- 1Laboratorio de Patogénesis Viral, Instituto de Biotecnología y Biología Molecular, Consejo Nacional de Investigaciones Científicas y Técnicas-Universidad Nacional de La Plata (CONICET-UNLP), La Plata, Argentina
- 2Department of Chemical and Structural Biology, Weizmann Institute of Science, Rehovot, Israel
- 3Galveston National Laboratory, Department of Pathology, University of Texas Medical Branch, Galveston, TX, United States
Editorial on the Research Topic
Mammarenaviruses: pathogenesis, transmission, and treatment
Lymphocytic choriomeningitis virus (LCMV) was the first arenavirus discovered in 1933. Decades later, several other viruses were found that shared common morphology, serology, biochemical characteristics, and natural history. This led to the recognition of the Arenaviridae family, named after the sandy (Latin arenosus) appearance of the ribosomes originally seen in electron microscopy. Some of these viruses caused hemorrhagic fevers in humans, such as Junin virus (JUNV), Argentine hemorrhagic fever (AHF) in Argentina, and Lassa virus (LASV), Lassa fever in several countries in West Africa, while others have not been associated with human disease. The Arenaviridae family is currently formed by the genera Mammarenavirus, Reptarenavirus, Hartmanivirus, Antennavirus, and Innmovirus. The mammarenaviruses infect mammals, mainly rodents, and their geographical distribution is related to their natural reservoirs. The Reptarenavirus and Hartmanivirus genera have been found in snakes, and some reptarenaviruses can cause disease in captive snakes. Antennaviruses, in turn, infect striped frogfish and salmon, while the natural reservoir of Innmovirus is still unknown.
Arenaviruses are single-stranded ambisense RNA viruses with some differences between the genera. Mammarenaviruses and reptarenaviruses have a bisegmented RNA with an ambisense coding strategy for four proteins: GPC and NP are coded in the S-segment and L and Z in the L-segment. Hartmaniviruses have a bisegmented RNA with an ambisense S segment coding for the GPC and NP proteins and a negative-sense RNA L segment coding for the L protein, but they have no homolog for the Z protein of mammarenavirus and reptarenavirus. Antennaviruses have genomes consisting of three genomic segments, a negative-sense S segment encoding NP, an ambisense segment encoding GPC and an unknown protein, and a negative-sense L segment that encodes the L protein but also has no homologous Z protein. Finally, Innmovirus has three negative-sense RNA segments, the S segment that codes for NP, the ambisense segment that codes for GPC and an unknown protein, and the L segment that codes for the L protein.
As far as the members of the Arenaviridae are concerned, it is very likely that more extensive and sensitive analyses and procedures will also lead to a rapid expansion of the family. The mammarenaviruses, in particular, pose a significant threat as emerging pathogens. Human activities such as deforestation and urbanization are leading to increased contact with wild rodents in new environments. This increased interaction increases the risk of future outbreaks and the discovery of new mammarenavirus isolates. As with other members of the genus, it is very likely that the family will expand rapidly with more extensive and sensitive analysis and methods.
In this Research Topics on recent advances in Mammarenaviruses: pathogenesis, transmission, and treatment, we have compiled a total of four articles. The only licensed vaccine against an arenavirus is the Candid#1 vaccine, which is used in Argentina to protect against AHF caused by JUNV. It is, therefore, understandable that we are making great efforts to improve our knowledge and develop drugs to help prevent or treat infections with mammarenaviruses. In this Research Topic, Iyer et al. provide an overview of the current state of knowledge on entry inhibitors as antiviral agents against arenaviruses. Homologous recombination (HR) is a fundamental genetic force that drives biological evolution. However, as it is a negative-stranded RNA virus, HR has hardly been studied in mammarenaviruses. Here, He et al. performed a bioinformatic analysis to determine whether HR occurs between LASVs and what influence it has on the occurrence of LF. The genetic code consists of 64 codons, 61 of which code for amino acids and 3 for stop signals in protein synthesis. Since there are only 20 common amino acids, the genetic code is degenerate, i.e., several codons are translated into the same amino acids, with the exception of methionine and tryptophan. However, not all synonymous codons are used with the same frequency. This unequal use of codons is called codon usage bias (CUB). Codon usage bias is an important measure of genome evolution. Several factors have been found to influence codon selection bias, with natural selection and mutational pressure in combination with genetic drift being the most important factors in viruses. In this Research Topic, Thomas et al. investigated the CUB of common genes of arenaviruses using in silico analyzes. Finally, Freitas Moraes Monteiro et al. studied viral diversity, including arenaviruses, in wild rodents in the northeastern Brazilian state of Para.
We hope that this Research Topic on mammarenaviruses will stimulate interest and the development of new studies on this genus, to which new members have been regularly added since its discovery.
Author contributions
RG: Writing – review & editing, Writing – original draft. RD: Writing – review & editing, Writing – original draft. SP: Writing – review & editing, Writing – original draft.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by the grants PICT 2020-0270 (RG) from the Agencia Nacional de Promoción Científica y Tecnológica (ANPCyT), Argentina. The funders had no role in study design, data collection and interpretation, or in the decision to submit the work for publication.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Keywords: arenavirus, mammarenavirus, entry blockers, homologus recombination, codon usage bias, viral diversity
Citation: Gómez RM, Diskin R and Paessler S (2025) Editorial: Mammarenaviruses: pathogenesis, transmission, and treatment. Front. Microbiol. 16:1615588. doi: 10.3389/fmicb.2025.1615588
Received: 21 April 2025; Accepted: 24 April 2025;
Published: 08 May 2025.
Edited and reviewed by: Anna Kramvis, University of the Witwatersrand, South Africa
Copyright © 2025 Gómez, Diskin and Paessler. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ricardo Martín Gómez, cm1nMTQyNkBnbWFpbC5jb20=