We have previously shown that 207-nm ultraviolet (UV) light has similar antimicrobial properties as typical germicidal UV light (254 nm), but without inducing mammalian skin damage. The biophysical rationale is based on the limited penetration distance of 207-nm light in biological samples (e.g. stratum corneum) compared with that of 254-nm light. Here we extended our previous studies to 222-nm light and tested the hypothesis that there exists a narrow wavelength window in the far-UVC region, from around 200–222 nm, which is significantly harmful to bacteria, but without damaging cells in tissues. We used a krypton-chlorine (Kr-Cl) excimer lamp that produces 222-nm UV light with a bandpass filter to remove the lower- and higher-wavelength components. Relative to respective controls, we measured: 1. in vitro killing of methicillin-resistant Staphylococcus aureus (MRSA) as a function of UV fluence; 2. yields of the main UV-associated premutagenic DNA lesions (cyclobutane pyrimidine dimers and 6-4 photoproducts) in a 3D human skin tissue model in vitro; 3. eight cellular and molecular skin damage endpoints in exposed hairless mice in vivo. Comparisons were made with results from a conventional 254-nm UV germicidal lamp used as positive control. We found that 222-nm light kills MRSA efficiently but, unlike conventional germicidal UV lamps (254 nm), it produces almost no premutagenic UV-associated DNA lesions in a 3D human skin model and it is not cytotoxic to exposed mammalian skin. As predicted by biophysical considerations and in agreement with our previous findings, far-UVC light in the range of 200–222 nm kills bacteria efficiently regardless of their drug-resistant proficiency, but without the skin damaging effects associated with conventional germicidal UV exposure.
The use of ultraviolet (UV) light for inactivating bacteria and viruses is well established (1, 2). However, UV radiations emitted by typical germicidal lamps with a peak emission at 254 nm represent a human health hazard, causing skin cancer (3, 4) and cataracts (5, 6).
We have developed an approach to kill bacteria without harming human cells in skin tissue models (7) and mouse skin in vivo (8) that employs single-wavelength UVC light generated by inexpensive filtered excilamps (9). The approach is based on the limited penetration distance of UVC light in the wavelength range of 200–222 nm in biological samples. Specifically, while far-UVC light has enough range to traverse microbes that are much smaller in size than human cells [less than 1 μm in diameter (10, 11), compared to the diameter of typical human cells ranging from about 10–25 μm (10)], it is strongly absorbed by the proteins in the cytoplasm of human cells (12, 13) and is drastically attenuated before reaching the human cell nucleus. It follows that far-UVC light is not able to penetrate the stratum corneum of skin and reach the underlying critical basal cells or melanocytes (4).
Another organ especially sensitive to UV damage is the lens; however, the lens is positioned distal to the cornea that is sufficiently thick [~500 μm (14))]. Therefore, penetration of far-UVC ~200-nm light through the cornea to the lens is predicted to be essentially zero (15).
The potential use of UVC light for microbe sterilization purposes in the presence of humans paves the way to numerous clinical applications, including reduction of surgical site infections (SSI) that are the second most common healthcare-associated infections resulting in read-missions, prolonged hospital stays, increased morbidity and mortality, and an overall higher medical cost (16, 17). A key factor contributing to the severity of SSI is the incidence of drug-resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA) (18, 19).
To address the issue of reducing SSI, we have developed an approach that involves the use of inexpensive excimer lamps that, appropriately filtered, emit monoenergetic wavelengths in the far-UVC range. A crucial property of UVC-mediated germicidal killing is that it is essentially independent of acquired drug resistance (20, 21).
We have previously shown that 207-nm light emitted by a filtered krypton-bromine (Kr-Br) excilamp has bactericidal efficacy while being minimally cytotoxic to human cells in a 3D skin tissue model in vitro (7) and in a hairless mouse skin model in vivo (8). Thus, continuous exposure of the wound to far-UVC light during surgery may inactivate the microbes alighting directly onto the surgical wound from the air. If proven to be safe to eyes as well as skin, continuous operation of far-UVC light would not require the use of cumbersome protective clothing, hoods and eye shields for the surgical staff and the patient (22, 23).
Here we extended those studies to a filtered krypton-chlorine (Kr-Cl) excimer lamp that produces essentially monoenergetic UV light at 222 nm and established that a wavelength window exist in the far-UVC region (from 200–222 nm) that inactivates bacteria efficiently but is not cytotoxic or mutagenic to mammalian cells.
We describe measurements of MRSA survival and of typical UV-induced premutagenic DNA lesions in a 3D human skin model immediately after exposure to different fluences of 222-nm light. We compared the results to those measured in samples exposed to similar fluences from a typical germicidal lamp emitting at 254 nm.
We further tested eight cellular and molecular endpoints relevant to skin damage in vivo in dorsal skin of hairless mice 48 h after exposure to 222-nm or 254-nm light used as positive control (8), at a fluence at which the 254-nm light is predicted to produce a significant decrease in SSI rates (22).
In agreement with our previous results using 207-nm light (7, 8), here we showed that 222-nm light has similar antimicrobial properties as a conventional germicidal lamp but without causing mammalian skin damage.
The finding that a far-UVC wavelength window (200–225 nm) is differentially cytotoxic to bacteria relative to mammalian cells is novel and can be used for various applications that would require the presence of humans, including room sterilization and reduction of surgical site infections, without the need of additional personal protective equipment.
MATERIALS AND METHODS
We used an excimer lamp based on a krypton-chlorine (Kr-Cl) gas mixture that emits principally at 222 nm. The lamp (High Current Electronics Institute, Tomsk, Russia) was air cooled with a 6,000-mm2 exit window (24). A custom bandpass filter (Omega Optical, Brattleboro, VT) was used to remove essentially all but the dominant 222-nm wavelength emission.
