Mehla Kusum, Ramana Jayashree
Department of Biotechnology and Bioinformatics, Jaypee University of Information Technology , Solan, Himachal Pradesh, India .
OMICS. 2015 Jun;19(6):354-60. doi: 10.1089/omi.2015.0030. Epub 2015 May 15.
Diarrhea is a highly common infection among children, responsible for significant morbidity and mortality rate worldwide. After pneumonia, diarrhea remains the second leading cause of neonatal deaths. Numerous viral, bacterial, and parasitic enteric pathogens are associated with diarrhea. With increasing antibiotic resistance among enteric pathogens, there is an urgent need for global surveillance of the mutations and resistance genes primarily responsible for resistance to antibiotic treatment. Single Nucleotide Polymorphisms are important in this regard as they have a vast potential to be utilized as molecular diagnostics for gene-disease or pharmacogenomics association studies linking genotype to phenotype. DBDiaSNP is a comprehensive repository of mutations and resistance genes among various diarrheal pathogens and hosts to advance breakthroughs that will find applications from development of sequence-based diagnostic tools to drug discovery. It contains information about 946 mutations and 326 resistance genes compiled from literature and various web resources. As of March 2015, it houses various pathogen genes and the mutations responsible for antibiotic resistance. The pathogens include, for example, DEC (Diarrheagenic E.coli), Salmonella spp., Campylobacter spp., Shigella spp., Clostridium difficile, Aeromonas spp., Helicobacter pylori, Entamoeba histolytica, Vibrio cholera, and viruses. It also includes mutations from hosts (e.g., humans, pigs, others) that render them either susceptible or resistant to a certain type of diarrhea. DBDiaSNP is therefore intended as an integrated open access database for researchers and clinicians working on diarrheal diseases. Additionally, we note that the DBDiaSNP is one of the first antibiotic resistance databases for the diarrheal pathogens covering mutations and resistance genes that have clinical relevance from a broad range of pathogens and hosts. For future translational research involving integrative biology and global health, the database offers veritable potentials, particularly for developing countries and worldwide monitoring and personalized effective treatment of pathogens associated with diarrhea. The database is accessible on the public domain at http://www.juit.ac.in/attachments/dbdiasnp/ .
腹泻是儿童中极为常见的感染性疾病,在全球范围内导致了相当高的发病率和死亡率。仅次于肺炎,腹泻仍是新生儿死亡的第二大主要原因。众多病毒、细菌和寄生虫性肠道病原体都与腹泻有关。随着肠道病原体对抗生素的耐药性不断增加,迫切需要对主要导致抗生素治疗耐药的突变和耐药基因进行全球监测。单核苷酸多态性在这方面很重要,因为它们具有巨大潜力,可被用作基因疾病或药物基因组学关联研究的分子诊断工具,将基因型与表型联系起来。DBDiaSNP是一个关于各种腹泻病原体和宿主中突变及耐药基因的综合数据库,旨在推动相关突破,这些突破将在基于序列的诊断工具开发到药物发现等领域得到应用。它包含从文献和各种网络资源中收集的946个突变和326个耐药基因的信息。截至2015年3月,它收录了各种病原体基因以及导致抗生素耐药的突变。这些病原体包括,例如,致泻性大肠杆菌、沙门氏菌属、弯曲杆菌属、志贺氏菌属、艰难梭菌、气单胞菌属、幽门螺杆菌、溶组织内阿米巴、霍乱弧菌以及病毒。它还包括宿主(如人类、猪等)的突变,这些突变使宿主对某种类型的腹泻易感或具有抗性。因此,DBDiaSNP旨在成为腹泻疾病研究人员和临床医生的综合开放获取数据库。此外,我们注意到DBDiaSNP是首批针对腹泻病原体的抗生素耐药数据库之一,涵盖了来自广泛病原体和宿主且具有临床相关性的突变和耐药基因。对于未来涉及整合生物学和全球健康的转化研究,该数据库具有切实的潜力,特别是对于发展中国家以及全球范围内监测和个性化有效治疗与腹泻相关的病原体而言。该数据库可在公共领域通过http://www.juit.ac.in/attachments/dbdiasnp/访问。