key: cord-0811070-luiilr5z
authors: de Lima, C.R.A.; Mirandolli, T.B.; Carneiro, L.C.; Tusset, C.; Romer, C.M.; Andreolla, H.F.; Baethgen, L.F.; Pasqualotto, A.C.
title: Prolonged respiratory viral shedding in transplant patients
date: 2013-12-02
journal: Transpl Infect Dis
DOI: 10.1111/tid.12167
sha: 0840f34ccae231d4df52a29267472fb6a8347901
doc_id: 811070
cord_uid: luiilr5z

Respiratory viral infections are frequent causes of morbidity in transplant patients. We screened symptomatic adult transplant recipients for respiratory viruses in a cohort of patients attending a referral medical center in Brazil. The duration of viral shedding and the prevalence of viral codetections were also determined. During a 1‐year period (2011–2012), swabs were obtained from 50 patients. An in‐house polymerase chain reaction panel designed to detect 10 viruses was used. Viruses were identified in 19 (38%) patients, particularly parainfluenza III (32%) and the respiratory syncytial virus (20%); multiple viruses were identified in 26% of patients. Prolonged viral shedding was observed with 60% of individuals excreting viruses for >10 days. The clinical and epidemiologic relevance of prolonged viral shedding remains to be determined.

Respiratory viral infections are usually associated with significant morbidity following organ transplantation (1) . Transplant patients could be infected by the same respiratory viruses that affect the overall population, including adenovirus (ADV), human bocavirus (hBOV), coronavirus, human metapneumovirus (hMPV), parainfluenza viruses (PIV), and respiratory syncytial virus (RSV) (2) . However, because of the state of immunosuppression, the rate of disease complication may be increased in the transplant population. The duration of viral shedding is an important determinant of viral infectivity and transmissibility; factors that provide vital information for effective infection control (3) (4) (5) (6) (7) (8) . In the transplant population, limited data are available regarding the duration of viral shedding following a respiratory tract infection. Here, we investigated the distribution of viruses causing acute respiratory syn-drome in transplant patients, to determine the outcome of these infections and the duration of viral excretion.

This was a prospective cohort study conducted between August 2011 and August 2012. The study was performed at Santa Casa de Misericordia de Porto Alegre, a reference transplant center located in Southern Brazil. Patients were included in or excluded from this research based on the Center for Disease Control and Prevention recommendations. Patients were studied if they presented fever, cough, and headache, plus at least 1 of the following symptoms: rhinorrhea, coryza, arthralgia, myalgia, prostration, sore throat, chest pain, abdominal pain, or nasal congestion (9) . Individuals were excluded in the presence of signs/ symptoms lasting >14 days. Informed written consent was obtained from all patients, and the study was approved by the local Ethics Committee (542/09).

Respiratory samples were obtained as recommended by the World Health Organization (10) . Briefly, rayon swabs were used to collect samples from nasopharyngeal and oropharyngeal sites. Swabs were transported in saline solution to the laboratory. Samples were stored at 4°C for a few hours until processing.

Total nucleic acids were extracted with PureLink â Viral RNA/DNA Mini Kit (Invitrogen TM ; Life Technologies, Grand Island, New York, USA) and stored at À80°C. The cDNAs of influenza A H3N2 (FluA), pandemic influenza A/H1N1 (pH1N1), influenza B (FluB), RSV, PIV I, II and III), and hMPV were synthesized by SuperScriptIII â First-Strand Synthesis SuperMix (Invitrogen TM ) with the following conditions: 10 min at 25°C, 50 min at 50°C, and 5 min at 85°C. Table 1 shows a list of the primers used in the study.

Real-time polymerase chain reaction (PCR) assay was performed using Platinum â SYBR â Green qPCR Su-perMix-UDG (Invitrogen TM ).

The real-time PCR conditions for all RNA viruses except for RSV were as follows: 2 min at 50°C, 5 min at 95°C, 45 cycles of 15 s at 95°C, and 30 s at 64°C, followed by 15 s at 95°, 1 min at 60°C, and 30 s at 95°C. For RSV, the condition was 2 min at 50°C, 5 min at 95°C, 45 cycles of 15 s at 95°C, 30 s at 56°C, and 15 s at 72°C. ADV and hBOV were detected by conventional PCR with Platinum Taq DNA Polymerase (Invitrogen TM ). The conditions used to amplify ADV and hBOV were 10 min at 95°C, 38 cycles of 30 s at 95°C, 30 s at 56°C, and 30 s at 72°C.

To determine the duration of viral shedding, patients with positive PCR tests were retested every 3-5 days, until a negative PCR test was obtained.

