- Research article
- Open Access
Activation of cytokines and NF-kappa B in corneal epithelial cells infected by respiratory syncytial virus: potential relevance in ocular inflammation and respiratory infection
© Bitko et al; licensee BioMed Central Ltd. 2004
- Received: 05 February 2004
- Accepted: 15 July 2004
- Published: 15 July 2004
Respiratory syncytial virus (RSV) is a major cause of lower respiratory tract infection, claiming millions of lives annually. The virus infects various cells of the respiratory tract as well as resident inflammatory cells such as macrophages. Infection activates a variety of cellular factors such as cytokines and the pro-inflammatory transcription factor, NF-kappa B, all of which are important players in the respiratory disease. However, the exact natural route of RSV infection and its etiology remain relatively unknown. In this paper, we test the hypothesis that human corneal epithelial cells, which constitute the outermost layer of the cornea, can be infected with RSV, and that the infection leads to the activation of proinflammatory macromolecules.
Corneal swabs obtained from pediatric patients with acute respiratory disease were found to contain RSV at a high frequency (43 positive out of 72 samples, i.e., 60%). Primary corneal epithelial cells in tissue culture supported robust infection and productive growth of RSV. Infection resulted in the activation of TNF-α, IL-6 and sixteen chemokines as well as NF-κB. Three proinflammatory CXC chemokines (MIG, I-TAC, IP-10) underwent the greatest activation.
The ocular epithelium is readily infected by RSV. The pro-inflammatory cytokines are likely to play critical roles in the etiology of inflammation and conjunctivitis commonly seen in pediatric patients with respiratory infections. RSV-eye interactions have important implications in RSV transmission, immunopathology of RSV disease, and in the management of conjunctivitis.
- A549 Cell
- Respiratory Syncytial Virus
- Respiratory Syncytial Virus Infection
- Corneal Epithelium
- Corneal Epithelial Cell
The respiratory syncytial virus (RSV), a nonsegmented negative-strand RNA virus of the Paramyxoviridae family, is the most important causative agent of pediatric respiratory disease worldwide [1–3]. Various cells of the upper and lower respiratory tracts can be infected by RSV, including cells of the lung and the nasal passage, and cells in transit such as alveolar macrophages [4–7]. Although major progress has been made in our understanding of ocular infections [8–10], the potential interaction of respiratory pathogens with the eye has remained largely neglected in spite of the anatomical connection between the optic and the nasal / upper respiratory tissues. More than a decade ago, Hall and coworkers found that use of eye goggles and nose masks significantly reduced transmission of RSV infection from patients to hospital workers . Moreover, when live RSV was instilled into the eye, nose, or mouth of adult volunteers, more respiratory infections occurred through eye or nose than through the mouth . Recently, conjunctival cells from patients with allergic conjunctivitis were shown to be more likely (23%) to contain RSV as compared to conjunctivitis-free individuals (5%) . Conjunctival tissue from RSV-infected eye also contained elevated levels of IL-4, an interleukin important in hypersensitivity [14, 15]. While these results suggested a susceptibility of the eye to RSV, the infectivity and response of the various kinds of ocular cells to RSV have not been systematically evaluated.
Respiratory cells infected with RSV elaborate cytokines and chemokines [6, 16, 17] that play important roles in the inflammatory response of the infected lung [2, 16, 18]. The chemokines are of particular interest because of their role in the recruitment of immune and inflammatory cells to the site of infection. Presently, the chemokines are divided into four subfamilies based on the number and spacing of conserved Cys residues in their primary structure: CXC (α chemokines), CC (β chemokines), C (γ chemokines) and CX3C (δ chemokines), where X can be any amino acid . In the unified nomenclature  the chemokines are viewed as ligands and given names such as CXCL, while their receptor names are indicated by the suffix R such as CXCR; both names are followed by a numeral.
A number of immunoregulatory genes require NF-κB for optimal transcription, and a major role of NF-κB in inflammation and septic shock has been well-documented . NF-κB subunits belong to the rel family of proteins  and the best-studied NF-κB species is a heterodimer consisting of RelA (formerly p65) and p50. RSV-infection of alveolar epithelial A549 cells was shown to promote nuclear translocation and activation of both RelA and p50 subunits [6, 22, 23]. In mouse as well as in A549 cells RSV infection led to the activation of NF-κB and this was essential for the transcriptional activation of various cytokine genes [6, 16, 22, 24, 25]. We, therefore, considered it important to determine if similar activation of NF-κB also occurs in HCE cells in response to RSV infection.
