scholarly journals Digging through the Obstruction: Insight into the Epithelial Cell Response to Respiratory Virus Infection in Patients with Cystic Fibrosis

2016 ◽  
Vol 90 (9) ◽  
pp. 4258-4261 ◽  
Author(s):  
Matthew R. Hendricks ◽  
Jennifer M. Bomberger
Keyword(s):  
Cystic Fibrosis ◽  
Lung Diseases ◽  
Respiratory Virus ◽  
Viral Infections ◽  
Molecular Diagnostic ◽  
Molecular Diagnostic Techniques ◽  
Virus Infections ◽  
Chronic Lung Diseases ◽  
Respiratory Viral Infections ◽  
Respiratory Virus Infections

Respiratory virus infections are common but generally self-limiting infections in healthy individuals. Although early clinical studies reported low detection rates, the development of molecular diagnostic techniques by PCR has led to an increased recognition that respiratory virus infections are associated with morbidity and acute exacerbations of chronic lung diseases, such as cystic fibrosis (CF). The airway epithelium is the first barrier encountered by respiratory viruses following inhalation and the primary site of respiratory viral replication. Here, we describe how the airway epithelial response to respiratory viral infections contributes to disease progression in patients with CF and other chronic lung diseases, including the role respiratory viral infections play in bacterial acquisition in the CF patient lung.

scholarly journals Cellular senescence: friend or foe to respiratory viral infections?

2020 ◽  
Vol 56 (6) ◽  
pp. 2002708
Author(s):  
William J. Kelley ◽  
Rachel L. Zemans ◽  
Daniel R. Goldstein
Keyword(s):  
Viral Replication ◽  
Cellular Senescence ◽  
Lung Diseases ◽  
Viral Infections ◽  
Respiratory Infections ◽  
Inflammatory Diseases ◽  
Cell Types ◽  
Chronic Lung Diseases ◽  
Respiratory Viral Infections ◽  
Immune Pathology

Cellular senescence permanently arrests the replication of various cell types and contributes to age-associated diseases. In particular, cellular senescence may enhance chronic lung diseases including COPD and idiopathic pulmonary fibrosis. However, the role cellular senescence plays in the pathophysiology of acute inflammatory diseases, especially viral infections, is less well understood. There is evidence that cellular senescence prevents viral replication by increasing antiviral cytokines, but other evidence shows that senescence may enhance viral replication by downregulating antiviral signalling. Furthermore, cellular senescence leads to the secretion of inflammatory mediators, which may either promote host defence or exacerbate immune pathology during viral infections. In this Perspective article, we summarise how senescence contributes to physiology and disease, the role of senescence in chronic lung diseases, and how senescence impacts acute respiratory viral infections. Finally, we develop a potential framework for how senescence may contribute, both positively and negatively, to the pathophysiology of viral respiratory infections, including severe acute respiratory syndrome due to the coronavirus SARS-CoV-2.

SEROLOGICAL EVIDENCE OF RESPIRATORY VIRUS INFECTIONS IN MOSCOW CHILDREN, 1948 TO 1956

PEDIATRICS ◽  
1966 ◽  
Vol 38 (3) ◽  
pp. 402-404
Author(s):  
V. V. Ritova ◽  
V. M. Zhdanov ◽  
E. I. Schastny
Keyword(s):  
Respiratory Disease ◽  
Respiratory Virus ◽  
Viral Infections ◽  
Mixed Infections ◽  
Virus Infections ◽  
Acute Respiratory Disease ◽  
Serological Evidence ◽  
Parainfluenza Viruses ◽  
Respiratory Virus Infections

1. The study of sera collected between 1948 and 1956 from children with acute respiratory disease showed that outbreaks were caused by adenoviruses, parainfluenza viruses, reoviruses, rhinoviruses, ECHO viruses, and Coxsackie viruses. 2. Adenovirus infections were the most prevalent. Other viral infections were prevalent in certain years. 3. Mixed infections with two viruses constituted about 10% of all cases.

