RSV A2 strain was grown in HEp-2 cells and purified by centrifugation on discontinuous sucrose gradients as described elsewhere (14). Titer of the purified RSV pools was 8 to 9 log₁₀ plaque-forming units (PFU)/ml using a methylcellulose plaque assay. No contaminating cytokines were found in these sucrose-purified viral preparations (15). The human metapneumovirus (hMPV) strain CAN97-83 was propagated and titrated in LLC-MK2 cells and sucrose-gradient purified as previously described (16). Virus pools were aliquoted, quick-frozen on dry ice/alcohol, and stored at −80°C until used. Virus pools were endotoxin free by routine tests using the limulus hemocyanin agglutination assay.

Female, 6- to 8-week-old BALB/c mice were purchased from Harlan (Houston, TX) and maintained in pathogen-free conditions at the animal research facility of the University of Texas Medical Branch (UTMB), Galveston, Texas. Mice were used under an experimental protocol approved by the UTMB Institutional Animal Care and Use Committee. Before inoculation with RSV, mice were lightly anesthetized by intraperitoneal administration of ketamine and xylazine. Mice were infected intranasally with 50 μl of RSV diluted in phosphate-buffered saline (PBS; 10⁷ PFU) or sham inoculated using the same volume of control buffer. For hMPV infection, mice were infected intranasally with 50 μl of hMPV (10⁷ PFU). Groups of mice were killed at various intervals after infection and BAL was collected by flushing the lungs twice with ice-cold sterile PBS (1 ml) as described (10). BAL fluid was centrifuged at 10,000 × g for 2 minutes at 4°C and stored at −80°C until further analysis. Lungs were removed, quickly frozen in liquid nitrogen, and stored at −80°C until further processing.

Sample of NPS were collected at UTMB from infants and children who were enrolled in an ongoing study on the pathogenesis of viral bronchiolitis. The study protocol and consent forms have been approved by the UTMB Institutional Review Board. The study population comprised groups of infants and children younger than 12 months old recruited from the UTMB Emergency Department, the pediatrics outpatient clinics, or inpatient areas of Children's Hospital. These subjects were assigned a diagnosis of upper respiratory tract infection (URTI) alone (absence of crackles or wheezing on auscultation of the chest, oxygen saturation ≥ 97% on room air, and normal chest radiograph when obtained), “nonhypoxic bronchiolitis” (defined for the purposes of this study as wheezing on auscultation with oxygen saturation > 95% on room air), or “hypoxic bronchiolitis” (wheezing on auscultation and oxygen saturation ≤ 95% on room air or, in the absence of wheezing, hyperinflation on chest radiograph and oxygen saturation ≤ 95% on room air). Hypoxia was assessed at the time that secretion samples were obtained, with subjects breathing ambient air without oxygen supplementation. Subjects with recurrent wheezing were not included, nor were those with history of chronic lung disease or congenital heart disease. Three infants who were intubated (VS, ventilatory support) because of acute respiratory failure caused by RSV infection were also included in the study. RSV infection was confirmed in all subjects by detection of viral antigen in NPS samples by antigen detection. All samples were obtained within the first 5 days of respiratory illness and within 24 hours after the onset of wheezing. Samples of NPS were obtained by passing size 5F feeding tubes into the nasopharynx and applying gentle suction. Secretions then were rinsed into collecting traps with 3 ml of PBS. After centrifugation to precipitate cells, samples were digested with sputolysin (Calbiochem, San Diego, CA), a mucolytic agent in 6.5 mM dithiothreitol in 100 mM phosphate buffer, pH 7.01, and stored at −80°C for subsequent protein and biomarker analysis.