Isolation of RSV from eyes of children with respiratory infection
We used RT-PCR for the initial screening of the large number of samples. However, RT-PCR does not distinguish dead virus or viral genome from live or infectious virus. To ensure that the PCR-positive samples reflected truly infectious RSV, we attempted to culture the virus by inoculating the samples into HEp-2 cell monolayers at low cell density (see Methods). Indeed, when the infected cells were subjected to immunoblot by a specific antibody against the viral P protein, the protein was discerned in nearly all (41 out of 43, i.e., 95%) of the PCR-positive swab samples (Fig. 1B). The fragility of RSV may explain the loss of infectivity in the remaining 5% samples. Furthermore, massive syncytia characteristic of RSV growth was seen in all samples that reacted positively in the immunoblot (Fig. 1C). Thus, we conclude that there is a strong statistical correlation (P < 0.02) between respiratory disease (n = 72) and our ability to isolate infectious RSV (n = 41) from the eye of the individual.
Growth of RSV in human corneal epithelial cells
Elaboration of interleukins by RSV-infected corneal epithelial cells
IL-1, a master-regulator cytokine, is often produced at the site of invasion/inflammation and then activates other cytokines including chemokines [28, 29]. IL-1β is generated by proteolytic processing of the pro-IL1β by IL-1β-converting enzyme or ICE [30, 31], which is a caspase homolog; the processed IL-1β is released and acts on surrounding cells to activate the synthesis and release of chemokines. IL-1α, in contrast, is activated mainly at the transcriptional level. Because the mRNAs of neither IL-1α nor β was elevated by RSV (Fig. 4), we tested the protein levels released in the extracellular medium at different times post-infection. As shown in Fig. 5B, while IL-1α was barely activated, IL-1β level in the medium reached its maximal concentration at 36 hr (460 pg/ml), accounting for nearly 90-fold activation over basal levels. Interestingly, IL-1β protein had an early kinetics of activation such that substantial extracellular amounts (~25 pg/ml) could be detected as early as 6 hr post-infection.
Activation of NF-κB in RSV-infected corneal epithelial cells
Next, in order to demonstrate the transcriptional activity of NF-κB, we employed a functional assay using the plasmid pNFκB-Luc, a specific NF-κB responsive reporter plasmid in which synthesis of luciferase is dependent on tandem promoter-proximal NF-κB sites . RSV infection of HCE cells transiently transfected with pNFκB-Luc resulted in a nearly 15-fold induction of luciferase activity over uninfected controls (Fig. 6B). No luciferase activity was detected using pfLuc, a control plasmid lacking the NF-κB sites [6, 32]. Induction of luciferase was inhibited by N-acetyl cysteine (NAC), an NF-κB inhibitor (Fig. 6B) as well as by sodium salicylate and acetylsalicylic acid (aspirin), two drugs that were previously shown to inhibit activation of NF-κB, including RSV-mediated activation in A549 cells [6, 32]. The NF-κB-dependence was further authenticated by the fact that negligible amounts (8–10%) of luciferase were produced when cells transfected with a control plasmid lacking NF-κB sites (pfLuc) were infected with RSV (data not shown). Taken together, these results demonstrate the functional activation of NF-κB (RelA) in corneal epithelial cells as a result of RSV infection.
Results presented here suggest that RSV, an established infectious agent of the lower respiratory tract, may be considered a pathogen of the eye as well. To our knowledge this is the first detailed report of a direct interaction of RSV with the ocular tissue. Interestingly, RSV infection of the corneal epithelium exhibited many features observed in the infection of the lung epithelium: (i) A strong correlation between respiratory infection and the presence of RSV in the eye (Fig. 1); (ii) A productive multiplication of the virus (Fig. 2, 3); (iii) Liberation of a variety of cytokines (Fig. 4, 5); and (iv) Strong activation of transcription factor NF-κB (Fig. 6). It is to be noted that RSV growth was slower in HCE cells compared to lung epithelial cells. Whereas the virus-induced syncytium is observed in about 36 hrs in A549 lung cells , it was not seen until about 48 hrs in HCE cells. The release of progeny virions and the induction of the cytokines also followed a parallel and slower kinetics in HCE cells (compare, for example, Fig. 2 with the kinetics in A549 cells [6, 23]). These results are in agreement with a role of viral macromolecular synthesis in the activation of these signaling pathways in HCE cells. It is to be mentioned here that specific RSV strains infect nonhuman mammals such as the cattle, sheep, pig and goat, and thus, an extension of these findings may have important relevance in agriculture. The implications of the viral regulation of corneal genes are briefly summarized below.
