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Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice
© The Author(s) 2010
- Received: 12 May 2010
- Accepted: 15 September 2010
- Published: 15 September 2010
Respiratory Syncytial Virus (RSV) infection is usually restricted to the respiratory epithelium. Few studies have documented the presence of RSV in the systemic circulation, however there is no consistent information whether virus detection in the blood correlates with disease severity.
Balb/c mice were inoculated with live RSV, heat-inactivated RSV or medium. A subset of RSV-infected mice was treated with anti-RSV antibody 72 h post-inoculation. RSV RNA loads were measured by PCR in peripheral blood from day 1-21 post-inoculation and were correlated with upper and lower respiratory tract viral loads, the systemic cytokine response, lung inflammation and pulmonary function. Immunohistochemical staining was used to define the localization of RSV antigens in the respiratory tract and peripheral blood.
RSV RNA loads were detected in peripheral blood from day 1 to 14 post-inoculation, peaked on day 5 and significantly correlated with nasal and lung RSV loads, airway obstruction, and blood CCL2 and CXCL1 expression. Treatment with anti-RSV antibody reduced blood RSV RNA loads and improved airway obstruction. Immunostaining identified RSV antigens in alveolar macrophages and peripheral blood monocytes.
RSV RNA was detected in peripheral blood upon infection with live RSV, followed a time-course parallel to viral loads assessed in the respiratory tract and was significantly correlated with RSV-induced airway disease.
- Respiratory Syncytial Virus
- Respiratory Syncytial Virus Infection
- Peripheral Blood Monocyte
- Nasal Wash
- Respiratory Syncytial Virus Disease
RSV is the most common cause of acute lower respiratory tract infection in infants and the leading cause of hospitalization in this age group [1, 2]. The clinical manifestations of the disease are thought to be a result of the direct viral cytopathic effect on the respiratory epithelium and the host immune response leading to significant inflammation of the respiratory tract [3–6].
Few reports, mostly in immunocompromised patients, have documented the possible dissemination of RSV outside the respiratory tract [7–12]. However, there are no studies that have examined in detail the potential relation between the presence of RSV RNA in the systemic circulation and whether it is correlated with RSV-induced acute airway disease. Other RNA respiratory viruses, such as the SARS-coronavirus, rhinoviruses, seasonal influenza or avian influenza (H5N1) viruses have been associated with detection of viral RNA in whole blood, blood fractions, serum or plasma in a subset of patients with acute or fatal disease, suggesting that viral dissemination may be associated with poor outcomes [11, 13–17].
We used a well-established experimental model of RSV infection to examine the significance of RSV dissemination in disease pathogenesis. We determined 1) whether RSV could be detected in peripheral blood during the acute phase of the disease, 2) its time course of detection compared with the upper and lower respiratory tract, and 3) whether the RSV-induced systemic cytokine response and clinical parameters of disease severity (airway obstruction and lung inflammation) were correlated with blood RSV RNA loads.
Virus, growth conditions and RSV quantification
Human RSV A2 (ATCC-1540) was grown on Hep-2 cells. RSV loads from brochoalveolar lavage (BAL) and nasal wash samples were measured by plaque assay with lower limit of detection of 1.7 log10 PFU/mL as described [18, 19]. RSV loads in BAL, whole lung, nasal wash and peripheral blood samples were measured by real-time PCR with lower limits of detection of 10 copies/reaction, as described [20, 21].
Animals and Inoculation
Seven-week old BALB/c mice were inoculated with 100 μL 107.6-8.3 PFU/mL of RSV, or heat inactivated RSV as described [18, 19, 21]. Uninfected controls were inoculated with 100 μL of 10% EMEM. All experiments were performed following the Institutional Animal Care and Research Advisory Committee guidelines.
