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    Oligonucleotidi sintetici per l'identificazione dei virus Herpes simplex e la tipizzazione dei virus Herpes simplex di tipo 1 e di tipo 2 mediante la tecnica di polymerase chain reaction (PCR) ed ibridazione molecolare, loro uso e kits diagnostici che li contengono.

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    La presente invenzione si riferisce ad oligonucleotidi sintetici che permettono di identificare i virus Herpes simplex e di tipizzare i virus Herpes simplex di tipo 1 e di tipo 2 mediante la tecnica di polymerase chain reaction (PCR) ed ibridazione molecolare. L’invenzione si riferisce inoltre al loro uso per le determinazioni e tipizzazioni suddette e a kits diagnostici che li contengono

    CV/BKV and SV40 viral load in lymphoid tissues of young immunocompetent children from an area of North-East Italy

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    Polyomavirus infection occurring during childhood is followed by a lifelong latency in immunocompetent subjects. The major site of polyomavirus persistence are the uroepithelial cells which leads to oral transmission. It has recently been hypothesized that tonsils could be a possible reservoir. The role of tonsil, adenoid, and peripheral blood mononuclear cells (PBMCs) as possible sites of JCV, BKV, and SV40 latency in young healthy children was assessed. Two hundred fifteen fresh specimens, including 57 tonsil, 80 adenoid, and 78 PBMC samples from 80 immunocompetent children (mean age 4.8 years) were analyzed to determine the viral load by quantitative real-time PCR. The human herpes virus 6 (HHV-6) was tested as a lymphotropic reference virus. Polyomavirus was detected in 5/ 80 (6.2%) children while HHV-6 infection affected 27/80 children (33.7%) (P<0.001). SV40 was detected in one adenoid sample, while footprints of BKV were found in one adenoid and three tonsil samples. JCV was never found in all samples. Polyomavirus sequences were not detected in the 78 blood samples. One adenoid and two tonsils from three children (1.4%) were positive for both polyomavirus and HHV-6. Infections were characterized by low replication rates ranging typically from 110e2/5.510e4 to 6.810e3/8.510e4 viral copies/number of cells. In conclusion, tonsils and adenoids of children could effectively harbor BKV and SV40, although only very few cells proved to be infected. Nevertheless, the low prevalence of polyomavirus, in comparison with the lymphotropic HHV-6, suggests that these tissues are unlikely to be the preferred site of polyomavirus latency, at least in younger children

    Molecular diagnosis of opportunistic pericardial infection in a patient treated with adalimumab: the role of next-generation sequencing

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    Biological immune-modulator drugs, especially inhibitors of tumor necrosis factor-α, are frequently encountered in modern clinical practice and opportunistic infections are therefore a common concern. Infective pericarditis has been described as a complication of these treatments with possible life-threatening consequences. In similar cases cultures may isolate multiple opportunistic bacteria from the pericardial fluid without specific identification of the responsible germ, representing a problem for targeted antibiotic therapy. We present a case of acute pericarditis evolving in pericardial constriction and cardiac tamponade in a patient treated with adalimumab for psoriatic arthritis overlapping with recurrent polychondritis. Next-generation sequencing allowed the identification of a common oral pathogen as the aetiological agent confirming its role in the identification of species that can be overlooked by common microbiological techniques
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