As noted in the Results (Fig. 4), a considerable number of chemokine genes of both CXC and CC families were induced in the RSV-infected HCE cells. The CX3C member, Fractalkine, was not up-regulated, and the C subfamily chemokines (Lymphotactin and SCM-1β) were not tested. The CXC subfamily  is further divided into two groups based on the presence or absence of the Glu-Leu-Arg (ELR) motif immediately preceding the first Cys residue near the amino terminus. The ELR+ CXC chemokines act primarily on neutrophils as chemoattractants and activators, inducing neutrophil degranulation with release of myeloperoxidase and other enzymes. In contrast, chemokines of the ELR- CXC and the CC subfamilies chemoattract and activate T- and B-lymphocytes and natural killer (NK) cells Interestingly, chemokines that exhibited the highest induction (in the hundreds of fold) by RSV (Fig. 4) belonged to the latter two subfamilies and included three ELR- chemokines, namely MIG (Monokine-induced by IFN-γ), I-TAC (IFN-γ-inducible T cell alpha chemoattractant) and IP-10 (IFN-γ-inducible protein of 10 kDa), and two CC chemokines, MIP-1α and MIP-1β. It is also noteworthy that whereas MIG, I-TAC and IP-10 are all IFN-γ inducible , RSV infection did not activate IFN-γ from the HCE cells (Fig. 4). Clearly, these chemokines must be induced via an IFN-γ-independent pathway activated by RSV, which needs to be elucidated further. It should be noted that recent studies have cast doubt on the original assumption that expression of these chemokines absolutely requires IFN-γ. For example, IFN-γ-independent activation of MIG and IP-10 has been observed in primary human umbilical vein endothelial cells (HUVECs) in response to infection by influenza virus . Moreover, studies in IFN-γ knockout mice have revealed that in the absence of IFN-γ, IFN-α and -β are able to induce MIG in response to a viral infection in vivo .
Although many chemokines can be pluripotent and exhibit redundant functions , we notice an interesting pattern in the HCE chemokines induced by RSV (Fig. 4). It appears that the some of most weakly induced ones (I-309, MDC, TARC) are agonists of CCR8 and CCR4, and therefore, likely to recruit Type 2 (Th2) lymphocytes characteristic of allergy. In contrast, the four most highly induced ones (MIG, I-TAC, IP-10 and MIP-1β) were CXCR3 and CCR5 agonists, and therefore, likely to recruit Th1 lymphocytes, characteristic of an inflammatory response . Further studies are needed to unravel how the Th1 and Th2 balance may affect the pathology of the RSV-infected eye.
The significantly higher induction of IL-1β (Fig. 5) deserves special mention. Ocular IL-1, by virtue of its multipotential nature, plays a regulatory and generally pro-inflammatory role in acute inflammation of the eye . First, because the IL-1β receptor (IL-1 RII) is found on monocytes, neutrophils and T cells , the elaborated IL-1β may directly recruit these cells to the infected cornea, thus promoting inflammation. Ocular chemokines have in fact been shown to play essential roles in blinding keratitis caused by herpes simplex and Pseudomonas aeruginosa [8–10]. Second, IL-1 has the potential to activate other cytokines, including chemokines such as IL-8, GROα, and MIP-1α, many of which may in turn recruit and/or activate inflammatory cells such as eosinophils and neutrophils at later times in the infected eye [8, 9, 36–40]. Results in Fig. 4 and 5 in fact suggest that IL-1β is activated through proteolytic processing by ICE relatively early (about 6 hr) in RSV infection of the corneal epithelial cells. Because the transcription of the IL-1β-inducible chemokines, such as IL-8, GRO, and MIP were all induced hours later (beginning around 12 hours) (Fig. 4, 5), it is quite possible that they were induced, at least in part, by IL-1β.
In a recent study , use of DNA microarray lead to the identification of a spectrum of chemokines inducible by RSV infection from two alveolar epithelial cell lines: A549, a type II-like cancer cell line, and SAE, a primary cell line of type I. In A549, the following chemokines mRNAs were induced: CC (I-309, Exodus-1, TARC, RANTES, MCP-1, MDC, and MIP-1α and -β), CXC (GRO-α, -β, and -γ, ENA-78, IL-8, and I-TAC) and CX3C (Fractalkine). Many of these chemokine mRNAs were also induced in SAE cells following RSV infection; however, important exceptions were MDC, TARC and MCP-1, suggesting that RSV-induced cytokine response differs between different types of airway-derived epithelial cells. The most notable differences between these airway cells and the HCE cells were the absence of induction of RANTES, ENA-78 and Fractalkine in the HCE cells (Fig. 4). Such differences may reflect the innate genetic difference between corneal and alveolar epithelial cells. In either case, just as the respiratory epithelium has been postulated to be a primary initiator of pulmonary inflammation , the corneal epithelium may also act as an initiator of ocular inflammation in RSV infection. Our conclusion should not be interpreted to mean that all conjunctivitis is caused by RSV; in chronic vernal keratoconjunctivitis, for example, RT-PCR analysis of conjunctival biopsy samples (n = 15) failed to detect RSV .
