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      Molecular and Functional Diversity of Crustin-Like Genes in the Shrimp Litopenaeus vannamei

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          Abstract

          Crustins are crustacean cationic cysteine-rich antimicrobial peptides that contain one or two whey acidic protein (WAP) domain(s) at the carboxyl terminus and mainly show antimicrobial and/or proteinase inhibitory activities. Here, we performed genome and transcriptome screening and identified 34 full-length crustin-like encoding genes in Litopenaeus vannamei. Multiple sequence analysis of the deduced mature peptides revealed that these putative crustins included 10 type Ia, two type Ib, one type Ic, 11 type IIa, three type IIb, four type III, one type IV, one type VI, and one type VII. These putative crustins were clustered into different groups. Phylogenetic analysis, considering their domain composition, showed that different types of crustin-like genes in crustaceans might be originated from the WAP core region, along with sequence insertion, duplication, deletion, and amino acid substitution. Tissue distribution analysis suggested that most crustin-like genes were mainly detected in immune-related tissues while several crustin-like genes exhibited tissue-specific expression patterns. Quantitative PCR analysis on 15 selected crustin-like genes showed that most of them were apparently upregulated after Vibrio parahaemolyticus or white spot syndrome virus (WSSV) infection. One type Ib crustin-like gene, mainly expressed in the ovary, showed the highest expression levels before the gastrula stage and was hardly detected after the limb bud stage, suggesting that it was a maternal immune effector. Collectively, the present data revealed the molecular and functional diversity of crustins and their potential evolutionary routes in crustaceans.

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          The co-evolution of host cationic antimicrobial peptides and microbial resistance.

          Endogenous cationic antimicrobial peptides (CAMPs) are among the most ancient and efficient components of host defence. It is somewhat of an enigma that bacteria have not developed highly effective CAMP-resistance mechanisms, such as those that inhibit many therapeutic antibiotics. Here, we propose that CAMPs and CAMP-resistance mechanisms have co-evolved, leading to a transient host-pathogen balance that has shaped the existing CAMP repertoire. Elucidating the underlying principles of this process could help in the development of more sustainable antibiotics.
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            Penaeid shrimp genome provides insights into benthic adaptation and frequent molting

            Crustacea, the subphylum of Arthropoda which dominates the aquatic environment, is of major importance in ecology and fisheries. Here we report the genome sequence of the Pacific white shrimp Litopenaeus vannamei, covering ~1.66 Gb (scaffold N50 605.56 Kb) with 25,596 protein-coding genes and a high proportion of simple sequence repeats (>23.93%). The expansion of genes related to vision and locomotion is probably central to its benthic adaptation. Frequent molting of the shrimp may be explained by an intensified ecdysone signal pathway through gene expansion and positive selection. As an important aquaculture organism, L. vannamei has been subjected to high selection pressure during the past 30 years of breeding, and this has had a considerable impact on its genome. Decoding the L. vannamei genome not only provides an insight into the genetic underpinnings of specific biological processes, but also provides valuable information for enhancing crustacean aquaculture.
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              New insights on Drosophila antimicrobial peptide function in host defense and beyond

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                Author and article information

                Journal
                Mar Drugs
                Mar Drugs
                marinedrugs
                Marine Drugs
                MDPI
                1660-3397
                13 July 2020
                July 2020
                : 18
                : 7
                : 361
                Affiliations
                [1 ]Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China; lishihao@ 123456qdio.ac.cn (S.L.); xjlubio@ 123456163.com (X.L.); yuyang@ 123456qdio.ac.cn (Y.Y.); xjzhang@ 123456qdio.ac.cn (X.Z.)
                [2 ]Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China
                [3 ]Center for Ocean Mega-Science, Chinese Academy of Sciences, Qingdao 266071, China
                [4 ]University of Chinese Academy of Sciences, Beijing 100049, China
                [5 ]The Innovation of Seed Design, Chinese Academy of Sciences, Wuhan 430072, China
                Author notes
                [* ]Correspondence: fhli@ 123456qdio.ac.cn
                Author information
                https://orcid.org/0000-0001-6399-4039
                Article
                marinedrugs-18-00361
                10.3390/md18070361
                7401287
                32668696
                b3508d6c-bc09-4007-9b2a-fe0c861c318d
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 26 April 2020
                : 08 July 2020
                Categories
                Article

                Pharmacology & Pharmaceutical medicine
                crustin,sequence diversity,immunological function,litopenaeus vannamei

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