Lung nuclear proteins were prepared as previously described (17, 18). Briefly, mouse lung tissue was homogenized in 5 ml ice-cold Buffer A (10 mM 2-hydroxyethyl-piperazine N′-2-ethanesulfonic acid [HEPES]–KOH, pH 7.9, 1.5 mM MgCl₂, 10 mM KCl, 0.5 mM dithiothreitol [DTT], 0.2 mM phemylmethyl sulfonyl fluoride [PMSF], 0.6% nonident P40 [NP-40]) and centrifuged at 350 × g, 4°C for 30 seconds. The supernatant was kept on ice for 5 minutes and centrifuged for 5 minutes at 6,000 × g at 4°C, and the pellet was resuspended in 200 μl Buffer B (10 mM HEPES–KOH, pH 7.9, 1.5 mM MgCl₂, 10 mM KCl, 1.2 M sucrose, 0.5 mM DTT, 0.2 mM PMSF). After centrifugation (13,000 × g, 4°C, 30 min), the pellet was resuspended in 100 μl Buffer C (20 mM HEPES–KOH, pH 7.9, 1.5 mM MgCl₂, 420 mM NaCl, 0.2 mM ethylenediamine-tetraacetic acid, 0.5 mM DTT, 0.2 mM PMSF, 2 mM benzamidine, 5 μg/ml leupeptin, 25% glycerol), incubated on ice for 20 minutes, and centrifuged (6,000 × g, 4°C, 2 min).

A lysis-lavage method described by Wheelock and colleagues was used to isolate epithelial cell proteins of conductive airways (19). Briefly, mice were killed and trachea was exposed and cannulated, lungs were then removed from the thorax and inflated with 0.5 ml agarose solution (0.75% low-melting agarose, 5% dextrose) immediately followed by 0.5 ml dextrose solution (1% dextrose, 2% protease inhibitor cocktail) through a three-way valve. Both solutions were preheated at 37°C. The inflated lungs were incubated in 5% dextrose for 15 minutes at room temperature. Dextrose solution was then removed by repeated steps of inversion of the lungs and gentle suction with a syringe. The airways were then lavaged with 0.5 ml of lysis buffer (2 M thiourea, 7 M urea, 4% 3-((3-cholamidopropyl)dimethylammonio)-1-propanesulfonic acid, 0.5% Triton X 100, 1% DTT, and protease inhibitors). The lysis buffer containing the proteins was immediately recovered, flash frozen on dry ice and stored at −80°C until further use.

Mouse BAL fluids and sputolysin-digested human NPS samples were lyophilized and reconstituted in 100 μl of reagent 1 procured from Bio-Rad (Hercules, CA; 50 mM Tris buffer), desalted using protein desalting columns from Pierce (Rockford, IL) (7,000 MW cutoff), followed by albumin depletion by a Montage albumin depletion kit. Then 200 μl of 1 mg/ml protein aliquots were isoelectrofocused (IEF) on 11 cm–long nonlinear precast immobilized pH gradient (IPG) strips (pH 3–10; Bio-Rad) using the IPGPhor isoelectrofocusing system. Protein samples were loaded onto an IPG strip and rehydrated overnight. IEF was performed at 20°C with the following parameters: 50 V for 11 hours, 250 V for 1 hour, 500 V for 1 hour, 1,000 V for 1 hour, 8,000 V for 2 hours, and 8,000 V for 6 hours, with a total of 48,000 V. After IEF, the IPG strips were stored at −80°C until two-dimensional sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) was performed. For the two-dimensional SDS-PAGE, the IPG strips were incubated in 4 ml of equilibration buffer (6 M urea, 2% SDS, 50 mM Tris-HCl [pH 8.8], 20% glycerol) containing 10 μl of 0.5 M TCEP [Tris(2-carboxyethyl) phosphine] for 15 minutes at 22°C with shaking. The strips were then incubated in another 4 ml of equilibration buffer with 25 mg of iodoacetamide/ml for 15 minutes at 22°C with shaking. Electrophoresis was performed at 150 V for 2.25 hours at 4°C with 8 to 16% precast polyacrylamide gels in Tris-glycine buffer (25 mM Tris-HCl, 192 mM glycine, 0.1% SDS [pH 8.3]). After two-dimensional gel electrophoresis (2DE), the gels were fixed (10% methanol [MeOH], 7% acetic acid in double-distilled water), stained with SYPRO Ruby (Bio-Rad), and destained (10% ethanol in double-distilled water).

