Shigella escapes lysosomal degradation through inactivation of Rab31 by IpaH4.5.

Jin Sun, Xiaolin Wang, Haotian Lin, Luming Wan, Ji Chen, Xiaopan Yang, Dongyu Li, Yanhong Zhang, Xiang He, Bin Wang, Mingxin Dong, Hui Zhong, Congwen Wei

Journal of medical microbiology 2021 Jul

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Introduction. Shigella flexneri is an intracellular bacterial pathogen that utilizes a type III secretion apparatus to inject effector proteins into host cells.Hypothesis/Gap Statement. The T3SS effector IpaH4.5 is important for the virulence of Shigella.Aim. This study aimed to elucidate the molecular mechanism and host target of the IpaH4.5 as well as its roles in S. flexneri infection.Methodology. The GAP assay was used to identify substrate Rab GTPases of IpaH4.5. A coimmunoprecipitation assay was applied to identify the interaction of Rab GTPases with IpaH4.5. A confocal microscopy analysis was used to assess the effects of IpaH4.5 on mannose 6-phosphate receptor (MPR) trafficking. To identify the effects of IpaH4.5 GAP activity on the activity of lysosomal cathepsin B, the Magic Red-RR assay was used. Finally, the intracellular persistence assay was used to identify IpaH4.5 GAP activity in S. flexneri intracellular growth.Results. We found that the effector IpaH4.5 disrupts MPR trafficking and lysosomal function, thereby counteracting host lysosomal degradation. IpaH4.5 harbours TBC-like dual-finger motifs and exhibits potent RabGAP activities towards Rab31. IpaH4.5 disrupts the transport of the cation-dependent mannose 6-phosphate receptor (CD-MPR) from the Golgi to the endosome by targeting Rab31, thereby attenuating lysosomal function. As a result, the intracellular persistence of S. flexneri requires IpaH4.5 TBC-like GAP activity to mediate bacterial escape from host lysosome-mediated elimination.Conclusion. We identified an unknown function of IpaH4.5 and its potential role in S. flexneri infection.

Citation

Jin Sun, Xiaolin Wang, Haotian Lin, Luming Wan, Ji Chen, Xiaopan Yang, Dongyu Li, Yanhong Zhang, Xiang He, Bin Wang, Mingxin Dong, Hui Zhong, Congwen Wei. Shigella escapes lysosomal degradation through inactivation of Rab31 by IpaH4.5. Journal of medical microbiology. 2021 Jul;70(7)