As mentioned earlier, RSV infection activates NF-kappa B in lung epithelial cells; however, the status of corneal NF-κB is relatively unknown. To our knowledge, the results presented here constitute the first documentation of NF-κB activation in HCE cells following a respiratory virus infection. Gene knock out studies have shown that the NF-κB kinase (IKK) – and by inference, NF-κB itself – is essential for the development of the mammalian cornea and conjunctiva . A basal expression of NF-κB in the HCE cells was also observed in our studies (Fig. 6). Thus, it is reasonable to conjecture that the increased NF-κB activity observed following RSV-infection might lead to transcriptional induction of cytokines such as IL-8, MIP-1α, MIP-1β and MCP (Fig. 4). We previously showed that non-steroidal anti-inflammatory drugs (NSAID) aspirin and salicylate inhibited NF-κB activation and induction of a number of cytokines from lung epithelial cells . A comparable ability of the NSAIDs to abrogate NF-κB activation in RSV-infected HCE cells (Fig. 6B) raises the interesting possibility that they may also help to resolve RSV-mediated inflammation of the eye. The other avenues of potential intervention would include inhibition of specific immunomodulatory cytokine(s) by a variety of available antagonists including, but not limited to, antibodies . Antiviral-antichemokine combination therapy is in fact a new strategy worth considering as a general therapeutic approach to viral infections [6, 43]. In a recent example , combination of an antiviral (ribavirin) and anti-CCL3 was synergistic and able to prevent mortality in mice infected with the highly lethal pneumonia virus of mice, a natural mouse pathogen that is very similar to RSV and belongs to the same genus, Pneumovirus.
Lastly, it will be interesting to determine whether RSV can travel from the infected outer cells of the eye to the inner layers and eventually to the respiratory tissues. Clearly, the short- and long-term effects of RSV on the ocular epithelium and their potential impact on vision and respiratory disease will open new directions in ocular immunopathology and the mechanism of RSV spread.
The outer layer of the eye can be productively infected by RSV ex vivo and in vivo. Our results thus establish a traditional respiratory virus as a bona fide eye pathogen. A large battery of cytokines and NF-κB, activated in RSV-infected corneal epithelium, may play strategic roles in producing conjunctivitis, frequently found in individuals with RSV infections. We also propose that the eye may serve as a gateway of RSV infection leading to and eventually infecting the upper and lower respiratory tracts. It is obvious that interactions between the eye and RSV are relevant in the etiology and pathology of the ocular as well as the respiratory disease.
Collection of eye swabs and detection of RSV
Children of 2–10 years age, admitted to the Department of Pediatrics, University of South Alabama, were screened for red, watery, and itchy eyes, and the common indicators of respiratory infection such as nasal congestion, bronchiolitis, cough, and wheezing. Age-matched controls consisted of children admitted to the same hospital for unrelated reasons (such as sports injury). Sample was collected from the surface of the eye (mainly corneal and conjunctival regions) with a sterile cotton swab (Q-tip) which was then dropped into 0.5 ml PBS; this suspension was subjected to two tests, viz., PCR and infectivity assay. The collection was pre-approved by the Institutional Review Board.
For PCR, 0.45 ml of the suspension was centrifuged at 120,000 × g in a table-top air-driven ultracentrifuge, and the supernatant discarded. The pellet (containing virions, if any) was resuspended in 5 μl of the following: 10 mM Tris-Cl (pH 8.3), 0.02% SDS, 0.05% Triton X-100, 0.5 mM EDTA, 2 mM DTT. To this, 30 pmole of each of the following oligodeoxynucleotide primers were added [25, 43]. For RSV: 5'TGTTATAGGCATATCATTGA3'; 5'TTAACCAGCAAAGTGTTAGA3' (221 bp product); for glyceraldehyde 3-phosphate dehydrogenase (GAPDH): 5'CCAAAAGGGTCATCATCTCTGG3' and 5'ATTTGGCAGGTTTTTCTAGACGG3' (417 bp product). Multiplex RT-PCR analyses have earlier revealed that the RSV primers, corresponding to the sequence of the fusion (F) glycoprotein gene of RSV, do not amplify any of the common viral and bacterial agents of acute respiratory infections [26, 45]. The mixture was heated at 95°C for 5 min and rapidly chilled in ice. To the annealed RNA-primer mixture the following were added: 2 μl of 5 × RT buffer [250 mM Tris-Cl (pH 8.3), 375 mM KCl, 25 mM MgCl2, 50 mM DTT], 0.5 μl RNasin (20 units), all four dNTPs (final concentration 1 mM each), M-MLV reverse transcriptase (200 units, 1 μl), and the volume was made up to 20 μl. The reverse transcription reaction was incubated for 30 min at 40°C.
