Comparison of sputum and nasopharyngeal swabs for detection of respiratory viruses
Diagnostic tests for respiratory viral infections use traditionally either nasopharyngeal washes or swabs. Sputum is representative of the lower respiratory tract but is used rarely for viral testing. The aim of this study was to compare the detection rates of respiratory viruses from nasopharyngeal...
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Published in | Journal of medical virology Vol. 86; no. 12; pp. 2122 - 2127 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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United States
Blackwell Publishing Ltd
01.12.2014
Wiley Subscription Services, Inc John Wiley and Sons Inc |
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Abstract | Diagnostic tests for respiratory viral infections use traditionally either nasopharyngeal washes or swabs. Sputum is representative of the lower respiratory tract but is used rarely for viral testing. The aim of this study was to compare the detection rates of respiratory viruses from nasopharyngeal swabs and sputum using a multiplex real‐time reverse transcription‐polymerase chain reaction (RT‐PCR). Adults who were admitted or presented to the clinics of Gil Medical Center with acute respiratory symptoms were recruited from 1 November 2012 to 31 March 2013. Paired specimens of nasopharyngeal swabs and sputum were obtained from 154 subjects, and RNA was extracted and tested for 16 different respiratory viruses using the Anyplex II RV16 Detection kit (Seegene, Seoul, Korea). The positive rate was 53% (81/154) for nasopharyngeal swabs and 68% (105/154) for sputum (P < 0.001). One hundred thirty‐four viruses were identified for 107 illnesses. Influenza A virus, RSV A, HRV, coronavirus OC43, and adenovirus were detected more frequently in sputum samples than in nasopharyngeal swabs (P < 0.001). Importantly, 12 of 44 (27%) influenza A infections and 11 of 27 (41%) RSV infections were positive in only sputum samples. The detection rates of respiratory viruses from sputum samples were significantly higher than those from nasopharyngeal swabs in adults using real‐time multiplex RT‐PCR. These findings suggest that sputum would benefit for the detection of respiratory viruses by nucleic acid amplification tests (NAATs) in patients who produce sputum. Further studies are needed to establish standardized RNA extraction methods from sputum samples. J. Med. Virol. 86:2122–2127, 2014. © 2014 Wiley Periodicals, Inc. |
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AbstractList | Diagnostic tests for respiratory viral infections use traditionally either nasopharyngeal washes or swabs. Sputum is representative of the lower respiratory tract but is used rarely for viral testing. The aim of this study was to compare the detection rates of respiratory viruses from nasopharyngeal swabs and sputum using a multiplex real-time reverse transcription-polymerase chain reaction (RT-PCR). Adults who were admitted or presented to the clinics of Gil Medical Center with acute respiratory symptoms were recruited from 1 November 2012 to 31 March 2013. Paired specimens of nasopharyngeal swabs and sputum were obtained from 154 subjects, and RNA was extracted and tested for 16 different respiratory viruses using the Anyplex II RV16 Detection kit (Seegene, Seoul, Korea). The positive rate was 53% (81/154) for nasopharyngeal swabs and 68% (105/154) for sputum (P < 0.001). One hundred thirty-four viruses were identified for 107 illnesses. Influenza A virus, RSV A, HRV, coronavirus OC43, and adenovirus were detected more frequently in sputum samples than in nasopharyngeal swabs (P < 0.001). Importantly, 12 of 44 (27%) influenza A infections and 11 of 27 (41%) RSV infections were positive in only sputum samples. The detection rates of respiratory viruses from sputum samples were significantly higher than those from nasopharyngeal swabs in adults using real-time multiplex RT-PCR. These findings suggest that sputum would benefit for the detection of respiratory viruses by nucleic acid amplification tests (NAATs) in patients who produce sputum. Further studies are needed to establish standardized RNA extraction methods from sputum samples.Diagnostic tests for respiratory viral infections use traditionally either nasopharyngeal washes or swabs. Sputum is representative of the lower respiratory tract but is used rarely for viral testing. The aim of this study was to compare the detection rates of respiratory viruses from nasopharyngeal swabs and sputum using a multiplex real-time reverse transcription-polymerase chain reaction (RT-PCR). Adults who were admitted or presented to the clinics of Gil Medical Center with