Detection of lumpy skin disease virus reads in the human upper respiratory tract microbiome requires further investigation

Lumpy skin disease virus (LSDV), a double‐stranded DNA virus from the Capripoxvirus genus, primarily affects Bos indicus, Bos taurus breeds, and water buffalo. Arthropod vectors, including mosquitoes and biting flies, are the main LSDV transmitters. Although LSDV is not zoonotic, this study unexpect...

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Veröffentlicht in:Journal of medical virology 2024-08, Vol.96 (8), p.e29829-n/a
Hauptverfasser: Tomar, Siddharth Singh, Khairnar, Krishna
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Khairnar, Krishna
description Lumpy skin disease virus (LSDV), a double‐stranded DNA virus from the Capripoxvirus genus, primarily affects Bos indicus, Bos taurus breeds, and water buffalo. Arthropod vectors, including mosquitoes and biting flies, are the main LSDV transmitters. Although LSDV is not zoonotic, this study unexpectedly detected LSDV reads in the upper respiratory tract microbiome of humans from rural and urban areas in Maharashtra, India. Nasopharyngeal and oropharyngeal swab samples collected for SARS‐CoV‐2 surveillance underwent whole‐genome metagenomics sequencing, revealing LSDV reads in 25% of samples. Split kmer analysis provided insights into sample relatedness despite the low coverage of LSDV reads with the reference genome. Our findings, which include the detection of LSDV contigs aligning to specific locations on the reference genome, suggest a common source for LSDV reads, potentially shared water sources, or milk/milk products. Further investigation is needed to ascertain the mode of transmission and reason for the detection of LSDV reads in human upper respiratory tract.
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Arthropod vectors, including mosquitoes and biting flies, are the main LSDV transmitters. Although LSDV is not zoonotic, this study unexpectedly detected LSDV reads in the upper respiratory tract microbiome of humans from rural and urban areas in Maharashtra, India. Nasopharyngeal and oropharyngeal swab samples collected for SARS‐CoV‐2 surveillance underwent whole‐genome metagenomics sequencing, revealing LSDV reads in 25% of samples. Split kmer analysis provided insights into sample relatedness despite the low coverage of LSDV reads with the reference genome. Our findings, which include the detection of LSDV contigs aligning to specific locations on the reference genome, suggest a common source for LSDV reads, potentially shared water sources, or milk/milk products. 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subjects Adult
Animals
Aquatic insects
Bos taurus
Bos taurus indicus
Capripoxvirus
COVID-19 - diagnosis
COVID-19 - virology
DNA viruses
Female
Gene sequencing
Genome, Viral - genetics
Genomes
Genomic analysis
Humans
human–animal interface
India
Lumpy skin disease
Lumpy Skin Disease - virology
lumpy skin disease virus (LSDV)
Lumpy skin disease virus - classification
Lumpy skin disease virus - genetics
Lumpy skin disease virus - isolation & purification
Male
Metagenomics
Metagenomics - methods
Microbiomes
Microbiota - genetics
Milk products
Nasopharynx - microbiology
Nasopharynx - virology
Oropharynx - microbiology
Oropharynx - virology
Respiratory System - microbiology
Respiratory System - virology
Respiratory tract
Respiratory tract diseases
SARS-CoV-2 - classification
SARS-CoV-2 - genetics
SARS-CoV-2 - isolation & purification
Severe acute respiratory syndrome coronavirus 2
Skin diseases
Transmitters
upper respiratory tract
Urban areas
Vectors
Viral diseases
Viruses
Whole Genome Sequencing
Zoonoses
title Detection of lumpy skin disease virus reads in the human upper respiratory tract microbiome requires further investigation
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