PCR was reconstituted in the same RT reaction tube by the addition of an equal volume (20 μl) of buffer containing 20 mM Tris-Cl (pH 8.3), 50 mM KCl, 2 mM MgCl2. PCR was performed for 40 cycles with the following parameters: 94°C, 2 min (denaturation); 48°C, 2 min (annealing); and 72°C, 20 sec (elongation). An initial melting step (also to inactivate the RT) of 94°C, 5 min and a final extension step of 72°C, 30 sec were added to the beginning and end, respectively. PCR was initiated by hot-start, i.e., by the addition of 2 units of Taq polymerase after the first 94°C step. The product (221 bp) was analyzed by standard agarose (0.8%) gel electrophoresis followed by staining with ethidium bromide.
For infectivity assay, 0.05 ml of the PBS suspension was directly added to each well of a 6-well HEp-2 monolayer at 30% confluency. The cells were then incubated for 3 days and routinely observed under microscope for syncytia formation, a hallmark of late-stage RSV infection. Once syncytia were recorded the monolayer was scraped off, the RSV-infected cells were spun down, and the pellet resuspended in SDS sample buffer . Portions of the sample (about 40 μg total protein) were resolved by SDS-PAGE followed by immunoblot analysis using rabbit antibody against the P protein of RSV  and anti-rabbit secondary antibody raised in goat. The Super Signal Ultra chemiluminescence procedure (Pierce, Rockford, IL) was used for detection of the signal as described previously .
Corneal epithelial cells and RSV infection
Normal eyes from human donors, free of known ocular infections, were purchased from National Disease Research Interchange (Philadelphia, PA). The corneal epithelia were isolated and the cells were dispersed and grown in monolayers essentially as described [36, 37]. Cells in this work were passaged no more than 4–5 times. When the monolayer reached a confluency of about 70%, RSV was added at a multiplicity of infection of 3.0 using standard procedures described earlier [6, 26]. The HCE monolayer was infected with human RSV (Long strain) . In all infection experiments described in this paper, control cells were "mock-infected" with a 120,000 × g supernatant of the viral preparation; such supernatants were previously shown to be free of detectable infectious virions .
The inoculum of human RSV was grown in HEp-2 cells and purified as described [6, 47], and progeny virions liberated from infected HCE cells were titered on HEp-2 by standard serial dilution and plaque counting [7, 48].
Cytokine and NF-κB Assays
For Real Time PCR experiments, RNA was isolated from RSV-infected HCE cells at 6, 12, 24, 36 and 48 h post-infection and the first-strand cDNA was made using the GeneAmp RNA PCR Core kit (Perkin Elmer-Applied Biosystems). Primers are designed by the Beacon Designer software v 2.13 from Premier Biosoft. Real Time PCR was performed on the iCycler iQ Quantitative PCR system from BioRad Laboratories (Hercules, CA) using the iQ Sybr Green SuperMix. Gene expression measurements were calculated using the manufacturer's software; GAPDH was used as an internal control.
Cytokines released in the culture media supernatant were assayed by the TransSignal Human Cytokine Antibody Array 3.0 from Panomics (Redwood City, CA) according to the manufacturer's protocol. Briefly, cytokine-specific antibodies were supplied immobilized on a membrane in an array configuration. Appropriate dilutions of the infected cell media were incubated with the array membrane and the captured cytokines were detected with a mixture of biotin-labeled anti-cytokine antibodies followed by streptavidin-HRP. The chemiluminescence (ECL) of the array dots was developed by the Pierce kit mentioned earlier and digitally captured and quantified using the Fujifilm LAS-1000 system and the Image Gauge 4.0 software. IL-1α and IL-1β were quantified by ELISA, using standardized assay kits from R&D Systems (Minneapolis, MN).
The various kinds of NF-κB analyses were carried out as described previously [6, 23]. Briefly, lysis of transfected and/or RSV-infected HCE cells and preparation of nuclear extracts were carried out essentially as described previously. Immunoblot analysis of 100 μg of nuclear extract was performed using rabbit antibodies against Sp1 and the p50 and p65 subunits of NF-κB (Santa Cruz Biotechnology, Santa Cruz, CA) . The NF-κB reporter plasmid (pNFκB-Luc) was constructed by cloning an additional synthetic NF-κB element (5'GGGGACTTTCCC3') into the plasmid pBIIxLuc by insertional mutagenesis using the Megaprimer method . The NF-κB-unresponsive plasmid, pfLuc, is missing the NF-κB response elements, but is otherwise identical to pNFκB-Luc [6, 32]. All plasmids were transfected into HCE cells using Fusgene (Roche Molecular Biochemicals, Indianapolis, IN) according to the manufacturer's protocol. At 15 hours post-transfection, RSV was added at a multiplicity of infection of 3, and at 18 h thereafter, processed for luciferase assay as described . Where used, NF-κB inhibitory drugs were added to the cells at the same time as the virus .
