| Literature DB >> 27513985 |
Lorenzo Zammarchi, Claudia Fortuna, Giulietta Venturi, Francesca Rinaldi, Teresa Capobianco, Maria Elena Remoli, Gian Maria Rossolini, Giovanni Rezza, Alessandro Bartoloni.
Abstract
Entities:
Keywords: Africa; Chikungunya virus; Europe; Italy; Somalia; traveler; viruses
Mesh:
Year: 2016 PMID: 27513985 PMCID: PMC5088032 DOI: 10.3201/eid2211.161225
Source DB: PubMed Journal: Emerg Infect Dis ISSN: 1080-6040 Impact factor: 6.883
Results of chikungunya virus testing for 2 persons who returned to Italy after traveling to Mogadishu, Somalia, 2016*
| Laboratory test performed | Place where test was performed | Results | |
|---|---|---|---|
| Patient 1† | Patient 2‡ | ||
| OnSite Chikungunya IgM Combo Rapid Test-Cassette (CTK Biotech, San Diego CA, USA)§ | Careggi University Hospital | Positive | Negative |
| Chikungunya virus IFA IgG (Euroimmun AG, Luebeck, Germany)¶ | Careggi University Hospital | Titer | Titer |
| Chikungunya virus IFA IgM (Euroimmun)** | Careggi University Hospital | Positive | Positive |
| Anti-CHIKV IgM ELISA (Euroimmun)†† | ISS, National Reference Laboratory for Arboviruses | Index 7.9‡‡ | Index 3.4‡‡ |
| PRNT for Chikungunya virus | ISS, National Reference Laboratory for Arboviruses | PRNT80 | PRNT80 |
*Testing was conducted on samples taken the day patients 1 and 2 sought care at the Infectious and Tropical Diseases Outpatient Unit at Careggi University Hospital in Florence, Italy. IFA, immunofluorescence assay; ISS, National Institute of Health in Rome, Italy; PRNT, plaque reduction neutralization test; PRNT80, 80% PRNT. †Samples were obtained 33 d after symptom onset. ‡Samples were obtained 52 d after symptom onset. §Sensitivity/specificity 90.3%/100% according to information reported in the kit data sheet (reference 10 in Technical Appendix, and 30%/73% according to an independent evaluation (reference 11 in Technical Appendix). ¶Sensitivity/specificity 100%/96% according to information reported in the kit data sheet (reference 12 in Technical Appendix). #Cut-off for positivity >1:10. **Sensitivity/specificity 95%/96% according to information reported in the kit data sheet (reference 12 in Technical Appendix). ††Sensitivity/specificity 98.1%/98.9% according to information reported in the kit data sheet (reference 13 in Technical Appendix) and 85%/82% according to an independent evaluation (reference 11 in Technical Appendix). ‡‡Cut-off for positivity >1.1. §§PRNT80 titers >1:10 are considered positive.