Exploring the antimicrobial peptidome of nematodes through phylum-spanning in silico analyses highlights novel opportunities for pathogen control.
Exploring the antimicrobial peptidome of nematodes through phylum-spanning in silico analyses highlights novel opportunities for pathogen control.
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通过跨门的计算机分析探索线虫的抗菌肽,为病原体控制提供了新的机会。
DOI:
10.1371/journal.pntd.0011618
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发表时间:
2023-09
影响因子:
3.8
通讯作者:
Mousley, Angela
中科院分区:
文献类型:
--
作者:
Irvine, Allister;Huws, Sharon A.;Atkinson, Louise E.;Mousley, Angela
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. Nematodes include some of the most abundant animals on Earth, found in almost every natural habitat. Globally, parasitic nematodes cause major impacts to human, animal and plant health. Little is known about how parasitic nematodes interact with microbes despite the microbe-rich environments that many of them inhabit. In other invertebrate animals, Antimicrobial Peptides (AMPs) are critical in defense against pathogenic microbes. By characterising nematode AMP diversity and exploring the role of nematode-derived AMPs we could reveal novel targets for antimicrobial and anthelmintic development. In this study we profiled the distribution of five known AMP groups across the nematode phylum. This homology-directed approach demonstrated that, nematodes appear rich in AMP diversity with major differences in the abundance and distribution of putative AMP-encoding genes across nematode lifestyles and clades. In addition, transcriptomic and proteomic analyses show that many of the identified AMP-encoding genes appear biologically relevant in nematode life stages that interact with the host. This study provides a database of potential nematode-derived AMPs which can drive functional analyses to explore the role of nematode AMPs.
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影响因子:
14.9
作者:
Babicki S;Arndt D;Marcu A;Liang Y;Grant JR;Maciejewski A;Wishart DS
通讯作者:
Wishart DS
影响因子:
--
作者:
Gabler, Felix;Nam, Seung-Zin;Alva, Vikram
通讯作者:
Alva, Vikram
影响因子:
2.9
作者:
Al Souhail Q;Hiromasa Y;Rahnamaeian M;Giraldo MC;Takahashi D;Valent B;Vilcinskas A;Kanost MR
通讯作者:
Kanost MR
影响因子:
5.2
作者:
Lim MP;Firdaus-Raih M;Nathan S
通讯作者:
Nathan S
影响因子:
30.8
作者:
Dieterich, Christoph;Clifton, Sandra W.;Schuster, Lisa N.;Chinwalla, Asif;Delehaunty, Kimberly;Dinkelacker, Iris;Fulton, Lucinda;Fulton, Robert;Godfrey, Jennifer;Minx, Pat;Mitreva, Makedonka;Roeseler, Waltraud;Tian, Huiyu;Witte, Hanh;Yang, Shiaw-Pyng;Wilson, Richard K.;Sommer, Ralf J.
通讯作者:
Sommer, Ralf J.