acute respiratory symptoms were recruited from 1 November 2012 to 31 March 2013. Paired specimens of nasopharyngeal swabs and sputum were obtained from 154 subjects, and RNA was extracted and tested for 16 different respiratory viruses using the Anyplex II RV16 Detection kit (Seegene, Seoul, Korea). The positive rate was 53% (81/154) for nasopharyngeal swabs and 68% (105/154) for sputum (P < 0.001). One hundred thirty-four viruses were identified for 107 illnesses. Influenza A virus, RSV A, HRV, coronavirus OC43, and adenovirus were detected more frequently in sputum samples than in nasopharyngeal swabs (P < 0.001). Importantly, 12 of 44 (27%) influenza A infections and 11 of 27 (41%) RSV infections were positive in only sputum samples. The detection rates of respiratory viruses from sputum samples were significantly higher than those from nasopharyngeal swabs in adults using real-time multiplex RT-PCR. These findings suggest that sputum would benefit for the detection of respiratory viruses by nucleic acid amplification tests (NAATs) in patients who produce sputum. Further studies are needed to establish standardized RNA extraction methods from sputum samples. Diagnostic tests for respiratory viral infections use traditionally either nasopharyngeal washes or swabs. Sputum is representative of the lower respiratory tract but is used rarely for viral testing. The aim of this study was to compare the detection rates of respiratory viruses from nasopharyngeal swabs and sputum using a multiplex real‐time reverse transcription‐polymerase chain reaction (RT‐PCR). Adults who were admitted or presented to the clinics of Gil Medical Center with acute respiratory symptoms were recruited from 1 November 2012 to 31 March 2013. Paired specimens of nasopharyngeal swabs and sputum were obtained from 154 subjects, and RNA was extracted and tested for 16 different respiratory viruses using the Anyplex II RV16 Detection kit (Seegene, Seoul, Korea). The positive rate was 53% (81/154) for nasopharyngeal swabs and 68% (105/154) for sputum ( P < 0.001). One hundred thirty‐four viruses were identified for 107 illnesses. Influenza A virus, RSV A, HRV, coronavirus OC43, and adenovirus were detected more frequently in sputum samples than in nasopharyngeal swabs ( P < 0.001). Importantly, 12 of 44 (27%) influenza A infections and 11 of 27 (41%) RSV infections were positive in only sputum samples. The detection rates of respiratory viruses from sputum samples were significantly higher than those from nasopharyngeal swabs in adults using real‐time multiplex RT‐PCR. These findings suggest that sputum would benefit for the detection of respiratory viruses by nucleic acid amplification tests (NAATs) in patients who produce sputum. Further studies are needed to establish standardized RNA extraction methods from sputum samples. J. Med. Virol. 86:2122–2127, 2014 . © 2014 Wiley Periodicals, Inc. Diagnostic tests for respiratory viral infections use traditionally either nasopharyngeal washes or swabs. Sputum is representative of the lower respiratory tract but is used rarely for viral testing. The aim of this study was to compare the detection rates of respiratory viruses from nasopharyngeal swabs and sputum using a multiplex real-time reverse transcription-polymerase chain reaction (RT-PCR). Adults who were admitted or presented to the clinics of Gil Medical Center with acute respiratory symptoms were recruited from 1 November 2012 to 31 March 2013. Paired specimens of nasopharyngeal swabs and sputum were obtained from 154 subjects, and RNA was extracted and tested for 16 different respiratory viruses using the Anyplex II RV16 Detection kit (Seegene, Seoul, Korea). The positive rate was 53% (81/154) for nasopharyngeal swabs and 68% (105/154) for sputum (P<0.001). One hundred thirty-four viruses were identified for 107 illnesses. Influenza A virus, RSV A, HRV, coronavirus OC43, and adenovirus were detected more frequently in sputum samples than in nasopharyngeal swabs (P<0.001). Importantly, 12 of 44 (27%) influenza A infections and 11 of 27 (41%) RSV infections were positive in only sputum samples. The detection rates of respiratory viruses from sputum samples were significantly higher than those from nasopharyngeal swabs in adults using real-time multiplex RT-PCR. These findings suggest that sputum would benefit for the detection of respiratory viruses by nucleic acid amplification tests (NAATs) in patients who produce sputum. Further studies are needed to establish standardized RNA extraction methods from sputum samples. J. Med. Virol. 