Literature detail

Surveillance and Molecular Characterization of SARS-CoV-2 Infection in Non-Human Hosts in Gujarat, India.

Dinesh Kumar1 Sejalben P Antiya2 Sandipkumar S Patel2 Ramesh Pandit1 Madhvi Joshi1 Abhinava K Mishra3 Chaitanya G Joshi1 Arunkumar C Patel2
Affiliations 3 institutions
  1. Gujarat Biotechnology Research Centre (GBRC), Sector-11, Gandhinagar 382011, Gujarat, India.
  2. Department of Veterinary Microbiology, College of Veterinary Science and Animal Husbandry, Sardarkrushinagar Campus, Kamdhenu University, Gandhinagar 382010, Gujarat, India.
  3. Molecular, Cellular and Developmental Biology Department, University of California Santa Barbara, Santa Barbara, CA 93106, USA.
PMID 36361271 2022 Int J Environ Res Public Health eng epublish
PubMed DOI Browse context

Article

Publication summary

Since December 2019, Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) has been spreading worldwide, triggering one of the most challenging pandemics in the human population. In light of the reporting of this virus in domestic and wild animals from several parts of the world, a systematic surveillance study was conceptualized to detect SARS-CoV-2 among species of veterinary importance. Nasal and/or rectal samples of 413 animals (dogs n= 195, cattle n = 64, horses n = 42, goats n = 41, buffaloes n = 39, sheep n = 19, cats n = 6, camels n = 6, and a monkey n = 1) were collected from different places in the Gujarat state of India. RNA was extracted from the samples and subjected to RT-qPCR-based quantification of the target sequences in viral nucleoprotein (N), spike (S), and ORF1ab genes. A total of 95 (23.79%) animals were found positive, comprised of n = 67 (34.35%) dogs, n= 15 (23.43%) cattle, and n = 13 (33.33%) buffaloes. Whole SARS-CoV-2 genome sequencing was done from one sample (ID-A4N, from a dog), where 32 mutations, including 29 single-nucleotide variations (SNV) and 2 deletions, were detected. Among them, nine mutations were located in the receptor binding domain of the spike (S) protein. The consequent changes in the amino acid sequence revealed T19R, G142D, E156-, F157-, A222V, L452R, T478K, D614G, and P681R mutations in the S protein and D63G, R203M, and D377Y in the N protein. The lineage assigned to this SARS-CoV-2 sequence is B.1.617.2. Thus, the present study highlights the transmission of SARS-CoV-2 infection from human to animals and suggests being watchful for zoonosis.

buffalo canine cattle delta variant RT-qPCR SARS-CoV-2 COVID-19 Animals Buffaloes Cattle Dogs Horses Humans Mutation Pandemics SARS-CoV-2 Sheep SARS-CoV-2 variants

Structured evidence records

Evidence records

8 total
3 records
Extraction confidence 0.95
Key finding

SARS-CoV-2 was transmitted from humans to dogs, cattle, and buffaloes in Gujarat, India, confirmed by RT-qPCR and sequencing of a canine sample belonging to lineage B.1.617.2.

Virus
Location
Supporting text

A total of 95 (23.79%) animals were found positive, comprised of 67 dogs, 15 cattle, and 13 buffaloes... Thus, the present study highlights the transmission of SARS-CoV-2 infection from human to animals.

Method
RNA extraction; RT-qPCR; whole genome sequencing
Study design
field surveillance
Transmission direction
human-to-animal
Geographic raw
Gujarat, India
Country inferred
India
Extraction confidence 0.95
Key finding

SARS-CoV-2 was transmitted from humans to cattle in Gujarat, India, confirmed by RT-qPCR detection of viral RNA.

Virus
Location
Supporting text

A total of 95 (23.79%) animals were found positive, comprised of 67 dogs, 15 cattle, and 13 buffaloes... Thus, the present study highlights the transmission of SARS-CoV-2 infection from human to animals.

Method
RNA extraction; RT-qPCR
Study design
field surveillance
Transmission direction
human-to-animal
Geographic raw
Gujarat, India
Country inferred
India
Extraction confidence 0.95
Key finding

SARS-CoV-2 was transmitted from humans to buffaloes in Gujarat, India, confirmed by RT-qPCR detection of viral RNA.

Virus
Location
Supporting text

A total of 95 (23.79%) animals were found positive, comprised of 67 dogs, 15 cattle, and 13 buffaloes... Thus, the present study highlights the transmission of SARS-CoV-2 infection from human to animals.

