Identification and characterization of chicken TRIM45 and its role as a negative regulator of ALV-J replication <i>in vitro</i>

Avian leukosis virus subgroup J (ALV-J) is an alpharetrovirus that infects chickens, causing immunosuppression and a decrease in production performance, leading to substantial economic losses in the poultry industry. ALV-J is also well-known for its oncogenic properties, inducing tumours such as myelomas and haemangiomas in infected chickens. TRIM45 has been identified as a potential tumour suppressor; however, the relationship between TRIM45 expression and ALV-J infection remains to be elucidated. This study aimed to dissect the molecular characteristics of the chicken TRIM45 gene and its modulation during ALV-J infection, as well as its influence on viral replication. We found that the chicken TRIM45 RING domain is significantly different from that of humans and other mammals. TRIM45 is expressed in all chicken tissues, with the highest levels in the heart. Subcellular localization studies indicated a cytoplasmic distribution of TRIM45, forming aggregates within cells. Our findings demonstrate that ALV-J infection significantly upregulates TRIM45 expression in DF-1 cells. To assess the functional role of TRIM45 in ALV-J replication, we employed both gene silencing and overexpression strategies. Strikingly, the overexpression of TRIM45, including a mutant lacking the RING domain, was found to markedly suppress ALV-J replication. In contrast, TRIM45 knockdown via siRNA resulted in an enhanced viral replication, highlighting the importance of TRIM45 limiting ALV-J replication. Mechanistically, overexpression of TRIM45 induces apoptosis in infected cells, independent of its RING domain function. In conclusion, our study demonstrates that chicken TRIM45 acts as a negative regulator of ALV-J replication <i>in vitro</i> by promoting apoptosis in infected cells.<b>RESEARCH HIGHLIGHTS</b>Chicken TRIM45 RING domain and protein localization significantly differ from humans.TRIM45 negatively regulates ALV-J replication <i>in vitro</i>.TRIM45 inhibits ALV-J replication by inducing apoptosis in infected cells.

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Publication Details

Journal
Avian Pathology
Published
2024-10-17
DOI
https://doi.org/10.1080/03079457.2024.2419039
Citations
4
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.96

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article

Identification and characterization of chicken TRIM45 and its role as a negative regulator of ALV-J replication in vitro

Ting Yang, Qiangzhou Wang, Xuan Huang, Guobin Chang et al.
4 citations
Avian Pathology
Immune Cell Function and Interaction
0.96
article

Identification and characterization of chicken TRIM45 and its role as a negative regulator of ALV-J replication in vitro

Ting Yang, Qiangzhou Wang, Xuan Huang, Guobin Chang, Jiaxing Wang, Yuyu Ping, Shihao Chen, Yulin Bi
article en
4 citations

Abstract

Avian leukosis virus subgroup J (ALV-J) is an alpharetrovirus that infects chickens, causing immunosuppression and a decrease in production performance, leading to substantial economic losses in the poultry industry. ALV-J is also well-known for its oncogenic properties, inducing tumours such as myelomas and haemangiomas in infected chickens. TRIM45 has been identified as a potential tumour suppressor; however, the relationship between TRIM45 expression and ALV-J infection remains to be elucidated. This study aimed to dissect the molecular characteristics of the chicken TRIM45 gene and its modulation during ALV-J infection, as well as its influence on viral replication. We found that the chicken TRIM45 RING domain is significantly different from that of humans and other mammals. TRIM45 is expressed in all chicken tissues, with the highest levels in the heart. Subcellular localization studies indicated a cytoplasmic distribution of TRIM45, forming aggregates within cells. Our findings demonstrate that ALV-J infection significantly upregulates TRIM45 expression in DF-1 cells. To assess the functional role of TRIM45 in ALV-J replication, we employed both gene silencing and overexpression strategies. Strikingly, the overexpression of TRIM45, including a mutant lacking the RING domain, was found to markedly suppress ALV-J replication. In contrast, TRIM45 knockdown via siRNA resulted in an enhanced viral replication, highlighting the importance of TRIM45 limiting ALV-J replication. Mechanistically, overexpression of TRIM45 induces apoptosis in infected cells, independent of its RING domain function. In conclusion, our study demonstrates that chicken TRIM45 acts as a negative regulator of ALV-J replication <i>in vitro</i> by promoting apoptosis in infected cells.<b>RESEARCH HIGHLIGHTS</b>Chicken TRIM45 RING domain and protein localization significantly differ from humans.TRIM45 negatively regulates ALV-J replication <i>in vitro</i>.TRIM45 inhibits ALV-J replication by inducing apoptosis in infected cells.

Avian PathologyVol. 54(2)
Yangzhou University (CN)
National Broiler Industrial and Technology System, National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 24%
Immune Cell Function and Interaction
0.96
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