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Drug Combinations against Borrelia burgdorferi Persisters In Vitro: Eradication Achieved by Using Daptomycin, Cefoperazone and Doxycycline

  • Jie Feng,

    Affiliation Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, United States of America

  • Paul G. Auwaerter,

    Affiliation Fisher Center for Environmental Infectious Diseases, School of Medicine, Johns Hopkins University, Baltimore, Maryland, United States of America

  • Ying Zhang

    Affiliation Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, United States of America

Drug Combinations against Borrelia burgdorferi Persisters In Vitro: Eradication Achieved by Using Daptomycin, Cefoperazone and Doxycycline

  • Jie Feng, 
  • Paul G. Auwaerter, 
  • Ying Zhang


Although most Lyme disease patients can be cured with antibiotics doxycycline or amoxicillin using 2-4 week treatment durations, some patients suffer from persistent arthritis or post-treatment Lyme disease syndrome. Why these phenomena occur is unclear, but possibilities include host responses, antigenic debris, or B. burgdorferi organisms remaining despite antibiotic therapy. In vitro, B. burgdorferi developed increasing antibiotic tolerance as morphology changed from typical spirochetal form in log phase growth to variant round body and microcolony forms in stationary phase. B. burgdorferi appeared to have higher persister frequencies than E. coli as a control as measured by SYBR Green I/propidium iodide (PI) viability stain and microscope counting. To more effectively eradicate the different persister forms tolerant to doxycycline or amoxicillin, drug combinations were studied using previously identified drugs from an FDA-approved drug library with high activity against such persisters. Using a SYBR Green/PI viability assay, daptomycin-containing drug combinations were the most effective. Of studied drugs, daptomycin was the common element in the most active regimens when combined with doxycycline plus either beta-lactams (cefoperazone or carbenicillin) or an energy inhibitor (clofazimine). Daptomycin plus doxycycline and cefoperazone eradicated the most resistant microcolony form of B. burgdorferi persisters and did not yield viable spirochetes upon subculturing, suggesting durable killing that was not achieved by any other two or three drug combinations. These findings may have implications for improved treatment of Lyme disease, if persistent organisms or detritus are responsible for symptoms that do not resolve with conventional therapy. Further studies are needed to validate whether such combination antimicrobial approaches are useful in animal models and human infection.


Lyme disease, caused by the spirochetal bacterium Borrelia burgdorferi, is the leading tick-borne infection of humans in the US [1]. The clinical manifestations of early Lyme disease are most often characterized by an erythema migrans rash often accompanied by flu-like symptoms. An inflammatory arthritis or neurological dysfunction can be frequent sequelae of untreated infection. Although the majority of patients with Lyme disease can be cured with antibiotics doxycycline or amoxicillin used for 2–4 weeks durations, a subset of patients experience persistent symptoms despite antimicrobial therapy including fatigue, neurocognitive difficulties or musculoskeletal pains. When symptoms last longer than 6 months after antibiotic treatment, this has been proposed as a non-infectious, post-treatment Lyme disease syndrome (PTLDS) due to the inability to find viable, remaining organisms and lack of substantial efficacy with longer term monotherapy with ceftriaxone, doxycycline or amoxicillin [13].

It is unclear what mechanisms promulgate this condition in these patients. Concepts raised have included host responses, although slow or ineffective killing of B. burgdorferi persisters has been voiced as a possible explanation though evidence of viable organisms present in PTLDS is lacking [4]. While PTLDS has only subjective symptom complexes, about 10% of patients with late Lyme arthritis have objective, persistent joint swelling despite antibiotic therapy [5]. Though part of this response may include autoimmune mimicry induced by B. burgdorferi in certain hosts, an additional explanation rests on immunological responses driven by continued infection or presence of antigenic debris [6]. The question of whether B. burgdorferi might still persist in some patients with suboptimal immune clearance after antibiotic therapy and further evade host immune clearance has been raised by some but is controversial [7, 8].

In various animal models such as mice, dogs and monkeys, antibiotic therapy with doxycycline, ceftriaxone or tigecycline could not fully eradicate detection of B. burgdorferi including by xenodiagnosis though viable organisms could not be cultured in conventional culture medium [912]. Recently demonstrated, post-antibiotic persistence was present with resurgence of non-culturable B. burgdorferi DNA found in mice 12 months after antibiotic treatment [11]. These observations suggest some form of persistent B. burgdorferi that antibiotic dosings employed in these animal models are not able to completely eradicate, though antibiotic levels in these animals may have been inadequate. A number of prospective, randomized clinical studies have found neither significant beneficial effect of additional prolonged antibiotic therapy with conventionally employed antibiotic monotherapy nor evidence of continued presence of B. burgdorferi in patients with long-term symptoms [3, 13]. Intriguingly, a recent study in humans demonstrated the recovery of B. burgdorferi DNA by xenodiagnosis in a single patient with PTLDS despite antibiotic treatment [14]. One study did report some improvement in fatigue symptoms with prolonged intravenous administration with ceftriaxone, though ultimately not thought to be worth the risks to administer for this benefit alone [15]. Ceftriaxone has recently been shown to be more active against B. burgdorferi persisters experimentally than doxycycline or amoxicillin [16].

B. burgdorferi is capable of a complex life style in vitro characterized by multiple pleomorphic forms including spirochetal, spheroplast (or L-form), and cyst or round body (RB) form and microcolony forms [8, 1720]. RB forms appear as coccoid atypical variants of B. burgdorferi, forming under experimental stress conditions such as starvation or antibiotic treatment in culture [17, 21]. These are relatively refractory to killing by many antibiotics including doxycycline and amoxicillin [16, 17], and can revert to classical helical spirochetal forms in fresh nonantibiotic-containing subculture [17, 22]. Atypical cystic or granular forms have been described in humans [19], but there is neither good evidence that such morphologic variants are common with human infection nor that additional antibiotics improves patients with persistent symptoms after initial treatment [23]. While frontline drugs doxycycline and amoxicillin kill replicating spirochetal form of B. burgdorferi quite effectively, they have little activity against non-replicating persisters or biofilm-like aggregates or microcolonies of B. burgdorferi enriched within stationary phase cultures [16, 24].

