The emergence and ongoing spread of antimicrobial-resistant bacteria is a major public health threat. Infections caused by antimicrobial-resistant bacteria are associated with substantially higher rates of morbidity and mortality compared to infections caused by antimicrobial-susceptible bacteria. The emergence and spread of these bacteria is complex and requires incorporating numerous interrelated factors which clinical studies cannot adequately address.
A model is created which incorporates several key factors contributing to the emergence and spread of resistant bacteria including the effects of the immune system, acquisition of resistance genes and antimicrobial exposure. The model identifies key strategies which would limit the emergence of antimicrobial-resistant bacterial strains. Specifically, the simulations show that early initiation of antimicrobial therapy and combination therapy with two antibiotics prevents the emergence of resistant bacteria, whereas shorter courses of therapy and sequential administration of antibiotics promote the emergence of resistant strains.
The principal findings suggest that (i) shorter lengths of antibiotic therapy and early interruption of antibiotic therapy provide an advantage for the resistant strains, (ii) combination therapy with two antibiotics prevents the emergence of resistance strains in contrast to sequential antibiotic therapy, and (iii) early initiation of antibiotics is among the most important factors preventing the emergence of resistant strains. These findings provide new insights into strategies aimed at optimizing the administration of antimicrobials for the treatment of infections and the prevention of the emergence of antimicrobial resistance.
Citation: D'Agata EMC, Dupont-Rouzeyrol M, Magal P, Olivier D, Ruan S (2008) The Impact of Different Antibiotic Regimens on the Emergence of Antimicrobial-Resistant Bacteria. PLoS ONE 3(12): e4036. doi:10.1371/journal.pone.0004036
Editor: Stefan Bereswill, Charité-Universitätsmedizin Berlin, Germany
Received: October 10, 2008; Accepted: November 17, 2008; Published: December 29, 2008
Copyright: © 2008 D'Agata et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported in part by the joint DMS/NIGMS Initiative through the National Institute of Health (NIH) grant R01GM083607 (E.M.C.D., S.R.) and the National Science Foundation (NSF) grant DMS-0715772 (S.R.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Antimicrobial resistance among bacteria has become a worldwide public health threat –. Despite substantial interventions aimed at preventing the emergence and spread of antimicrobial-resistant bacteria, the rates continue to rise rapidly . The geographic locations affected by antimicrobial resistance are mounting . The economic impact of antimicrobial resistance is substantial . Infections caused by these antimicrobial-resistant bacteria are associated with substantially higher mortality rates, longer hospital stays and greater hospital costs, compared to infections caused by antimicrobial-susceptible bacteria , . In 1998, it was estimated that the annual cost of antimicrobial resistance in hospitals due to Staphylococcus aureus was already $122 million and of nosocomial infections was $4.5 billion , . A recent estimate showed that there were 18,650 deaths in patients with invasive methicillin-resistant S. aureus in the United Sates in 2005, exceeding the total number of deaths due to HIV/AIDS in the same year .
In the last decade, mathematical models have been increasingly used as tools to identify factors responsible for observed patterns of antimicrobial resistance, to predict the effect of various factors on the prevalence of antimicrobial resistance, and to help design effective control and intervention programs –. We also refer to the surveys on this topic , , –. Most of these studies have used differential equations models, which aggregate patient and health-care worker populations into compartments such as colonized or uncolonized patients and contaminated or uncontaminated health-care workers. Interventions proposed by these studies have focused on reducing the transmission of antimicrobial-resistant bacteria between patients thereby preventing de novo acquisition. Antimicrobial treatments have also been evaluated in some of these studies. For example, Bonhoeffer et al.  considered two models for treatment and resistance with a single and two drugs, respectively. They found that when more than one antibiotic is employed, sequential (cycling) use of different antibiotics is not as good as that with a combination of antibiotics. Bergstrom et al.  further developed a mathematical model to study the efficacy of cycling program and found that cycling is unlikely to reduce the spread of antimicrobial resistance. Se also , .
