Interleukin-2 enhancer binding factor 2 (ILF2) in pacific white shrimp (Litopenaeus vannamei): Alternatively spliced isoforms with different responses in the immune defenses against vibrio infection. (May 2021)

• Record Type: Journal Article
• Authors: Jiang, Xiao; Zhang, Xin; Ren, Chunhua; Ruan, Yao; Lu, Yongtong; Yuan, Lihong; Li, Jiaxi; Yan, Aifen; Wang, Yanhong; Luo, Peng; Hu, Chaoqun; Chen, Ting
• Is Part Of: Developmental and comparative immunology. Volume 118(2021)
• Publication Date: 2021-05
• Subjects: Interleukin-2 enhancer binding factor 2 -- Litopenaeus vannamei -- Alternatively splicing -- Vibrio -- Immune defense -- Crustacean; Immunology -- Periodicals; Developmental immunology -- Periodicals; 616.079
• DOI: 10.1016/j.dci.2020.103975
• Languages: English
• ISSNs: 0145-305X

Abstract

Abstract: Alternative splicing is an essential molecular mechanism that increase the protein diversity of a species to regulate important biological processes. As a transcription factor, Interleukin-2 enhancer binding factor 2 (ILF2) regulates the functions of interleukin-2 (IL-2) at the levels of transcription, splicing and translation, and plays other critical roles in the immune system. ILF2 is well-documented in vertebrates, while little is currently known in crustacean species such as the Pacific white shrimp ( Litopenaeus vannamei ). In the present study, five cDNA for spliced isoforms of Lv- ILF2 were identified, in which four of them are the full-length long isoforms ( Lv- ILF2-L1, Lv- ILF2-L2, Lv- ILF2-L3 and Lv- ILF2-L4) and one of them is a truncated short isoform ( Lv- ILF2-S). The whole sequence of ILF2 gene from L. vannamei was obtained, which is 11, 680 bp in length with 9 exons separated by 8 introns. All five isoforms contain a domain associated with zinc fingers (DZF). Two alternative splicing types (alternative 5′ splice site and alternative 3′ splice site) were identified in the five isoforms. The Lv-ILF2 mRNA showed a broad distribution in all detected tissues, and the Lv-ILF2-L transcript levels were higher than those of Lv-ILF2-S in corresponding tissues. The mRNA levels of Lv-ILF2-S in the hepatopancreas, heart, muscle and stomach, but not in the eyestalk, were significantly increased after challenges with Vibrio harveyi or lipopolysaccharide (LPS), while no significant changes were observed for the transcript levels of Lv-ILF2-L in these tissues under the same immune stimulants. On the contrary, the transcript levels of neither Lv-ILF2-S nor Lv-ILF2-L were affected by challenges of polyinosinic: polycytidylic acid [Poly (I:C)]. In addition, after knockdown of the Lv-ILF2 mRNA level by siRNA, the mortality of shrimp and the hepatopancreatic bacterial numbers were significantly increased under V. harveyi challenge, indicating that Lv -ILF2 might participate in the immune defenses against V. harveyi invasion. Collectively, our study here supplied the first evidence for a novel splicing mechanism of ILF2 transcripts, and provided a functional link between the Lv- ILF2 isoforms and the capacity against pathogenic Vibrio in penaeid shrimp. Highlights: Five ILF2 isoforms were first identified in Pacific white shrimp. Lv-ILF2 transcripts were generated by a novel alternative splicing mechanism. The capacities of Lv- ILF2 isoforms against pathogenic Vibrio were analyzed. The Lv-ILF2 plays a crucial role in the immune defense mechanisms of crustaceans.