Cryptic Mutation in the Genome of Salmonella enterica to Acquire AMR Genes With Alteration of Amino Acid Sequences: A Pathogenomics Study.

IF 2.7 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Smaranika Pattnaik
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引用次数: 0

Abstract

The Mahanadi river is a freshwater sink of Odisha which has taken its course through the Western Odisha and finally end in the Bay of Bengal. However, the river water is receiving pathogenic bacterial strains due to anthropogenic activities and therefore health of the common man is severely affected with regular outbreaks. This present pursuit had aimed to carry out pathogenomics of a bacterial isolate perpetuating in the said river water near a local tertiary care hospital, Burla, Odisha, India. Relevant procedures and experiments were carried out, and a strain of Salmonella enterica was identified. The whole genome of said isolate was sequenced using NGS approaches. It was observed that there was alteration of amino acids leading genome with acquire of AMR genes. There was a change in nucleotide codon from CTA reversed back to CTA, amino acid from I > P, position in contig, 143183-146332 at node 15, and the eluted gene was acrB with identity 99.97%. In addition, AGC reversed back to ACC amino acid from T > S at node 17 position in contig, with elution of genes, pmrA (109013-10968) and pmrB (109691-110761) in contig. It was further observed that there was depiction of nucleotide codon change from ATG to ACG, GTC to GCC, GGC to AGC, GTA to ATA, ATT to GTT, and GCG to ACG. As a result of which, methionine to threonine (M > T), valine to alanine (V > A), glycine to serine (G > S), valine to isoleucine (V > I), isoleucine to valine (I > V), and alanine to threonine (A > T) were changed without any change in respect to AMR gene consociation.

肠沙门氏菌基因组的隐性突变以氨基酸序列改变获得AMR基因:一项病理基因组学研究。
Mahanadi河是奥里萨邦的一个淡水汇,它流经奥里萨邦西部,最终流入孟加拉湾。然而,由于人为活动,河水正在感染致病菌株,因此普通人的健康受到严重影响,经常爆发。目前的研究目的是对印度奥里萨邦Burla当地一家三级保健医院附近的上述河水中存在的一种细菌分离物进行病理基因组学研究。经过相关程序和实验,鉴定出一株肠道沙门氏菌。该分离物的全基因组测序采用NGS方法。结果表明,随着AMR基因的获得,其基因组中氨基酸发生了改变。CTA的核苷酸密码子反转回CTA,氨基酸从I b> P,序列143183 ~ 146332,15节点,洗脱基因为acrB,同源性99.97%。此外,AGC在contig的17节点位置从T > S逆转回ACC氨基酸,洗脱了contig中的pmrA(109013-10968)和pmrB(109691-110761)基因。进一步观察到ATG到ACG、GTC到GCC、GGC到AGC、GTA到ATA、ATT到GTT、GCG到ACG的核苷酸密码子变化。结果表明,蛋氨酸到苏氨酸(M > T)、缬氨酸到丙氨酸(V b> a)、甘氨酸到丝氨酸(G b> S)、缬氨酸到异亮氨酸(V > I)、异亮氨酸到缬氨酸(I > V)和丙氨酸到苏氨酸(a > T)在AMR基因关联方面没有变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biotechnology and applied biochemistry
Biotechnology and applied biochemistry 工程技术-生化与分子生物学
CiteScore
6.00
自引率
7.10%
发文量
117
审稿时长
3 months
期刊介绍: Published since 1979, Biotechnology and Applied Biochemistry is dedicated to the rapid publication of high quality, significant research at the interface between life sciences and their technological exploitation. The Editors will consider papers for publication based on their novelty and impact as well as their contribution to the advancement of medical biotechnology and industrial biotechnology, covering cutting-edge research in synthetic biology, systems biology, metabolic engineering, bioengineering, biomaterials, biosensing, and nano-biotechnology.
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