One of the main limitations in providing guidance with antibiotic administration is the paucity of data regarding optimal duration of therapy and patterns of use which would reduce the emergence and spread of resistant bacteria. This lack of data is due to the fact that patient-oriented clinical studies cannot fully address the multitude of factors that are involved in the treatment of infections, the emergence of resistance and the role of the immune system in eradicating the infection. D'Agata et al.  integrated an individual-based model and a deterministic model to provide a quantitative analysis of the emergence and spread of antimicrobial resistant bacteria and demonstrated that early initiation of treatment and minimization of its duration mitigates antimicrobial resistance epidemics in hospitals.
Mathematical models have also developed to study pharmacodynamics of various antimicrobial therapies –. Lipsitch and Levin  presented a simple mathematical model of pharmacokinetics and bacterial population dynamics that is designed to address the problem of suppressing the emergence of resistance during treatment. They restricted their consideration to treatment with bactericidal antibiotics and the evaluation of resistance by mutation. Via mathematical modelling and computer simulations, the effect of mutation in antimicrobial resistance has further investigated by Levin and Rozen  who showed non-inherited resistance could extend the duration of antimicrobial treatment, cause treatment failure and promote the generation and ascent of inherited resistance in treated patients.
Bacteria can also develop antimicrobial resistance through the acquisition of new genetic material from other resistant organisms, such as horizontal gene transfer , . The widespread dissemination of antimicrobial resistance genes are the results of improper and excessive administration of antibiotics, combined with the ready bacterial ability to transfer antimicrobial resistance genes through plasmids and transposons and the presence of large transfer communities such as hospitals . Compared to the mathematical modelling on population dynamics of the antimicrobial resistance bacteria, there are few models describing the horizontal transfer of antimicrobial resistance genes , which could help better understand the mechanisms of antimicrobial resistance in bacteria and provide more effective treatment.
Multidrug-resistant bacteria can colonize specific sites in the host and evade immune surveillance . The nature of the host immune response to multidrug-resistant bacterial infection is complex. To the best of our knowledge, the combined effect of immune response, horizontal gene transfer and antibiotic treatment has not been modelled and explored. In this article, we develop a new mathematical model which incorporates three key aspects in the emergence of resistance caused by antibiotic exposure: the response of the host's immune system, horizontal transfer of resistance genes and patterns of antibiotic treatment regimens. Specifically, we want to propose a model for the bacterial population and study the within-host dynamics that would provide critical information regarding the optimal regimens for antibiotics administration in the treatment of infections in order to prevent the emergence of antimicrobial resistant bacteria. By mathematical modelling and numerical simulations, we demonstrate the importance and significance of the necessary length of antimicrobial treatment, the early initiation of treatment, and the combination of antibiotics in preventing antimicrobial resistant bacterial infections in treated patients.
(A) Model with immune response and single antibiotic treatment
We first present an ideal case of a homogenous bacterial population within a host treated by an antimicrobial agent. Since a growing bacterial population will eventually saturate due to the limitation of nutrients and space, we use the logistic growth to describe the population dynamics of the bacteria. Also assume that the bacteria are killed by the antimicrobial agent at a constant rate proportional to the density of the bacteria population.
Let B(t) be the number of bacteria at time t. Let δ (day−1) be the division rate and μ (day−1) the mortality rate due to antibiotic treatment. So λ = δ−μ is net growth rate and λκ is the carrying capacity of the bacteria, the term describes the limitation of space and food available to the bacteria. The bacterium Escherichia coli is chosen for this model since baseline parameters pertaining to its biology are available from the literature. For E. coli, the average in vivo doubling time (AV) is 0.4 day, based on data from several studies , , . The growth rate is λ = ln2/ AV = 2.7726 day−1. The maximum number is set at bacteria . Thus, .
Now we consider the response of the host's immune system to the invading bacteria. The innate immunity is characterised by a rapid action of the host's effectors cells including leukocytes, which will limit the multiplication of bacteria and destroy them. Assume that the killing rate of bacteria by leukocytes satisfies the Monod function , . In our model, the minimal infecting dose, or threshold of bacteria required to overcome the immune system, will be addressed. This value implies that above the threshold, the immune response is ineffective against bacterial growth and the infection progresses.