This research was supported in part by a R01 grant (EY013826) from the National Eye Institute and by a NRSA Postdoctoral Fellowship (F32 AI049682), both from the National Institutes of Health, USA.
- Thompson WW, Shay DK, Weintraub E, Brammer L, Cox N, Anderson LJ, Fukuda K: Mortality associated with influenza and respiratory syncytial virus in the United States. JAMA. 2003, 289: 179-186. 10.1001/jama.289.2.179.View ArticlePubMedGoogle Scholar
- Maggon K, Barik S: New drugs and treatment for respiratory syncytial virus. Rev Med Virol. 2004, 14: 149-168. 10.1002/rmv.423.View ArticlePubMedGoogle Scholar
- Marriott AC, Easton AJ: Reverse genetics of the Paramyxoviridae. Adv Virus Res. 1999, 53: 321-340.View ArticlePubMedGoogle Scholar
- Welliver RC: Respiratory syncytial virus and other respiratory viruses. Pediatr Infect Dis J. 2003, 22: S6-S12. 10.1097/00006454-200302001-00002.PubMedGoogle Scholar
- Greenough A: Respiratory syncytial virus infection: clinical features, management, and prophylaxis. Curr Opin Pulm Med. 2002, 8: 214-217. 10.1097/00063198-200205000-00011.View ArticlePubMedGoogle Scholar
- Bitko V, Velazquez A, Yang L, Yang YC, Barik S: Transcriptional activation of multiple cytokines by respiratory syncytial virus requires activation of NF-κB and is inhibited by sodium salicylate and aspirin. Virology. 1997, 232: 369-378. 10.1006/viro.1997.8582.View ArticlePubMedGoogle Scholar
- Bitko V, Oldenburg A, Garmon NE, Barik S: Profilin is required for viral morphogenesis, syncytium formation, and cell-specific stress fiber induction by respiratory syncytial virus. BMC Microbiol. 2003, 3: 9-10.1186/1471-2180-3-9.PubMed CentralView ArticlePubMedGoogle Scholar
- Tumpey TM, Cheng H, Cook DN, Smithies O, Oakes JE, Lausch RN: Absence of macrophage inflammatory protein-1 alpha prevents the development of blinding herpes stromal keratitis. J Virol. 1998, 72: 3705-3710.PubMed CentralPubMedGoogle Scholar
- Kumaraguru U, Davis I, Rouse BT: Chemokines and ocular pathology caused by corneal infection with herpes simplex virus. J Neurovirol. 1999, 5: 42-47.View ArticlePubMedGoogle Scholar
- Pearlman E: Chemokines in ocular allergy and inflammation. In: Chemokines in Allergic Disease. Edited by: Rothenberg ME. 2000, New York: Marcel Dekker, 435-452.Google Scholar
- Gala CL, Hall CB, Schnabel KC, Pincus PH, Blossom P, Hildreth SW, Betts RF, Douglas RG: The use of eye-nose goggles to control nosocomial respiratory syncytial virus infection. JAMA. 1986, 256: 2706-2708. 10.1001/jama.256.19.2706.View ArticlePubMedGoogle Scholar
- Hall CB, Douglas RG, Schnabel KC, Geiman JM: Infectivity of respiratory syncytial virus by various routes of inoculation. Infect Immun. 1981, 33: 779-783.PubMed CentralPubMedGoogle Scholar
- Fujishima H, Okamoto Y, Saito I, Tsubota K: Respiratory syncytial virus and allergic conjunctivitis. J Allergy Clin Immunol. 1995, 95: 663-667.View ArticlePubMedGoogle Scholar
- Fujishima H, Saito I, Okamoto Y, Takeuchi T, Tsubota K: Respiratory syncytial virus- induced interleukin-4 production by human conjunctival epithelial cells contributes to allergy: preliminary study. Curr Eye Res. 1998, 17: 656-662. 10.1076/ceyr.17.6.656.5181.View ArticlePubMedGoogle Scholar
- Fujishima H: Respiratory syncytial virus may be a pathogen in allergic conjunctivitis. Cornea. 2002, 21: S39-45. 10.1097/00003226-200203001-00009.View ArticlePubMedGoogle Scholar
- Tian B, Zhang Y, Luxon BA, Garofalo RP, Casola A, Sinha M, Brasier AR: Identification of NF-kappaB-dependent gene networks in respiratory syncytial virus-infected cells. J Virol. 2002, 76: 6800-6814. 10.1128/JVI.76.13.6800-6814.2002.PubMed CentralView ArticlePubMedGoogle Scholar