The destained gels were scanned at a 100-μm resolution using the Perkin-Elmer (Boston, MA) ProXPRESS ProFinder Proteomic Imaging System with 480-nm excitation and 620-nm emission filters. The exposure time was adjusted to achieve a value of approximately 55,000- to 63,000-pixel intensity on the most intense protein spots on the gel. The 2DE gel images were subsequently analyzed using Progenesis Discovery software version 2006.03 (Nonlinear Dynamics, Ltd., Newcastle Upon Tyne, UK). An average gel was created from gels run on BAL proteins from three separate samples from mock-infected mice (control) and three separate samples from RSV-infected mice (24 hours). For human samples, an average gel was created from gels run on NPS proteins from infants with URTI, nonhypoxic bronchiolitis, bronchiolitis with hypoxia, and patients on VS. The software automatically selected one of the six gels for mice experiment and one of the four gels for human NPS as the base image of the reference gel. The gel with the highest number of spots was set as the reference gel. Unmatched spots present in five of the six other gels were subsequently added to the reference gel image by the software to give a comprehensive reference gel. Subsequent to automatic spot detection, spot filtering was also manually performed. The matching of spots between the gels was manually reviewed and adjusted as necessary. Moreover, the log-transformed spot volumes were normally distributed, indicating that nonparametric statistical comparisons, such as t tests, could be applied to identify those proteins whose expression was significantly changed by infection. The spot volumes were normalized based on the total spot volume for each gel, and the control and RSV-infected samples were compared.

Protein gel spots were excised and prepared for matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF-MS) analysis using Genomic Solutions' ProPic and ProPrep robotic instruments following the manufacturer's protocols. Briefly, gel pieces were incubated with trypsin (20 μg/ml in 25 mM ammonium bicarbonate, pH 8.0; Promega Corp., Madison, WI) at 37°C for 4 hours. The peptide mixture was purified with an in-tip reversed-phase column (C18 Zip-Tip; Millipore) to remove salts and impurities (20). MALDI-TOF-MS was performed using an Applied Biosystems Voyager model DE STR (Applied Biosystems, Framingham, MA) for peptide mass fingerprinting. The peptide masses were matched with the theoretical peptide masses of all the proteins from mouse and human species of the Swiss-Prot and National Center for Biotechnology database. Protein identification was performed using a Bayesian algorithm, in which high-probability matches are indicated by an expectation score, an estimate of the number of matches that would be expected in that database if the matches were completely random (21).

Equal amount of proteins (10–20 μg, depending on the antibody used) from mouse BAL, conductive airway epithelial cells or human NPS were loaded and separated by SDS-PAGE, and transferred onto Hybond-polyvinylidene difluoride membrane (Amersham Pharmacia Biotech, Piscataway, NJ). Nonspecific binding was blocked by immersing the membrane in Tris-buffered saline-Tween (TBST) blocking solution (10 mM Tris-HCl, pH 7.6, 150 mM NaCl, 0.05% Tween-20 [v/v]) containing 5% skim milk powder for 30 minutes. After a short wash in TBST, the membranes were incubated with the primary antibody overnight at 4°C, followed by the appropriate secondary antibody (Santa Cruz Biotechnology, Santa Cruz, CA), diluted 1:5–10,000 in TBST for 1 hour at room temperature. After washing, the proteins were detected using enhanced-chemiluminescence assay (Amersham Biosciences, Piscataway, NJ) according to the manufacturer's recommendations. The primary antibodies used for Western blots were anti-SOD 1, 2, and 3 rabbit polyclonal antibodies (Stressgen Bioreagents, Ann Arbor, MI), anti-catalase rabbit polyclonal antibody, and anti-lamin B mouse monoclonal antibody (Calbiochem), anti-Nrf2 (C20) rabbit polyclonal (Santa Cruz Biotechnology), and anti–β-actin mouse monoclonal antibody from Sigma-Aldrich (Saint Louis, MO). The anti-GST rabbit polyclonal antibody was a generous gift from Dr. Yogesh Awasthi, University of North Texas Health Science Center.

