ABSTRACT
OBJECTIVE: This research work was conducted for the molecular characterization of the circulating foot-and-mouth disease (FMD) virus in Bangladesh and revealed out their serotype. MATERIALS AND METHODS: The VP1 gene of six field isolates of FMD virus (FMDV) serotypes (two serotypes O, two serotypes A, and two serotypes Asia 1) was subjected for sequencing and phylogenetic analysis. Neighbor-joining trees were constructed by using the Molecular Evolutionary Genetics Analysis 6, having the field nucleotide sequences of FMDV and related sequences available in the GenBank. RESULTS: The nucleotide sequences of the VP1 genes of serotypes O, A, and Asia-1 of the isolates revealed that overall isolates were 91%-100% similar to the isolates reported from Bangladesh and other neighboring countries. Among the isolates reported from Bangladesh, serotype O had 98%-100% identity, serotype A had 91%-100% identity, and serotype Asia-1 had 94%-100% identity. A phylogenetic analysis revealed that the FMDV serotype O PanAsia-02 sub-lineage was confirmed in Bangladesh under the Middle East-South Asian (ME-SA) topotype. On the other hand, we identified genotype VII (18) of Asia topotype (serotype A) and lineage C (serotype Asia-1). CONCLUSION: The FMDV serotype O PanAsia-02 sub-lineage was confirmed in Bangladesh under the ME-SA topotype for the first time. The extensive cross-border animal movement from neighboring countries may act as the source of diversified FMDV serotypes in Bangladesh.
ABSTRACT
OBJECTIVE: This study was conducted to estimate the prevalence of Trichomonas gallinae infection in pigeon and determination of spatial factors related with T. gallinae infection among smallholder farms at Abhaynagar and Monirampur Upazillas, Jessore District, Bangladesh. MATERIALS AND METHODS: This cross-sectional study has undertaken from November 24, 2017 to February 28, 2018 on randomly selected 60 pigeons from 12 smallholder farms. Wet smear technique has been used to identify T. gallinae, from swab samples collected from oropharynx and crop of the sampled birds. RESULTS: The overall prevalence was 60% (95% CI: 46.5-72.4) in which 75% (95% CI: 55.1-89.3), 50% (95% CI: 23.0-76.9), and 44.4% (95% CI: 21.5-69.2) were in squab, adult male, and adult female, respectively. The prevalence, in the case of dead pigeons (n = 13), 69.2% showed positive to the protozoan infection in the study. On the basis of spatial distribution, T. gallinae infection in the rural area was 64% (n = 25) followed by urban area 57.1% (n = 35) of the district. The prevalence of T. gallinae was insignificantly higher at Abhaynagar upazilla in contrast to Monirampur upazilla (30%) of Jessore district. CONCLUSION: This research finding suggests that a significant level of (57.4%) T. gallinae infection is circulating among the pigeon population of Bangladesh. Therefore, proper housing, feeding, and disease management should be ensured by the owner to prevent this problem.
ABSTRACT
Avian influenza viruses (AIVs) continue to pose a global threat. Waterfowl are the main reservoir and are responsible for the spillover of AIVs to other hosts. This study was conducted as part of routine surveillance activities in Bangladesh and it reports on the serological and molecular detection of H5N1 AIV subtype. A total of 2169 cloacal and 2191 oropharyngeal swabs as well as 1725 sera samples were collected from live birds including duck and chicken in different locations in Bangladesh between the years of 2013 and 2014. Samples were tested using virus isolation, serological tests and molecular methods of RT-PCR. Influenza A viruses were detected using reverse transcription PCR targeting the virus matrix (M) gene in 41/4360 (0.94%) samples including both cloacal and oropharyngeal swab samples, 31 of which were subtyped as H5N1 using subtype-specific primers. Twenty-one live H5N1 virus isolates were recovered from those 31 samples. Screening of 1,868 blood samples collected from the same birds using H5-specific ELISA identified 545/1603 (34%) positive samples. Disconcertingly, an analysis of 221 serum samples collected from vaccinated layer chicken in four districts revealed that only 18 samples (8.1%) were seropositive for anti H5 antibodies, compared to unvaccinated birds (n=105), where 8 samples (7.6%) were seropositive. Our result indicates that the vaccination program as currently implemented should be reviewed and updated. In addition, surveillance programs are crucial for monitoring the efficacy of the current poultry vaccinations programs, and to monitor the circulating AIV strains and emergence of AIV subtypes in Bangladesh.