Taking advantage of a newly developed SYBR Green I/PI viability assay, we recently screened an FDA-approved drug library against stationary phase B. burgdorferi persisters and identified 27 drug candidates that individually have higher activity than the currently recommended Lyme antibiotics doxycycline or amoxicillin [16]. Among the top 27 confirmed drug candidates, daptomycin, clofazimine, carbomycin, sulfa drugs such as sulfamethoxazole, and certain cephalosporins such as cefoperazone showed higher activity against B. burgdorferi persisters [16]. Interestingly, some drug candidates such as daptomycin and clofazimine with the highest activity against non-growing persisters had poor activity against actively growing B. burgdorferi with high MICs, at 12.5–25 μg/ml and 6.25 μg/ml, respectively [16]. Although these drug candidates active against persisters may not have good activity when used alone due to their poor activity against growing B. burgdorferi, it raises the question whether they may be used with another antibiotic such as doxycycline that is effective at inhibiting or killing the growing forms of B. burgdorferi. Such combinations may yield more effective treatment of Lyme disease.

Experimentally, since a stationary phase culture contains mixed populations of growing and non-growing bacteria that have different morphological variants such as round bodies and microcolonies that are tolerant to antibiotics [16, 17, 24], it is most likely that a single drug may not effectively kill all bacterial populations including morphological variants. In this study, we evaluated a range of drug combinations with the aim to identify optimal drug combinations that are most effective at killing B. burgdorferi persisters.


B. burgdorferi culture possesses different proportions of morphological variants including round body and microcolony forms as the culture ages

As shown in our previous study [16], the stationary phase culture was enriched with morphological variants such as round body form and biofilm-like aggregated microcolony form in increasing proportions in contrast to individual spirochetes found in log phase culture (Fig. 1). To more accurately assess the proportion of different morphological variant forms, we examined representative images of each sample taken from cultures of different ages to measure the percentage of different morphological forms of B. burgdorferi (Table 1). We found that the log phase (3 day old) B. burgdorferi culture consisted almost entirely of spirochetal form (96%), with few round body form (4%) and no aggregated microcolony form (Fig. 1A). In the 7 day old stationary phase culture of B. burgdorferi, there were 38% spirochetal form, 23% round body form, and 39% microcolony form (Fig. 1B). When B. burgdorferi stationary phase culture was cultured for 10 days, the percentage of the microcolony form increased to 64%, and the spirochetal form and the round body form were 20% and 16%, respectively (Fig. 1C).

Figure 1. Representative images of 3 day old log phase (A), 7 day (B) and 10 day (C) old stationary phase B. burgdorferi cultures.

The B. burgdorferi cultures of varying ages were stained with SYBR Green I/PI assay and observed under the microscope (400 × magnification). The arrows indicate the spirochete (s), round body (r), and microcolony (m) forms of B. burgdorferi in stationary phase cultures.

Table 1. Varying degrees of susceptibility of different forms of B. burgdorferi to commonly used Lyme antibiotics.

Persister frequencies in log phase and stationary phase cultures

Because B. burgdorferi does not form colonies easily on agar plates, the conventional method to assay persister frequency after antibiotic exposure by calculating the percentage of bacteria killed by a bacteriocidal antibiotic cannot be applied to B. burgdorferi. Therefore, we assessed the frequency of B. burgdorferi persisters in log phase and stationary phase cultures using SYBR Green I/PI viability assay after exposure of the cultures to antimicrobials. We used E. coli culture as a control after exposure to antibiotics to validate the SYBR Green I/PI viability assay for persister frequency assessment. The persister frequency of the log phase E. coli culture with exposure to 50 µg/ml amoxicillin for 3 hours was 4.4% for the SYBR Green I/PI assay and 0.9% for the CFU assay (Table 1). Using SYBR Green I/PI assay the persister frequencies of B. burgdorferi ranged from 5–10% for log phase cultures, but ranged 16–27% in stationary phase cultures treated with ceftriaxone, doxycycline or amoxicillin (Table 1). Given the SYBR Green I/PI viability assay seemed to give about 5 fold (4.4%/0.9%) overestimation of the persister frequency over the CFU assay with the E. coli control, the real persister frequencies of B. burgdorferi are likely to be in the range of 1–2% for B. burgdorferi log phase cultures and 3–5.5% for stationary phase cultures.

Microcolony form is more tolerant to antibiotics than free-living spirochetal and round body forms

Our previous study showed that the stationary phase B. burgdorferi was more resistant or tolerant to antibiotics than the log phase culture [16]. In view of the heterogeneity of the morphological variants of the stationary phase culture (Fig. 1B, 1C), we determined the susceptibility of different variant forms of B. burgdorferi to commonly employed antibiotics for Lyme disease (doxycycline, amoxicillin, and ceftriaxone) in a more quantitative manner. Interestingly, we found that different variant forms had differing susceptibilities to these antibiotics (Table 1). The log phase culture (3 day old) primarily consisting of spirochetal form was highly susceptible to these antibiotics, whereas the stationary phase (7 and 10 day old) cultures comprising mainly of round body and biofilm-like microcolony forms were less sensitive to these antibiotics, as shown by increasing proportion of viable cells remaining after the antibiotic exposure (Table 1).