For the immune system to be ineffective and the infection to progress, the bacterial population need to be above the minimal infecting dose, or threshold, which is related to the number of phagocytes. Indeed, we can consider the following equation:(1)where P is the equilibrium number of activated phagocytes, and γ (day−1) is the maximal killing rate of bacteria by activated phagocytes. We assume that the number of phagocytes remains constant. The main consequence of this assumption is that the threshold of invasion and the threshold of bacterial eradication are the same . For other values see Table 1.
Model (1) has at most three non-negative equilibria. is always an equilibrium, which is stable if λ = δ−μ>0 and unstable if λ = δ−μ<0. There eventually exist two other equilibria which are solutions of the quadratic equation . It has two roots if , where corresponds to the invasion threshold and corresponds to the maximal bacterial load. In practice, we fix  and corresponding to the experimental value obtained in previous studies . Notice that with parameter values in Table 1, is unstable and is stable. Thus, the asymptotic behavior of solutions of Model (A) depends on the location of the initial value. If the initial bacterial load is between 106 and 1015, then the solution will increase and approach as time involves. However, treatment can change the dynamics (see simulations in Results).
(B) Model with resistant strains to one antibiotic through horizontal gene transfer
Antimicrobial resistance among bacteria can be intrinsic or acquired either through de novo mutations or via the acquisition of antimicrobial-resistance genes . The latter occurs through horizontal gene transfer of mobile genetic elements including plasmids, integrons and transposons37. Acquisition of resistance genes is among the main mechanism of antimicrobial resistance among E. coli isolates –.
Let and BR(t) denote the population levels of antibiotic-sensitive (plasmid free) and antibiotic-resistant (plasmid bearing) bacteria at time t, respectively, so that is the total bacterial load in a host. Thus, is the fraction of bacteria that are antibiotic-sensitive and is the fraction of bacteria that are antibiotic-resistant. Let τ be the recombination rate (i.e. horizontal gene transfer rate) of plasmid free and plasmid bearing to plasmid bearing. Then represents the recombination process. Let p be the probability that a plasmid is lost, which varies after 50 generations from 0, 40 or 100% – and depends on the type of plasmid, its stability and copy number, and the presence of the antibiotic pressure. In practice this leads to the estimation of as the reversion rate of plasmid bearing to plasmid free, where is the division rate of the antibiotic-resistant bacteria. Let be the division rate of the antibiotic-sensitive bacteria, and be the mortality rates of plasmid free and plasmid bearing bacteria, respectively.
Extending the model of Webb et al.  to include the immune response, we obtain the following:(2)The rate of horizontal gene transfer occurs at a rate ranging from 10−1 to 10−6 genes per cell per generation –. In this model, we assume that gene transfer occurs at a rate of 10−3/day. Since plasmid-bearing bacteria have a longer generation time than plasmid-free bacteria, we assumed a 40% increase in generation time among the plasmid-bearing bacteria , . In the absence of antibiotic pressure, plasmids carrying antimicrobial resistance genes are lost to minimize costs associated with replication and conservation, as shown in several studies –. In our model, plasmid loss during bacterial replication is set at 10−5 per cell and per generation , , . In absence of antibiotics, we can assume that . In this case B(t) satisfies Model (1). So we observe that .
Note that we have extinction when or invasion when and (, BR(t)) converges to () as time t increases, where and . The proportion of antibiotic-susceptible and -resistant bacteria can therefore be quantified in function of the parameter in absence of antibiotics.
(C) Model with different antibiotic treatments and multidrug-resistant (MDR) strains
Finally we consider the situation when the bacteria are multidrug-resistant. We will model different antibiotic treatments and study the combined treatment regimens. Denote
- BS(t)–the number of antibiotic-sensitive (plasmid-free) bacteria at time t
- BA(t)–the number of bacteria resistant to antibiotic A but not resistant to antibiotic B (i.e. bacteria bearing only plasmid A)
- BB(t)–the number of bacteria resistant to antibiotic B but not resistant to antibiotic A (i.e. bacteria bearing only plasmid B)
- BAB(t)–the number of bacteria resistant to both antibiotics A and B (i.e. bacteria bearing both plasmids A and B) .