- Zhang Y, Luxon BA, Casola A, Garofalo RP, Jamaluddin M, Brasier AR: Expression of respiratory syncytial virus-induced chemokine gene networks in lower airway epithelial cells revealed by cDNA microarrays. J Virol. 2001, 75: 9044-9058. 10.1128/JVI.75.19.9044-9058.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Haeberle HA, Kuziel WA, Dieterich HJ, Casola A, Gatalica Z, Garofalo RP: Inducible expression of inflammatory chemokines in respiratory syncytial virus-infected mice: role of MIP-1alpha in lung pathology. J Virol. 2001, 75: 878-890. 10.1128/JVI.75.2.878-890.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Baggiolini M: Chemokines in pathology and medicine. J Intern Med. 2001, 250: 91-104. 10.1046/j.1365-2796.2001.00867.x.View ArticlePubMedGoogle Scholar
- Bacon K, Baggiolini M, Broxmeyer H, Horuk R, Lindley I, Mantovani A, Maysushima K, Murphy P, Nomiyama H, Oppenheim J, Rot A, Schall T, Tsang M, Thorpe R, Van Damme J, Wadhwa M, Yoshie O, Zlotnik A, Zoon K: IUIS/WHO Subcommittee on Chemokine Nomenclature. Chemokine/chemokine receptor nomenclature. J Interferon Cytokine Res. 2002, 22: 1067-1068. 10.1089/107999002760624305.View ArticlePubMedGoogle Scholar
- Perkins ND: The Rel/NF-kappa B family: friend and foe. Trends Biochem Sci. 2000, 25: 434-440. 10.1016/S0968-0004(00)01617-0.View ArticlePubMedGoogle Scholar
- Garofalo R, Sabry M, Jamaluddin M, Yu RK, Casola A, Ogra PL, Brasier AR: Transcriptional activation of the interleukin-8 gene by respiratory syncytial virus infection in alveolar epithelial cells: nuclear translocation of the RelA transcription factor as a mechanism producing airway mucosal inflammation. J Virol. 1996, 70: 8773-8781.PubMed CentralPubMedGoogle Scholar
- Bitko V, Barik S: Persistent activation of RelA by respiratory syncytial virus involves protein kinase C, underphosphorylated IκBβ, and sequestration of protein phosphatase 2A by the viral phosphoprotein. J Virol. 1998, 72: 5610-5618.PubMed CentralPubMedGoogle Scholar
- Mastronarde JG, He B, Monick MM, Mukaida N, Matsushima K, Hunninghake G: Induction of IL-8 gene expression by respiratory syncytial virus involves activation of NF-κB and NF-IL-6. J Infect Dis. 1996, 174: 262-267.View ArticlePubMedGoogle Scholar
- Fiedler MA, Wernke-Dollries K, Stark JM: Inhibition of viral replication reverses respiratory syncytial virus-induced NF-kappa B activation and interleukin-8 gene expression in A549 cells. J Virol. 1996, 70: 9079-9082.PubMed CentralPubMedGoogle Scholar
- Bitko V, Barik S: Phenotypic silencing of cytoplasmic genes using sequence-specific double-stranded short interfering RNA and its application in the reverse genetics of wild type negative-strand RNA viruses. BMC Microbiol. 2001, 1: 34-10.1186/1471-2180-1-34.PubMed CentralView ArticlePubMedGoogle Scholar
- Bitko V, Barik S: An endoplasmic reticulum-specific stress-activated caspase (caspase-12) is implicated in the apoptosis of A549 epithelial cells by respiratory syncytial virus. J Cell Biochem. 2001, 80: 441-454. 10.1002/1097-4644(20010301)80:3<441::AID-JCB170>3.0.CO;2-C.View ArticlePubMedGoogle Scholar
- Dinarello CA: Anti-cytokine therapeutics and infections. Vaccine. 2003, 21 (Suppl 2): S24-34.View ArticlePubMedGoogle Scholar
- O'Neill LA: Signal transduction pathways activated by the IL-1 receptor/toll-like receptor superfamily. Curr Top Microbiol Immunol. 2002, 270: 47-61.PubMedGoogle Scholar
- Burns K, Martinon F, Tschopp J: New insights into the mechanism of IL-1beta maturation. Curr Opin Immunol. 2003, 15: 26-30. 10.1016/S0952-7915(02)00017-1.View ArticlePubMedGoogle Scholar
- Thornberry NA, Bull HG, Calaycay JR, Chapman KT, Howard AD, Kostura MJ, Miller DK, Molineaux SM, Weidner JR, Aunins J, Elliston KO, Ayala JM, Casano FJ, Chin J, Ding GJF, Egger LA, Gaffney EP, Limjuco G, Palyha OC, Raju SM, Rolando AM, Salley JP, Yamin TT, Lee TD, Shively JE, MacCross M, Mumford RA, Schmidt JA, Tocci MJ: A novel heterodimeric cysteine protease is required for interleukin-1 beta processing in monocytes. Nature. 1992, 356: 768-774. 10.1038/356768a0.View ArticlePubMedGoogle Scholar