When the 10 day old stationary phase culture, consisting of mixed populations of spirochetal form in minor portions and round body form and microcolony form in major proportions, was exposed to various antibiotics, the microcolony form was more tolerant to antibiotics than the free-living spirochetal form and the round body form. Daptomycin at 10 μg/ml, a drug with high activity against B. burgdorferi persisters [16] killed all planktonic forms (spirochetal and round body) of stationary phase cells (Fig. 2A, h) but could only partially kill the microcolony form of B. burgdorferi persisters as shown by the presence of significant numbers of red cells (dead cells) mixed with some green cells (viable cells) in the microcolony (Fig. 2A, g). The other persister active drug cefoperazone [16] had weaker activity than daptomycin since it had some activity for the planktonic form cells (52% cells were green cells) but little activity for the microcolony form of persisters where most of the microcolony cells remained as green (live) cells (Fig. 2A, e). In contrast, doxycycline had the least activity against stationary phase B. burgdorferi persisters where about 71% free-living planktonic cells including spirochetal form and round body form were not killed by doxycycline as shown by green (live) cells (Fig. 2A, Panel d) but the microcolony form was almost all live (Fig. 2A, Panel c). These findings suggest there is a differential tolerance or resistance in different variant forms of persisters in vitro (spirochetal form, round body form and microcolony in increasing order of resistance) to both current Lyme disease antibiotics and also even persister active antibiotics daptomycin and cefoperazone, with the microcolony form being the most tolerant to antibiotics.

Figure 2. Effect of antibiotics alone and in combinations on aggregated microcolony form and planktonic forms of B. burgdorferi.

Stationary phase B. burgdorferi culture (10 day old) was treated with 10 μg/ml drugs (labeled on the image) for 7 days followed by staining by SYBR Green I/PI assay. Green cells indicate live cells whereas red cells dead cells. (A) B. burgdorferi aggregated microcolony (MC) form was more resistant to different antibiotics or their combinations than planktonic form (round body and spirochetal form) (PT) as observed by fluorescence microscopy at 400 × magnification. (B) Susceptibility of B. burgdorferi microcolony form to antibiotics and antibiotic combinations was assessed by fluorescence microscopy at 200 × magnification. The luminance of individual RB is much weaker than that of microcolony, which makes the individual cells hard to be observed when the microcolonies were being examined. Abbreviation: Dox, doxycycline; CefP, cefoperazone; Cfz, clofazimine; Dap, daptomycin; Smx, sulfamethoxazole; Cab, carbencillin; Car, carbomycin.

Effect of drug combinations on stationary phase B. burgdorferi persisters

Despite the powerful anti-persister activity of daptomycin and cefoperazone, they had limited activity to kill the most resistant microcolony form of persisters at 10 μg/ml (Fig. 2). These findings suggest that these FDA-approved persister drugs may have limited potential if used alone against B. burgdorferi. To identify more effective drug combinations that kill different variant forms of B. burgdorferi stationary phase persisters, we evaluated 81 drug combinations including FDA-approved drugs on a 10 day old B. burgdorferi culture enriched with microcolony and round body forms at 10 μg/ml of each individual drug (close to or lower than MIC). The results showed that some drug combinations were indeed much more effective than single drugs alone (Table 2). Among them, daptomycin highlighted itself as having the best activity against stationary phase B. burgdorferi persisters when combined with other drugs.

Table 2. Effect of drug combinations on stationary phase B. burgdorferi culturea.

Daptomycin (10 μg/ml) alone could not eliminate the microcolonies by itself (Fig. 2A, g), but daptomycin in combination with doxycycline or beta-lactams was very effective against B. burgdorferi planktonic persisters and also against microcolonies (Table 2, Fig. 2B). However, daptomycin in combination with doxycycline or cefoperazone produced better bacteriocidal activity against the microcolony form than either of these agents alone or drug combinations without daptomycin, such as doxycycline + cefoperazone or even doxycycline + cefoperazone + sulfamethoxazole as shown by more red cells (dead cells) being produced after treatment with daptomycin drug combinations (Fig. 2B, panel f, g, i, j, k and l). Nevertheless, daptomycin used as part of two drug combinations did not completely eradicate the more resistant microcolony form of persisters (Fig. 2B, panel f and g). Remarkably, daptomycin in a three drug combination with doxycycline and cefoperazone eradicated all microcolonies, whereas other daptomycin-containing three drug combinations using cefoperazone + either sulfamethoxazole or carbenicillin or carbomycin or clofazimine still had some traces of green/yellow cells remaining after treatment (Fig. 2B, panel h, i, j, k and l).

In addition to doxycycline and beta-lactams, some clinical drugs such as vancomycin, ofloxacin, clarithromycin, and hydroxychloroquine, which are not recommended for treating Lyme disease, also exhibited some weak activity on the 10 day old stationary phase B. burgdorferi culture, either alone or in combination with doxycycline and cefoperazone. Rifampin alone did not have significant activity for B. burgdorferi persisters but in combination with doxycycline, amoxicillin, ceftriaxone or cefoperazone had higher activity for B. burgdorferi persisters (Table 2). Among all the other non-daptomycin drug combinations, the only two drug combinations that are close to daptomycin drug combinations in killing B. burgdorferi persisters were Dox + either cefoperazone or miconazole or sulfamethoxazole (Table 2). In addition, clofazimine showed good activity against stationary phase B. burgdorferi persisters when combined with doxycycline and cefoperazone (Table 2). It is worth noting that the activity of carbenicillin, vancomycin, ofloxacin, clarithromycin, tigecycline, nisin, and hydroxychloroquine when combined with doxycycline only marginally enhanced doxycycline activity and their anti-persister activities were not as effective as when they were combined with daptomycin (Table 2).

Subculture of antibiotic-treated B. burgdorferi

In our previous study, we found that daptomycin at 50 μM (equivalent to 81 μg/ml, a high dose to achieve in humans) had remarkable anti-persister activity that seemed to kill all B. burgdorferi persisters, as shown by all red cells stained by PI (Fig. 3D in Feng et al., 2014)[16]. To confirm that these red cells are indeed dead, we performed subculture test in fresh BSK-H medium and found that indeed these red cells treated with 50 μM daptomycin were dead as they failed to grow in the subculture test as shown by lack of any visible green spirochetes after 15 day subculture (data not shown). Having established the subculture test as a reliable assay for assessing the viability of antibiotic treated cells, we next proceeded to validating the above results obtained with select antibiotics or antibiotic combinations that produced the best bacteriocidal effects against persisters (Fig. 2).