Experimental design and sample collection
Four to six mice per time point, per group were evaluated on days 1, 3, 4, 5, 6, 7, 10, 14 and 21 after inoculation. Mice were inoculated with: 1) live RSV; 2) heat-inactivated (HI)-RSV or 3) EMEM. In a second set of experiments, a group RSV-infected mice was treated with an anti-RSV monoclonal antibody (moAb; motavizumab) administered intraperitoneally (IP; 2.50 mg/per mouse or 100 mg/kg in 100 μl) at 72 h post-inoculation . Mice were euthanized with an IP injection of ketamine and acepromazine prior to cardiac puncture. Blood, nasal wash, BAL and whole lung samples were collected for viral load quantification by culture and real-time PCR. To assess the severity of the pneumonia and the distribution of RSV antigens in the lungs we performed lung histologic evaluation and immunohistochemical (IHC) staining. Systemic CCL2, CXCL1 (innate immunity cytokines), IFN-γ (Th-1) and IL-4 (Th-2) mRNA expression was measured sequentially from days 1 to 7 post-inoculation.
Blood samples (~500 μL/mouse) were obtained by cardiac puncture, mixed in RNA stabilization reagent (Tempus® solution; ABI, Foster City, CA) and stored at -20°C until analysis. On day 5, the peak of RSV disease in this model [18, 19, 21], peripheral blood samples from two separate experiments were placed in EDTA tubes (BD vacutainer) for RSV antigen detection by IHC staining. Nasal wash and BAL specimens were obtained by infusing 500 μl of 10% EMEM through a 25-gauge needle as previously described [19, 23]. Lungs were rinsed with 3 mL of PBS 1× prior to sample collection and fixed with either 10% buffered formalin for histologic evaluation or placed in RNAlater stabilization reagent (Quiagen, Valencia, CA) for viral load quantification [20, 21]. Results represent aggregate data from four independent experiments; each included 4-6 mice per time-point per group.
Pulmonary Function Tests and Lung Histopathology
Enhanced pause (Penh), a measure of airway obstruction (AO), was assessed daily until day 10, and then weekly until day 21 using a whole-body plethysmograph (Buxco Inc, Wilmington, NC) [19, 21, 24]. For histologic evaluation lung samples were fixed in formalin, embedded in paraffin, and whole-mount sections were stained with H&E. Histopathologic scores (HPS) were determined by a pathologist who was unaware of the infection status of the mice. This scoring system has been previously validated in the RSV mouse model [18, 19, 21].
Immunohistochemical Staining (IHC)
Whole lung samples and blood cells were processed following a similar protocol. Briefly, samples were fixed in 10% buffered formalin for 30 min and re-suspended in liquefied histogel. Four-μm sections blocks were cut and placed onto positively charged slides. After deparafinization, sections were incubated at 95-100°C for 36 min for antigen retrieval. After antibody block, a primary goat anti-RSV polyclonal antibody (Biodesign International, Saco, ME) was incubated for 1 h at room temperature followed by incubation with a rabbit secondary antibody (Abcam, Cambridge, MA) and with horseradish peroxidase conjugated anti-rabbit for 24 min (Ventana, Tucson, AZ). Slides were developed using a DAB chromogen-based detection kit from Ventana and hematoxylin used as a counterstain. Lung sections from RSV infected and uninfected mice were used as positive and negative controls respectively.
Real-time Polymerase Chain Reaction (PCR)
One sample per mouse was evaluated as a single specimen and RNA detection performed by an operator who was blinded to the sample's identification. Samples subjected to RNA detection met the requirements for quantity and quality/purity assessed with the NanoDrop spectrophotometer (Wilmington, DE). No false positives were detected in a total of 1,007 samples analyzed. RNA was obtained from nasal wash, BAL and whole-lung specimens and extracted using ion-exchange mini-columns (Qiagen, Valencia, CA). Whole blood RNA was extracted using the Tempus Spin RNA kit (ABI, Foster City, CA) according to the manufacturer's instructions. RNA reverse transcription, amplification and quantification of a conserved region of the N gene was performed as described [20–22].
Semi-quantitative real-time PCR for Cytokine analysis
Quantification of blood IFN-γ (Mm 00801778_m1), IL-4 (Mm 00445259_m1), KC/CXCL1 (Mm 00433859_m1), MCP-1/CCL2 (Mm 99999056_m1), was performed by real-time PCR in ABI 7300 HT sequence detector. Relative mRNA expression was calculated using the comparative ΔΔCt method [21, 25, 26].