Considering exposure to two antibiotics and generalizing the Model (2) which includes the effect of the saturation due to food or space limitation, and the effect of immune system, we have the following model:(3)To simplify, we will assume that and the mortality rates are shown in Table 1.
By carrying out numerical simulations of Models (1)–(3), we study the impact of several factors, such as the immune response, duration of antimicrobial therapy, initiation and interruption of treatment, delay and sequential antimicrobial regimens, and combination of antimicrobial therapies, on the progress of an infection within a host. Note that in all simulations, the initial values are chosen near the equilibrium values of these models.
(A) Immune system response and duration of antimicrobial therapy
The first simulation (Model (1)) demonstrates the importance of longer antimicrobial therapies required to prevent the progression of an infection. When the bacterial load is below the minimal infecting dose, the immune system is effective in killing bacteria and the patient does not develop an infection. When the duration of an antimicrobial therapy is for 9 days, the bacterial load is reduced below the threshold and progression of the infection is prevented. However, a shorter antimicrobial therapy of 6-day courses does not reduce the bacterial load to below the threshold and therefore an infection is not prevented (Figure 1).
The initial value is chosen between 106 and 1015, so the solution increases initially. The green line represents the threshold of bacterial load above which an infection develops. Below this threshold, the phagocyte density is sufficient to prevent the progression to infection. (a) Treatment starts at the 4th day after an infection and lasts for 9 days. The bacterial load decreases to below the threshold and the infection is prevented. (b) Treatment starts at the 4th day after an infection and lasts for only 6 days. The bacterial load decreases to close to the threshold, but stays above it and increases again. The infection becomes more progressive.
(B) Initiation and interruption of treatment and resistant strains to one antibiotic
The second simulation (Model (2)) addresses the issue of the importance of the timing of antibiotic initiation in the progression to an infection. The model includes the susceptible strain and a strain that is resistant to antibiotic A. Antibiotics are administered for a total of 9 days to optimize the duration of therapy, as shown in Figure 1.
In Figure 2(a), the treatment starts at the first day of an infection and in Figure 2(b), treatment is delayed and starts at the third day of the infection. The treatment occurs with antibiotic A which is ineffective against the resistant strain A. The simulations show that if the initiation of a therapy is delayed the infection will progress. If the antimicrobial therapy starts early, the infection can be treated successfully, with both the susceptible and resistant strains.
(a) Treatment starts at the 1st day after an infection and lasts for 9 days. The bacterial load decreases to below the threshold and the infection is prevented. (b) Treatment starts at the 3rd day after an infection and lasts for 9 days. The bacterial load decreases slightly, but stays above the threshold and increases even during the treatment.
The third simulation (Model (2)) addresses the issue of treatment interruption and its impact on the progression of an infection. The importance of initiating appropriate antibiotic therapy at the start of infection is addressed in these simulations. In both Figures 3(a) and 3(b) the treatment duration is for 9 days, but in Figure 3(a) the treatment is interrupted for one day at day 3 and in Figure 3(b) the interruption occurs at day 5. These simulations demonstrate that early interruption of therapy results in the progression of an infection with the resistant strain since the bacterial load of the resistant strain exceeds the threshold of the minimum infecting dose prior to treatment interruption.
(a) Treatment is interrupted for 1 day at day 3 and continues for the rest of the 9-day therapy. The bacterial load does not change much and increases afterward, the infection is progressive. (b) Treatment is interrupted for 1 day at day 5 and continues for the rest of the 9-day therapy. The bacterial load decreases steadily and the infection can be prevented.