Figure 3. Subculture (15 days) of 10 day old B. burgdorferi stationary phase culture treated with different antibiotics alone or in combinations.

Representative images were taken with fluorescence microscopy (400 × magnification) using SYBR Green I/PI staining. Only Dox+Dap+CefP completely killed all forms including the microcolony form of B. burgdorferi persisters as shown by lack of any viable green spirochetal form after 15 day subculture. Abbreviation: Dox, doxycycline; CefP, cefoperazone; Cfz, clofazimine; Dap, daptomycin; Smx, sulfamethoxazole.

To do this, we subjected a 7-day old stationary phase B. burgdorferi culture to exposure with select antibiotics and antibiotic combinations for 7 days, followed by subculture in fresh BSK-H medium for 7 days or 15 days. Microscope counting showed that drug-free controls and samples treated with single drug grew in the 7 day subculture. Samples treated with two drug combinations grew more slowly (Table 3). However, after 7 day subculture, all the three drug combinations, e.g., doxycycline+daptomycin+ either cefoperozone or sulfamethoxazole or clofazimine did not show any sign of growth as no visible spirochetal form was observed, whereas other drug combinations all had visible green spirochetes under the microscope. After 15 day subculture, there were about 6×106 spirochetes in the control sample and about 5×106 spirochetes in doxycycline or amoxicillin treated samples (Table 3). Interestingly, daptomycin alone, or two drug combinations doxycycline+cefoperazone and doxycycline+daptomycin, or even three drug combination doxycycline+daptomycin+clofazimine, could not sterilize the B. burgdorferi persisters, as they all had visible spirochetes growing after subculture (Fig. 3).

Table 3. Subculture tests to assess the viability of drug-treated stationary phase B. burgdorferi.a

However, doxycycline+daptomycin+sulfamethoxazole significantly reduced the number of spirochetes with very few spirochetes being visible after 15 day subculture (Fig. 3h). By far the best result was achieved with daptomycin in combination with doxycycline and cefoperazone, which killed all B. burgdorferi persisters with no viable bacteria observed (Fig. 3i). This is demonstrated by a decrease in the green/red fluorescence and lack of any viable green spirochetes, in contrast to samples treated with other drugs alone or drug combinations which all had higher Green/Red fluorescence and visible green spirochetal bacteria (Table 3, Fig. 3). Importantly, this drug combination could eliminate not only planktonic stationary phase B. burgdorferi persisters (spirochetal and round body forms) but also the more resistant biofilm-like microcolonies (Table 3, Fig. 3). Subculturing the sample treated with this drug combination showed no sign of any detectable organisms by microscopy (detection limit < 105) even after 15 days of subculture (Table 3, Fig. 3i). These findings indicate that the microcolony structures are not eliminated by monotherapy (doxycycline, amoxicillin, persister active drugs), two drug combinations or even some three drug combinations, but could be eradicated by the drug combination of doxycycline, cefoperazone and daptomycin.


In this study, we conducted the first in vitro drug combination study using persister active drugs [16] in combination with the currently recommended Lyme antibiotics such as doxycycline or amoxicillin or other antibiotics to achieve more effective eradication of B. burgdorferi persisters. We found it is more effective to kill B. burgdorferi persisters by drug combination than single antibiotic, but bacteriocidal activity depended on the particular antibiotics used (Table 2). It is interesting to note that although persister active antibiotics such as the lipopeptide daptomycin and beta-lactam cefoperazone themselves were quite active against planktonic B. burgdorferi persisters (both spirochetal and round body forms), they were unable to eradicate the more resistant microcolony form when used alone or even in combination with some drugs (Fig. 2). Previous studies showed that tinidazole, metronidazole, and tigecycline were more active against B. burgdorferi round body and microcolonies than doxycycline and amoxicillin, but they could not completely kill the microcolonies even at high concentrations of antibiotics [24], indicating the limited activity of these individual antibiotics against B. burgdorferi persisters. Although tigecycline was the most active antibiotic against the round body form compared with tinidazole and metronidazole in that study [24], we found that by itself tigecycline was not very effective at killing the biofilm-like microcolonies (Table 2).

Remarkably, we found that daptomycin in combination with doxycycline and cefoperazone was able to completely eradicate the most resistant microcolonies (Fig. 2), and this was further confirmed by subculture studies which showed lack of any growth (Fig. 3). While various drug combinations showed improved activity against stationary phase B. burgdorferi persisters, daptomycin combinations had the best activity among drug combinations against persisters (Table 2). The only non-daptomycin regimens that were close to daptomycin combinations contained cefoperazone (Fig. 2, Table 2). Unexpectedly, other antibiotics such as sulfamethoxazole, clofazimine and miconazole also had more activity against stationary phase B. burgdorferi persisters in combination with doxycycline and cefoperazone. These drugs are not currently used as antibiotics for treatment of Lyme disease clinically [2, 25]. Although sulfa drugs are bacteriostatic when used alone for growing bacteria, they could kill non-growing round body or aggregated microcolony form of B. burgdorferi during long-term treatment. Clofazimine with high anti-persister activity improved the combination with daptomycin or daptomycin plus doxycycline (Table 2) which may be due to its multiple mechanisms of action including membrane destabilization, reactive oxygen species production, and inhibition of membrane energy metabolism in M. tuberculosis [26]. We also found that miconazole, an imidazole antifungal drug, had high activity against B. burgdorferi persisters when combined with doxycycline and cefoperazone (Table 2). Miconazole has been shown to alter the integrity of lipid membrane [27] and therefore may facilitate the penetration of other drugs such as doxycycline and cefoperazone for improved activity against B. burgdorferi persisters (Table 2).

