A novel positive-sense
RNA virus named Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)
was identified in December 2019 in China. It is a systemic disease that
includes severe respiratory distress, coronavirus disease 19 (Covid-19). The
primary way of transmitting this virus is person-to-person contact via respiratory
droplets, but it can also be transmitted by contaminated surfaces. Symptoms
range from mild to severe, and the virus spreads quickly. On 11 March 2020
Covid-19 was declared a pandemic by the World Health Organization. The standard
way to identify the presence of the virus is to detect its genome using
real-time reverse transcriptase polymerase chain reaction (RT-PCR). It can be
applied to respiratory tract samples such as nasopharyngeal swabs, sputum and
bronchoalveolar lavage. In order to identify contact with the virus and
immunological response of the individual, tests based on immunoassays were
developed. Many of those tests were produced in short periods of time and they
mostly differ on the sample that can be used (serum, plasma or whole blood), complexity
and/or expense, and the class of the antibody they detect. The reliability of
such tests is of high importance for epidemiological surveys as well as for the
development of a vaccine. The aim of this study was to compare three
commercially available immunoassay tests. Our results show that different
serological tests have different sensitivity and specificity, and that the
rapid option, which is the easiest to perform and has the lowest cost, provides
the least reliable results.