We assume that the patient is harbouring a sensitive strain (AsBs) and a strain that is resistant to antibiotic A but susceptible to antibiotic B (ArBs). The effects of varying treatment sequences with antibiotics A and B are simulated in Figure 4. Treatment with antibiotic A is ineffective and the infection progresses, but subsequent treatment with antibiotic B is effective in eradicating the infection (Figure 4(a)). Concurrent therapy with antibiotics A and B is more effective as the patient is treated with an effective antibiotic against ArBs (Figure 4(b)).
In both simulations, treatment starts at the 4th day after the infection and lasts for 9 days. (a) If antibiotic A fails in the first therapy, then a second treatment with antibiotic B has to be administrated to prevent the infection. (b) A combination of both antibiotics A and B can bring the bacterial level below the threshold and the infection can be prevented.
(C) Delay and sequential antibiotic regimens on the emergence of MDR strains
The impact of early initiation of therapy is addressed in the final model (Model (3)) for treating two-drug resistant strains, since this treatment was effective in eliminating the single-drug resistant strain (Figure 2(a)). We assume that the patient is colonized with three E. coli populations: a strain that is sensitive to both antibiotics A and B (AsBs), a second strain that is sensitive to antibiotic A and resistant to antibiotic B (AsBr), and a third strain which is resistant to antibiotic B and sensitive to antibiotic A (AsBr). The impact of concurrent or sequential therapies with antibiotics A and B and its effect on the emergence of the two-drug resistant strains (ArBr) is assessed.
We consider two scenarios: (i) The patient is treated with the antibiotic A and than immediately with the antibiotic B, followed by both antibiotics simultaneously (Figure 5(a)). (ii) Treatment starts at the first day after the infection (Figure 5(b)). Simulations demonstrate that early initiation of therapy, on day 1, can eliminate the two-drug resistant strain ArBr irrespective of the sequence of antibiotic therapies (Figure 5(b)). In this scenario, the bacterial load of ArBr always remains below threshold. Thus, early initiation of therapy and combined antimicrobial therapy are the key measures to prevent and control infections with multi-drug resistant strains.
(a) Treatment with antibiotic A starts at the 3rd day after the infection and lasts for 10 days, right after that antibiotic B is administrated for 10 days, and at the 40th day both antibiotics A and B are used for 10 days. (b) Same therapies except that the first treatment starts at the 1st day after the infection.
To further simulate the early initiation of therapy and the effect of combined therapy, in Figure 6(a) the patient is treated on the 3rd day after infection with both antibiotics A and B simultaneously. In Figure 6(b) the patient is treated on the 10th day after infection with both antibiotics A and B simultaneously.
(a) A combined therapy with both antibiotics A and B did not start until the 10th day after the infection. After 10 days, the treatment prevents the progression of the infection. (b) A combined therapy of both antibiotics A and B starts at the 3rd day after the infection and lasts for 10 days.
In these simulations (Figures 5 and 6), the antibiotic regimens that eradicate the infection and eliminate the resistant strains are therapies using antibiotics A and B simultaneously. In Figure 5(b) and Figure 6, as opposed to Figure 5(a), the bacterial loads of AsBr and ArBs decrease during therapy with antibiotic A and B, respectively. The decrease in bacterial quantity diminishes the rate of horizontal gene transfer, thereby preventing the emergence of ArBr, despite ineffective therapy against two-drug resistant strain. The efficacy of initiating therapy with both antibiotics simultaneously is persistent even if therapy is delayed (Figure 6(a)). The optimal regimen in treating the two-drug resistant strains is demonstrated in Figure 6(b): early treatment with a combination of two antibiotics.
Antimicrobial exposure is central to the emergence and spread of antimicrobial-resistant bacteria. We have presented a model delineating the interrelated factors of antimicrobial therapy, the immune system and resistance gene transfer, and their effect on the emergence of antimicrobial-resistant bacterial strains. The model delineates novel findings with regards to the timing and sequence of antibiotic therapy in preventing the emergence of resistant strains. First, the model shows that shorter lengths of antibiotic therapy and early interruption of antibiotic therapy provide an advantage for the resistant strains and result in infections caused by these resistant bacteria to progress. Second, the model outlines the optimal antibiotic regimens which prevent the progression of infection with a resistant strain. Our model demonstrates that combination therapy with two antibiotics prevents treatment failure and the emergence of resistant strains, as opposed to sequential therapy. Third, the model shows that a delay in the start of therapy is one of the key factors in promoting the rapid rise in resistant strains. The early timing is even more important than the type of antibiotic regimen since early initiation of antimicrobials will prevent emergence of resistance regardless of whether antibiotics are administered sequentially or concurrently. Using a model system which incorporated population-level factors, D'Agata et al.  also demonstrated that early initiation of therapy is key to preventing the spread of antibiotic-resistant bacteria within a hospital setting.