Catalase, GST, GPx, and SOD activities were determined in BAL fluids using specific biochemical assays (Cayman Chemical, Ann Arbor, MI; Catalog No. 707002, 703302, 703102, and 706002, respectively, for catalase, GST, GPx, and SOD), according to the manufacturer's instructions. The quantification of catalase activity in BAL was based on the reaction of the enzyme with methanol in the presence of an optimal concentration of H₂O₂. The formaldehyde produced is measured spectrophotometrically with 4-amino-3-hydrazino-5-mercapto-124-triazole as the chromogen. The catalase activity was expressed as nmol/min/mg of protein in the sample. The total GST activity was quantified by measuring the conjugation of 1-chloro-2,4-dinitrobenzene with reduced glutathione. The conjugation is accompanied by an increase in absorbance at 340 nm. The rate of increase is directly proportional to the GST activity in the sample. The GST activity was expressed as nmol/min/mg of protein in the sample. The GPx activity was determined spectrophotometrically in BAL through an indirect coupled reaction with glutathione reductase. Oxidized glutathione, produced on reduction of hydroperoxide by GPx, is recycled to its reduced state by glutathione reductase and NADP reduced. The oxidation of NADP reduced to NADP⁺ is accompanied by a decrease in absorbance at 340 nm. Under conditions in which the GPx activity is rate limiting, the rate of decrease in the A₃₄₀ is directly proportional to the GPx activity in the sample. SOD activity was determined by using tetrazolium salt for the detection of superoxide radicals generated by xanthine oxidase and hypoxanthine. One unit of SOD is defined as the amount of enzyme needed to exhibit 50% dismutation of the superoxide radical.

Measurement of F₂ 8-isoprostane in human NPS was performed using a competitive enzyme immunoassay from Cayman Chemical Co. according to manufacturer's instructions. Measurement of malondialdehyde (MDA) was performed using a spectrophotometric assay (Oxis Research, Burlingame, CA).

All results are expressed as mean ± SEM. Data were analyzed using the GraphPad Instat Biostatistics 3.0 software. Student t test using a 95% confidence level was used to determine the level of differences in RSV-infected versus sham-inoculated mice. Differences between RSV illness groups were assessed by use of ANOVA.

ROS generation due to the respiratory burst of activated phagocytic cells recruited to the airways during viral infections is an important antiviral defense. However, a robust production of ROS can lead to depletion of antioxidants and cause oxidative stress. In previous studies, we have shown that RSV infection causes significant oxidative stress damage as demonstrated by the increase of the lipid peroxidation markers F₂ 8-isoprostane, MDA, and 4-hydroxynonenal in cultured airway epithelial cells and in the lung of experimentally infected mice (8, 10). More recently, we have demonstrated a significant reduction in the expression of several antioxidant enzymes, such as SOD 1, SOD 3, catalase, and GST, in airway epithelial cells as a result of RSV infection, suggesting that oxidative stress could be the result of imbalance between ROS production and antioxidant cellular defenses (11). To determine whether RSV infection results in decreased expression of antioxidant proteins in vivo, similar to our observation in cultured cells, groups of BALB/c mice were infected intranasally with RSV or sham-inoculated. BAL was collected at Days 1, 3, 5, and 9 after infection to assess levels of catalase, GST-mu, and SOD 1, 2, and 3 by Western blot. As shown in Figure 1 and by densitometric analysis in Figure E1 in the online supplement, RSV-infected mice showed a significant reduction in the expression levels of most of the tested enzymes at Days 1 and/or 3 after infection compared with control animals. SOD 3 was decreased at Days 3 and 5 after infection in most but not all of the RSV-infected animals and therefore did not reach statistical significance. Overall, levels of AOE in RSV-infected mice returned to control levels by Day 9 after infection, with the exception of SOD 2, whose expression normalized earlier (Day 5 after infection). A similar reduction in AOE expression in the lung was also observed in mice infected with hMPV, a paramyxovirus that causes a significant proportion of lower respiratory tract infections in young infants and children (22) (Figure E4).

