This study aimed to determine the prevalence of FPV and CPV infections among cats and dogs in Gujarat, India, compare the diagnostic performance of rapid antigen testing (RAT), conventional polymerase chain reaction (PCR), and quantitative PCR (qPCR), charact…
Abstract / descriptionThis study aimed to determine the prevalence of FPV and CPV infections among cats and dogs in Gujarat, India, compare the diagnostic performance of rapid antigen testing (RAT), conventional polymerase chain reaction (PCR), and quantitative PCR (qPCR), characterize circulating viral variants through VP2 gene sequencing and phylogenetic analysis, and investigate evidence of cross-species circulation.
This study aimed to determine the molecular prevalence of T. orientalis in cattle and their naturally infesting ticks in Wasit Province, Iraq; identify host-associated risk factors; and characterize the genetic diversity and phylogenetic relationships of loca…
Abstract / descriptionThis study aimed to determine the molecular prevalence of T. orientalis in cattle and their naturally infesting ticks in Wasit Province, Iraq; identify host-associated risk factors; and characterize the genetic diversity and phylogenetic relationships of local isolates relative to global reference strains.
This study aimed to detect FMDV in clinically affected cattle in Aceh, Indonesia, using serological and molecular approaches and to characterize the phylogenetic relationship of the detected virus based on the VP1 gene.
Abstract / descriptionThis study aimed to detect FMDV in clinically affected cattle in Aceh, Indonesia, using serological and molecular approaches and to characterize the phylogenetic relationship of the detected virus based on the VP1 gene.
This cross-sectional laboratory-based study aimed to detect MDR E. coli from quail cloacal swabs in Surabaya's traditional markets and screen MDR isolates for the iroN gene, highlighting market level risks within a One Health framework.
Abstract / descriptionThis cross-sectional laboratory-based study aimed to detect MDR E. coli from quail cloacal swabs in Surabaya's traditional markets and screen MDR isolates for the iroN gene, highlighting market level risks within a One Health framework.
This study aimed to develop a three-part histopathological exam using light microscopy, polarized light microscopy, and Nile Red (NR) fluorescence, and to analyze MP distribution and linked tissue effects in mussels collected from industrial shoreline areas i…
Abstract / descriptionThis study aimed to develop a three-part histopathological exam using light microscopy, polarized light microscopy, and Nile Red (NR) fluorescence, and to analyze MP distribution and linked tissue effects in mussels collected from industrial shoreline areas in Rayong Province.
This study aimed to characterize the diversity of Ovar-DRB1 exon 2 alleles in Edilbay sheep and to identify novel allelic variants using Sanger sequencing.
Abstract / descriptionThis study aimed to characterize the diversity of Ovar-DRB1 exon 2 alleles in Edilbay sheep and to identify novel allelic variants using Sanger sequencing.
This study aimed to develop and validate a regionally adapted sandwich enzyme-linked immunosorbent assay (ELISA) based on monoclonal and polyclonal antibodies (pAbs) raised against a recombinant p60 antigen derived from a Kazakhstani L. monocytogenes field is…
Abstract / descriptionThis study aimed to develop and validate a regionally adapted sandwich enzyme-linked immunosorbent assay (ELISA) based on monoclonal and polyclonal antibodies (pAbs) raised against a recombinant p60 antigen derived from a Kazakhstani L. monocytogenes field isolate.
This study aimed to clone, express, and evaluate recombinant serine proteases from Trichinella spiralis (rTsp-LE) to Trichinella nativa (rTnsp-4E), and to assess their diagnostic performance compared with ES antigens and a commercial kit.
Abstract / descriptionThis study aimed to clone, express, and evaluate recombinant serine proteases from Trichinella spiralis (rTsp-LE) to Trichinella nativa (rTnsp-4E), and to assess their diagnostic performance compared with ES antigens and a commercial kit.
This study aimed to detect, characterize, and analyze the AMR patterns and resistance genes of Klebsiella spp. and Enterobacter spp. isolated from slaughtered guinea pigs intended for human consumption in Colombia.
Abstract / descriptionThis study aimed to detect, characterize, and analyze the AMR patterns and resistance genes of Klebsiella spp. and Enterobacter spp. isolated from slaughtered guinea pigs intended for human consumption in Colombia.
This study aimed to detect Shiga toxin-producing E. coli (STEC) in wild rats captured from slum-adjacent urban areas of Banyuwangi District, Indonesia.
Abstract / descriptionThis study aimed to detect Shiga toxin-producing E. coli (STEC) in wild rats captured from slum-adjacent urban areas of Banyuwangi District, Indonesia.
This study aimed to (i) establish a nested reverse transcription polymerase chain reaction (RT-PCR) assay targeting the open reading frame 7 (ORF7) gene to detect and differentiate PRRSV-1 and PRRSV-2, and (ii) refine the genetic classification of PRRSV-2 str…
Abstract / descriptionThis study aimed to (i) establish a nested reverse transcription polymerase chain reaction (RT-PCR) assay targeting the open reading frame 7 (ORF7) gene to detect and differentiate PRRSV-1 and PRRSV-2, and (ii) refine the genetic classification of PRRSV-2 strains circulating in Thailand through ORF5-based phylogenetic analysis.
This study aimed to identify and characterize B. canis vogeli in naturally infected dogs in Khon Kaen, Thailand, to compare the diagnostic performance of two primer sets (Bab7/Bab9 and Babf/Babc), and to perform phylogenetic analysis of the isolates.
Abstract / descriptionThis study aimed to identify and characterize B. canis vogeli in naturally infected dogs in Khon Kaen, Thailand, to compare the diagnostic performance of two primer sets (Bab7/Bab9 and Babf/Babc), and to perform phylogenetic analysis of the isolates.
This study aimed to develop a sensitive and specific duplex quantitative polymerase chain reaction (qPCR) assay targeting the env gene of BLV with β-actin as an internal control and apply it for molecular surveillance and genotyping of BLV in cattle from six …
Abstract / descriptionThis study aimed to develop a sensitive and specific duplex quantitative polymerase chain reaction (qPCR) assay targeting the env gene of BLV with β-actin as an internal control and apply it for molecular surveillance and genotyping of BLV in cattle from six regions of Kazakhstan.