Method
RNA extraction; RT-qPCR
Study design
field surveillance
Transmission direction
human-to-animal
Geographic raw
Gujarat, India
Country inferred
India
3 records
Extraction confidence 0.98
Key finding

Surveillance by RT-qPCR detected SARS-CoV-2 RNA in dogs in Gujarat, India, with 67 of 195 animals testing positive.

Virus
Location
Supporting text

Nasal and/or rectal samples of 413 animals (dogs n=195, cattle n=64, horses n=42, goats n=41, buffaloes n=39, sheep n=19, cats n=6, camels n=6, and a monkey n=1) were collected from different places in the Gujarat state of India. RNA was extracted from the samples and subjected to RT-qPCR-based quantification... A total of 95 animals were found positive, comprised of n=67 dogs, n=15 cattle, and n=13 buffaloes.

Method
RT-qPCR
Sample type
nasal; rectal
Geographic raw
Gujarat
Country inferred
India
Extraction confidence 0.98
Key finding

Surveillance by RT-qPCR detected SARS-CoV-2 RNA in cattle in Gujarat, India, with 15 of 64 animals testing positive.

Virus
Host
Location
Supporting text

Nasal and/or rectal samples of 413 animals (dogs n=195, cattle n=64, horses n=42, goats n=41, buffaloes n=39, sheep n=19, cats n=6, camels n=6, and a monkey n=1) were collected from different places in the Gujarat state of India. RNA was extracted from the samples and subjected to RT-qPCR-based quantification... A total of 95 animals were found positive, comprised of n=67 dogs, n=15 cattle, and n=13 buffaloes.

Method
RT-qPCR
Sample type
nasal; rectal
Geographic raw
Gujarat
Country inferred
India
Extraction confidence 0.98
Key finding

Surveillance by RT-qPCR detected SARS-CoV-2 RNA in buffaloes in Gujarat, India, with 13 of 39 animals testing positive.

Virus
Host
Location
Supporting text

Nasal and/or rectal samples of 413 animals (dogs n=195, cattle n=64, horses n=42, goats n=41, buffaloes n=39, sheep n=19, cats n=6, camels n=6, and a monkey n=1) were collected from different places in the Gujarat state of India. RNA was extracted from the samples and subjected to RT-qPCR-based quantification... A total of 95 animals were found positive, comprised of n=67 dogs, n=15 cattle, and n=13 buffaloes.

Method
RT-qPCR
Sample type
nasal; rectal
Geographic raw
Gujarat
Country inferred
India
1 records
Extraction confidence 0.80
Key finding

Whole genome sequencing of SARS-CoV-2 from a dog in Gujarat revealed multiple spike and nucleocapsid mutations characteristic of the Delta lineage (B.1.617.2).

Virus
Location
Not specified
Supporting text

Whole SARS-CoV-2 genome sequencing was done from one sample (ID-A4N, from a dog), where 32 mutations, including 29 single-nucleotide variations (SNV) and 2 deletions, were detected. Among them, nine mutations were located in the receptor binding domain of the spike (S) protein. The lineage assigned to this SARS-CoV-2 sequence is B.1.617.2.

Genes or proteins
spike (S); nucleoprotein (N)
Analysis methods
whole genome sequencing
1 records
Extraction confidence 0.85
Key finding

A dog-derived SARS-CoV-2 genome (delta variant, B.1.617.2) exhibited several amino acid changes in the spike receptor binding domain and nucleoprotein, including T19R, L452R, T478K, D614G, and P681R, suggesting molecular adaptation features.

Virus
Host
Not specified
Location
Not specified
Supporting text

Whole SARS-CoV-2 genome sequencing was done from one sample (ID-A4N, from a dog), where 32 mutations, including 29 single-nucleotide variations (SNV) and 2 deletions, were detected. Among them, nine mutations were located in the receptor binding domain of the spike (S) protein. The consequent changes in the amino acid sequence revealed T19R, G142D, E156-, F157-, A222V, L452R, T478K, D614G, and P681R mutations in the S protein and D63G, R203M, and D377Y in the N protein.

Genes or proteins
spike; nucleoprotein
Mutations
T19R; G142D; E156-; F157-; A222V; L452R; T478K; D614G; P681R; D63G; R203M; D377Y
Mechanism types
receptor_binding; molecular_adaptation