Population-level models quantifying the factors promoting the spread of resistant bacteria have been instrumental in identifying the preventive strategies most effective at decreasing cross-transmission between patients –. These models have shown the impact of overall antimicrobial exposure on the spread of resistant bacteria. In our individual-level model, we extend the analysis of antimicrobial exposure and treatment regimen to further our understanding of the type and sequence of antimicrobial exposure to provide guidance on the optimal prescribing patterns.
Clinical studies do not provide conclusive evidence of the benefit of combination therapy in the treatment of infections with the exception of tuberculosis and HIV . In these cases, combination therapy is effective due to the high bacterial burden and high rate of emergence of resistance during therapy through mutations . For other bacteria is remains unclear from clinical studies whether combination therapy provides a benefit in reducing resistance. Thus, current guidelines for improving antibiotic use from the Infectious Disease Society of America and the Society for Healthcare Epidemiology do not recommend use of combination therapy . However, we would like to point out that in clinical practice, when laboratory tests confirm the co-existence of different antimicrobial-resistant bacteria with different antimicrobial susceptibility profiles, combination therapy is used to target each pathogen. In our paper, combination therapy referred to the use of two antimicrobials both of which would have efficacy against the infecting organism. In fact, our model supports the use of combination therapy in preventing the emergence of multiple resistant strains within an individual , , , , . The effect of widespread combination therapy on the emergence and spread of resistant bacteria to other patients however was not addressed. Future models should incorporate both individual- and population level analysis to determine the impact of the spread of resistant bacteria within a community or hospital setting.
For the purpose of numerical simulations, in Model (1) we assumed that the growth of bacteria satisfies the specific logistic equation and the immune response satisfies the specific Monod function. It should be pointed out that Model (1) can be generalized to include a general bacteria growth term g(B) and a general immune response function p(B), where g(B) is continuously differentiable and satisfies g(0) = g(K) = 0 for a positive constant K, and g′(0)>0, g′(K)<0. p(B) is also continuously differentiable and satisfies p(B)>0 and p′(B)>0. Similar extensions apply to Models (2) and (3).
Our conclusions were mainly based on the numerical simulations of Models (1)–(3). It would be very interesting and helpful to perform qualitative analysis of these models and provide theoretical support for our numerical simulations and thus our conclusions. Studies on the dynamics of these models are under consideration and will be reported somewhere else.
Conceived and designed the experiments: ED MMDR PM DO. Analyzed the data: ED MMDR PM SR. Contributed reagents/materials/analysis tools: ED MMDR PM DO SR. Wrote the paper: ED MMDR PM SR.
- 1. Cassel GH, Mekalanos J (2001) Development of antimicrobial agents in the era of new and reemerging infectious diseases and increasing antibiotic resistance. JAMA 285: 601–605.
- 2. Levy SB, Marshall B (2004) Antibacterial resistance worldwide: Causes, challenges and responses. Nat Med 10: S122–S129.
- 3. Spellberg B, et al. (2008) The epidemic of antibiotic-resistant infections: a call to action for the medical community from the Infectious Diseases Society of America. Clin Infect Dis 46: 155–164.
- 4. Siegel JD, Rhinehart E, Jackson M, Chiarello L (2007) Management of multidrug-resistant organisms in health care settings, 2006. Am J Infect Control 35: S165–193.
- 5. Daxboeck F, et al. (2006) Economic burden associated with multi-resistant Gram-negative organisms compared with that for methicillin-resistant Staphylococcus aureus in a university teaching hospital. J Hosp Infect 62: 214–218.
