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Published on: November 8, 2011
Distinctive Epstein-Barr virus variants associated with benign and malignant pediatric pathologies: LMP1 sequence
Mario Alejandro Lorenzetti1, Magdalena Gantuz, Jaime Altcheh
1Molecular Biology Laboratory, Pathology Division, Ricardo Gutiérrez Children Hospital, Gallo 1330 Buenos Aires, Argentina. marioloren@yahoo.com.ar
Abstract:
The ubiquitous Epstein-Barr virus (EBV) is related to the development of lymphoma and is also the etiological agent for infectious mononucleosis (IM). Sequence variations in the gene encoding LMP1 have been deeply studied in different pathologies and geographic regions. Controversial results propose the existence of tumor-related variants, while others argued in favor of a geographical distribution of these variants. Reports assessing EBV variants in IM were performed in adult patients who displayed multiple variant infections. In the present study, LMP1 variants in 15 pediatric patients with IM and 20 pediatric patients with EBV-associated lymphomas from Argentina were analyzed as representatives of benign and malignant infections in children, respectively. A 3-month follow-up study of LMP1 variants in peripheral blood cells and in oral secretions of patients with IM was performed. Moreover, an integrated linkage analysis was performed with variants of EBNA1 and the promoter region of BZLF1. Similar sequence polymorphisms were detected in both pathological conditions, IM and lymphoma, but these differ from those previously described in healthy donors from Argentina and Brazil. The results suggest that certain LMP1 polymorphisms, namely, the 30-bp deletion and high copy number of the 33-bp repeats, are associated with EBV-related pathologies, either benign or malignant, instead of just being tumor related. Additionally, this is the first study to describe the Alaskan variant in EBV-related lymphomas that previously was restricted to nasopharyngeal carcinomas from North America.
Insights
Epstein-Barr virus (EBV) LMP1 gene variations are linked to both benign infectious mononucleosis (IM) and malignant lymphomas in children. Specific polymorphisms, like the 30-bp deletion, are associated with these EBV-related diseases.
Area of Science:
- Virology
- Genetics
- Pediatric Oncology
Background:
- Epstein-Barr virus (EBV) is linked to lymphoma and infectious mononucleosis (IM).
- LMP1 gene sequence variations have been studied in various pathologies and regions with conflicting results.
- Previous studies on EBV variants in IM focused on adult patients with multiple infections.
Purpose of the Study:
- To analyze LMP1 variants in pediatric patients with IM and EBV-associated lymphomas in Argentina.
- To conduct a follow-up study of LMP1 variants in IM patients.
- To perform linkage analysis with EBNA1 and BZLF1 variants.
Main Methods:
- Analysis of LMP1 variants in 15 pediatric IM patients and 20 pediatric EBV-lymphoma patients.
- 3-month follow-up of LMP1 variants in blood and oral secretions of IM patients.
- Integrated linkage analysis with EBNA1 and BZLF1 variants.
Main Results:
- Similar sequence polymorphisms were found in both IM and lymphoma, differing from healthy donors.
- The 30-bp deletion and high copy number of 33-bp repeats in LMP1 are associated with EBV pathologies (benign and malignant).
- The Alaskan EBV variant was identified in EBV-related lymphomas, previously only seen in North American nasopharyngeal carcinomas.
Conclusions:
- Certain LMP1 polymorphisms are associated with EBV-related diseases, not exclusively tumors.
- This study identifies specific EBV variants linked to pediatric pathologies in Argentina.
- The findings contribute to understanding EBV variant distribution and disease association.
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