Mohammad Siddique
University of Dhaka
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Featured researches published by Mohammad Siddique.
Genome Announcements | 2014
Munawar Sultana; Mohammad Siddique; Samina Momtaz; Arafat Rahman; H. Ullah; Shuvro Prokash Nandi; M.A. Hossain
ABSTRACT Foot-and-mouth disease (FMD) is a highly infectious enzootic disease caused by FMD virus. The complete genome sequence of a circulatory FMD virus (FMDV) serotype O isolated from Natore, Bangladesh, is reported here. Genomic analysis revealed antigenic heterogeneity within the VP1 region, a fragment deletion, and insertions at the 5′ untranslated region (UTR) and 3A region compared to the genome of the available vaccine strain.
Genome Announcements | 2014
H. Ullah; Mohammad Siddique; Munawar Sultana; M.A. Hossain
ABSTRACT The complete genome sequence of a foot-and-and mouth disease virus (FMDV) type A strain (BAN/GA/Sa-197/2013), isolated from Gazipur in Bangladesh, revealed an 84-nucleotide insertion within the 5′-untranslated region (UTR), a lengthened poly(C) tract, and amino acid substitutions at the VP1 region compared to the available genome sequence of the vaccine strain (GenBank accession no. HM854025).
Letters in Applied Microbiology | 2015
H. Ullah; Mohammad Siddique; Md. Al Amin; B.C. Das; Munawar Sultana; M.A. Hossain
Foot‐and‐mouth disease virus (FMDV) serotypes O, A and Asia1 are responsible for significant number of disease outbreaks in Bangladesh; however serotype Asia1 has not been reported in circulation since 1996. The present investigation reports the detection of serotype FMDV Asia1 from local farms in 2012 and 2013 outbreaks. The farms were located in Jessore and Gazipur districts, and one of these farms was under vaccine control programme. Phylogenetic analysis of the complete VP1 gene revealed that FMDV Asia1 is under genetic lineage C having close similarity to the Asia1 sequences of Indian origin. The circulatory genotype Asia1 showed VP1 protein sequence heterogeneity of eight amino acid substitutions within the G‐H loop with the vaccine strain [IND 63/72 (AY304994)] used in vaccination programme. ELISA assay revealed that, of seven, only one local field serum sample (cattle vaccinated 38 days earlier) was positive at a titre level of >2·4 (log10) but failed to protect the cattle from infection occurred by the virus. This investigation focused that the eight amino acid substitution in VP1 protein at G‐H loop of the locally circulated FMDV serotype Asia1 strain may be a reason for current vaccination failure.
Genome Announcements | 2016
M. Rahmat Ali; H. Ullah; Mohammad Siddique; Munawar Sultana; M. Anwar Hossain
ABSTRACT In this article, we document the first pig-isolated complete genome sequence of foot-and-mouth disease virus type O in Bangladesh. The complete viral genome revealed a potential serotypic recombination at the 5′ untranslated region (UTR). Conventional amino acid deletion was lacking in 3A region, and antigenic heterogeneity to circulatory type O existed within the VP1 region.
Letters in Applied Microbiology | 2015
Anwar Hossain; Shuvro Prokash Nandi; Mohammad Siddique; Santonu Kumar Sanyal; Munawar Sultana; M.A. Hossain
White Spot Syndrome Virus (WSSV) is a dsDNA virus causing White Spot Syndrome Disease (WSSD) in shrimp with almost 100% morality rate within 3–10 days. In Bangladesh, WSSD is one of the major impediments of shrimp farming. This study first investigated the prevalence and distribution of WSSV in cultured shrimps of the coastal regions in Bangladesh. A total of 60 shrimp samples, collected from the 25 shrimp farms of different coastal regions (Satkhira, Khulna, Bagerhat and Coxs Bazar), were analysed during 2013–2014 by conventional PCR using VP28 and VP664 gene‐specific primers; 39 of 60 samples were found WSSV positive. SYBR green real‐time PCR using 71‐bp amplicon for VP664 gene correlated well with conventional PCR data. The prevalence rates of WSSV among the collected 60 samples were Satkhira 79%, Khulna 50%, Bagerhat 38% and Coxs Bazar 25%. Sequencing of WSSV‐positive PCR amplicons of VP28 showed 99% similarity with WSSV NCBI Ref/Seq Sequences. Molecular analysis of the VP28 gene sequences of WSSV revealed that Bangladeshi strains phylogenetically affiliated to the strains belong to India. This work concluded that WSSV infections are widely distributed in the coastal regions cultured shrimp in Bangladesh.
Transboundary and Emerging Diseases | 2018
Mohammad Siddique; M. R. Ali; A. S. M. R. U. Alam; H. Ullah; A. Rahman; R. P. Chakrabarty; M. A. Amin; Sirajul Hoque; Shuvro Prokash Nandi; Munawar Sultana; M.A. Hossain
Foot-and-mouth disease (FMD) is endemic in Bangladesh, and the implementation of a control programme for this disease is at an early stage, according to the FAO- and OIE-proposed Progressive Control Pathway for FMD (PCP-FMD) Roadmap. To develop an effective control programme, understanding of foot-and-mouth disease virus (FMDV) serotypes, even subtypes within the serotypes is essential. The present investigation aims at viral VP1 coding region sequence-based analysis of FMD samples collected from 34 FMD outbreaks during 2012-2016 in Bangladesh. Foot-and-mouth disease virus (FMDV) serotype O was responsible for 82% of the outbreaks in Bangladesh, showing its dominance over serotype A and Asia1. The VP1 phylogeny revealed the emergence of two novel sublineages of serotype O, named as Ind2001BD1 and Ind2001BD2, within the Ind2001 lineage along with the circulation of Ind2001d sublineage in Bangladesh, which was further supported by the multidimensional scaling with distinct clusters for each sublineage. The novel sublineages had evident genetic variability with other established sublineages within Ind2001 lineage. Ten mutations with three or more amino acid variations were detected within B-C loop, G-H loop and C-terminal region of the VP1 protein of FMDV serotype O viruses isolated exclusively from Bangladesh. Furthermore, two amino acid substitutions at positions 197 and 198 within the VP1 C-terminal region are unique to the novel sublineages. The existence of widespread genetic variations among circulatory FMDV serotype O viruses makes the FMD control programme complex in Bangladesh. Adequate epidemiological data, disease reporting, animal movement control, appropriate vaccination and above all stringent policies of the government are necessary to combat FMD in Bangladesh.
Genome Announcements | 2017
M. Rahmat Ali; A. S. M. Rubayet Ul Alam; M. Al Amin; H. Ullah; Mohammad Siddique; Samina Momtaz; Munawar Sultana; M. Anwar Hossain
ABSTRACT The complete genome sequence of foot-and-mouth disease virus (FMDV) serotype Asia1 isolated from Bangladesh is reported here. Genome analysis revealed amino acid substitutions in the VP1 antigenic region and deletions in both the 5′ and 3′ untranslated regions (UTRs) compared to the genome of the existing vaccine strain (GenBank accession no. AY304994).
Journal of Applied and Emerging Sciences | 2016
Mohammad Siddique; Mohammad Amin
Bangladesh Journal of Microbiology | 2016
Mohammad Siddique; H. Ullah; Shuvro Prokash Nandi; Debaraj Chakma; Munawar Sultana; M. Anwar Hossain
Bangladesh Journal of Microbiology | 2016
Anwar Hossain; Santonu Kumar Sanyal; Mohammad Siddique; Raj Kumar Biswas; Munawar Sultana; M. Anwar Hossain