Evidence map›Paper›PMID 42232907›Full record

ArticleFrontiers in microbiology2026

Genetic variability, N-glycosylation, and recombination in sublineage 1A of

Rony Yunior Cotaquispe Nalvarte, Miriam Legua Barrios, Edgard De la Cruz Vásquez, Julio Cesar Ecos Espino, Erick Llona García, Ayda Liliana Reyes Ruiz, Merici Ingrid Medina Guerrero, Felicita Karina Camargo Paredes, Hilda Victoria Coila De la Cruz, Elvia Mejía Vargas and 3 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Rony Yunior Cotaquispe NalvarteUniversidad Privada de Ciencias y Humanidades, Lima, Peru.
Miriam Legua BarriosUniversidad Privada San Juan Bautista, Ica, Peru.
Edgard De la Cruz VásquezUniversidad Privada Autónoma de Ica, Ica, Peru.
Julio Cesar Ecos EspinoUniversidad Privada San Juan Bautista, Ica, Peru.
Erick Llona GarcíaUniversidad Privada San Juan Bautista, Ica, Peru.
Ayda Liliana Reyes RuizUniversidad Nacional San Luis Gonzaga, Ica, Peru.
Merici Ingrid Medina GuerreroUniversidad Privada Autónoma de Ica, Ica, Peru.
Felicita Karina Camargo ParedesUniversidad Nacional San Luis Gonzaga, Ica, Peru.
Hilda Victoria Coila De la CruzUniversidad Nacional José Faustino Sánchez Carrión, Lima, Peru.
Elvia Mejía VargasHospital Felix Torrealva Gutiérrez, Ica, Peru.
Cesar Augusto Mendoza YáñezUniversidad Nacional San Luis Gonzaga, Ica, Peru.
Carmen Lucy Cabrel PalomaresUniversidad Nacional José Faustino Sánchez Carrión, Lima, Peru.
Jennifer Toskano HurtadoMolecular Research and Biosciences Laboratory (IMBIOS), Department of Research & Development, Corporación Montana S.A., Lima, Peru.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) is highly variable, and emerging variants have been responsible for severe outbreaks with unprecedented economic losses. Lima represents a major center of pig production; however, the absence of a structured epidemiological surveillance program has facilitated the spread of divergent variants in commercial farms. The present study provides an initial assessment of GP5 variability in a high-risk production setting. The aim of this study was to characterize the genetic variability, N-glycosylation sites, and recombination events within this region. Bioinformatic tools and servers were used for phylogenetic analyses, revealing that all 24 analyzed strains clustered within sublineage 1A, with evidence of divergent variants. Several amino acid substitutions were identified in domains associated with neutralizing and non-neutralizing antibody responses, including A27V/S (12/24), A31T (1/24), N32S/G/R/E (16/24), S34N/T (3/24), S35N/I (6/24), H38L (1/24), L39F (7/24), Q40L/R (6/24), L41Y/V (3/24), I42V (1/24), Y43H (4/24), N44I (4/24), L45R (4/24), T46A (4/24), K58E/V/R (15/24), and S59H/R/N (8/24) in GP5. Nine N-glycosylation patterns (A-I) were identified, with nine putative sites at N30, N32, N33, N34, N35, N44, N50, N51, and N57. Patterns A, B, E, and G exhibited five to six potential glycosylation sites in 12/24 strains. A recombination event was detected in strain RC05088942.1_montana/PERU/2019-R, with RC05088941.1_montana/PERU/2019 as the putative major parent (96.1% similarity) and an unidentified minor parent; however, strain RC05088939.1_montana/PERU/2019 showed the closest phylogenetic relationship. Genetic diversity analysis revealed 172 polymorphic sites. Tajima's D test yielded a value of -0.84020, which was not statistically significant (

Indexed as

genetic diversityN-glycosylationORF5RDP4.101recombinationsublineage 1A

Identifiers

PMID42232907
PMCPMC13224472

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.