The Hidden Truths of Fungal Virulence and Adaptation on Hosts: Unraveling the Conditional Dispensability of Minichromosomes in the Hemibiotrophic Colletotrichum Pathogens.
Vijai BhadauriaManyu ZhangWendi MaJun YangWen-Sheng ZhaoYou-Liang PengPublished in: International journal of molecular sciences (2023)
Colletotrichum spp. are ascomycete fungi and cause anthracnose disease in numerous crops of economic significance. The genomes of these fungi are distributed among ten core chromosomes and two to three minichromosomes. While the core chromosomes regulate fungal growth, development and virulence, the extent to which the minichromosomes are involved in these processes is still uncertain. Here, we discuss the minichromosomes of three hemibiotrophic Colletotrichum pathogens, i.e., C. graminicola , C. higginsianum and C. lentis . These minichromosomes are typically less than one megabase in length, characterized by containing higher repetitive DNA elements, lower GC content, higher frequency of repeat-induced point mutations (RIPMs) and sparse gene distribution. Molecular genetics and functional analyses have revealed that these pathogens harbor one conditionally dispensable minichromosome, which is dispensable for fungal growth and development but indispensable for fungal virulence on hosts. They appear to be strain-specific innovations and are highly compartmentalized into AT-rich and GC-rich blocks, resulting from RIPMs, which may help protect the conditionally dispensable minichromosomes from erosion of already scarce genes, thereby helping the Colletotrichum pathogens maintain adaptability on hosts. Overall, understanding the mechanisms underlying the conditional dispensability of these minichromosomes could lead to new strategies for controlling anthracnose disease in crops.
Keyphrases
- antimicrobial resistance
- gram negative
- escherichia coli
- pseudomonas aeruginosa
- staphylococcus aureus
- biofilm formation
- genome wide
- cell wall
- high frequency
- genome wide identification
- cystic fibrosis
- high glucose
- drug induced
- single cell
- endothelial cells
- high resolution
- cell free
- diabetic rats
- oxidative stress
- transcription factor
- circulating tumor