BimABm positivity in melioidosis and its impact on clinical profile, and outcomes: a retrospective cohort study

IF 1.7 Q4 INFECTIOUS DISEASES
Nitin Gupta , Tirlangi Praveen Kumar , Soumi Chowdhury , Chiranjay Mukhopadhyay
{"title":"BimABm positivity in melioidosis and its impact on clinical profile, and outcomes: a retrospective cohort study","authors":"Nitin Gupta ,&nbsp;Tirlangi Praveen Kumar ,&nbsp;Soumi Chowdhury ,&nbsp;Chiranjay Mukhopadhyay","doi":"10.1016/j.ijregi.2025.100723","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>Melioidosis, caused by <em>Burkholderia pseudomallei</em> presents with diverse clinical features. Neurological involvement, though rare, is a severe complication. The BimA<sub>Bm</sub> allele, a variant of the <em>Burkholderia</em> intracellular motility A (BimA) virulence gene, has been linked to neurotropism, but data from India on this association are limited.</div></div><div><h3>Methods</h3><div>We conducted a retrospective cohort study of 138 culture-confirmed melioidosis patients at a tertiary care center in southern India. A polymerase chain reaction assay was used to detect the BimA<sub>Bm</sub> allele in archived isolates. Clinical features and 28-day mortality were compared between BimA<sub>Bm</sub> -positive and -negative groups.</div></div><div><h3>Results</h3><div>The BimA<sub>Bm</sub> allele was detected in 5.8% of isolates. Neurological involvement was significantly more common in BimA<sub>Bm</sub>-positive patients (50% [4/8] vs 2.3% [3/130], <em>P</em> &lt; 0.001). No significant differences in comorbidities or 28-day mortality were observed between the two groups.</div></div><div><h3>Conclusions</h3><div>Although uncommon, the BimA<sub>Bm</sub> allele is strongly associated with neurological melioidosis in southern India.</div></div>","PeriodicalId":73335,"journal":{"name":"IJID regions","volume":"16 ","pages":"Article 100723"},"PeriodicalIF":1.7000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IJID regions","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772707625001584","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives

Melioidosis, caused by Burkholderia pseudomallei presents with diverse clinical features. Neurological involvement, though rare, is a severe complication. The BimABm allele, a variant of the Burkholderia intracellular motility A (BimA) virulence gene, has been linked to neurotropism, but data from India on this association are limited.

Methods

We conducted a retrospective cohort study of 138 culture-confirmed melioidosis patients at a tertiary care center in southern India. A polymerase chain reaction assay was used to detect the BimABm allele in archived isolates. Clinical features and 28-day mortality were compared between BimABm -positive and -negative groups.

Results

The BimABm allele was detected in 5.8% of isolates. Neurological involvement was significantly more common in BimABm-positive patients (50% [4/8] vs 2.3% [3/130], P < 0.001). No significant differences in comorbidities or 28-day mortality were observed between the two groups.

Conclusions

Although uncommon, the BimABm allele is strongly associated with neurological melioidosis in southern India.
类鼻炎患者BimABm阳性及其对临床表现和结果的影响:一项回顾性队列研究
目的假性伯克霍尔德菌引起的类鼻疽病临床表现多样。神经系统受累虽然罕见,但却是一种严重的并发症。BimABm等位基因是伯克霍尔德氏菌胞内运动a (BimA)毒力基因的一种变体,与嗜神经性有关,但来自印度的这一关联的数据有限。方法:我们对印度南部一家三级保健中心138例经培养证实的类鼻疽患者进行了回顾性队列研究。采用聚合酶链反应法检测存档分离株的BimABm等位基因。比较BimABm阳性组和阴性组的临床特征和28天死亡率。结果在5.8%的分离株中检出BimABm等位基因。神经系统受累在bimabm阳性患者中更为常见(50% [4/8]vs 2.3% [3/130], P < 0.001)。两组患者的合并症和28天死亡率无显著差异。结论BimABm等位基因虽然不常见,但与印度南部神经性类鼻瘤病密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
IJID regions
IJID regions Infectious Diseases
CiteScore
1.60
自引率
0.00%
发文量
0
审稿时长
64 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信