2014
DOI: 10.1007/s00705-014-2045-z
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Molecular epidemiology of rabies virus in Poland

Abstract: The paper describes a phylogenetic study of 58 Polish isolates of rabies virus collected between 1992 and 2010. Sequences of the nucleoprotein (N) and glycoprotein (G) genes approximately 600 bp long were compared with reference sequences (GenBank) of European rabies viruses from neighbouring countries. The study confirmed a very high level of homology (94.4–100 %) of the Polish rabies virus strains irrespective of the date of isolation. Two variants of rabies virus: NEE (Northeastern Europe variant) and CE (C… Show more

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Cited by 9 publications
(8 citation statements)
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“…The majority of the Baltic rabies isolates grouped with the North-East European lineage (NEE), forming one strongly supported group (bootstrap value of 83). The NEE group consisted of 52 samples from the Baltic States and 21 published viral sequences ( S1 Table ) [ 38 , 49 51 ]. Both wild and domestic species fell in the NEE group.…”
Section: Resultsmentioning
confidence: 99%
“…The majority of the Baltic rabies isolates grouped with the North-East European lineage (NEE), forming one strongly supported group (bootstrap value of 83). The NEE group consisted of 52 samples from the Baltic States and 21 published viral sequences ( S1 Table ) [ 38 , 49 51 ]. Both wild and domestic species fell in the NEE group.…”
Section: Resultsmentioning
confidence: 99%
“…This amino acid replacement was reported in one rabies related virus isolate from Poland having accession number AF298142. 26 The amino acid replacement N375K was found in all studied sequences and Delhi sequences of the year 2013 and other Indian states like Uttar Pradesh, Andhra Pradesh and Rajasthan. This is also exhibited in neighboring countries isolates like Nepal (JX944593) and Pakistan (HE802675).…”
Section: Discussionmentioning
confidence: 75%
“…The amplification of G gene fragment of 590-bp of RABV was carried out using one step RT-PCR kit (Qiagen, Germany) on ABI 9700 Thermal cycler (Applied Biosystems, USA) using primers Gp2L (5'-AGT AGA GGG AAG AGA GCATCC A-3') and Gp2P (5'-GAG GAT AGG AAC AAC TCCAT-3'). 26 The thermal profile for the amplification was as follows: first cycle of reverse transcription at 50 0 C for 30 min, followed by initial denaturation at 95 0 C for 15 min; 35 cycles of denaturation at 95 0 C for 30 s, annealing at 62 0 C for 30 s, and elongation at 72 0 C for 1 min and a final extension at 72 0 C for 10 min. The amplified PCR products (590-bp) were run in ethidium bromide (0.5 μg/mL) stained 1.2% agarose gel and were visualized under UV transilluminator (Gel Documentation System, Alpha Imager EC, USA).…”
Section: Reverse Transcription-polymerase Chain Reaction (Rt-pcr)mentioning
confidence: 99%
“…RABV RNA codes five proteins and the N gene-coding nucleoprotein is the most conservative fragment within the RABV genome (13). Traditionally, the N gene was utilised as the favourite not only for RABV detection but also for viral speciation and phylogenetic analysis (4,20,21). Partial or full nucleoprotein gene sequencing using the Sanger method is mostly valuable for preliminary phylogenetic studies and identification of RABV species.…”
Section: Introductionmentioning
confidence: 99%