Figure 1. Antioxidant enzymes are reduced in bronchoalveolar lavage (BAL) of respiratory syncytial virus (RSV)-infected mice. Groups of mice were infected with RSV or sham inoculated with saline (Control) and BAL was collected at Days 1, 3, 5, and 9. BAL proteins were resolved on 10% sodium dodecyl sulfate–polyacrylamide gel electrophoresis and Western blots were performed using antibodies against superoxide dismutase (SOD) 1, SOD 2, SOD 3, catalase, and glutathione S-transferase (GST)-mu. Membranes were stripped and reprobed for β-actin as an internal control for protein integrity and loading. Lanes 1 to 4 are BAL from four control and 5 to 8 from four RSV-infected mice at each time point. Densitometric analysis of Western blot band intensities is presented in Figure E1. The figure is representative of three independent experiments, each experiment with four mice per group at each time point.

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To determine whether levels of AOE detected in the BAL reflected changes in the AOE in airway epithelium, a major target of RSV infection, we performed Western blot analysis of SOD 1, 2, and 3 in proteins isolated from airway epithelial cells of infected mice. We found a significant decrease of SOD 1 and 3 in epithelial proteins of RSV-infected mice compared with epithelial proteins from control mice (Figure 2). On the other hand, SOD 2 levels were similar in epithelial proteins of RSV-infected and control mice, suggesting that the reduction of such enzymes observed in Western blots of infected BAL samples may reflect a nonepithelial source/cell target of such enzymes after RSV infection (see Discussion).

Figure 2. Superoxide dismutase (SOD) 1, SOD 2, and SOD 3 in conductive airway epithelial cells. (A) Proteins of conductive airway epithelial cells were obtained by lysis-lavage from respiratory syncytial virus (RSV)-infected or control mice (Day 1 after infection). Proteins were analyzed by Western blot for content of SOD 1, SOD 2, and SOD 3 as in Figure 1. (B) Densitometric analysis of Western blot band intensities was performed using Alpha Ease software, version 2200 (2.2d) (Alpha Innotech Co., San Leandro, CA). Bands in RSV-infected samples were normalized to uninfected control sample background and are presented as mean ± SEM of n = 4. *P < 0.05; ***P < 0.001 relative to control mice.

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To determine whether changes in AOE protein expression resulted in changes in their activities in response to RSV infection, BAL was collected from groups of RSV-infected or sham-inoculated mice at Days 1, 3, 5, and 9 after infection, and total SOD, catalase, GST, and GPx enzymatic activity were assessed by biochemical assays. There was a significant reduction of all AOE activities in RSV-infected mice compared with control animals (Figure 3). In particular, in RSV-infected mice, total SOD and GPx activities decreased significantly at Days 1 (86 and 59%, respectively) and 3 (52 and 46%, respectively), compared with sham-inoculated mice, with levels returning to those in control mice by Day 9. In addition, catalase and GST activities were significantly lower in RSV-infected mice compared with control mice at all tested time points, but different from our findings with SOD and GPx, they did not return to control levels by Day 9 (76, 63, 37, and 50% reduction for catalase and 75, 59, 50, and 48% reduction for GST at Days 1, 3, 5, and 9 after infection). Overall, these results indicate that RSV significantly reduces antioxidant defenses of the airways.

Figure 3. Respiratory syncytial virus (RSV) infection inhibits antioxidant enzyme activity in the lung. Specific biochemical assays were used to determine total superoxide dismutase (SOD), catalase, glutathione peroxidase (GPx), and glutathione S-transferase (GST) activity in bronchoalveolar lavage of groups of mice that were RSV infected or sham inoculated as in Figure 1. The figure is representative of three independent experiments, each experiment with four to five mice per group at each time point. Data are presented as mean ± SEM of four mice per group at each time point. *P < 0.05; **P < 0.01 and ***P < 0.001 relative to control mice.