Reduction in Rate of Nosocomial Respiratory Virus Infections in a Children’s Hospital Associated With Enhanced Isolation Precautions

2018 ◽  
Vol 39 (2) ◽  
pp. 152-156 ◽  
Author(s):  
Lorry G. Rubin ◽  
Nina Kohn ◽  
Susan Nullet ◽  
Margaret Hill
Keyword(s):  
Respiratory Virus ◽  
Viral Infections ◽  
Respiratory Infections ◽  
Medical Center ◽  
Tertiary Care ◽  
Virus Infections ◽  
Children's Hospital ◽  
Children’S Hospital ◽  
Respiratory Virus Infections ◽  
Hospital Days

OBJECTIVETo determine whether the use of enhanced isolation precautions (droplet and contact precautions) for inpatients with respiratory tract viral infections is associated with a reduction in rate of nosocomial viral respiratory infections.DESIGNQuasi-experimental study with the rate of nosocomial respiratory virus infection as the primary dependent variable and rate of nosocomialClostridium difficileinfection as a nonequivalent dependent variable comparator.SETTINGCohen Children’s Medical Center of NY, a tertiary-care children’s hospital attached to a large general hospital.INTERVENTIONDuring years 1 and 2 (July 2012 through June 2014), the Centers for Disease Control and Prevention/Healthcare Infection Control Practices Advisory Committee’s recommended isolation precautions for inpatients with selected respiratory virus infections were in effect. Enhanced isolation precautions were in effect during years 3 and 4 (July, 2014 through June, 2016), except for influenza, for which enhanced precautions were in effect during year 4 only.RESULTSDuring the period of enhanced isolation precautions, the rate of nosocomial respiratory virus infections with any of 4 virus categories decreased 39% from 0.827 per 1,000 hospital days prior to enhanced precautions to 0.508 per 1,000 hospital days (P<.0013). Excluding rhinovirus/enterovirus infections, the rates decreased 58% from 0.317 per 1,000 hospital days to 0.134 per 1,000 hospital days during enhanced precautions (P<.0014). During these periods, no significant change was detected in the rate of nosocomialC. difficileinfection.CONCLUSIONSEnhanced isolation precautions for inpatients with respiratory virus infections were associated with a reduction in the rate of nosocomial respiratory virus infections.Infect Control Hosp Epidemiol2018;39:152–156

scholarly journals Home Self-Collection of Nasal Swabs for Diagnosis of Acute Respiratory Virus Infections in Children With Cystic Fibrosis

2013 ◽  
Vol 2 (4) ◽  
pp. 345-351 ◽  
Author(s):  
Julia Emerson ◽  
Elizabeth Cochrane ◽  
Sharon McNamara ◽  
Jane Kuypers ◽  
Ronald L. Gibson ◽  
...  
Keyword(s):  
Cystic Fibrosis ◽  
Respiratory Virus ◽  
Virus Infections ◽  
Nasal Swabs ◽  
Respiratory Virus Infections

scholarly journals 1182. Clinical Outcomes of Hospital-Associated Respiratory Virus Infections

2019 ◽  
Vol 6 (Supplement_2) ◽  
pp. S423-S424
Author(s):  
Joshua G Petrie ◽  
Adam S Lauring ◽  
Keith S Kaye
Keyword(s):  
Respiratory Syncytial Virus ◽  
Clinical Outcomes ◽  
Influenza A ◽  
Respiratory Virus ◽  
Diagnostic Testing ◽  
Direct Result ◽  
Molecular Diagnostic ◽  
Virus Infections ◽  
Syncytial Virus ◽  
Respiratory Virus Infections

