Genetic Determinants Analysis of PB1 and PB2 Genes in H5N1 Avian Influenza Strains from Romania.

Maria Rodica Gurău1 Florica Bărbuceanu1,2 Alexandru Gligor3 Cosmin Șonea1 Georgeta Ștefan1 Doina Daneș1 Elena Negru1 Iosif Nicodim Fiț4 Kalmár Zsuzsa4 Doru Valentin Hristescu2 Vlad Barbu Vuță2 Raluca Burlacu2 Ionica Iancu3 Viorel Herman3,5 Stelian Bărăităreanu1
Affiliations 5 institutions
  1. Faculty of Veterinary Medicine, University of Agronomical Sciences and Veterinary Medicine, 050097 Bucharest, Romania.
  2. Institute for Diagnosis and Animal Health (IDAH), 050557 Bucharest, Romania.
  3. Faculty of Veterinary Medicine, University of Life Sciences "King Mihai I" from Timişoara, 300645 Timişoara, Romania.
  4. Faculty of Veterinary Medicine, University of Agriculture Sciences and Veterinary Medicine, 400372 Cluj Napoca, Romania.
  5. Academy of Romanian Scientists (AOSR), Str. Ilfov, Nr. 3, Sector 5, 050044 Bucharest, Romania.

Abstract

Avian influenza is a highly contagious viral disease affecting domestic and wild birds, caused by influenza A viruses of the family Orthomyxoviridae. Continuous genetic surveillance is essential for monitoring viral evolution and identifying molecular determinants associated with pathogenicity and host adaptation. In this study, the PB1 and PB2 polymerase genes of highly pathogenic avian influenza (HPAI) H5N1 viruses detected in Romania between 2017 and 2024 were genetically characterized. A total of 18 organ samples collected from domestic and wild birds in several Romanian counties were analyzed by real-time RT-PCR, followed by conventional RT-PCR, Sanger sequencing, mutational analysis, and phylogenetic reconstruction. High-quality sequence data were obtained for six PB1 and eight PB2 gene fragments. Sequence analysis revealed a high degree of conservation within the PB1 gene, particularly across regions involved in viral replication, indicating strong evolutionary constraints. In contrast, the PB2 gene exhibited several amino acid substitutions, including changes at positions 464 and 678 in selected isolates. Notably, all analyzed strains lacked the mammalian adaptation marker E627K. Phylogenetic analysis clustered the Romanian isolates within Eurasian H5N1 lineages and demonstrated close genetic relationships with contemporary strains circulating in Eastern Europe and Russia. These findings highlight the genetic stability of PB1, the ongoing diversification of PB2, and the importance of continuous molecular surveillance for the early detection of viral variants with potential implications for host adaptation and zoonotic risk.

Supporting text Virus Host Location
avian influenza 57 H5N1 82 molecular epidemiology 28 PB1 1 PB2 9 phylogenetic analysis 66

Evidence records

2 total
Zoonotic Surveillance
1 records · 1 evidence types
Evidence type
1 records
OVE11878
Key finding

HPAI H5N1 viral RNA was detected in organ samples from domestic and wild birds in Romania (2017–2024) using real-time RT-PCR, with subsequent sequencing of PB1 and PB2 fragments.

Virus
Host
Natural host
Location
Supporting text

A total of 18 organ samples collected from domestic and wild birds in several Romanian counties were analyzed by real-time RT-PCR, followed by conventional RT-PCR, Sanger sequencing... In this study, the PB1 and PB2 polymerase genes of highly pathogenic avian influenza (HPAI) H5N1 viruses detected in Romania between 2017 and 2024 were genetically characterized.

Method
real-time RT-PCR | conventional RT-PCR | Sanger sequencing | mutational analysis | phylogenetic reconstruction
Sample type
organ samples
Geographic raw
Romania | Romanian counties
Country inferred
ROU
Genomic Evolution
1 records · 1 evidence types
Evidence type
1 records
OVE11879
Key finding

Romanian H5N1 isolates cluster within Eurasian H5N1 lineages and are closely related to contemporary strains from Eastern Europe and Russia.

Virus
Host
Location
Not specified
Supporting text

A total of 18 organ samples collected from domestic and wild birds in several Romanian counties were analyzed by real-time RT-PCR, followed by conventional RT-PCR, Sanger sequencing, mutational analysis, and phylogenetic reconstruction. Phylogenetic analysis clustered the Romanian isolates within Eurasian H5N1 lineages and demonstrated close genetic relationships with contemporary strains circulating in Eastern Europe and Russia.

Genes or proteins
PB1 | PB2
Analysis methods
real-time RT-PCR | conventional RT-PCR | Sanger sequencing | mutational analysis | phylogenetic reconstruction | phylogenetic analysis