Protein and transcriptional biomarker profiling may inform treatment strategies in lower respiratory tract infections by indicating bacterial-viral differentiation

被引:1
作者
Sivakumaran, Dhanasekaran [1 ]
Jenum, Synne [1 ,2 ]
Markussen, Dagfinn Lunde [1 ,3 ,4 ]
Serigstad, Sondre [3 ,5 ]
Srivastava, Aashish [6 ]
Saghaug, Christina Skar [1 ,4 ]
Ulvestad, Elling [1 ,4 ]
Knoop, Siri Tandberg [1 ,4 ]
Grewal, Harleen M. S. [1 ,4 ]
机构
[1] Univ Bergen, Dept Clin Sci, Bergen Integrated Diagnost Stewardship Cluster, Bergen, Norway
[2] Oslo Univ Hosp, Dept Infect Dis, Oslo, Norway
[3] Haukeland Hosp, Emergency Care Clin, Bergen, Norway
[4] Haukeland Hosp, Dept Microbiol, Bergen, Norway
[5] Univ Bergen, Dept Clin Med, Bergen, Norway
[6] Univ Bergen, Haukeland Univ Hosp, Clin Lab K2, Genome Core Facil, Bergen, Norway
关键词
acute respiratory infections; bacterial vs viral diagnosis; host-based biomarkers; biosignatures; antibiotic treatment; COMMUNITY-ACQUIRED PNEUMONIA; REQUIRING HOSPITALIZATION; ETIOLOGY; IMPACT; VALIDATION; DISCOVERY; VIRUSES; ADULTS;
D O I
10.1128/spectrum.02831-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Lower respiratory tract infections (LRTIs) remain a significant global cause of infectious disease-related mortality. Accurate discrimination between acute bacterial and viral LRTIs is crucial for optimal patient care, prevention of unnecessary antibiotic prescriptions, and resource allocation. Plasma samples from LRTI patients with bacterial (n = 36), viral (n = 27; excluding SARS-CoV-2), SARS-CoV-2 (n = 22), and mixed bacterial-viral (n = 38) etiology were analyzed for protein profiling. Whole-blood RNA samples from a subset of patients (bacterial, n = 8; viral, n = 8; and SARS-CoV-2, n = 8) were analyzed for transcriptional profiling. Lasso regression modeling identified a seven-protein signature (CRP, IL4, IL9, IP10, MIP1 alpha, MIP1 beta, and TNF alpha) that discriminated between patients with bacterial (n = 36) vs viral (n = 27) infections with an area under the curve (AUC) of 0.98. When comparing patients with bacterial and mixed bacterial-viral infections (antibiotics clinically justified; n = 74) vs patients with viral and SARS-CoV-2 infections (antibiotics clinically not justified; n = 49), a 10-protein signature (CRP, bFGF, eotaxin, IFN gamma, IL1 beta, IL7, IP10, MIP1 alpha, MIP1 beta, and TNF alpha) with an AUC of 0.94 was identified. The transcriptional profiling analysis identified 232 differentially expressed genes distinguishing bacterial (n = 8) from viral and SARS-CoV-2 (n = 16) etiology. Protein-protein interaction enrichment analysis identified 20 genes that could be useful in the differentiation between bacterial and viral infections. Finally, we examined the performance of selected published gene signatures for bacterial-viral differentiation in our gene set, yielding promising results. Further validation of both protein and gene signatures in diverse clinical settings is warranted to establish their potential to guide the treatment of acute LRTIs.IMPORTANCEAccurate differentiation between bacterial and viral lower respiratory tract infections (LRTIs) is vital for effective patient care and resource allocation. This study investigated specific protein signatures and gene expression patterns in plasma and blood samples from LRTI patients that distinguished bacterial and viral infections. The identified signatures can inform the design of point-of-care tests that can aid healthcare providers in making informed decisions about antibiotic prescriptions in order to reduce unnecessary use, thereby contributing to reduced side effects and antibiotic resistance. Furthermore, the potential for faster and more accurate diagnoses for improved patient management in acute LRTIs is compelling. Accurate differentiation between bacterial and viral lower respiratory tract infections (LRTIs) is vital for effective patient care and resource allocation. This study investigated specific protein signatures and gene expression patterns in plasma and blood samples from LRTI patients that distinguished bacterial and viral infections. The identified signatures can inform the design of point-of-care tests that can aid healthcare providers in making informed decisions about antibiotic prescriptions in order to reduce unnecessary use, thereby contributing to reduced side effects and antibiotic resistance. Furthermore, the potential for faster and more accurate diagnoses for improved patient management in acute LRTIs is compelling.