86:2122-2127, 2014. copyright 2014 Wiley Periodicals, Inc. Diagnostic tests for respiratory viral infections use traditionally either nasopharyngeal washes or swabs. Sputum is representative of the lower respiratory tract but is used rarely for viral testing. The aim of this study was to compare the detection rates of respiratory viruses from nasopharyngeal swabs and sputum using a multiplex real‐time reverse transcription‐polymerase chain reaction (RT‐PCR). Adults who were admitted or presented to the clinics of Gil Medical Center with acute respiratory symptoms were recruited from 1 November 2012 to 31 March 2013. Paired specimens of nasopharyngeal swabs and sputum were obtained from 154 subjects, and RNA was extracted and tested for 16 different respiratory viruses using the Anyplex II RV16 Detection kit (Seegene, Seoul, Korea). The positive rate was 53% (81/154) for nasopharyngeal swabs and 68% (105/154) for sputum (P < 0.001). One hundred thirty‐four viruses were identified for 107 illnesses. Influenza A virus, RSV A, HRV, coronavirus OC43, and adenovirus were detected more frequently in sputum samples than in nasopharyngeal swabs (P < 0.001). Importantly, 12 of 44 (27%) influenza A infections and 11 of 27 (41%) RSV infections were positive in only sputum samples. The detection rates of respiratory viruses from sputum samples were significantly higher than those from nasopharyngeal swabs in adults using real‐time multiplex RT‐PCR. These findings suggest that sputum would benefit for the detection of respiratory viruses by nucleic acid amplification tests (NAATs) in patients who produce sputum. Further studies are needed to establish standardized RNA extraction methods from sputum samples. J. Med. Virol. 86:2122–2127, 2014. © 2014 Wiley Periodicals, Inc. Diagnostic tests for respiratory viral infections use traditionally either nasopharyngeal washes or swabs. Sputum is representative of the lower respiratory tract but is used rarely for viral testing. The aim of this study was to compare the detection rates of respiratory viruses from nasopharyngeal swabs and sputum using a multiplex real-time reverse transcription-polymerase chain reaction (RT-PCR). Adults who were admitted or presented to the clinics of Gil Medical Center with acute respiratory symptoms were recruited from 1 November 2012 to 31 March 2013. Paired specimens of nasopharyngeal swabs and sputum were obtained from 154 subjects, and RNA was extracted and tested for 16 different respiratory viruses using the Anyplex II RV16 Detection kit (Seegene, Seoul, Korea). The positive rate was 53% (81/154) for nasopharyngeal swabs and 68% (105/154) for sputum (P < 0.001). One hundred thirty-four viruses were identified for 107 illnesses. Influenza A virus, RSV A, HRV, coronavirus OC43, and adenovirus were detected more frequently in sputum samples than in nasopharyngeal swabs (P < 0.001). Importantly, 12 of 44 (27%) influenza A infections and 11 of 27 (41%) RSV infections were positive in only sputum samples. The detection rates of respiratory viruses from sputum samples were significantly higher than those from nasopharyngeal swabs in adults using real-time multiplex RT-PCR. These findings suggest that sputum would benefit for the detection of respiratory viruses by nucleic acid amplification tests (NAATs) in patients who produce sputum. Further studies are needed to establish standardized RNA extraction methods from sputum samples. |
Author | Jeong, Sung Hwan Kim, Kyung Hee Lee, Sang Min Park, Jeong Woong Seo, Yiel Hea Jeong, Ji Hun |
AuthorAffiliation | 1 Department of Laboratory Medicine Gachon University Gil Medical Center Incheon Korea 2 Department of Pulmonary Medicine Gachon University Gil Medical Center Incheon Korea |
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Keywords | nasopharyngeal swab reverse transcription-polymerase chain reaction sputum |
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References | Desjardin L, Perkins M, Teixeira L, Cave M, Eisenach K. 1996. Alkaline decontamination of sputum specimens adversely affects stability of mycobacterial mRNA. J Clin Microbiol 34:2435-2439. Kim SR, Ki CS, Lee NY. 2009. Rapid detection and identification of 12 respiratory viruses using a dual priming oligonucleotide system-based multiplex PCR assay. J Virol Methods 156:111-116. Pérez-Ruiz M, Pedrosa-Corral I, Sanbonmatsu-Gámez S, Navarro-Marí M. 2012. Laboratory detection of respiratory viruses by automated techniques. Open Virol J 6:151-159. Roa PL, Rodríguez-Sánchez B, Catalán P, Giannella M, Alcalá L, Padilla B, Viedma DG, Muñoz P, Bouza E. 2012. Diagnosis of influenza in intensive care units: Lower respiratory tract samples are better than nose-throat swabs. Am J Respir Crit Care Med 186:929-930. Gharabaghi F, Hawan A, Drews S, Richardson S. 2011. Evaluation of multiple commercial molecular and conventional diagnostic