Sigma Stat 2008 software (SPSS Science, San Rafael, CA) was used for analyses. Differences between groups were tested using the one-way ANOVA or Kruskal-Wallis test according to data distribution. When these tests demonstrated a significant difference between groups (p < 0.05), the Tukey test to correct for multiple comparisons was used. Pearson or Spearman Rank Order test were used for correlations. In all analyses, a two-tailed p value < 0.05 was considered to be statistically significant.
Dynamics of RSV RNA detection in the in the upper and lower respiratory tract
To document the presence of replicative virus, viral loads were measured by plaque assay in BAL and nasal wash samples during the acute infection. Viral loads in both BAL (p = 0.03) and nasal wash samples (p < 0.01) increased from day 1 to days 3-4 post-inoculation, providing evidence of active viral replication, then decreased and remained below the limit of detection of the assay after day 7 post-inoculation, as previously shown in this model [18, 19, 21]. Overall, viral loads measured in BAL samples were higher than in nasal wash. This difference reached statistical significance on days 1 and 5 post-inoculation (Fig. 1B).
As previously reported, mice inoculated with HI-RSV had significantly lower RSV RNA loads in BAL and whole lung samples compared with mice infected with live RSV and no viable virus was recovered by plaque assay (data not shown) .
RSV RNA is detected in peripheral blood during acute RSV infection and follows a time-course similar to RSV RNA loads measured in the respiratory tract
The dynamics of RSV RNA in the blood mirrored RSV loads detected in the respiratory tract, although at significant lower concentrations (p < 0.05). On day 5, the peak of RSV RNA detection in peripheral blood, blood RSV RNA loads significantly correlated with nasal wash and whole lung RSV RNA loads (p < 0.05; r = 0.65-0.76), but not with those measured in BAL specimens.
RSV Antigens are detected in Peripheral Blood Monocytes
Systemic Cytokine Profiles During Acute RSV Infection
Compared with non-infected controls and mice inoculated with HI-RSV, blood CCL2 and CXCL1 mRNA peaked on day 1 (p < 0.01), they leveled off on days 4-5, and decreased by day 7 post-inoculation in mice infected with live RSV (Fig 4A and 4B). On the other hand, the systemic expression of IFN-γ increased on day 4 and remained significantly elevated thereafter (Fig. 4C). IL-4 expression was below the limit of detection or was detected at very low levels from day 1 to 5, but showed a significant increase on day 7 post-inoculation compared with controls. Expression levels of these 4 cytokines were comparable in non-infected controls and mice inoculated with HI-RSV at all time points evaluated (Fig. 4A-D).
There was a significant but inverse correlation between blood RSV RNA loads and blood expression of CCL2 and CXCL1 on day 4 post-inoculation (p < 0.05, r = -0.9/-1).
Blood RSV RNA Loads Correlates with the Severity of Acute RSV Disease
To determine the significance of blood RSV RNA detection in the context of disease pathogenesis, we assessed disease severity by measuring pulmonary function abnormalities and lung inflammation, and determined whether they were correlated with peripheral blood RSV RNA loads.
Treatment with anti-RSV neutralizing antibody reduced blood RSV RNA loads and improved acute airway obstruction
Our current understanding of the ability of RSV to spread from the respiratory tract to the systemic compartment, the time course of detection in peripheral blood, and whether this has implications for disease pathogenesis is limited. Using a mouse model of RSV infection, we found that: 1) inoculation with live RSV was consistently associated with detection of RSV RNA in peripheral blood; 2) the time course of RSV RNA detection in peripheral blood mirrored viral replication in the respiratory tract; 3) RSV antigens were detected in peripheral blood monocytes and lung alveolar macrophages during the acute phase of the disease; 4) blood RSV RNA loads correlated with acute airway obstruction; and 5) administration of an anti-RSV antibody significantly decreased the peak and duration of peripheral blood RSV RNA loads and was associated with improved airway obstruction.