- 6. Schwaber MJ, et al. (2006) Clinical and economic impact of bacteremia with extended- spectrum-beta-lactamase-producing Enterobacteriaceae. Antimicrob Agents Chemother 50: 1257–1262.
- 7. Institute of Medicine (1998) Antimicrobial Resistance: Issues and Options. Washingto DC: National Academic Press.
- 8. Klevens RM, et al. (2007) Invasive methicillin-resistant Staphylococcu aureus infections in the United States. JAMA 298: 1763–1771.
- 9. Austin DJ, Anderson RM (1999) Studies of antibiotic resistance within the patient, hospitals and the community using simple mathematical models. Phil Trans R Soc Lond B 354: 721–738.
- 10. Bonhoeffer S, Liptsitch M, Levin BR (1997) Evaluating treatment protocols to prevent antibiotic resistance. Proc Natl Acad Sci USA 94: 12106–12111.
- 11. Bergstrom CT, Lo M, Lipsitch M (2004) Ecological theory suggests that antimicrobial cycling will not reduce antimicrobial resistance in hospitals. Proc Natl Acad Sci USA 101: 13285–13290.
- 12. D'Agata EMC, Magal P, Olivier D, Ruan S, Webb GF (2007) Modeling antibiotic resistance in hospitals: The impact of minimizing treatment duration. J Theor Biol 249: 487–499.
- 13. Boldin B, Bonten MJ, Diekmann O (2007) Relative effects of barrier precautions and topical antibiotics on nosocomial bacterial transmission: Results of multi-compartment models. Bull Math Biol 69: 2227–2248.
- 14. Consortium REX (2007) Structure of the scientific community modelling the evolution of resistance. PLoS ONE 2(12): e1275. doi:10.1371/journal.pone.0001275.
- 15. Temime L, et al. (2008) The rising impact of mathematical modeling in epidemiology: Antibiotic resistance research as a case study. Epidemiol Infec 136: 289–298.
- 16. Webb GF, D'Agata EMC, Magal P, Ruan S (2005) A model of antibiotic-resistant bacterial epidemics in hospitals. Proc Natl Acad Sci USA 102: 13343–13348.
- 17. Bonten MJM, Austin DJ, Lipsitch M (2001) Understanding the spread of antibiotic resistant pathogens in hospitals: mathematical models as tools for control. Clin Infect Dis 33: 1739–1746.
- 18. Grundmann H, Hellriegel B (2006) Mathematical modeling: A tool for hospital infection control. Lancet Infect Dis 6: 39–45.
- 19. Levin BR (2001) Minimizing potential resistance: A population dynamics view. Clin Infect Dis 33: S161–S169.
- 20. Austin DJ, White NJ, Anderson RM (1998) The dynamics of drug action on the within-host population growth of infectious agents: melding pharmacokinetics with pathogen population dynamics. J Theoret Biol 194: 313–339.
- 21. Imran M, Smith HL (2007) The dynamics of bacterial infection, innate immune response and antibiotic treatment. Discrete Cont Dynamical Systems B 8: 127–143.
- 22. Lipsitch M, Levin BR (1997) The population dynamics of antimicrobial chemotherapy. Antimicrob Agent Chemother 41: 363–373.
- 23. Levin BR, Rozen DE (2006) Non-inherited antibiotic resistance. Nat Rev Microbiol 4: 556–562.
- 24. Smets BF, Barkay T (2005) Horizontal gene transfer: Perspectives at a crossroads of scientific disciplines. Nat Rev Microbiol 3: 675–678.
- 25. Walsh C (2000) Molecular mechanisms that confer antibacterial drug resistance. Nature 406: 775–781.
- 26. Monack DM, Mueller A, Falkow S (2004) Persistent bacterial infections: The interface of pathogen and the host immune system. Nat Rev Microbiol 2: 747–765.
- 27. Freter R, et al. (1983) Survival and implantation of Escherichia coli in the intestinal tract. Infect Immun 39: 686–703.