The complete eradication of the B. burgdorferi biofilm-like microcolonies by the three drug combination of daptomycin+doxycycline+cefoperazone has not been achieved with any single, dual or even some three drug combinations in this study or any other previous studies. The mechanism by which this three drug combination was able to achieve this remarkable activity is worth commenting. Doxycycline and cefoperazone inhibits protein synthesis and cell wall peptidoglycan synthesis respectively [21]. Either may be needed to kill the growing forms present in the B. burgdorferi microcolonies or those occasionally revert to growing forms from microcolonies, but these drugs are less effective against the round body or microcolony persisters themselves [16, 17, 24]. This inability could be because of the reduced drug penetration into the microcolony structure, efflux mechanism [17, 28], or decreased protein or cell wall synthesis in persisters. The high efficacy of daptomycin against B. burgdorferi persisters could be due to its effect on membrane disruption or depolarization, resulting in a loss of membrane potential and inhibition of energy metabolism [16, 29], which is required for persister survival [30]. Prior studies have suggested that the combination of beta-lactams plus daptomycin increase effectiveness even with daptomycin resistant Gram-positive infections [31]. While drugs traditionally active against Gram-positive organisms are not thought to have activity against B. burgdorferi, in vitro studies have previously documented activity with drugs such as vancomycin [32, 33] but not teicoplanin or daptomycin, though this study was performed examining not persisters but log phase cultures. Though daptomycin is not used for Gram-negative pathogens, a drug such as colistin has been suggested to improve polyanionic lipopeptide activity due to outer membrane permeabilization [34]. Regardless, our studies suggest that combined use of these agents that kill or inhibit both growing organisms (doxycycline and cefoperazone) and non-replicating organisms (daptomycin and cefoperazone) may be important for good activity against the highly resistant microcolonies, which is consistent with the proposition to use drugs targeting both growing and non-growing microbial populations for improved treatment of persistent infections [30].

It is worth noting that short term incubation in subculture studies of antibiotic treated B. burgdorferi is not sufficient to assess the stable eradication of persisters. This is shown by 7 day subculture of B. burgdorferi persister cells treated with 3 drug combinations daptomycin+doxycycline+cefoperazone or Smx or Cfz, which all produced no detectable levels of any residual growth (Table 3). However, extended incubation to 15 days of subculture showed that only daptomycin, doxycycline and cefoperazone combination was able to completely eradicate biofilm-like microcolonies with no detectable spirochetes (Fig. 3i). These findings suggest that longer incubation to 15 days or more in post-antibiotic exposure may be needed to thoroughly assess the drug combinations that stably eradicate the persister forms without relapse. The subculture results do validate the SYBR Green I/PI viability assay and is a useful and more sensitive technique to assess the viability of B. burgdorferi persisters or microcolonies after drug treatment in identifying optimal drug combinations for killing more resistant persisters.

B. burgdorferi spirochetes could develop morphological variants as in vitro cultures age or are subjected to adverse conditions [16, 17, 20, 24, 35]. The proportions of these variants have not been well characterized over time in culture conditions. With careful measurement, the percentages of morphological variants were determined as they transitioned from spirochetes to progressively round body form to then microcolony form as log phase culture grew to stationary phase (7–10 days) (Fig. 1). Although previous studies reported the round body form or biofilm-like microcolony form is more resistant to antibiotics [16, 17, 24], their relative resistance was not fully studied. Here, we found a hierarchy or varying levels of stationary phase B. burgdorferi persisters in terms of their levels of persistence as the morphology of the variants changes from spirochetes, to round body, and to microcolony forms, with increasing antibiotic tolerance (Table 1). Future studies are needed to address the molecular basis of morphological transitions and their relationship to persistence in vivo.

The finding that persister frequencies are higher in stationary phase B. burgdorferi cultures than in log phase cultures is consistent with studies in other bacteria. However, the persister frequencies in B. burgdorferi log phase culture (5–10%) and stationary phase cultures (16–27%) determined by SYBR Green I/PI assay seem to be higher than those reported for E. coli [36]. CFU is the gold standard of current persister assays for bacteria that form colonies readily on agar plates. However, because B. burgdorferi does not form colonies easily on plates, especailly after antibiotic treatment, we have to rely on viability staining using microscope counting of green cells stained by viability dye SYBR Green even though CFU and viability by viability staining are two different measures of bacterial viability. To more accurately assess the percentage of B. burgdorferi persisters after antibiotic treatment, we used E. coli as a control to determine the correlation between the CFU assay and the SYBR Green assay. We found that the SYBR Green I/PI assay tended to overestimate the persister frequency by about 5 fold based on the E. coli data (4.4% persisters by SYBR Green viability assay versus 0.9% persisters by CFU assay) (Table 1). The overestimation of the persister frequency by SYBR Green I/PI assay may be due to some live persisters and/or injured cells that are unable to recover and form colonies on agar plates. Assuming the same correlation holds true for B. burgdorferi, the converted persister frequencies of 1–2% and 3–5% for B. burgdorferi log phase and stationary phase cultures would still suggest higher persister frequencies with B. burgdorferi than E. coli, which has 0.001% persisters in log phase and 1% in stationary phase [36]. In this study, the log phase E. coli had a considerably higher persister frequency of 0.9% by the CFU assay, and this could reflect differences in the higher inoculum and use of non-shaking condition, which could greatly increase the persister frequency. On the other hand, the higher persister frequencies for B. burgdorferi than E. coli could indicate that B. burgdorferi may form persisters more readily or reflect differences in the speed of growth of the organisms, the age of culture when antibiotic is added, and the dilution factor which affects the number of persisters carried over during the subculture. In addition, we found that the persister frequencies vary according to antibiotic exposure, with the more effective antibiotic ceftriaxone having a lower persister frequency than amoxicillin (Table 1), a finding that is consistent with previous studies [30, 37]. It remains to be determined if there are differences in persistence of B. burgdorferi strains and if the high persister frequencies in B. burgdorferi strains are associated with recalcitrance to antibiotic therapies.

