 to 128 mg/liter (eightfold) for the Enterobacter aerogenes MDR strain EA27 (8); the remainder of the plants are less active and reduce the MIC of chloramphenicol from between two- and fourfold (see the supplemental material). Due to the ability of the essential oil derived from H. italicum to reduce the chloramphenicol resistance of EA27 to a level that is close to that of the control phenylalanine arginine β-naphthylamide (PAβN) (5), it was selected for further study that would evaluate its ability to reduce the antibiotic resistance of other gram-negative bacteria. As demonstrated in Table 1, the essential oil derived from H. italicum is more effective than PAβN in reducing the resistance of Acinetobacter baumannii strains to chloramphenicol. In the case of the highly chloramphenicol-resistant Pseudomonas aeruginosa strains, although it reduces resistance to essentially the same degree as that produced in A. baumannii, it is not as effective as PAβN. The ability of the H. italicum essential oil to significantly reduce the chloramphenicol resistance of three very pathogenic MDR gram-negative bacteria (1, 12) supports the prediction of similar activities against other gram-negative pathogens.

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TABLE 1. Effect of Helichrysum italicum essential oil on the susceptibilities of gram-negative species to chloramphenicol

Evaluation of potential EPIs is best conducted with bacteria that overexpress a specific efflux pump that renders the bacterium MDR. The ability of the H. italicum essential oil to reduce chloramphenicol resistance of EA27, a strain that overexpresses its AcrAB efflux pump (11), suggests that this essential oil contains an agent with the activity of an EPI. That this suggestion is correct is evident from the data summarized in Table 2. The essential oil not only reduces chloramphenicol resistance of the MDR E. aerogenes strain EAEP289 that overexpresses efflux pumps (11) but also reduces intrinsic chloramphenicol resistance of the wild-type controls E. aerogenes ATCC 13048 and Escherichia coli AG100. Moreover, a strong restoration was observed for E. aerogenes strain CM-64 that overproduced AcrAB (13) and also for the MDR E. aerogenes strain EAEP294 that has its acrAB operon deleted (11) but still has other active efflux pumps (2). In contrast to these effects, the E. coli mutant AG100A, which has its acrAB operon deleted (9), is not affected by the essential oil. Because the resistance of the acrAB-deleted progeny, which has been induced to high-level resistance to chloramphenicol, is due to the overexpression of the AcrEF system (13), the reduced resistance to chloramphenicol noted for the acrAB Tet^r mutant suggests that the essential oil is active against AcrEF. Regardless, from the data summarized in Table 2, it is clear that the essential oil derived from H. italicum contains one or more agents that have EPI activity, and hence, an attempt to isolate that agent or agents was made (see the supplemental material).

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TABLE 2. Effect of H. italicum essential oil on susceptibilities of E. aerogenes and E. coli efflux mutant strains to chloramphenicol

To our knowledge, none of the compounds identified in the essential oil (see the supplemental material) have been previously evaluated for EPI activity. Therefore, the evaluation of the main fractions of the essential oil derived from H. italicum for EPI activity against the MDR EAEP289 strain was conducted, and Table 3 shows a summary of the results obtained. Briefly, whereas the hydrocarbon and F1 fractions are devoid of any EPI activity (i.e., reduction of chloramphenicol resistance) when used alone against the MDR EAEP289 strain (data not shown), fractions F2 and F3 produce twofold reductions of chloramphenicol resistance. However, when fractions F2 and F3 are combined, they reduce chloramphenicol resistance from an initial MIC of 1,024 to 128 mg/liter. Reduction of resistance can also be achieved with combinations of PAβN with either the F2 or F3 fraction, with combinations of the latter producing the greatest reduction that is comparable to a complete reversal of chloramphenicol resistance expected of a chloramphenicol hypersusceptible strain (i.e., a MIC of less than 0.25 mg/liter). Identical evaluation of each fraction alone or in combination with each other or with PAβN for EPI activity against the acrAB derivative EAEP294 strain demonstrated the very strong activity of fraction F3. We thus decided to perform chloramphenicol susceptibility testing in the presence of various compounds of F3 that were available (see the supplemental material). Among the compounds tested, geraniol produced significant restoration of susceptibility of the MDR strain EAEP289 to chloramphenicol by as much as 16-fold. When combined with PAβN, it rendered the organism fully susceptible to chloramphenicol, i.e., it completely reversed initial resistance (Table 3). Interestingly, geraniol restored the susceptibility of the acrAB derivative EAEP294 to the same extent as the combination of F3 and PAβN (Table 3). The other compounds identified in F3 did not significantly reduce the resistance to chloramphenicol (data not shown).

