What to know
- Many laboratories can test for human adenoviruses, but the extent of testing capability can vary.
- If typing or specialized testing is needed, contact your state health department to discuss available testing options.
Laboratory guidelines
Laboratories can detect and type human adenoviruses using:
- Molecular detection (e.g., Nucleic Acid Amplification Tests (NAATs), such as PCR)
- Partial or full genome sequencing
- Antigen detection
- Virus isolation
- Virus neutralization with type-specific antisera
Additional information on adenovirus testing at ÐÇ¿ÕÓéÀÖ¹ÙÍø is available at Submitting Specimens to ÐÇ¿ÕÓéÀÖ¹ÙÍø.
Specimen collection
The types of specimens you should collect for human adenovirus detection depend on the patient's clinical presentation and type of infection.
Before collecting any specimens, discuss with a laboratory and a clinician familiar with adenovirus. To improve human adenovirus detection, you should collect specimens within a week of symptom onset.
Respiratory Infections
For respiratory infections, you should typically collect upper respiratory specimens such as a nasopharyngeal swab and/or oropharyngeal (throat) swab. If there is evidence of a lower respiratory infection, you should also collect a lower respiratory specimen such as sputum. In some instances, a serum specimen may be helpful.
Eye Infections
If there is clinical evidence of a conjunctival or eye infection, you should collect a conjunctival swab.
Gastroenteritis Infections
See Recommendations for Collection of Laboratory Specimens Associated with Outbreaks of Gastroenteritis (cdc.gov).
- National Center for Immunization and Respiratory Diseases, NCIRD Divisions and Offices
- Lu X and Erdman DD. Molecular typing of human adenovirus by PCR and sequence of a partial region of the hexon gene. Arch Virol. 2006; 151(8):1587-602.
- Lu X, Trujillo-Lopez E, Lott L, Erdman DD. J Clin Microbiol. 2013; 51(4):1089-1093.
- Lu X and Erdman DD. Quantitative real-time PCR assays for identification of species C human adenoviruses. J Virol. Method. 2016; 237:174-178.