粪肠球菌中调节适应性和致病性的血红素降解酶的特性。

IF 5.1 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-05-14 Epub Date: 2025-04-11 DOI:10.1128/mbio.00146-25
Debra N Brunson, Haider Manzer, Alexander B Smith, Joseph P Zackular, Todd Kitten, José A Lemos
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引用次数: 0

摘要

粪肠球菌是一种肠道共生菌,是机会性感染的主要原因。它的毒性与它在恶劣环境中茁壮成长的能力有关,其中包括宿主施加的金属饥饿。我们最近发现,粪肠杆菌通过五种专门的转运体来逃避铁饥饿,这些转运体共同从宿主组织中清除铁。有趣的是,血红素,人体中最丰富的铁来源,支持缺乏所有五种铁转运蛋白的菌株的生长(Δ5Fe)。为了从血红素中释放铁,许多细菌病原体利用血红素加氧酶来降解血红素中协调铁离子的卟啉环。虽然粪肠杆菌缺乏这些酶,但生物信息学揭示了在大肠杆菌和其他一些革兰氏阴性菌中发现的厌氧血红素降解酶厌氧素合成酶的潜在同源物。在这里,我们证明了在粪肠杆菌(ΔRS05575)或Δ5Fe背景(Δ5FeΔRS05575)中OG1RF_RS05575的缺失导致厌氧条件下细胞内血红素积累和超敏反应,这表明RS05575编码厌氧菌合成酶,这是革兰氏阳性细菌中首次描述的厌氧菌合成酶。此外,RS05575的缺失,无论是单独缺失还是在Δ5Fe背景下缺失,都会削弱粪肠球菌在小鼠胃肠道中的定植以及小鼠腹膜炎和兔感染性心内膜炎模型中的毒力。这些结果支持了RS05575负责血红素厌氧降解的建议,并将这种相对较新的酶类确定为细菌发病的新因素。本研究的发现可能具有广泛的意义,因为在其他革兰氏阳性兼性厌氧菌中也发现了RS05575的同源物。重要性:血红素是细菌病原体的重要营养物质,主要是因为其在感染过程中作为铁源的能力。虽然已知细菌利用血红素加氧酶从血红素中释放铁,但最近在革兰氏阴性细菌中发现了一种新的厌氧血红素降解酶家族。在这里,我们报道了革兰氏阳性细菌厌氧血红素降解的第一个描述,机会致病菌粪肠球菌,并将这种酶的活性与它们定植和感染宿主的能力联系起来。我们还发现这种酶的同源物存在于许多革兰氏阳性兼性厌氧菌中,这意味着在厌氧条件下降解血红素的能力可能是细菌病原体被忽视的适应性和毒力因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of a heme-degrading enzyme that mediates fitness and pathogenicity in Enterococcus faecalis.

Enterococcus faecalis, a gut commensal, is a leading cause of opportunistic infections. Its virulence is linked to its ability to thrive in hostile environments, which includes host-imposed metal starvation. We recently showed that E. faecalis evades iron starvation using five dedicated transporters that collectively scavenge iron from host tissues. Interestingly, heme, the most abundant source of iron in the human body, supported the growth of a strain lacking all five iron transporters (Δ5Fe). To release iron from heme, many bacterial pathogens utilize heme oxygenase enzymes to degrade the porphyrin ring that coordinates the iron ion of heme. Although E. faecalis lacks these enzymes, bioinformatics revealed a potential ortholog of the anaerobic heme-degrading enzyme anaerobilin synthase, found in Escherichia coli and a few other gram-negative bacteria. Here, we demonstrated that deletion of OG1RF_RS05575 in E. faecalis (ΔRS05575) or in the Δ5Fe background (Δ5FeΔRS05575) led to intracellular heme accumulation and hypersensitivity under anaerobic conditions, suggesting RS05575 encodes an anaerobilin synthase, the first of its kind described in gram-positive bacteria. Additionally, deletion of RS05575, either alone or in the Δ5Fe background, impaired E. faecalis colonization in the mouse gastrointestinal tract and virulence in mouse peritonitis and rabbit infective endocarditis models. These results support the proposal that RS05575 is responsible for the anaerobic degradation of heme and identifies this relatively new enzyme class as a novel factor in bacterial pathogenesis. The findings from this study are likely to have broad implications, as homologues of RS05575 are found in other gram-positive facultative anaerobes.

Importance: Heme is an important nutrient for bacterial pathogens, mainly for its ability to serve as an iron source during infection. While bacteria are known to release iron from heme using enzymes called heme oxygenases, a new family of anaerobic heme-degrading enzymes has been described recently in gram-negative bacteria. Here, we report the first description of anaerobic heme degradation by a gram-positive bacterium, the opportunistic pathogen Enterococcus faecalis, and link activity of this enzyme to their ability to colonize and infect the host. We also show that homologs of this enzyme are found in many gram-positive facultative anaerobes, implying that the ability to degrade heme under anaerobic conditions may be an overlooked fitness and virulence factor of bacterial pathogens.

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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
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