Patients' charts were reviewed in an attempt to obtain clinical and demographic information. To compare the distribution of respiratory viruses infecting the overall Respiratory viruses were detected in 19 patients (38.0%), mostly in fall and winter months. Multiple viruses were identified in 5 individuals (26.3%), including 1 patient who had 3 viruses detected. The most prevalent virus was PIV III (32%), followed by RSV (20%), hBOV (12%), hMPV (12%), pH1N1 (8%), ADV (8%), FluA (4%), and FluB (4%). The viral distribution differed from what was observed for the overall population, in which RSV was the predominant agent (54.5%). The prevalence of viral codetection in the general population was 35%, with 5 patients in the group showing concomitantly 4 respiratory viruses. Table 2 presented the duration of viral shedding per patient studied. Viral shedding ranged from 6 days (hBOV; n = 1) to 44 days (hMPV; n = 1). The average duration of viral shedding was 10 days for pH1N1 (n = 2), 17 days for PIV III (n = 3), and 13 days for RSV (n = 3). (11) . Recent studies reported a frequency of 21.4% and 10% of dual respiratory viral infection in children with bronchiolitis after molecular assays were added to the diagnostic list of clinical laboratories (12, 13) . Therefore, when using modern and sensitive methods, such as real-time PCR, in the diagnosis of respiratory tract infections, even higher rates of viral codetection are anticipated to be found in the transplant setting (11) . As shown before (11) , the detection of multiple respiratory viruses in transplant recipients was not associated with a poor prognosis in these patients. In our study, PIV III was the most frequent virus detected in transplant patients (31.6%), followed by RSV (20%), hBOV (12%), hMPV (12%), pH1N1 (8%), and ADV (8%). In previous investigations, using conventional diagnostic methods (i.e., direct immunofluorescence and viral culture), the incidence of PIV III infection following transplantation varied from 2-9% (4, 14) . On the other hand, studies based on PCR revealed a higher frequency of PIV III infection, as high as 14.0% (4). In contrast to transplant patients, in whom PIV III was the predominant virus, RSV was the main cause of respiratory infections in the non-transplant population (54.5%), referred to the same hospital. The high RSV frequency detected in non-transplant patients suggests that most of these patients were probably children, which is in accordance with the literature that suggests that RSV is one of the most common causes of severe lower respiratory disease in young children (15) . Human rhinoviruses and coronaviruses are frequently associated with the common cold and are generally considered to replicate principally within the upper respiratory tract (16) . Despite the high frequency of these viruses in the population, the real importance of these agents in the transplant population remains to be determined (16) .

In this study, hBOV, hMPV, ADV, FluA, and FluB were detected in 12%, 12%, 8%, 4%, and 4% of transplant patients, respectively. These frequencies were in agreement with the literature data (17) (18) (19) (20) (21) (22) (23) . In contrast, pH1N1 was detected in only 8% of transplant patients. The low percentage of pH1N1 detection in this study may be justified by the massive FluA/pH1N1 immunization campaign that had occurred in Brazil few months before the study was initiated.

Information about the duration of viral shedding is important to establish effective infection control measures in the hospital environment. In this work, we reported a prolonged shedding in this cohort of transplant patients, with 60% of individuals excreting viruses for >10 days. This finding is in agreement with the literature, in which a prolonged shedding has been reported for PIV III (6-42 days), RSV (5-39 days), and hMPV (7-24 days) infections (3) (4) (5) (6) (7) (8) . Even though a previous study showed prolonged hBOV shedding in non-transplant children (7), only 1 patient with hBOV infection was included in our study, and therefore, we were not able to properly evaluate hBOV shedding in our transplant cohort. The current data on pH1N1 shedding are in agreement with a previous report, which suggested that the presence of pH1N1 was a significant risk factor for prolonged viral shedding (median of 27 days) (8) .

Limitations of this work included the inability to test for rhinovirus in this cohort of patients, and the difficulty to follow these individual for a prolonged period of time. Another limitation was the small number of transplant patients studied. We only included patients who presented with acute respiratory illness (symptoms lasting for <14 days, as based on the CDC recommendations). Because viral shedding is prolonged in these patients (as demonstrated by the current study), this criterion could have reduced the number of patients enrolled in our study (9) . Furthermore, it is already known that transplant patients have fewer and milder symptoms. Because of this fact, we could have missed some patients with mild to no symptoms, which could affect the estimated duration of shedding.

This work demonstrated that respiratory viruses are a significant cause of morbidity in transplant patients. The use of molecular tools in clinical practice may facilitate the management of such patients, particularly when infection control measures are being considered. Transplant patients have demonstrated prolonged viral sheddingthe clinical relevance of that, and the potential for intrahospital dissemination of disease remain to be determined.

Thanks: We would like to thank the following team members involved in sample collection: Edimar Silveira Barbosa, Felipe Silveira Rodrigues, Helena Krummenauer da Silveira, Julia Wladeska Caldieraro, Leonardo Disconzi Barboza, and Michele Metz. We are grateful to all ISCMPA professionals for the notification of patients with viral respiratory symptoms, and to colleagues at the molecular biology laboratory for their cooperation.

Conflict of interest: The authors declare no conflicts of interest that could be perceived as prejudicing the impartiality of the research reported.

Funding: This work was supported by a Governmental Research grant (FAPERGS 09/0571-9 to A.C.P).

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