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TABLE 3. EPI activity of H. italicum fractions alone or in combination with each other or with the EPI PAβN against E. aerogenes strains

Chloramphenicol was used in this study to reveal efflux inhibition. However, this antibiotic is not currently used as therapeutic agent against gram-negative bacteria. β-Lactams and quinolones are actually mostly used, even though resistance to these agents is becoming a major concern (1). Herein we have assayed the efficacy of geraniol in restoring antibiotic susceptibility, or at least increasing the susceptibility of EAEP289 and EAEP294 to the β-lactams ampicillin and penicillin and to the fluoroquinolone norfloxacin. The results are summarized in Table 4). As shown, the MICs of these antibiotics are very high, especially for the two β-lactams. When geraniol was added, we were not able to observe a change in the susceptibility of strain EAEP289. However, for EAEP294, the AcrAB-deficient strain, a very strong increase in susceptibility was observed in the presence of geraniol and a β-lactam. This indicated that the geraniol had a synergistic effect with β-lactams. Moreover, the same results were obtained with the fluoroquinolone norfloxacin, thus demonstrating a pleiotropic effect of geraniol against the MDR phenotype in E. aerogenes. Taken together, these results suggest that PAβN and geraniol have an inhibitory effect on different mechanisms that are altogether involved in resistance.

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TABLE 4. EPI activity of geraniol on susceptibilities of two β-lactams and a quinolone

In this study, we demonstrated that the essential oil from Helichrysum italicum contains compounds that modulate drug resistance in several gram-negative bacterial species by targeting efflux mechanisms. This conclusion is based on the following evidence. First, H. italicum decreases the chloramphenicol MIC for E. aerogenes isolates (Tables 1 and 2) in addition to A. baumannii and P. aeruginosa strains (Table 1). Second, H. italicum decreases the MIC of chloramphenicol for a strain that overproduced the tripartite efflux pump AcrAB-TolC (the E. aerogenes strain CM-64) (Table 2), and in addition it is able to restore susceptibility in a strain that overexpresses efflux pumps different from AcrAB, the E. coli strain AG100A Tet^r (Table 2). The two fractions (Table 3) that are the most active contain compounds that have not been previously described as modulators (see the supplemental material). Among these compounds, geraniol appeared to be a potent inhibitor of efflux mechanisms (Tables 3 and 4). Interestingly, the inhibition efficiency of geraniol that was first assayed for chloramphenicol resistance (Table 3) was also observed for resistance to β-lactams and to the fluoroquinolone norfloxacin that are more clinically important antibiotics (Table 4). Moreover, a ranking of the EPI activity demonstrated that geraniol is a very potent inhibitor of resistance in an acrAB mutant compared to PAβN (see the supplemental material), thus suggesting that these two molecules have different targets. Together, these findings provide a new source of drugs that may help in therapy, and also geraniol may help to create a better understanding of MDR in gram-negative bacteria that continue to pose a threat to public health.

 
We are indebted to the Collectivité de Corse, the COST Action BM0701 ATENS, the Université de la Méditerranée, and the Service de Santé des Armées for financial support.

We gratefully acknowledge M. Pierre Alessandri, who supplied the commercial sample of essential oil. We deeply acknowledge Jean-Marie Desjobert for his excellent technical assistance in chromatography. We thank Luc Dedieu, Myrielle Dupont, Laurent Mamelli, Jean Panighi, Solange Quenin, and Paul-Georges Rossi for helpful advice and fruitful discussions. Chloé James is deeply acknowledged for her help with the English.

 
* Corresponding author. Mailing address: UMR-MD1, Faculté de Médecine, 27 Bd Jean Moulin, 13385 Marseille Cedex 05, France. Phone: (33) 4 91 32 44 40. Fax: (33) 4 91 32 46 06. E-mail: Jean-Michel.Bolla{at}medecine.univ-mrs.fr

Published ahead of print on 2 March 2009.

Supplemental material for this article may be found at http://aac.asm.org/.

Present address: Université de Corse, Laboratoire de Biochimie et de Biologie Moléculaire du Végétal, UMR-CNRS 6134, Quartier Grossetti, BP 52, 20250 Corte, France.

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Antimicrobial Agents and Chemotherapy, May 2009, p. 2209-2211, Vol. 53, No. 5
0066-4804/09/$08.00+0     doi:10.1128/AAC.00919-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

This Article Abstract Full Text (PDF) Supplemental material Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Lorenzi, V. Articles by Bolla, J.-M. Search for Related Content PubMed PubMed Citation Articles by Lorenzi, V. Articles by Bolla, J.-M. Pubmed/NCBI databases Compound via MeSH Substance via MeSH Medline Plus Health Information Antibiotics Hazardous Substances DB CHLORAMPHENICOL GERANIOL