Orf virus (ORFV) infection in a three-dimensional human skin model: Characteristic cellular alterations and interference with keratinocyte differentiation
ORF virus (ORFV) is the causative agent of contagious ecthyma, a pustular dermatitis of small ruminants and humans. Even though the development of lesions caused by ORFV was extensively studied in animals, only limited knowledge exists about the lesion development in human skin. The aim of the present study was to evaluate a three-dimensional (3D) organotypic culture (OTC) as a human skin model for ORFV infection considering lesion development, replication of the virus, viral gene transcription and modulation of differentiation of human keratinocytes by ORFV. ORFV infection of OTC was performed using the ORFV isolate B029 derived from a human patient. The OTC sections showed a similar structure of stratified epidermal keratinocytes as human foreskin and a similar expression profile of the differentiation markers keratin 1 (K1), K10, and loricrin. Upon ORFV infection, OTCs exhibited histological cytopathic changes including hyperkeratosis and ballooning degeneration of the keratinocytes. ORFV persisted for 10 days and was located in keratinocytes of the outer epidermal layers. ORFV-specific early, intermediate and late genes were transcribed, but limited viral spread and restricted cell infection were noticed. ORFV infection resulted in downregulation of K1, K10, and loricrin at the transcriptional level without affecting proliferation as shown by PCNA or Ki-67 expression. In conclusion, OTC provides a suitable model to study the interaction of virus with human keratinocytes in a similar structural setting as human skin and reveals that ORFV infection downregulates several differentiation markers in the epidermis of the human skin, a hitherto unknown feature of dermal ORFV infection in man.
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Univ Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, BrazilUniv Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, Brazil
Isaac, Cesar
Mathor, Monica Beatriz
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Univ Sao Paulo, IPEN, Inst Nucl Energy Res, Sao Paulo, BrazilUniv Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, Brazil
Mathor, Monica Beatriz
Bariani, Giovani
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Univ Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, BrazilUniv Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, Brazil
Bariani, Giovani
Paggiaro, Andre Oliveira
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Univ Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, BrazilUniv Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, Brazil
Paggiaro, Andre Oliveira
Herson, Marisa Roma
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Univ Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, BrazilUniv Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, Brazil
Herson, Marisa Roma
Goldenstein-Schainberg, Claudia
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Univ Sao Paulo, Sao Paulo Med Sch, Dept Rheumatol, Sao Paulo, BrazilUniv Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, Brazil
Goldenstein-Schainberg, Claudia
Carrasco, Solange
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Univ Sao Paulo, Sao Paulo Med Sch, Dept Rheumatol, Sao Paulo, BrazilUniv Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, Brazil
Carrasco, Solange
Teodoro, Walcy Rosolia
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Univ Sao Paulo, Sao Paulo Med Sch, Dept Rheumatol, Sao Paulo, BrazilUniv Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, Brazil
Teodoro, Walcy Rosolia
Yoshinari, Natalino Hajime
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Univ Sao Paulo, Sao Paulo Med Sch, Dept Rheumatol, Sao Paulo, BrazilUniv Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, Brazil
Yoshinari, Natalino Hajime
Ferreira, Marcus Castro
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Univ Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, BrazilUniv Sao Paulo, Fac Med, Cell Culture & Wound Healing Res Lab, Div Plast Surg, Sao Paulo, Brazil