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对印度小鼷鹿(Urva auropunctata)中的汉赛巴尔通体(Bartonella henselae)进行序列分型。

Sequence typing of Bartonella henselae in small Indian mongooses (Urva auropunctata).

机构信息

Biomedical Sciences Department, One Health Center for Zoonoses and Tropical Veterinary Medicine, Ross University School of Veterinary Medicine, West Farm, Saint Kitts and Nevis.

Intracellular Pathogens Research Laboratory, Department of Clinical Sciences, College of Veterinary Medicine, Comparative Medicine Institute, North Carolina State University, Raleigh, NC, USA.

出版信息

Sci Rep. 2024 Aug 12;14(1):18654. doi: 10.1038/s41598-024-69909-z.

Abstract

This study aimed to determine the sequence type (ST) of Bartonella henselae infecting small Indian mongooses from Saint Kitts via multi-locus sequence typing (MLST). This investigation used stored EDTA blood (n = 22) samples from mongooses previously identified as positive for B. henselae. Chocolate agar plates were enriched with Bartonella alpha-Proteobacteria growth medium (BAPGM) to culture and isolate Bartonella from the blood samples. To perform MLST, DNA was extracted and purified from isolates followed by amplification by conventional PCR (300-500 bp) for eight genes (16S rDNA, batR, gltA, groEL, ftsZ, nlpD, ribC, and rpoB). Bartonella henselae STs were deposited in the PubMLST repository. Out of 22 B. henselae-positive blood samples, isolates were obtained from 12 mongooses (54.5%; 12/22). Each mongoose was infected with one ST. The studied mongoose population was infected with sequence types ST2, ST3, ST8, and a novel ST represented by ST38. Bartonella henselae ST2, ST3 and ST8 infecting mongooses are known to circulate in humans and cats, with ST2 and ST8 associated with Cat Scratch Disease (bartonellosis) in humans. The results presented herein denote the circulation of B. henselae STs with zoonotic potential in mongooses with risk of B. henselae transmission to humans.

摘要

本研究旨在通过多位点序列分型(MLST)确定从圣基茨感染印度小长尾狸的汉赛巴尔通体的序列型(ST)。本研究使用先前鉴定为汉赛巴尔通体阳性的小长尾狸的储存 EDTA 血液(n=22)样本。巧克力琼脂平板用 Bartonella alpha-Proteobacteria 生长培养基(BAPGM)进行富集,以从血液样本中培养和分离巴尔通体。为了进行 MLST,从分离物中提取和纯化 DNA,然后通过常规 PCR(300-500 bp)扩增 8 个基因(16S rDNA、batR、gltA、groEL、ftsZ、nlpD、ribC 和 rpoB)。汉赛巴尔通体 ST 已存入 PubMLST 存储库。在 22 份汉赛巴尔通体阳性血液样本中,从 12 只长尾狸(54.5%,12/22)中获得了分离物。每只长尾狸都感染了一种 ST。研究的长尾狸种群感染了 ST2、ST3、ST8 和一种由 ST38 代表的新型 ST。感染长尾狸的汉赛巴尔通体 ST2、ST3 和 ST8 已知在人类和猫中循环,ST2 和 ST8 与人类的猫抓病(巴尔通体病)有关。本文介绍的结果表明,具有人类感染风险的汉赛巴尔通体 ST 存在于长尾狸中,存在汉赛巴尔通体向人类传播的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9dc/11319332/52ce1cd9f04d/41598_2024_69909_Fig1a_HTML.jpg

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