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In recent years, proteomic analysis has advanced our knowledge of BAL proteins and their degradation products present at the alveolar level. These proteins may be plasma derived or locally produced and are released under normal or pathological conditions by inflammatory, immune, and tissue-resident cells (23). Thus, with the intent to gain a more global insight into the lung antioxidant response in the course of a viral infection, we investigated differential protein expression in BAL of RSV-infected mice compared with control uninfected animals by 2DE. Comparison of SYPRO Ruby-stained 2DE gels of RSV-infected and uninfected BAL proteins showed significant changes in the protein spot profile, as shown in the master gel images of 2DE BAL proteins from control (Figure 4A) and RSV-infected mice (Figure 4B) at Day 3 after infection. Overall, more than 1,300 protein spots with pH range 3 to 10 and relative molecular masses range of 10 to 250 kD were detected on our 2DE. BAL protein spots found to be significantly different in expression level between RSV-infected and control mice (either increased or decreased) were excised from the gels, trypsinized, and analyzed by MALDI-TOF-MS. Among the spots that we were able to identify with high probability score there were several antioxidant enzymes that were decreased in the BAL of RSV-infected mice compared with control mice. We found reduced expression of several other AOE, including peroxiredoxin enzymes (listed with their corresponding spot number in Figure 4C), in addition to catalase, SOD 1, GPx 1, and GST-mu (whose change in expression is better shown in Figure E2). Table 1 summarizes all antioxidant proteins whose expression in BAL changed during the course of RSV infection. Most of the AOE levels were significantly reduced as early as Day 1 (with the exception of peroxiredoxin 2), and they were significantly lower throughout the acute phase of RSV infection, compared with control mice, to return to basal or slightly above basal levels by Day 25 after infection. Thioredoxin 1 was the only AOE substantially unchanged in infected mice compared with control mice. These results confirm and extend our findings by Western blots, indicating that RSV significantly diminishes antioxidant defenses in the lung.

Figure 4. Two-dimensional gel electrophoresis (2DE) of bronchoalveolar lavage (BAL) proteins reveals a global reduction in antioxidant enzyme expression after respiratory syncytial virus (RSV) infection. SYPRO Ruby–stained 2DE of BAL from (A) control and (B) RSV-infected mouse at Day 3 after infection Desalted and albumin-depleted proteins (200 μl at 1 mg/ml concentration) were fractionated over immobilized pH gradients from 3 to 10 in the horizontal dimension, followed by sodium dodecyl sulfate–polyacrylamide gel electrophoresis in the vertical dimension. Left, migration of molecular mass standards (kDa). The spot volumes were normalized based on the total spot volume for each gel, and the control and RSV-infected samples were compared. The numbers indicate differentially expressed spots identified by tryptic peptide mass fingerprinting and listed in C.

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Recent findings have demonstrated that Nrf2 is a crucial transcription factor that binds to antioxidant responsive element (ARE) sequences and regulates the expression of antioxidant and phase 2 metabolizing enzymes in response to oxidative stress (12) (24, 25). To examine the effect of RSV infection on Nrf2 activation, we performed Western blot analysis of mouse lung nuclear extracts. Groups of BALB/c mice were infected with RSV or sham inoculated, and nuclear extracts were obtained from lungs at 12, 24, 48, and 72 hours after infection. There was a significant decrease of Nrf2 nuclear abundance in RSV-infected mice compared with control mice at 12 hours and 24 hours after infection (average percentage change of Nrf2 in RSV over control is 61 and 97% at 12 and 24 hours, respectively) (Figure 5), with nuclear levels in RSV-infected mice still below control at 48 and 72 hours after infection (data not shown). These results suggest that decreased AOE expression after RSV infection could be due to reduced basal activation of Nrf2 in the airways of mice.

Figure 5. Respiratory syncytial virus (RSV) infection is associated with decreased levels of nuclear Nrf2 in the lung. Mice were infected with RSV or sham inoculated and lungs were harvested at 12 and 24 hours to isolate nuclear proteins. Equal amounts of nuclear proteins were analyzed by Western blot using anti-Nrf2 antibody. Membranes were stripped and reprobed for Lamin B, as control for equal loading of the samples. Lanes 1 to 3 are lung nuclear proteins from control and 4 to 6 from RSV-infected mice at each time point. The figure is representative of three independent experiments, each experiment with four to five mice per group at each time point. Densitometric analysis of Western blot band intensities was performed using Alpha Ease software presented as mean ± SEM of n = 3. *P < 0.05; **P < 0.01 relative to control mice.