Abstract Background Influenza and respiratory syncytial virus (RSV) are recognized as important causes of hospital-acquired infection. Increased use of multiplex molecular diagnostic testing is shedding light on the incidence of other hospital-associated respiratory virus infections (HA-RVI). However, the incidence and clinical impact of HA-RVI are not well understood. Methods We identified hospitalized patients admitted between July 1, 2017 and June 30, 2018 who were clinically tested to diagnose respiratory virus infections. HA-RVI were defined as respiratory virus positivity beginning more than 48 hours after hospital admission. The clinical outcomes of HA-RVI were compared with respiratory virus infections that were not considered hospital-associated (non-HA-RVI). Results Respiratory virus testing was performed on 4,690 individuals during 5,942 inpatient encounters. At least 1 virus was identified in 1,871 (31%) encounters, and 229 (12%) were defined as HA-RVI (median hours from admission to positivity [IQR]: 154 [79, 308]). Among the patients with a respiratory virus infection, 56% were adults, 52% were male, 77% were non-Hispanic white, and the median Charlson score was 2 (IQR: 1, (4); HA-RVI patients were more likely to be male (59% vs. 51%, P = 0.01) and had higher median Charlson scores (3 vs. 2, P < 0.001). All 14 respiratory viruses in the diagnostic panel were positive for at least one HA-RVI (Figure 1), but rhino/enterovirus (99), influenza A (27), human metapneumovirus (22) and respiratory syncytial virus (20) were most common. Compared with non-HA-RVI patients, those with HA-RVI had longer post-infection lengths of stay (median: 9 vs. 4 days, P < 0.001) and were more likely to die during hospitalization (odds ratio [95% confidence interval]: 3.4 [2.0, 5.7]) (Table 1). Conclusion A substantial number of HA-RVI were identified during the 2017–2018 respiratory virus season, and they were associated with a striking number of severe outcomes. More in depth analyses are required to determine whether severe outcomes are a direct result of HA-RVI or whether HA-RVI are more common in critically ill patients and serve as a marker for severe morbidity. A broader understanding of HA-RVI transmission and prevention strategies is needed. Disclosures All authors: No reported disclosures.

scholarly journals Are Respiratory Viruses Involved in Preseasonal Symptoms or Severity in Japanese Cedar Pollinosis?

2016 ◽  
Vol 7 (2) ◽  
pp. ar.2016.7.0157 ◽  
Author(s):  
Hirokuni Otsuka ◽  
Hiroyuki Tsukagoshi ◽  
Hirokazu Kimura ◽  
Ikuo Takanashi ◽  
Kimihiro Okubo
Keyword(s):  
Respiratory Virus ◽  
Viral Infections ◽  
Japanese Cedar ◽  
Respiratory Viruses ◽  
Virus Infections ◽  
Significant Difference ◽  
Syncytial Virus ◽  
Japanese Cedar Pollinosis ◽  
Respiratory Virus Infections ◽  
The Relationship

Background Respiratory virus infections are involved in asthma exacerbations. However, there are no reports of the relationship between respiratory virus infections and Japanese cedar pollinosis. Objective We studied the relationship between respiratory viral infection and the appearance of preseasonal symptoms and the severity of seasonal symptoms in Japanese cedar pollinosis. Methods In 36 patients with asthma and with no symptoms (PreAsyP) and 54 patients with asthma and with symptoms (PreSyP) before the cedar pollen shedding commenced (preseason), and 37 patients with mild-to-moderate severity (InMild/Mod) and 45 patients with severe to extreme severity (InSev/Ext) after cedar shedding commenced (in season), the occurrence of respiratory viruses and nasal smear cytology were examined. Results In total, seven infections with respiratory viruses were detected among the subjects. Human rhinovirus (HRV) C infection was detected in one subject in each of the PreAsyP and PreSyP groups, and one HRVA infection occurred in the InMild/Mod group. In the InSev/Ext group, one HRVA, one HRVC, one respiratory syncytial virus, and one human metapneumovirus were detected. There was no significant difference in the rate of detection of viral infections between the PreAsyP and the PreSyP groups (p = 0.077), and between the InMild/Mod group and the InSev/Ext group (p = 0.24, Wilcoxon rank sum test). When cells types in nasal smears were identified and their abundance examined, the rate of neutrophilia in the subjects in the PreSyP group was 54%, which was statistically higher (p < 0.01) than the subjects in the PreAsyP group (25%). Interestingly, in the subjects in the InSev/Ext group, the proportion of eosinophils (40%) was larger (p < 0.05) than in the subjects in the InMild/Mod group (19%). Conclusion These results provided no evidence that respiratory virus infections contributed to preseasonal symptoms and severity in season of Japanese cedar pollinosis. Nasal neutrophilia was related to preseasonal symptoms, whereas nasal eosinophilia was related to severity of symptoms during the pollen season.

scholarly journals Respiratory Viral Infections in Chronic Lung Diseases

2017 ◽  
Vol 38 (1) ◽  
pp. 87-96 ◽  
Author(s):  
Clemente J. Britto ◽  
Virginia Brady ◽  
Seiwon Lee ◽  
Charles S. Dela Cruz
Keyword(s):  
Lung Diseases ◽  
Viral Infections ◽  
Chronic Lung Diseases ◽  
Respiratory Viral Infections
Sign in / Sign up

Export Citation Format

Share Document