Evidence map›Paper›PMID 42902023›Full record

ArticleFunctional & integrative genomics2026

Genome-wide identification and characterization of the PE/PPE gene family in Mycobacterium abscessus.

Panqi Gao, Xinyu Wang, Longxiang Xie, Quanxin Long

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Article in Functional & integrative genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

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4 authors.

Panqi Gao *Key Laboratory of Molecular Biology for Infectious Diseases (Ministry of Education), Institute for Viral Hepatitis, Department of Infectious Diseases, The Second Affiliated Hospital of ChongqingMedical University, Chongqing, China.
Xinyu Wang *Department of Predictive Medicine, School of Basic Medical Sciences, Institute of Biomedical Informatics, Bioinformatics Center, Henan Provincial Engineering Center for Tumor Molecular Medicine, Henan University, Kaifeng, 475004, China.
Longxiang XieDepartment of Predictive Medicine, School of Basic Medical Sciences, Institute of Biomedical Informatics, Bioinformatics Center, Henan Provincial Engineering Center for Tumor Molecular Medicine, Henan University, Kaifeng, 475004, China.
Quanxin LongKey Laboratory of Molecular Biology for Infectious Diseases (Ministry of Education), Institute for Viral Hepatitis, Department of Infectious Diseases, The Second Affiliated Hospital of ChongqingMedical University, Chongqing, China. longqx@cqmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycobacterium abscessus (Mab) is a rapidly growing non-tuberculous mycobacterium that causes opportunistic infections and exhibits extensive intrinsic antibiotic resistance. The proline-glutamate (PE) and proline-proline-glutamate (PPE) protein families are mycobacteria-specific virulence factors implicated in immune modulation, antigenic variation, and persistence. While Mycobacterium tuberculosis (Mtb) harbors approximately 170 PE/PPE members, the repertoire of PE/PPE genes in Mab remains largely uncharacterized. Here, we performed a genome-wide survey of PE/PPE genes in Mab ATCC 19,977 and identified 18 candidate family members, representing a relatively small fraction of the genome compared with slow-growing mycobacteria. Most predicted proteins harbor canonical PE or PPE domains and display acidic physicochemical properties. Phylogenetic analysis resolved the proteins into three subfamilies: PE, PPE, and PE-PPE, revealing moderate structural diversity but limited family expansion. Motif and gene structure analyses supported the evolutionary conservation. Notably, no PE_polymorphic GC-rich repetitive sequence (PE_PGRS) or PPE_major polymorphic tandem repeat (PPE_MPTR) members were detected, suggesting lineage-specific genomic reduction relative to other pathogenic mycobacteria. AlphaFold predictions revealed conserved N-terminal folds and variable C-terminal regions, which may contribute to functional diversification. Subcellular localization predictions indicated that most proteins are extracellular. Synteny analysis revealed no detectable collinearity among these genes. Transcriptomic analyses revealed condition-dependent expression of PE/PPE genes during amoeba and macrophage infection and under artificial sputum medium and metal ion stress, suggesting roles in environmental adaptation and host interaction. This study provides the first systematic overview of PE/PPE gene repertoire in Mab and lays the groundwork for elucidating their roles in intracellular survival, host interaction, and antimicrobial resistance.

Indexed as

Bacterial ProteinsMycobacterium abscessusGenome, BacterialMultigene FamilyPhylogenyBacterial Proteinsgene expression profilegenome-wide analysisMycobacterium abscessusPE/PPE gene family

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.