A UV spectrometer (Photon Control, BC, Canada) sensitive in the wavelength range from 200–360 nm was used to characterize the wavelength spectra emitted by the excimer lamp, and a deuterium lamp standard with a NIST-traceable spectral irradiance (Newport Corp, Stratford, CT) was used to calibrate the UV spectrometer.
Studies were also carried out with a conventional mercury germicidal lamp (Hygeaire, Atlantic Ultraviolet Corporation, Hauppauge, NY) with peak emission at 254 nm and used as positive control. An ILT1400 sensor equipped with a SEL220 detector (International Light Technologies, Peabody, MA) was used to measure the fluence rate from both lamps. For acute exposures (MRSA and 3D tissues), the 222- and 254-nm lamps were positioned 9 and 99 cm, respectively, from the sample at which corresponded a power density of 0.036 mJ/cm2. For chronic exposures of mice, delivery of 157 mJ/cm2 in a 7 h period was obtained by locating the 222- and the 254-nm lamps 41 and 205 cm from the samples, respectively; the corresponding power densities were 0.0062 mJ/cm2 for the 222-nm lamp and 0.0008 mJ/cm2 in the case of the conventional germicidal lamp.
Figure 1 shows the measured spectra emitted from the Kr-Cl excimer lamp that, together with the main excimer emission at 222 nm, also includes lower fluences of higher wavelength light (i.e. ~237 and ~258 nm). To remove these more penetrating higher wavelengths and therefore potentially more harmful to human cells, we used a custom bandpass filter (Omega Optical, Brattleboro, VT). As shown in the inset in Fig. 1, the filtered lamp effectively emitted only the characteristic single wavelength of 222 nm.
IN VITRO STUDIES
MRSA Cell Survival
We used methicillin-resistant S. aureus (MRSA USA300, multilocus sequence type 8, clonal complex 8, staphylococcal cassette chromosome mec type IV), which is a major cause of both community and nosocomial infections (25–27). Survival of MRSA as a function of UVC fluence was assessed immediately after exposure with the standard colony forming unit (CFU) assay, as previously reported (7).
UV-Associated Premutagenic DNA Lesions in a 3D Human Skin Model
We used a 3D human skin model EpiDerm-FT (MatTek Corp., Ashland, MA) consisting of stratum corneum and 8–12 human cell layers to reproduce human epidermis and dermis (28). We measured induction of the two most abundant premutagenic DNA lesions in the epidermis, cyclobutane pyrimidine dimers (CPD) and pyrimidine-pyrimidone 6-4 photoproducts (6-4PP) (4), as a function of UVC fluence in 3D human skin constructs immediately after exposure using the immunohistochemical approach previously described (7).
IN VIVO STUDIES
We used six- to eight-week-old male hairless mice (SKH1-Elite strain 477, Charles River Laboratories, Stone Ridge, NY); the strain has UV action spectra for histological, physical and visible changes similar to those of human skin (29, 30). Moreover, the typical thickness of the stratum corneum of SKH1 mice (5–10 μm) (31, 32) is comparable to that of human skin (5–20 μm) (33).
One group of three mice was exposed to fluence of 157 mJ/cm2 from 222 nm light delivered in a 7 h period by a filtered Kr-Cl excimer lamp while another group of three mice was sham irradiated to zero UV fluence. Mice exposed to 157 mJ/cm2 delivered in 7 h period from 254 nm light represented the positive controls (8).
All animal procedures were carried out in accordance with federal guidelines and protocols approved by the Columbia University Medical Center IACUC.
Mouse Skin Safety-Specific Endpoints
Following the same protocols described in our previous mouse skin safety study (8), 48 h after UV exposure we measured the following endpoints: 1. Epidermal thickness measured in hematoxylin and eosin stained samples; 2. The percentage of proliferating keratinocytes expressing the Ki-67 antigen (34, 35). 3. Yields of UV-induced cyclobutane pyrimidine dimers (CPD) and 6-4 photoproducts (6-4PP); 4. The number of neutrophils and mast cells as markers of skin inflammation (36); 5. The expression of keratin (K) K6A as marker of skin differentiation (37, 38).
Tissues were examined with an Olympus IX70 microscope equipped with a Photometrics® PVCAM high-resolution, high-efficiency digital camera; Image-Pro Plus 6.0 software and Fiji/Image J software were used to analyze the images. For each mouse, each endpoint was measured in at least six randomly selected fields of view.
Comparisons of mean values between treatment groups and controls were performed using Student’s t test, and comparison of proportions were assessed with standard χ2 tests.
IN VITRO RESULTS
We measured MRSA survival immediately after exposure to different fluences of 222-nm light generated by a filtered Kr-Cl excimer lamp (Fig. 2). We compared the results to survival of MRSA exposed to similar fluences from a conventional germicidal UV lamp (254 nm) (7). As illustrated in Fig. 2, at relatively high fluences at which the 254-nm light is predicted to produce a significant decrease in SSI rates (1), 222-nm light kills MRSA almost as efficiently as a conventional germicidal UV lamp. However, 254-nm light is almost equally efficient at killing human cells (7).
Induction of Premutagenic DNA Lesions in Human Skin
Figure 3 shows the comparison of the induced yields of CPD (left panel) and 6-4PP (right panel) in 3D skin tissue models exposed to 222-nm or 254-nm light. Unlike conventional germicidal light (254 nm), exposure to the 222-nm light at any of the studied fluences did not induce yields of either lesions that was significantly higher than the sham-irradiated samples.