Volume 9, Issue 1 e12278
ORIGINAL ARTICLE

No detectable human herpesvirus-8 oral shedding in seronegative-healthy, immunocompetent individuals from non-endemic regions for Kaposi's sarcoma: A pilot study

Tânia R. Tozetto-Mendoza

Tânia R. Tozetto-Mendoza

Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo, Brazil

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Laura M. Sumita

Laura M. Sumita

Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo, Brazil

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Michelle Palmieri

Michelle Palmieri

Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil

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Mariana Ornaghi

Mariana Ornaghi

Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil

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Alan M. do Canto

Alan M. do Canto

Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil

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Paulo H. Braz-Silva

Corresponding Author

Paulo H. Braz-Silva

Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo, Brazil

Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil

Correspondence

Professor Paulo H. Braz-Silva, Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil.

Email: [email protected]

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First published: 20 June 2017
Citations: 4

Abstract

Aim

Saliva can play an important role in human herpesvirus-8 (HHV-8) transmission in endemic regions for Kaposi's sarcoma (KS). Little is known about HHV-8 oral shedding in immunocompetent individuals from non-endemic regions for KS.

Methods

We conducted a prospective study of HHV-8 salivary excretion among 59 healthy, immunocompetent individuals from São Paulo, Brazil, followed up weekly for 4 months, resulting in 16 saliva samples from each participant. Antibodies to HHV-8 latency-associated nuclear antigen (LANA) and lytic-phase antigens were investigated with immunofluorescence assays (IFA). HHV-8 DNA detection was performed using real-time polymerase chain reaction (PCR).

Results

All 59 individuals were seronegative to LANA and lytic antibodies. HHV-8 DNA was undetectable in saliva samples in 100% of the participants, totaling 944 samples and being consistently negative during the different periods of sampling, which lasted approximately 120 days. No sequences of HHV-8 DNA were detected in the saliva samples of healthy, immunocompetent adults by using real-time PCR, with the resulting data being consistent with IFA-based serological tests.

Conclusions

Unlike other herpesviruses, HHV-8 is not excreted in the saliva of healthy individuals from non-endemic regions for KS.

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