The Calicophoron daubneyi genome provides new insight into mechanisms of feeding, eggshell synthesis and parasite-microbe interactions.

IF 4.4 1区 生物学 Q1 BIOLOGY BMC Biology Pub Date : 2025-01-13 DOI:10.1186/s12915-025-02114-0
Shauna M Clancy, Mark Whitehead, Nicola A M Oliver, Kathryn M Huson, Jake Kyle, Daniel Demartini, Allister Irvine, Fernanda Godoy Santos, Paul-Emile Kajugu, Robert E B Hanna, Sharon A Huws, Russell M Morphew, J Herbert Waite, Sam Haldenby, Mark W Robinson
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Abstract

Background: The rumen fluke, Calicophoron daubneyi, is the major paramphistome species infecting ruminants within Europe. Adult flukes reside within the rumen where they are in direct contact with a unique collection of microorganisms. Here, we report a 1.76-Gb draft genome for C. daubneyi, the first for any paramphistome species.

Results: Several gene families have undergone specific expansion in C. daubneyi, including the peptidoglycan-recognition proteins (PGRPs) and DM9 domain-containing proteins, which function as pattern-recognition receptors, as well as the saposin-like proteins with putative antibacterial properties, and are upregulated upon arrival of the fluke in the microbe-rich rumen. We describe the first characterisation of a helminth PGRP and show that a recombinant C. daubneyi PGRP binds to the surface of bacteria, including obligate anaerobes from the rumen, via specific interaction with cell wall peptidoglycan. We reveal that C. daubneyi eggshell proteins lack L-DOPA typically required for eggshell crosslinking in trematodes and propose that C. daubneyi employs atypical eggshell crosslinking chemistry that produces eggs with greater stability. Finally, although extracellular digestion of rumen ciliates occurs within the C. daubneyi gut, unique ultrastructural and biochemical adaptations of the gastrodermal cells suggest that adult flukes also acquire nutrients via uptake of volatile fatty acids from rumen fluid.

Conclusions: Our findings suggest that unique selective pressures, associated with inhabiting a host environment so rich in microbial diversity, have driven the evolution of molecular and morphological adaptations that enable C. daubneyi to defend itself against microorganisms, feed and reproduce within the rumen.

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Calicophoron daubneyi的基因组为摄食、蛋壳合成和寄生虫-微生物相互作用的机制提供了新的见解。
背景:瘤胃吸虫(Calicophoron daubneyi)是感染欧洲反刍动物的主要类腹虫。成年吸虫居住在瘤胃内,在那里它们与一种独特的微生物直接接触。在这里,我们报告了一个1.76 gb的C. daubneyi基因组草图,这是所有副虫物种中第一个。结果:几个基因家族在C. daubneyi中发生了特异性扩增,包括作为模式识别受体的肽聚糖识别蛋白(PGRPs)和DM9结构域蛋白,以及具有抗菌特性的皂苷样蛋白,当吸虫到达微生物丰富的瘤胃时,这些基因家族的表达上调。我们描述了蠕虫PGRP的第一个特征,并表明重组C. daubneyi PGRP通过与细胞壁肽聚糖的特异性相互作用结合到细菌表面,包括来自瘤胃的专门厌氧菌。我们发现C. daubneyi蛋壳蛋白缺乏典型的吸虫蛋壳交联所需的L-DOPA,并提出C. daubneyi采用非典型的蛋壳交联化学,产生更稳定的鸡蛋。最后,尽管瘤胃纤毛虫的细胞外消化发生在C. daubneyi肠道内,但胃真皮细胞独特的超微结构和生化适应表明,成年吸虫也通过从瘤胃液中摄取挥发性脂肪酸来获取营养。结论:我们的研究结果表明,独特的选择压力,与居住在微生物多样性丰富的宿主环境有关,推动了C. daubneyi分子和形态适应的进化,使其能够抵御微生物,在瘤胃内进食和繁殖。
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来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
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