- 28. Gibbons RJ, Kapsimalis B (1967) Estimates of the overall rate of growth of the intestinal microflora of hamsters, guinea pigs, and mice. J Bacteriol 93: 510–512.
- 29. Hartl DL, Dykhuizen DE (1984) The population genetics of Escherichia coli. Annu Rev Genet 18: 31–68.
- 30. Pilyugin SS, Antia R (2000) Modeling immune response with handling time. Bull Math Biol 62: 869–890.
- 31. Poulsen LK, et al. (1995) Physiological state of Escherichia coli BJ4 growing in the large intestines of streptomycin-treated mice. J Bacteriol 177: 5840–5845.
- 32. Sorensen TL, et al. (2001) Transient intestinal carriage after ingestion of antibiotic-resistant Enterococcus faecium from chicken and pork. N Engl J Med 345: 1161–1166.
- 33. Bahl MI, et al. (2004) Quantification of plasmid loss in Escherichia coli cells by use of flow cytometry. FEMS Microbiol Lett 232: 45–49.
- 34. Haneda T, Okada N, Miki T, Danbara H (2004) Sequence analysis and characterization of sulfonamide resistance plasmid pRF-1 from Salmonella enterica serovar Choleraesuis. Plasmid 52: 218–224.
- 35. Sorensen SJ, et al. (2005) Studying plasmid horizontal transfer in situ: a critical review. Nat Rev Microbiol 3: 700–710.
- 36. Smith MA, Bidochka MJ (1998) Bacterial fitness and plasmid loss: the importance of culture conditions and plasmid size. Can J Microbiol 44: 351–355.
- 37. Dutta C, Pan A (2002) Horizontal gene transfer and bacterial diversity. J Biosci 27: 27–33.
- 38. Leverstein-van Hall MA, et al. (2003) Multidrug resistance among Enterobacteriaceae is strongly associated with the presence of integrons and is independent of species or isolate origin. J Infect Dis 187: 251–259.
- 39. Livermore DM, et al. (2007) CTX-M: changing the face of ESBLs in Europe. J Antimicrob Chemother 59: 165–174.
- 40. Walsh TR (2005) The emergence and implications of metallo-beta-lactamases in Gram-negative bacteria. Clin Microbiol Infect 11: (Suppl 6)2–9.
- 41. Kurland GC, Canback B, Berg OG (2003) Horizontal gene transfer: a critical view. Proc Natl Acad Sci USA 100: 9658–9662.
- 42. Spratt BG, Hanage WP, Feil EJ (2001) The relative contributions of recombination and point mutation to the diversification of bacterial clones. Curr Opin Microbiol 4: 602–606.
- 43. Waters VL (1999) Conjugative transfer in the dissemination of beta-lactam and aminoglycoside resistance. Front Biosci 4: D433–456.
- 44. Lenski RE (1998) Bacterial evolution and the cost of antibiotic resistance. Int Microbiol 1: 265–270.
- 45. Nordstrom K (2006) Plasmid R1–replication and its control. Plasmid 55: 1–26.
- 46. Nordstrom K, Aagaard-Hansen H (1984) Maintenance of bacterial plasmids: comparison of theoretical calculations and experiments with plasmid R1 in Escherichia coli. Mol Gen Genet 197: 1–7.
- 47. Dellit TH, et al. (2007) Infectious Diseases Society of America and the Society for Healthcare Epidemiology of America guidelines for developing an institutional program to enhance antimicrobial stewardship. Clin Infect Dis 44: 159–177.
- 48. Cottarel G, Wierzbowski J (2007) Combinatioon drugs, an emerging option for antibacterial therapy. TRENDS Biotechnol 25: 547–555.
- 49. Lipsitch M, Bergstrom CT (2002) Modeling of antibiotic resistance in the ICU–U.S. slant. In: Weinstein RA, Benten M, editors. Infection Control in the ICU Environment. Dordrecht, The Netherlands: Kluwer. pp. 1–16.
- 50. Reluga TC (2005) Simple models of antibiotic cycling. Math Med Biol 22: 187–208.