# Two Phytophthora effectors mitigate plant immunity by manipulating intracellular pH through interaction with V-ATPase in potato

**Authors:** Xiaojing Xue, Xiao Chen, Xin Wang, Tao Wang, Rui Liao, Haifeng Liu, Changxiang Zhu, Jonathan D. G. Jones, Zhaohui Chu

PMC · DOI: 10.1186/s43897-025-00184-w · Molecular Horticulture · 2026-01-09

## TL;DR

This study shows how two proteins from a potato pathogen manipulate plant cell pH to weaken immunity and promote disease, while plants evolved immune proteins to counteract this.

## Contribution

The study identifies a new mechanism of effector-triggered susceptibility and immunity through intracellular pH regulation by Phytophthora effectors and plant NLRs.

## Key findings

- AL3 and Avr2 effectors manipulate V-ATPase activity to acidify and alkalinize the cytoplasm, promoting disease in potato.
- Plants evolved NLRs R2 and Rpi-mcq1 to guard against these effectors and mitigate late blight.
- The findings reveal a new arms race between plants and oomycetes centered on intracellular pH homeostasis.

## Abstract

Plant V-ATPase serves as a primary active proton pump of the endomembrane system and is crucial for the stress response. However, the role of the C subunit of V-ATPase (VHA-C) in effector-triggered immunity remains poorly understood. Here, we reveal that Phytophthora infestans evolved a pair of RxLR effectors, AL3 and Avr2, which are expressed sequentially and both target the host VHA-C (StATP6V1C1) and StBSL1. In the early stage of P. infestans infection, AL3 promotes the assembly of StATP6V1C1 with subunits G and E, leading to increased V-ATPase activity and cytoplasmic acidification. Subsequently, Avr2 inhibits the StWNK10-catalyzed Ser-261 phosphorylation of StATP6V1C1, thereby retarding V-ATPase activity and causing intracellular alkalinization. In cultivars absence of two immune receptors, this pH shift facilitates the interactions of the two effectors with downstream susceptibility factors of StBSL1 at various stages of infection, which may promote the onset and development of the disease. As coping strategy, plants independently evolve two NLRs, R2 and Rpi-mcq1, guard both StATP6V1C1 and StBSLs to perceive effectors thereby mitigating the risk of late blight. Our findings establish a new arms race battlefield between plants and oomycetes, highlighting the role of intracellular pH homeostasis in both effector-triggered susceptibility (ETS) and effector-triggered immunity (ETI).

The online version contains supplementary material available at 10.1186/s43897-025-00184-w.

## Linked entities

- **Genes:** Vha16-1 (Vacuolar H[+] ATPase 16kD subunit 1) [NCBI Gene 44307], CD1E (CD1e molecule) [NCBI Gene 913]
- **Proteins:** VhaSFD (Vacuolar H[+]-ATPase SFD subunit), AL3 (alfin-like 3), AVR2 (avidin related protein 2)
- **Species:** Phytophthora infestans (taxon 4787)

## Full-text entities

- **Diseases:** infection (MESH:D007239), late blight (MESH:D000067562)
- **Chemicals:** proton (MESH:D011522)
- **Species:** Phytophthora infestans (potato late blight agent, species) [taxon 4787], Solanum tuberosum (potatoes, species) [taxon 4113]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12784495/full.md

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Source: https://tomesphere.com/paper/PMC12784495