In conclusion, we found there is a hierarchy of B. burgdorferi persisters with increasing antibiotic tolerance as the culture ages from log phase to stationary phase with morphological changes from spirochetal form to round body and microcolony forms. Importantly, we identified drug combinations that have high activity against B. burgdorferi persisters with daptomycin-containing combinations achieving the best activity. The most effective drug combination used daptomycin, cefoperazone and doxycycline which appeared to render resistant microcolony forms of B. burgdorferi unable to resuscitate viability upon subculture, a feature not previously described using any other antibiotic singly or in combinations. While important to state that the role of any persister organisms in human disease is far from elucidated, these findings may have implications for the treatment of certain Lyme disease patients with slow to resolve- or antibiotic-refractory arthritis or possibly stubborn ongoing symptoms. Direct extrapolation of these in vitro findings to human treatment would be unwise and premature. Future studies are needed to confirm whether such combination drug therapy yields benefit in animal models and possibly then in clinical studies.

Materials and Methods

Strain, media and culture

Borrelia burgdorferi B31 strain (ATCC 35210) was obtained from American Type Tissue Collection. Low passage (≤ 8) B. burgdorferi was cultured in BSK-H media (HiMedia Laboratories Pvt. Ltd.), with 6% rabbit serum (Sigma-Aldrich). All culture media were filter-sterilized by 0.2 μm filter. Cultures were incubated in sterile 50 ml conical tubes (BD Biosciences, California, USA) at 33°C without antibiotics. After incubation for 7–10 days stationary-phase B. burgdorferi cultures (100 μl, 1 × 106 cells) were transferred into 96-well tissue culture microplate for evaluating effect of antibiotic treatment.


Doxycycline (Dox), amoxicillin (Amo), cefoperazone (CefP), clofazimine (Cfz), miconazole (Mcz), polymyxin B (Pmb), sulfamethoxazole (Smx), daptomycin (Dap), carbomycin (magnamycin A), vancomycin, nisin, carbencillin, ofloxacin, tigecycline, hydroxychloroquine, rifampin, and clarithromycin (Sigma-Aldrich, St. Louis, USA) were dissolved in suitable solvents [38] to obtain stock solutions. The antibiotic stocks were filter-sterilized by 0.2 μm filter except clofazimine which was dissolved in DSMO (dimethylsulfoxide) and not filtered. Then the stocks were stored at -20°C.

Microscopy techniques

Specimens were examined on a Nikon Eclipse E800 microscope equipped with differential interference contrast (DIC) and epi-fluorescence illumination, and recorded with a Spot slider color camera. Cell proliferation assays were performed by direct counting using a bacterial counting chamber (Hausser Scientific Partnership, PA, USA) and DIC microscopy. SYBR Green I/PI assay was performed to assess the viability of B. burgdorferi as described [39]. The ratio of live (green) and dead (red) B. burgdorferi was calculated by counting these cells using a bacterial counting chamber and epi-fluorescence microscopy. The three representative images of every sample were captured for quantitative analysis. Image Pro-Plus software was applied to select green (including yellow) and red (including orange) areas of different morphological forms with calculation of the integrated fluorescence intensity (equal to area × average density or average intensity) of red and green portions as previously described [40].

Antibiotic exposure assay

To qualitatively determine the effect of antibiotics, 10 μl of each compound from the pre-diluted plate or pre-diluted stock was added to stationary phase B. burgdorferi culture in the 96-well plate. The final volume per well was adjusted to 100 μl at a concentration of 10 μg/ml for each antibiotic. Plates were sealed and placed in 33°C incubator for 7 days. SYBR Green I/ PI viability assay was used to assess the live and dead cells after antibiotic exposure as described [16]. Briefly, 10 μl of SYBR Green I (10,000 × stock, Invitrogen) was mixed with 30 μl propidium iodide (PI, 20 mM) into 1.0 ml of sterile dH2O. Then, 10 μl of staining mixture was added to each well and mixed thoroughly. The plates were incubated at room temperature in the dark for 15 minutes followed by plate reading at excitation wavelength at 485 nm and the fluorescence intensity at 535 nm (green emission) and 635 nm (red emission) in microplate reader (HTS 7000 plus Bio Assay Reader, PerkinElmer Inc., USA). With least-square fitting analysis, the regression equation and regression curve of the relationship between percentage of live bacteria and green/red fluorescence ratios was obtained. The regression equation was used to calculate the percentage of live cells in each well of the 96-well plate. Each value is the mean of three replicates and the standard t-test was used for comparing the drug treated group and the drug-free control group.

For persister frequency assay, E. coli W3110 was diluted 1:100 in LB broth and shaken at 37°C. After 3-hour incubation, log phase culture was withdrawn, washed with LB broth, and spotted on LB agar plate to obtain the beginning colony counts. Meanwhile amoxicillin was added at a final concentration of 50 μg/ml, and shaken at 37°C. After 3-hour incubation, samples were withdrawn, washed with LB broth, and spotted on LB agar plate for colony counts.

Subculture of antibiotic-treated B. burgdorferi to assess viability of the organisms

Seven day old B. burgdorferi culture (1×107 spirochetes/ml) (500 μl) was treated with drugs or drug combinations in Eppendorf tubes. After incubation at 33°C for 7 days without shaking, the cells were collected by centrifugation and rinsed with 1 ml fresh BSK-H medium followed by resuspension in 500 μl fresh BSK-H medium without antibiotics. Then 50 μl of cell suspension was transferred to 1 ml fresh BSK-H medium for subculture at 33°C for 2 weeks. Cell proliferation was assessed using SYBR Green I/PI assay and bacterial counting chamber (Hausser Scientific Partnership, PA, USA) by microscopy as described above.