assays for the detection of respiratory viruses in children. Clin Microbiol Infect 17:1900-1906. Lieberman D, Shimoni A, Keren-Naus A, Steinberg R, Shemer-Avni Y. 2009. Identification of respiratory viruses in adults: Nasopharyngeal versus oropharyngeal sampling. J Clin Microbiol 47:3439-3443. Yu X, Lu R, Wang Z, Zhu N, Wang W, Julian D, Chris B, Lu J, Tan W. 2012. Etiology and clinical characterization of respiratory virus infections in adult patients attending an emergency department in Beijing. PLoS ONE 7:e32174. Monto AS. 2002. Epidemiology of viral respiratory infections. Am J Med 112:4-12. Xiang X, Qiu D, Hegele RD, Tan WC. 2001. Comparison of different methods of total RNA extraction for viral detection in sputum. J Virol Methods 94:129-135. Falsey AR, Formica MA, Walsh EE. 2012. Yield of sputum for viral detection by reverse transcriptase PCR in adults hospitalized with respiratory illness. J Clin Microbiol 50:21-24. Bogoch II, Andrews JR, Zachary KC, Hohmann EL. 2013. Diagnosis of influenza from lower respiratory tract sampling after negative upper respiratory tract sampling. Virulence 4:82-84. Storch GA. 2000. Diagnostic virology. Clin Infect Dis 31:739-751. Drews SJ, Blair J, Lombos E, DeLima C, Burton L, Mazzulli T, Low DE. 2008. Use of the Seeplex RV Detection kit for surveillance of respiratory viral outbreaks in Toronto, Ontario, Canada. Ann Clin Lab Sci 38:376-379. Loens K, Van Heirstraeten L, Malhotra-Kumar S, Goossens H, Ieven M. 2009. Optimal sampling sites and methods for detection of pathogens possibly causing community-acquired lower respiratory tract infections. J Clin Microbiol 47:21-31. Landis JR, Koch GG. 1977. The measurement of observer agreement for categorical data. Biometrics 33:159-174. Zhang G, Hu Y, Wang H, Zhang L, Bao Y, Zhou X. 2012. High incidence of multiple viral infections identified in upper respiratory tract infected children under three years of age in Shanghai, China. PloS one 7:e44568. 2012; 50 2009; 47 2012; 186 2001; 94 2013; 4 2008; 38 2002; 112 2000; 31 2009; 156 1977; 33 2011; 17 2012; 6 2012; 7 1996; 34 |
References_xml | – reference: Desjardin L, Perkins M, Teixeira L, Cave M, Eisenach K. 1996. Alkaline decontamination of sputum specimens adversely affects stability of mycobacterial mRNA. J Clin Microbiol 34:2435-2439. – reference: Bogoch II, Andrews JR, Zachary KC, Hohmann EL. 2013. Diagnosis of influenza from lower respiratory tract sampling after negative upper respiratory tract sampling. Virulence 4:82-84. – reference: Landis JR, Koch GG. 1977. The measurement of observer agreement for categorical data. Biometrics 33:159-174. – reference: Loens K, Van Heirstraeten L, Malhotra-Kumar S, Goossens H, Ieven M. 2009. Optimal sampling sites and methods for detection of pathogens possibly causing community-acquired lower respiratory tract infections. J Clin Microbiol 47:21-31. – reference: Monto AS. 2002. Epidemiology of viral respiratory infections. Am J Med 112:4-12. – reference: Falsey AR, Formica MA, Walsh EE. 2012. Yield of sputum for viral detection by reverse transcriptase PCR in adults hospitalized with respiratory illness. J Clin Microbiol 50:21-24. – reference: Roa PL, Rodríguez-Sánchez B, Catalán P, Giannella M, Alcalá L, Padilla B, Viedma DG, Muñoz P, Bouza E. 2012. Diagnosis of influenza in intensive care units: Lower respiratory tract samples are better than nose-throat swabs. Am J Respir Crit Care Med 186:929-930. – reference: Zhang G, Hu Y, Wang H, Zhang L, Bao Y, Zhou X. 2012. High incidence of multiple viral infections identified in upper respiratory tract infected children under three years of age in Shanghai, China. PloS one 7:e44568. – reference: Lieberman D, Shimoni A, Keren-Naus A, Steinberg R, Shemer-Avni Y. 2009. Identification of respiratory viruses in adults: Nasopharyngeal versus oropharyngeal sampling. J Clin Microbiol 47:3439-3443. – reference: Gharabaghi F, Hawan A, Drews S, Richardson S. 2011. 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SubjectTerms | Adenovirus Adult Body fluids Clinical Laboratory Techniques - methods Coronavirus Diagnostic tests Female Humans Influenza A virus Male Middle Aged Multiplex Polymerase Chain Reaction - methods nasopharyngeal swab Nasopharynx - virology Respiratory diseases Respiratory Tract Infections - diagnosis Respiratory Tract Infections - virology Reverse Transcriptase Polymerase Chain Reaction - methods reverse transcription-polymerase chain reaction Ribonucleic acid RNA Sensitivity and Specificity sputum Sputum - virology Virology Virology - methods Viruses - isolation & purification |
Title | Comparison of sputum and nasopharyngeal swabs for detection of respiratory viruses |
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