Table 1.
Patient | Days from symptom onset | PCR result (viral copies/reaction) a | Sampling site | Serology result (realized on serum samples) b |
---|---|---|---|---|
1 | 8 | Positive (unknown) | NPS | |
32 | Negative | NPS | ||
35 | Negative | NPS | ||
39 | Positive (590,000) | BAL | IgG 1.22 (doubtful) | |
Positive (54) | Serum | IgA 0.89 (doubtful) | ||
42 | Positive (478,000) | ETA | ||
Negative | NPS | |||
48 | Positive (9,700) | BAL | ||
Positive (60,000) | ETA | |||
Negative | NPS | |||
55 | Positive (11,950,000) | ETA | ||
Positive (62) | NPS | |||
67 | Positive (low) | NPS | ||
68 | Negative | Serum | IgG 0.74 (doubtful) | |
IgA 8.24 (positive) | ||||
73 | Negative | NPS | ||
77 | Negative | NPS | ||
2 | 1 | Positivec | NPS | |
34 | Negative | NPS | ||
35 | Positive (24,630,000) | BAL | IgG 0.61 (doubtful) | |
Negative | Serum | IgA 5.34 (positive) | ||
41 | Negative | NPS | ||
43 | / | IgG 1.16 (doubtful) | ||
IgA 2.97 (positive) | ||||
45 | Positive (97) | Plasma | ||
54 | Negative | Serum |
Abbreviations: BAL, bronchoalveolar lavage; ETA, endotracheal aspirate; IgA, immunoglobulin A; IgG, immunoglobulin G; NPS, nasopharyngeal swab; PCR, polymerase chain reaction; RT‐PCR, reverse transcription PCR; SARS‐CoV‐2, severe acute respiratory syndrome coronavirus 2.
SARS‐CoV‐2 was identified via RT‐PCR according to the current guidelines (Institut Pasteur and the WHO technical guidance). The assay targets two regions of the viral RNA‐dependent RNA polymerase (RdRp) gene and has the threshold limit of detection of 10 copies per reaction.
SARS‐CoV‐2 serological diagnostic was performed according manufacturer instructions:
– IgA were detected using the Euroimmun assays (negative: ratio <0.8; doubtful: 0.8‒1.1; positive: >1.1).
– IgG were detected using the Abbott architect assay (negative: ratio <0.49; doubtful: 0.49‒1.4; positive: >1.4).
Viral load was not available for this sample; the threshold cycle value was 27.