Despite that the systemic spread of other paramyxoviruses has been frequently reported in the literature [30, 31], limited efforts have been dedicated to characterize the significance of the detection of RSV in peripheral blood in experimental models or patients with naturally acquired infection. Three studies documented the presence of RSV RNA by real-time PCR in blood or peripheral blood mononuclear cells (PBMCs) in a subset of neonates and children with RSV lower respiratory tract infection [8–10]. In those studies, RSV RNA was also found in the blood of a small percentage of children with no evidence of RSV infection, and the association between the detection of RSV in the blood and parameters of disease severity was inconclusive. On the other hand, the detection of RSV RNA in the serum of a 2-month old with RSV bronchiolitis was associated with the development of hepatitis, indicating the possible dissemination of RSV in severe forms of the disease . More recently, a study conducted in hematopoietic cell transplant (HCT) recipients with respiratory virus-associated pneumonia showed that compared with bronchoalveolar lavage (BAL) viral loads, serum RSV, hMPV and influenza virus RNA loads were significantly associated with the need for mechanical ventilation and death, . In the present study, the detection of peripheral blood RSV RNA gradually increased from day 1 to day 5, with detection in 100% of samples on day 5 post-inoculation which correlated with the peak of clinical disease in this model defined by increased airway obstruction.
The detection of RSV antigens by immunofluorescence prior to the implementation of PCR assays has been previously described in PBMCs of children and calves with acute RSV infection [32, 33]. In agreement with those studies, using IHC staining we identified peripheral blood monocytes bearing RSV antigens on day 5, the peak of RSV RNA detection in blood. Similarly, on days 4 to 6 post-infection the distribution of RSV antigens in the lungs was predominant in alveolar macrophages. Hence, it is possible that during the acute infection immune cells bearing RSV antigens may migrate from the respiratory tract to the systemic compartment, and this migration may explain the detection of RSV RNA in peripheral blood.
Despite that RSV antigens were detected in peripheral monocytes, blood RSV RNA loads were inversely correlated with blood CXCL1 (neutrophil chemoattractant) and CCL2 (monocyte chemoattractant) on day 4 post-inoculation and there were no correlations with IFN-γ and IL-4, key Th1/Th2 adaptive immunity cytokines [19, 29, 34]. The fact that CXCL1 and CCL2 peaked early on the infection when blood RSV RNA was detected at very low levels, and inversely correlated with the peak of RSV RNA loads on day 4 may reflect the different dynamics of viral replication and cytokine production in RSV disease.
Unexpectedly, the peak of blood RSV RNA loads did not correlate with the severity of lung inflammation, suggesting that the different components of RSV-induced lung disease may have different pathogenic mechanisms or follow different dynamics. It also suggests that the detection of RSV RNA in the blood might be an earlier event in disease pathogenesis that precedes the establishment of severe pulmonary inflammation. If this is the case, detection of RSV RNA in peripheral blood may help identifying the more severe forms of RSV disease in an early stage.
Our study has a number of limitations. We did not document viral replication in the blood using traditional cell culture, which may be due to the limited sensitivity of the culture assay with small sample volumes. Nevertheless, RSV RNA was consistently detected only in peripheral blood of mice inoculated with live RSV, suggesting that live viral infection is required for pathogenic viral dissemination. We further documented the presence of RSV by a completely different methodology, and identified a cell subtype, monocytes, bearing RSV antigens in peripheral blood. It is possible that the high RSV inoculum used caused severe lung inflammation and cell damage with subsequent leakage of RSV particles, which may have been engulfed by peripheral blood monocytes. However, the decrease of blood RSV RNA loads after treatment directed against RSV suggests that the detection of RSV RNA in peripheral blood truly reflected the spread of the virus to the systemic compartment. Lastly, the identification of RSV RNA was limited to the respiratory tract and peripheral blood but not to other organs, which could have help to indirectly assess the systemic spread of RSV during the acute infection, and warrants further studies to determine whether other organs are also affected in severe RSV disease.
We acknowledge Emilio Flaño, PhD (Nationwide Children's Hospital, Columbus, OH) from his critical review of the manuscript and insightful advice. Jason Skinner PhD (Baylor Institute for Immunology and Research, Dallas, TX) and Samir Gupta MD (UT Southwestern Medical Center, Dallas, TX) for their suggestions, and Evangeline Brock, (Children's Medical Center, Dallas, TX) for her help with viral cultures.
This work was presented in part at the 48th Annual ICAAC/IDSA 46th Annual Meeting, Washington DC, October 25-28, 2008. AM was supported in part by institutional grants and the RGK foundation. OR was supported in part by research grants from Medimmune.
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