Prevalence of Torque teno virus in healthy donors of Paraná State, southern Brazil

OBJECTIVE: To determine the prevalence of the Torque teno virus in healthy donors in the northern and northwestern regions of the state of Paraná, southern Brazil.METHODS: The Torque teno virus was detected by a nested polymerase chain reaction using a set of oligoprimers for the N22 region.RESULTS: The prevalence of the virus was 69% in 551 healthy blood donors in southern Brazil. There was no statistically significant difference between the presence of the virus and the variables gender, ethnicity and marital status. There was significant difference in the prevalence of the virus regarding the age of the donors (p-value = 0.024) with a higher incidence (74.7%) in 18- to 24-year-old donors.CONCLUSION: A high prevalence of Torque teno virus was observed in the population studied. Further studies are needed to elucidate the routes of contamination and the clinical implications of the virus in the healthy population.

Prevalência e diversidade genética do torque teno vírus em pacientes com lúpus eritematoso sistêmico em serviço de referência no Mato Grosso do Sul / Prevalence and genetic diversity of torque teno virus in patients with systemic lupus erythematosus in a reference service in Mato Grosso do Sul

Estudos recentes sobre o torque teno vírus (TTV), gênero Anellovirus, permitiram construir a hipótese de que esse vírus pode ser um desencadeante ou tenha algum papel patogênico nas doenças reumáticas autoimunes. OBJETIVOS: Verificar a frequência da infecção pelo TTV em pacientes com lúpus eritematoso sistêmico (LES), e sua diversidade gênica, a existência de correlação entre a infecção pelo TTV e as manifestações clínicas do LES, sua evolução clínica e o perfil sorológico. PACIENTES E MÉTODOS: Foram obtidas 46 amostras de soro de pacientes com LES atendidos no Ambulatório de Reumatologia do Hospital Universitário de Campo Grande (NHU/FAMED/UFMS). Para os controles, utilizaram-se 46 amostras de soro de doadores de sangue. O DNA viral foi extraído das amostras utilizando o QIAamp DNA Blood Mini Kit (QIAGEN, Hilden, Alemanha), e amplificado utilizando a técnica de nested PCR. RESULTADOS: Foi encontrada positividade para o TTV em 17 (37 por cento) dos pacientes lúpicos, e em apenas sete (15,2 por cento) dos controles (teste z, P = 0,03). Não houve correlação entre a infecção pelo TTV, as manifestações clínicas, o perfil sorológico e a evolução clínica dos pacientes avaliados neste estudo. CONCLUSÃO: A presença do TTV nos pacientes com LES necessita ser mais bem compreendida a partir deste estudo inicial.

Recent studies on the torque teno virus (TTV), genus Anellovirus, have allowed formulating the hypothesis that TTV may trigger autoimmune rheumatic diseases or have some pathogenic role in them. OBJECTIVES: To determine the frequency of TTV infection in patients with systemic lupus erythematosus (SLE), the genetic diversity of TTV, the correlation between TTV infection and SLE clinical manifestations, and SLE clinical course and serological profile. PATIENTS AND METHODS:Serum samples were obtained from 46 SLE patients treated at the University-Affiliated Hospital of Campo Grande (NHU/FAMED/UFMS), Brazil. For controls, serum samples were obtained from 46 healthy volunteer blood donors. Viral DNA was extracted from samples using the QIAamp DNA Blood Mini Kit (QIAGEN, Hilden, Germany) and amplified using nested PCR. RESULTS: Positivity for TTV was found in 17 (37 percent) of SLE patients and in only seven (15.2 percent) of the controls (z test, P = 0.03). There was no correlation between TTV infection, SLE clinical manifestations, SLE clinical course, and the serological profile of the patients evaluated. CONCLUSION: Further studies on the presence of TTV in SLE patients are required.

Detection Rate and Genetic Variability of Small Anellovirus DNA from Blood Donors at a Tertiary Hospital / 대한수혈학회지

BACKGROUND: Small anellovirus (SAV) is a new member of the genus Anellovirus and this virus can infect humans. SAV could be transmissible by transfusion. However, there have been no studies about the genotypes of SAV among the blood donors in Korea. In this paper, the detection rate and genotypes of SAV were investigated among the blood donors at a tertiary hospital. METHODS: A total of 286 plasma samples from blood donors were tested. SAV DNA was amplified using primers derived from the open reading frame 1 (ORF1) region. Simultaneously, Torquetenovirus (TTV) and torquetenominivirus (TTMV) DNA were detected from the SAV DNA positive plasma samples by using nested PCR. Sequencing of amplicons (n=41) was carried out to investigate the SAV genotypes. RESULTS: SAV DNA was detected in 28.7% (82/286) of the blood donors. TTV or TTMV DNA was detected in 37.8% (31/82) of the SAV DNA positive blood donors. Twenty-four sequences were determined and compared with those deposited in the databases (GenBanK) and they revealed a high degree of genetic variability among the SAV DNA (nucleotide similarity: mean 69.3, range 61.2~99.3%). Phylogenetic analysis demonstrated the existence of three main clusters, which were tentatively assigned to genotype 1 (G1), genotype 2 (G2), and genotype 3 (G3), respectively. Genotype G1 was most prevalent and this was followed by G2 and G3. CONCLUSION: The detection rate of SAV DNA among Koreans seems to be higher than that stated in the previous reports from some other countries. Moreover, we determined the genotype distribution of SAV among Korean blood donors.

Detection of Small Anellovirus DNA from Blood Products / 대한수혈학회지

BACKGROUND: The small anellovirus (SAV) is a new member of the genus Anellovirus infecting humans. SAV can be transmissible by transfusion. However there are no reports on SAV infections in Korea. The aim of this study was to determine the prevalence of SAV in blood products. METHODS: A total of 90 plasma samples from blood products (each 30 units of Red blood cell, whole blood, and platelet concentrate) and 30 serum samples from non-A to C hepatitis patients were tested. SAV DNA was detected using nested polymerase chain reaction (PCR). At the same time, TTV and TTMV DNA were detected using nested PCR. RESULTS: SAV DNA was detected in 34% (31/90) of blood products. TTV and TTMV DNA were detected in 66% (54/90) and 29% (26/90) of blood products, respectively. One of the three anelloviruses (SAV, TTV, TTMV) was detected in a total of 77 blood products (86%). SAV DNA was detected in 40% (12/30) of hepatitis patients. TTV and TTMV DNA were detected in 73% (22/30) and 33% (10/30) of those patients, respectively. One of the three anelloviruses (SAV, TTV, TTMV) was detected in 97% (29/30) of hepatitis patients. CONCLUSION: Blood products are frequently infected with SAV and (or) other anelloviruses (TTV/TTMV) in Korea, and can be transmissible with a high probability.