Exploring the antimicrobial peptidome of nematodes through phylum-spanning in silico analyses highlights novel opportunities for pathogen control.

IF 3.8 2区 医学 Q1 Medicine PLoS Neglected Tropical Diseases Pub Date : 2023-09-06 eCollection Date: 2023-09-01 DOI:10.1371/journal.pntd.0011618
Allister Irvine, Sharon A Huws, Louise E Atkinson, Angela Mousley
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Abstract

Antimicrobial Peptides (AMPs) are key constituents of the invertebrate innate immune system and provide critical protection against microbial threat. Nematodes display diverse life strategies where they are exposed to heterogenous, microbe rich, environments highlighting their need for an innate immune system. Within the Ecdysozoa, arthropod AMPs have been well characterised, however nematode-derived AMP knowledge is limited. In this study the distribution and abundance of putative AMP-encoding genes was examined in 134 nematode genomes providing the most comprehensive profile of AMP candidates within phylum Nematoda. Through genome and transcriptome analyses we reveal that phylum Nematoda is a rich source of putative AMP diversity and demonstrate (i) putative AMP group profiles that are influenced by nematode lifestyle where free-living nematodes appear to display enriched putative AMP profiles relative to parasitic species; (ii) major differences in the putative AMP profiles between nematode clades where Clade 9/V and 10/IV species possess expanded putative AMP repertoires; (iii) AMP groups with highly restricted profiles (e.g. Cecropins and Diapausins) and others [e.g. Nemapores and Glycine Rich Secreted Peptides (GRSPs)] which are more widely distributed; (iv) complexity in the distribution and abundance of CSαβ subgroup members; and (v) that putative AMPs are expressed in host-facing life stages and biofluids of key nematode parasites. These data indicate that phylum Nematoda displays diversity in putative AMPs and underscores the need for functional characterisation to reveal their role and importance to nematode biology and host-nematode-microbiome interactions.

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通过跨门的计算机分析探索线虫的抗菌肽组,为病原体控制提供了新的机会。
抗菌肽(AMPs)是无脊椎动物先天免疫系统的关键成分,可提供抵御微生物威胁的关键保护。线虫表现出不同的生活策略,它们暴露在异质的、富含微生物的环境中,这突出了它们对先天免疫系统的需求。在Ecdysozoa中,节肢动物AMP已经得到了很好的表征,但线虫衍生的AMP知识有限。在这项研究中,在134个线虫基因组中检测了推定的AMP编码基因的分布和丰度,提供了线虫门内最全面的AMP候选图谱。通过基因组和转录组分析,我们揭示了线虫门是推定AMP多样性的丰富来源,并证明了(i)受线虫生活方式影响的推定AMP组谱,其中自由生活的线虫似乎显示出相对于寄生物种丰富的推定AMP谱;(ii)线虫分支之间推定AMP图谱的主要差异,其中分支9/V和10/IV物种具有扩大的推定AMP库;(iii)具有高度限制性图谱的AMP基团(例如Cecropins和Diapausins)和分布更广泛的其他基团[例如Nemapores和富含甘氨酸的分泌肽(GRPS)];(iv)CSαβ亚群成员分布和丰度的复杂性;和(v)假定的AMP在主要线虫寄生虫的面向宿主的生命阶段和生物流体中表达。这些数据表明,线虫门在假定的AMP中表现出多样性,并强调了功能表征的必要性,以揭示其在线虫生物学和宿主-线虫-微生物组相互作用中的作用和重要性。
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来源期刊
PLoS Neglected Tropical Diseases
PLoS Neglected Tropical Diseases Medicine-Infectious Diseases
CiteScore
7.40
自引率
10.50%
发文量
723
审稿时长
2-3 weeks
期刊介绍: PLOS Neglected Tropical Diseases publishes research devoted to the pathology, epidemiology, prevention, treatment and control of the neglected tropical diseases (NTDs), as well as relevant public policy. The NTDs are defined as a group of poverty-promoting chronic infectious diseases, which primarily occur in rural areas and poor urban areas of low-income and middle-income countries. Their impact on child health and development, pregnancy, and worker productivity, as well as their stigmatizing features limit economic stability. All aspects of these diseases are considered, including: Pathogenesis Clinical features Pharmacology and treatment Diagnosis Epidemiology Vector biology Vaccinology and prevention Demographic, ecological and social determinants Public health and policy aspects (including cost-effectiveness analyses).
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