Author Contributions

Conceived and designed the experiments: YZ JF. Performed the experiments: JF. Analyzed the data: JF YZ PA. Wrote the paper: JF YZ PA.


  1. 1. CDC (2014) Lyme Disease website. Available: Accessed 2014 Sep 13.
  2. 2. Wormser GP, Dattwyler RJ, Shapiro ED, Halperin JJ, Steere AC, et al. (2006) The clinical assessment, treatment, and prevention of lyme disease, human granulocytic anaplasmosis, and babesiosis: clinical practice guidelines by the Infectious Diseases Society of America. Clin Infect Dis 43: 1089–1134. doi: 10.1086/508667. pmid:17029130
  3. 3. Klempner MS, Baker PJ, Shapiro ED, Marques A, Dattwyler RJ, et al. (2013) Treatment trials for post-Lyme disease symptoms revisited. Am J Med 126: 665–669. doi: 10.1016/j.amjmed.2013.02.014. pmid:23764268
  4. 4. Berndtson K (2013) Review of evidence for immune evasion and persistent infection in Lyme disease. Int J Gen Med 6: 291–306. doi: 10.2147/IJGM.S44114. pmid:23637552
  5. 5. Steere AC, Glickstein L (2004) Elucidation of Lyme arthritis. Nat Rev Immunol 4: 143–152. doi: 10.1038/nri1267. pmid:15040587
  6. 6. Bockenstedt LK, Gonzalez DG, Haberman AM, Belperron AA (2012) Spirochete antigens persist near cartilage after murine Lyme borreliosis therapy. J Clin Invest 122: 2652–2660. doi: 10.1172/JCI58813. pmid:22728937
  7. 7. Hodzic E, Feng S, Holden K, Freet KJ, Barthold SW (2008) Persistence of Borrelia burgdorferi following antibiotic treatment in mice. Antimicrobial Agents and Chemotherapy 52: 1728–1736. doi: 10.1128/AAC.01050-07. pmid:18316520
  8. 8. Diterich I, Rauter C, Kirschning CJ, Hartung T (2003) Borrelia burgdorferi-induced tolerance as a model of persistence via immunosuppression. Infect Immun 71: 3979–3987. doi: 10.1128/IAI.71.7.3979-3987.2003. pmid:12819085
  9. 9. Barthold SW, Hodzic E, Imai DM, Feng S, Yang X, et al. (2010) Ineffectiveness of tigecycline against persistent Borrelia burgdorferi. Antimicrobial Agents and Chemotherapy 54: 643–651. doi: 10.1128/AAC.00788-09. pmid:19995919
  10. 10. Embers ME, Barthold SW, Borda JT, Bowers L, Doyle L, et al. (2012) Persistence of Borrelia burgdorferi in rhesus macaques following antibiotic treatment of disseminated infection. PLoS One 7: e29914. doi: 10.1371/journal.pone.0029914. pmid:22253822
  11. 11. Hodzic E, Imai D, Feng S, Barthold SW (2014) Resurgence of Persisting Non-Cultivable Borrelia burgdorferi following Antibiotic Treatment in Mice. PLoS One 9: e86907. doi: 10.1371/journal.pone.0086907. pmid:24466286
  12. 12. Straubinger RK, Summers BA, Chang YF, Appel MJ (1997) Persistence of Borrelia burgdorferi in experimentally infected dogs after antibiotic treatment. Journal of clinical microbiology 35: 111–116. pmid:8968890
  13. 13. Fallon BA, Keilp JG, Corbera KM, Petkova E, Britton CB, et al. (2008) A randomized, placebo-controlled trial of repeated IV antibiotic therapy for Lyme encephalopathy. Neurology 70: 992–1003. doi: 10.1212/01.WNL.0000284604.61160.2d. pmid:17928580
  14. 14. Marques A, Telford SR III, Turk SP, Chung E, Williams C, et al. (2014) Xenodiagnosis to Detect Borrelia burgdorferi Infection: A First-in-Human Study. Clin Infect Dis 58: 937–945. doi: 10.1093/cid/cit939. pmid:24523212
  15. 15. Krupp LB, Hyman LG, Grimson R, Coyle PK, Melville P, et al. (2003) Study and treatment of post Lyme disease (STOP-LD): a randomized double masked clinical trial. Neurology 60: 1923–1930. doi: 10.1212/01.WNL.0000071227.23769.9E. pmid:12821734
  16. 16. Feng J, Wang T, Shi W, Zhang S, Sullivan D, et al. (2014) Identification of Novel Activity against Borrelia burgdorferi Persisters Using an FDA Approved Drug Library. Emerg Microb Infect July 2, 2014: 3, e49.
  17. 17. Brorson O, Brorson SH, Scythes J, MacAllister J, Wier A, et al. (2009) Destruction of spirochete Borrelia burgdorferi round-body propagules (RBs) by the antibiotic tigecycline. Proc Natl Acad Sci U S A 106: 18656–18661. doi: 10.1073/pnas.0908236106. pmid:19843691
  18. 18. Sapi E, Bastian SL, Mpoy CM, Scott S, Rattelle A, et al. (2012) Characterization of biofilm formation by Borrelia burgdorferi in vitro. PLoS One 7: e48277. doi: 10.1371/journal.pone.0048277. pmid:23110225
  19. 19. Miklossy J, Kasas S, Zurn AD, McCall S, Yu S, et al. (2008) Persisting atypical and cystic forms of Borrelia burgdorferi and local inflammation in Lyme neuroborreliosis. J Neuroinflammation 5: 40. doi: 10.1186/1742-2094-5-40. pmid:18817547
  20. 20. Alban PS, Johnson PW, Nelson DR (2000) Serum-starvation-induced changes in protein synthesis and morphology of Borrelia burgdorferi. Microbiology 146 ( Pt 1): 119–127. pmid:10658658
