key: cord-0684900-xi34ogmk
authors: Scagnolari, Carolina; Bitossi, Camilla; Frasca, Federica; Viscido, Agnese; Oliveto, Giuseppe; Scordio, Mirko; De Vito, Corrado; Trancassini, Maria; Midulla, Fabio; Cimino, Giuseppe; Pierangeli, Alessandra; Antonelli, Guido
title: No detection of SARS-CoV-2 in cystic fibrosis patients at the Regional (Lazio) Reference Center for CF in Italy
date: 2020-06-23
journal: J Cyst Fibros
DOI: 10.1016/j.jcf.2020.06.018
sha: 83b5b02643bb51a8a6d6becb572a64a4c542caec
doc_id: 684900
cord_uid: xi34ogmk

nan

The newly emergent human coronavirus (HCoV), known as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has become a worldwide threat and the most severe public healthcare concern. The impact of SARS-CoV-2 on cystic fibrosis (CF) remains poorly understood, still there are serious concerns over its potential effect due to deficiencies in respiratory tract physiology of CF patients that prevent efficient clearance of pathogens from the airways. SARS-CoV-2 infections have been observed in few CF patients and were associated to a not severe infection [1] . Moreover, an asymptomatic case of COVID-19 in an infant with CF has been recently reported [2] .

Hence, we retrospectively investigated the incidence of SARS-CoV-2 in a cohort of patients with CF (n=265) who attended clinic visits at the Regional (Lazio) CF Reference Center, either with respiratory disease that required medical attention or in stable conditions, from November 2019 to March 2020, before and after the Italian government restrictions for COVID-19. Three groups of patients were investigated, where a residual amount of respiratory sample was sufficient for respiratory viruses detection: young children (n=43 ≤10 years of age), adolescents (n=39 11-18 years), and adults (n=183 >18 years, Table 1 ). The local ethics committee approved the study protocol (Sapienza University of Rome, Policlinico Umberto I Hospital); all adults patients and parents/guardians gave informed consent to participate in the study and patients' data were anonymized. Respiratory tract samples were analyzed for common and emerging microorganisms genes of SARS-CoV-2 were developed in-house following published protocols [3] . No SARS-CoV-2 positive result was identified in the respiratory samples analyzed; we retain that testing all 3 samples with two primer-probe sets [3] warranted a low rate of false-negative results. By contrast, 95/265 samples (35.8%) were positive for one or more non-SARS-CoV-2 viruses (Table 1) .

Among virus positive samples, 8.4% (n=8/95) were simultaneously infected by 2 viruses. HRV was the most frequently detected viruses (n=56; 58.9%), followed by RSV (n=11; 11.6%), and FluA (n=10; 10.5%). Less frequently detected respiratory viruses were HCoV-229E (n=7; 7.3%) and

HCoV-HKU1 (n=3; 3.2%). A coinfection between HRV and other respiratory viruses (RSV A/B, FluA and HCoV-HKU1) was found in 6 respiratory samples (6.3%); moreover, 2 samples were positive to both RSV A and RSV B (2.1%). The rates of HRV and RSV infections were Evidences across several countries from the early pandemic period suggested that CF condition does not represent a higher risk of SARS-CoV-2 infection and that disease course does not seem to differ from the general population [1, 2, 4] .

From this study data, it is difficult to identify specific factor(s) that could have contributed to the apparent low spread of SARS-CoV-2 in CF. The implementation of social distancing and preventive measures might have mitigated the diffusion of the SARS-CoV-2 in CF individuals. In the Italian COVID-19 decree effective since March 10, the general population was requested to stay home, unless strictly necessary; as a consequence, routine clinic appointments at the Regional (Lazio) CF Reference Center were cancelled and only visits for emergency were performed. Beside the lower number of CF patients attending the Center in March, the virus positivity rate was also the lowest of the study period, because the decrease in social interactions may have caused a reduction in respiratory disease incidence. However, virus positivity distribution in the study period, lower in November and March and peaking in January, may be consistent also with the seasonal circulation 4 of many respiratory viruses. As regards SARS-CoV-2 circulation in March, on 32846 molecular tests performed in Lazio Region, 2914 (8.9%) tested positive for SARS-CoV-2 (from http://www.salute.gov.it/imgs/C_17_notizie_4362_0_file.pdf). Taken together, these figures would suggest that SARS-CoV-2 circulated in Lazio Region and that CF patients had a chance to be infected. Of course, we cannot exclude that asymptomatic or mild SARS-CoV-2 infections in CF individuals eventually happened but did not induce them to attend the CF Reference Center for care, given the Government restriction measures.

In conclusion, this study, conducted in an early pandemic period in Italy, showed that SARS-CoV-2 was not present in CF patients of different ages in stable conditions or with respiratory signs and symptoms, differently from common respiratory viruses. These findings encourage further studies to determine the prevalence of SARS-CoV2 in CF patients across a broad range of age, not just among individuals seeking medical attention, due to the possible severe disease course, to understand more fully the burden of this novel pathogen and to develop adequate preventive measures against this infection. 

The authors declare that they have no conflicts of interests. 24 (9.1%) 5 (11.6%) 5 (12.9%) 14 (7.7%) Detection of one or more respiratory virus, n (%)

A multinational report to characterise SARS-CoV-2 infection in people with cystic fibrosis

Asymptomatic case of Covid-19 in an infant with cystic fibrosis

Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR

Impact of COVID-19 on people with cystic fibrosis

HRV, n (%) 56/95 (58.9%)

N.A.: not applicable. (▲) =p<0.01 by Chi-Squared test (viral detection higher in children) (■) =p<0.001 by Chi-Squared test (HRV detection higher in children) (•) =<0.05 by Chi-Squared test (RSV detection higher in children) (♦) FluA n=3/11