Discovering the secrets of the Candida albicans agglutinin-like sequence (ALS) gene family – a sticky pursuit
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The agglutinin-like sequence (ALS) family of Candida albicans includes eight genes that encode large cell-surface glycoproteins. The high degree of sequence relatedness between the ALS genes and the tremendous allelic variability often present in the same C. albicans strain complicated definition and characterization of the gene family. The main hypothesis driving ALS family research is that the genes encode adhesins, primarily involved in host-pathogen interactions. Although adhesive function has been demonstrated for several Als proteins, the challenge of studying putative adhesins in a highly adhesive organism like C. albicans has led to varying ideas about how best to pursue such investigations, and results that are sometimes contradictory. Recent analysis of alsdelta/alsdelta strains suggested roles for Als proteins outside of adhesion to host surfaces, and a broader scope of Als protein function than commonly believed. The availability and use of experimental methodologies to study C. albicans at the genomic level, and the ALS family en masse, have advanced knowledge of these genes and emphasized their importance in C. albicans biology and pathogenesis.
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The enriched set includes several members in each of three cell wall gene families important for biofilm formation and virulence: Hyr/Iff proteins, ALS adhesins, and PGA-30-like proteins.
“including several members in each of three cell wall gene families important for biofilm formation and virulence (Hoyer et al., 2008): the Hyr/Iff proteins (HYR1 and 3, IFF8 and 6), the ALS adhesins (ALS1-4,7,9), and the PGA-30-like proteins (seven genes)”
From The evolution of drug resistance in clinical isolates of Candida albicans. (2015) · cites this paper as Hoyer et al., 2008
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- Authors
- Hoyer, L. L., Green, C. B., Oh, S.-H., & Zhao, X.
- Affiliations
- University of Illinois Urbana-Champaign (US)
- Venue
- Medical Mycology
- Publisher
- Oxford University Press (OUP)
- Published
- 2008-01
- Volume
- 46
- Issue
- 1
- Pages
- 1-15
- ISSN
- 0268-1218 (ISSN-L)
- 1369-3786
- 1460-2709
- PMC
- PMC2742883
- OpenAlex
- W2067631595
- Cited by
- 356
- References
- 85
- Citations by year
- 2026: 9 · 2025: 17 · 2024: 19 · 2023: 11 · 2022: 14 · 2021: 15 · 2020: 18 · 2019: 20 · 2018: 18 · 2017: 15 · 2016: 13 · 2015: 20 · 2014: 29 · 2013: 17 · 2012: 31
- FWCI
- 2.24
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Medical Mycology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Dental and Craniofacial Research (R01DE014158, DE 14158)
- National Center for Research Resources (C06 RR16515-01, C06RR016515)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
- Keywords
- Candida albicans, cell surface glycoproteins, adhesins, host-pathogen interaction, allelic variation, fungal pathogenesis, gene family characterization
- MeSH terms
- Agglutinins, Alleles, Bacterial Adhesion, Candida, Candida albicans, Candidiasis, Fungal Proteins, Multigene Family, Humans, Gene Expression Regulation, Fungal, Genome, Fungal, Adhesins, Bacterial
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