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We have previously shown that RSV is a potent inducer of ROS in airway epithelial cells in vitro (8) and causes significant oxidative stress damage in vivo, as demonstrated by the increase of lipid peroxidation markers F₂ 8-isoprostane, MDA, and 4-hydroxynonenal in the lung of experimentally infected mice (10). These data along with the findings presented herein showing a global down-regulation of the lung antioxidant capacity as a consequence of RSV infection prompted us to conduct a study in children to determine whether the virus is capable of inducing oxidative stress damage in naturally acquired infections. Thus, we measured the levels of F₂ 8-isoprostane and MDA in NPS of children with RSV-proven infections of increasing clinical severity, from milder URTI to bronchiolitis without or with hypoxia (demographics of the study population described in Table 2). The group of children with hypoxic bronchiolitis included also three subjects who required intubation and VS because of respiratory failure. As shown in Figure 6A, concentration of F₂ 8-isoprostane in NPS was slightly increased in subjects with mild bronchiolitis compared with those with URTI, but the difference was not statistically significant. However, subjects with hypoxic bronchiolitis had significantly more F₂ 8-isoprostane in NPS than did subjects with URTI alone (P < 0.01) or with nonhypoxic bronchiolitis (P < 0.001). A similar trend was observed for MDA concentrations in a smaller number of NPS samples that were tested (Figure 6B).

Figure 6. Concentrations of the oxidative stress markers in nasopharyngeal secretions (NPS) of infants with naturally acquired respiratory syncytial virus (RSV) infections. NPS collected from infants and young children with RSV-proven upper respiratory tract infections (URTI) and bronchiolitis were tested for (A) F2-isoprostane or (B) malondialdehyde (MDA) concentrations. Horizontal lines indicate the mean concentration. **P < 0.01 and ***P < 0.001 compared with URTI.

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To determine whether natural RSV infection along with an oxidative stress response may cause reduction of antioxidant defenses as we observed in experimentally infected mice, we measured levels of SOD 1, 2, and 3, catalase, and GST-mu in NPS of infected children by Western blot (Figure 7). For this analysis, infants on VS (i.e., those with most severe illness) were included in a separate group. SOD 1 levels were lower in infants with bronchiolitis, hypoxic bronchiolitis, and VS compared with those with URTI alone. The VS group showed also significantly lower levels of SOD 3, catalase, and GST-mu compared with the other illness groups. SOD 2 levels were similar in all illness groups.

Figure 7. Antioxidant enzyme expression in nasopharyngeal secretions (NPS) of infants with naturally acquired respiratory syncytial virus (RSV) infections. (A) Western blot analysis of superoxide dismutase (SOD) 1, SOD 2, and SOD 3, catalase, and glutathione S-transferase (GST)-mu in NPS of children with upper respiratory tract infections (URTI), bronchiolitis (BR), bronchiolitis with hypoxia (BR + H), and patients on ventilatory support (VS). β-actin was used as a control for protein integrity and equal loading of the samples. Densitometric analysis of Western blot band intensities was performed using Alpha Ease software. *P < 0.05; **P < 0.01, compared with URTI.

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To further investigate the spectrum of AOE changes in NPS samples from RSV-infected children, NPS proteins from the four groups described above were separated by high-resolution 2DE followed by MALDI-TOF-MS. We found that the antioxidant protein spots corresponding to SOD 1 and catalase were clearly present in URTI and bronchiolitis but significantly decreased in patients with hypoxic bronchiolitis and patients on VS, in agreement with the data of the Western blot analysis. Peroxiredoxin 1 expression was also significantly lower in children with bronchiolitis with hypoxia and VS compared with those with URTI and bronchiolitis (Figure E3).