The Major Facilitator Superfamily Transporter HAP12 Is Critical in Toxoplasma gondii Survival and Virulence

As an important zoonotic pathogen, <i>Toxoplasma gondii</i> relies on a unique organelle known as the apicoplast, which has garnered significant attention as a potential drug target for anti-<i>Toxoplasma</i> therapy. To better understand the structure and function of the apicoplast, we previously constructed a membrane protein database of the apicoplast. During this process, we identified the major facilitator superfamily (MFS) transporter protein HAP12, which partially colocalizes with the apicoplast. Evolutionary analysis revealed that HAP12 is highly conserved across the <i>Apicomplexa</i> family and model organisms. HAP12 depletion impaired <i>T</i>. <i>gondii</i> invasion and survival but did not affect the stability of several key organelles, including the apicoplast. Moreover, depletion of HAP12 resulted in a characteristic delayed-death phenotype in the apicoplast. Mouse virulence assays confirmed that HAP12 is an essential protein for parasite survival. This study provides new insights into potential drug and vaccine targets for combating <i>Toxoplasma</i> infections.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-04-21
DOI
https://doi.org/10.3390/ijms26083910
Citations
2
Primary Topic
Toxoplasma gondii Research Studies
Type
article
Field-Weighted Citation Impact
4.10
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article

The Major Facilitator Superfamily Transporter HAP12 Is Critical in Toxoplasma gondii Survival and Virulence

Shaojun Long, Tao Tang, Xiaowei Chen, Xun Suo et al.
2 citations
International Journal of Molecular Sciences
Toxoplasma gondii Research Studies
4.10
article

The Major Facilitator Superfamily Transporter HAP12 Is Critical in Toxoplasma gondii Survival and Virulence

Shaojun Long, Tao Tang, Xiaowei Chen, Xun Suo, Hui Dong, Hui-Yong Ding
article en
2 citations

Abstract

As an important zoonotic pathogen, <i>Toxoplasma gondii</i> relies on a unique organelle known as the apicoplast, which has garnered significant attention as a potential drug target for anti-<i>Toxoplasma</i> therapy. To better understand the structure and function of the apicoplast, we previously constructed a membrane protein database of the apicoplast. During this process, we identified the major facilitator superfamily (MFS) transporter protein HAP12, which partially colocalizes with the apicoplast. Evolutionary analysis revealed that HAP12 is highly conserved across the <i>Apicomplexa</i> family and model organisms. HAP12 depletion impaired <i>T</i>. <i>gondii</i> invasion and survival but did not affect the stability of several key organelles, including the apicoplast. Moreover, depletion of HAP12 resulted in a characteristic delayed-death phenotype in the apicoplast. Mouse virulence assays confirmed that HAP12 is an essential protein for parasite survival. This study provides new insights into potential drug and vaccine targets for combating <i>Toxoplasma</i> infections.

International Journal of Molecular SciencesVol. 26(8)
Sun Yat-sen University (CN), Tarim University (CN), China Agricultural University (CN)
Good health and well-being
Openalex Percentile: Top 8%
Toxoplasma gondii Research Studies
4.10
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