- Kopp E, Ghosh S: Inhibition of NF-κB by sodium salicylate and aspirin. Science. 1994, 265: 956-959.View ArticlePubMedGoogle Scholar
- Ishiguro N, Takada A, Yoshioka M, Ma X, Kikuta H, Kida H, Kobayashi K: Induction of interferon-inducible protein-10 and monokine induced by interferon-gamma from human endothelial cells infected with influenza A virus. Arch Virol. 2004, 149: 17-34. 10.1007/s00705-003-0208-4.View ArticlePubMedGoogle Scholar
- Mahalingam S, Chaudhri G, Tan CL, John A, Foster PS, Karupiah G: Transcription of the interferon gamma (IFN-gamma)-inducible chemokine Mig in IFN-gamma-deficient mice. J Biol Chem. 2001, 276: 7568-7574. 10.1074/jbc.M005773200.View ArticlePubMedGoogle Scholar
- Staats HF, Lausch RN: Cytokine expression in vivo during murine herpetic stromal keratitis. Effect of protective antibody therapy. J Immunol. 1993, 151: 277-283.PubMedGoogle Scholar
- Cubitt CL, Lausch RN, Oakes JE: Differential induction of GROα gene expression in human corneal epithelial cells and keratinocytes exposed to proinflammatory cytokines. Invest Opthalmol Vis Sci. 1997, 38: 1149-1158.Google Scholar
- Cubitt CL, Tang Q, Monterio CA, Lausch RN, Oakes JE: IL-8 gene expression in cultures of human corneal epithelial cells and keratocytes. Invest Opthalmol Vis Sci. 1993, 34: 3199-3206.Google Scholar
- Arrunategui-Correa V, Baltatzis S, Foster CS: The role of cytokines in experimental herpes simplex keratitis. Acta Virol. 1999, 43: 325-329.PubMedGoogle Scholar
- Yan XT, Tumpey TM, Kunkel SL, Oakes JE, Lausch RN: Role of MIP-2 in neutrophil migration and tissue injury in the herpes simplex virus-1-infected cornea. Invest Ophthalmol Vis Sci. 1998, 39: 1854-1862.PubMedGoogle Scholar
- Hendricks RL: Immunopathogenesis of viral ocular infections. Chem Immunol. 1999, 73: 120-136.View ArticlePubMedGoogle Scholar
- Koulikovska M, van der Ploeg I, Herrmann B, Montan PG: Respiratory syncytial virus and chlamydia are not detectable by PCR in ongoing vernal keratoconjunctivitis. Ocul Immunol Inflamm. 2001, 9: 253-257. 10.1076/ocii.126.96.36.19955.View ArticlePubMedGoogle Scholar
- Yoshida K, Hu Y, Karin M: IkappaB kinase alpha is essential for development of the mammalian cornea and conjunctiva. Invest Ophthalmol Vis Sci. 2000, 41: 3665-3669.PubMedGoogle Scholar
- Glass WG, Rosenberg HF, Murphy PM: Chemokine regulation of inflammation during acute viral infection. Curr Opin Allergy Clin Immunol. 2003, 3: 467-473. 10.1097/00130832-200312000-00008.View ArticlePubMedGoogle Scholar
- Bonville CA, Easton AJ, Rosenberg HF, Domachowske JB: Altered pathogenesis of severe pneumovirus infection in response to combined antiviral and specific immunomodulatory agents. J Virol. 2003, 77: 1237-1244. 10.1128/JVI.77.2.1237-1244.2003.PubMed CentralView ArticlePubMedGoogle Scholar
- Grondahl B, Puppe W, Hoppe A, Kuhne I, Weigl JA, Schmitt HJ: Rapid identification of nine microorganisms causing acute respiratory tract infections by single-tube multiplex RT-PCR: feasibility study. J Clin Microbiol. 1999, 37: 1-7.PubMed CentralPubMedGoogle Scholar
- Laemmli UK: Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970, 227: 680-685.View ArticlePubMedGoogle Scholar
- Barik S, McLean T, Dupuy L: Phosphorylation of Ser232 directly regulates the transcriptional activity of the P protein of human respiratory syncytial virus: Phosphorylation of Ser237 may play an accessory role. Virology. 1995, 213: 405-412. 10.1006/viro.1995.0013.View ArticlePubMedGoogle Scholar
- Burke E, Dupuy L, Wall C, Barik S: Role of cellular actin in the gene expression and morphogenesis of human respiratory syncytial virus. Virology. 1998, 252: 137-148. 10.1006/viro.1998.9471.View ArticlePubMedGoogle Scholar
- Barik S: Mutagenesis and gene fusion by megaprimer PCR. Methods Mol Biol. 1997, 67: 173-181.PubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.