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页数:15
相关论文
共 47 条
[1]  
Abbafati C, 2020, LANCET, V396, P1135, DOI 10.1016/S0140-6736(20)31404-5
[2]  
[Anonymous], 2021, NASJONAL FAGLIG RETN
[3]  
[Anonymous], 2018, R LANG ENV STAT COMP
[4]   Novel point-of-care biomarker combination tests to differentiate acute bacterial from viral respiratory tract infections to guide antibiotic prescribing: a systematic review [J].
Carlton, Henry C. ;
Savovic, Jelena ;
Dawson, Sarah ;
Mitchelmore, Philip J. ;
Elwenspoek, Martha M. C. .
CLINICAL MICROBIOLOGY AND INFECTION, 2021, 27 (08) :1096-1108
[5]   The etiology of community-acquired pneumonia in Australia: Why penicillin plus doxycycline or a macrolide is the most appropriate therapy [J].
Charles, Patrick G. P. ;
Whitby, Michael ;
Fuller, Andrew J. ;
Stirling, Robert ;
Wright, Alistair A. ;
Korman, Tony M. ;
Holmes, Peter W. ;
Christiansen, Keryn J. ;
Waterer, Grant W. ;
Pierce, Robert J. P. ;
Mayall, Barrie C. ;
Armstrong, John G. ;
Catton, Michael G. ;
Nimmo, Graeme R. ;
Johnson, Barbara ;
Hooy, Michelle ;
Grayson, M. L. .
CLINICAL INFECTIOUS DISEASES, 2008, 46 (10) :1513-1521
[6]   Diagnostic accuracy of the FebriDx host response point-of-care test in patients hospitalised with suspected COVID-19 [J].
Clark, Tristan W. ;
Brendish, Nathan J. ;
Poole, Stephen ;
Naidu, Vasanth V. ;
Mansbridge, Christopher ;
Norton, Nicholas ;
Wheeler, Helen ;
Presland, Laura ;
Ewings, Sean .
JOURNAL OF INFECTION, 2020, 81 (04) :607-613
[7]   Epidemiology of lower respiratory tract infections in adults [J].
Feldman, Charles ;
Shaddock, Erica .
EXPERT REVIEW OF RESPIRATORY MEDICINE, 2019, 13 (01) :63-77
[8]   Clinical Utility of On-Demand Multiplex Respiratory Pathogen Testing among Adult Outpatients [J].
Green, Daniel A. ;
Hitoaliaj, Letiana ;
Kotansky, Brian ;
Campbell, Sheldon M. ;
Peaper, David R. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2016, 54 (12) :2950-2955
[9]   Epidemiology of community-acquired pneumonia in adult patients at the dawn of the 21st century:: a prospective study on the Mediterranean coast of Spain [J].
Gutiérrez, F ;
Masiá, M ;
Rodríguez, JC ;
Mirete, C ;
Soldán, B ;
Padilla, S ;
Hernández, I ;
De Ory, F ;
Royo, G ;
Hidalgo, AM .
CLINICAL MICROBIOLOGY AND INFECTION, 2005, 11 (10) :788-800
[10]   Etiology of community-acquired pneumonia and diagnostic yields of microbiological methods: a 3-year prospective study in Norway [J].
Holter, Jan C. ;
Muller, Fredrik ;
Bjorang, Ola ;
Samdal, Helvi H. ;
Marthinsen, Jon B. ;
Jenum, Pal A. ;
Ueland, Thor ;
Froland, Stig S. ;
Aukrust, Pal ;
Husebye, Einar ;
Heggelund, Lars .
BMC INFECTIOUS DISEASES, 2015, 15