  21. 21. Kersten A, Poitschek C, Rauch S, Aberer E (1995) Effects of penicillin, ceftriaxone, and doxycycline on morphology of Borrelia burgdorferi. Antimicrob Agents Chemother 39: 1127–1133. doi: 10.1128/AAC.39.5.1127. pmid:7625800
  22. 22. Brorson O, Brorson SH (1998) In vitro conversion of Borrelia burgdorferi to cystic forms in spinal fluid, and transformation to mobile spirochetes by incubation in BSK-H medium. Infection 26: 144–150. doi: 10.1007/BF02771839. pmid:9646104
  23. 23. Lantos PM, Auwaerter PG, Wormser GP (2014) A systematic review of Borrelia burgdorferi morphologic variants does not support a role in chronic Lyme disease. Clin Infect Dis 58: 663–671. doi: 10.1093/cid/cit810. pmid:24336823
  24. 24. Sapi E, Kaur N, Anyanwu S, Luecke DF, Datar A, et al. (2011) Evaluation of in-vitro antibiotic susceptibility of different morphological forms of Borrelia burgdorferi. Infect Drug Resistance 4: 97–113.
  25. 25. Hunfeld KP, Brade V (2006) Antimicrobial susceptibility of Borrelia burgdorferi sensu lato: what we know, what we don′t know, and what we need to know. Wien Klin Wochenschr 118: 659–668. doi: 10.1007/s00508-006-0693-z. pmid:17160604
  26. 26. Xu J, Lu Y, Fu L, Zhu H, Wang B, et al. (2012) In vitro and in vivo activity of clofazimine against Mycobacterium tuberculosis persisters. Int J Tuberc Lung Dis 16: 1119–1125. doi: 10.5588/ijtld.11.0752. pmid:22691726
  27. 27. Vanden Bossche H, Marichal P, Gorrens J, Coene MC, Willemsens G, et al. (1989) Biochemical approaches to selective antifungal activity. Focus on azole antifungals. Mycoses 32 1: 35–52. doi: 10.1111/j.1439-0507.1989.tb02293.x. pmid:2561184
  28. 28. Casjens S (2000) Borrelia genomes in the year 2000. J Mol Microbiol Biotechnol 2: 401–410. pmid:11075912
  29. 29. Pogliano J, Pogliano N, Silverman JA (2012) Daptomycin-mediated reorganization of membrane architecture causes mislocalization of essential cell division proteins. J Bacteriol 194: 4494–4504. doi: 10.1128/JB.00011-12. pmid:22661688
  30. 30. Zhang Y (2014) Persisters, Persistent Infections and the Yin-Yang Model. Emerg Microb Infect (Nature Publishing Group) 3, e3. doi: 10.1038/emi.2014.3.
  31. 31. Dhand A, Bayer AS, Pogliano J, Yang SJ, Bolaris M, et al. (2011) Use of antistaphylococcal beta-lactams to increase daptomycin activity in eradicating persistent bacteremia due to methicillin-resistant Staphylococcus aureus: role of enhanced daptomycin binding. Clin Infect Dis 53: 158–163. doi: 10.1093/cid/cir340. pmid:21690622
  32. 32. Hall Snyder A, Werth BJ, Barber KE, Sakoulas G, Rybak MJ (2014) Evaluation of the novel combination of daptomycin plus ceftriaxone against vancomycin-resistant enterococci in an in vitro pharmacokinetic/pharmacodynamic simulated endocardial vegetation model. The Journal of antimicrobial chemotherapy 69: 2148–2154. doi: 10.1093/jac/dku113. pmid:24777900
  33. 33. Dever LL, Jorgensen JH, Barbour AG (1993) In vitro activity of vancomycin against the spirochete Borrelia burgdorferi. Antimicrob Agents Chemother 37: 1115–1121. doi: 10.1128/AAC.37.5.1115. pmid:8517700
  34. 34. Morris CM, George A, Wilson WW, Champlin FR (1995) Effect of polymyxin B nonapeptide on daptomycin permeability and cell surface properties in Pseudomonas aeruginosa, Escherichia coli, and Pasteurella multocida. J Antibiot (Tokyo) 48: 67–72. doi: 10.7164/antibiotics.48.67.
  35. 35. Murgia R, Cinco M (2004) Induction of cystic forms by different stress conditions in Borrelia burgdorferi. APMIS: acta pathologica, microbiologica, et immunologica Scandinavica 112: 57–62. doi: 10.1111/j.1600-0463.2004.apm1120110.x. pmid:14961976
  36. 36. Keren I, Kaldalu N, Spoering A, Wang Y, Lewis K (2004) Persister cells and tolerance to antimicrobials. FEMS Microbiol Lett 230: 13–18. doi: 10.1016/S0378-1097(03)00856-5. pmid:14734160
  37. 37. Li Y, Zhang Y (2007) PhoU is a persistence switch involved in persister formation and tolerance to multiple antibiotics and stresses in Escherichia coli. Antimicrob Agents Chemother 51: 2092–2099. doi: 10.1128/AAC.00052-07. pmid:17420206
  38. 38. Clinical and Laboratory Standards Institute (2007) Performance Standards for Antimicrobial Susceptibility Testing; Seventeenth Informational Supplement. CLSI document M100-S17 27: 154–161.
  39. 39. Feng J, Wang T, Zhang S, Shi W, Zhang Y (2014) An Optimized SYBR Green I/PI Assay for Rapid Viability Assessment and Antibiotic Susceptibility Testing for Borrelia burgdorferi. PLoS ONE 9(11): e111809. doi: 10.1371/journal.pone.0111809. pmid:25365247
  40. 40. Shopov A, Williams SC, Verity PG (2000) Improvements in image analysis and fluorescence microscopy to discriminate and enumerate bacteria and viruses in aquatic samples. Aquatic Microbial Ecology 22: 103–110. doi: 10.3354/ame022103.