Coffee is a significant traded commodity for developing countries. Among the various diseases affecting coffee, anthracnose caused by Colletotrichum spp. has re-emerged as a major constraint on global coffee production. To better understand the Colletotrichum species complex associated with coffee anthracnose, we characterized Colletotrichum spp. using a combination of phenotypic traits, MAT1-2 (ApMat) gene analysis, multi-locus phylogenetic (ITS, ACT, CHS-1, and GAPDH), and pathogenicity assays. A total of 74 Colletotrichum isolates were collected from coffee plants exhibiting anthracnose symptoms across nine coffee plantations in China. Among these, 55 isolates were identified as the C. gloeosporioides species complex using the ApMat locus, while the remaining 19 isolates were identified through multi-locus phylogenetic analyses. The isolates represented seven Colletotrichum species from five species complexes: C. gloeosporioides (including C. siamense, C. nupharicola, and C. theobromicola), C. boninens (C. karstii), C. gigasporum (C. gigasporum), C. orchidearum (C. cliviicola), and C. magnum (C. brevisporum). This is the first report of C. nupharicola and C. cliviicola causing coffee anthracnose worldwide, and the first report of C. nupharicola in China. Pathogenicity tests confirmed that all seven species were capable of infecting coffee leaves. This research enhances our understanding of the Colletotrichum species responsible for coffee anthracnose, and provides valuable insights for developing effective disease management strategies.

Coffee is one of the most popular beverages around the world, which is mainly produced from the allopolyploid Coffea arabica. The genomes of C. arabica and its two ancestors C. canephora and C. eugenioides have been released due to the development of next generation sequencing. However, few studies on C. arabica are related to the PIN-FORMED (PIN) auxin efflux transporter despite its importance in auxin-mediated plant growth and development. In the present study, we conducted a genome-wide analysis of the PIN gene family in the three coffee species. Totals of 17, 9 and 10 of the PIN members were characterized in C. Arabica, C. canephora and C. eugenioides, respectively. Phylogenetic analysis revealed gene loss of PIN1 and PIN2 homologs in C. arabica, as well as gene duplication of PIN5 homologs during the fractionation process after tetraploidy. Furthermore, we conducted expression analysis of PIN genes in C. arabica by in silico and qRT-PCR. The results revealed the existence of gene expression dominance in allopolyploid coffee and illustrated several PIN candidates in regulating auxin transport and homeostasis under leaf rust fungus inoculation and the tissue-specific expression pattern of C. arabica. Together, this study provides the basis and guideline for future functional characterization of the PIN gene family.

Phytophthora-induced crop diseases, commonly known as “plant plagues”, pose a significant threat to global food security. In this study, strain ASG80 was isolated from sisal roots and demonstrated a broad-spectrum antagonistic activity against several Phytophthora species and fungal pathogens. Strain ASG80 was identified as Streptomyces luteireticuli via phylogenetic analysis, digital DNA–DNA hybridization (dDDH), and average nucleotide identity (ANI). Whole-genome sequencing identified 40 biosynthetic gene clusters (BGCs) related to secondary metabolite production, including antimicrobial compounds. Strain ASG80 extract exhibited broad-spectrum inhibitory activity against Phytophthora nicotianae, P. vignae, P. cinnamomi, and P. sojae. Pot experiments showed that strain ASG80 extract significantly reduced sisal zebra disease incidence, with an efficacy comparable to the fungicide metalaxyl. These findings suggest that strain ASG80 is a promising biocontrol agent with substantial potential for managing Phytophthora-related diseases in agriculture.

Coffee (Coffea arabica L.) is a very important crop in China and in the global economy. During March 2019, symptoms of leaf blight were observed on coffee planted at Hainan and Yunnan Provinces in ...

Brown rot disease caused by Pyrrhoderma noxium is a widespread disease that severely affects the roots of rubber trees (Hevea brasiliensis Muell. Arg.). The economic losses, along with environmental and health problems arising from the use of disease control chemicals, have raised the interest of scholars to explore the use of biological control agents for the effective control of fungal pathogen P. noxium. Here, the inhibition effect of the culture filtrate of B. subtilis Czk1 on P. noxium was demonstrated. The findings indicate that the antifungal activity of this strain is mediated wholly or partly by compounds produced in the culture filtrate. The combined use of liquid chromatography–tandem mass spectrometry and antifungal activity assays rapidly identified compounds produced by B. subtilis Czk1. Metabolic profiles were assessed and used to identify major metabolites based on the scores of variable importance in the projection and the plot scores of principal component analysis. A total of 296 differential metabolites were screened, including 208 in positive ion mode and 88 in negative ion mode. Two key metabolites, diacetyl and trans-2-octenoic acid, were screened from 29 metabolites by antifungal activity assays. The median effective concentration (EC₅₀) of trans-2-octenoic acid and diacetyl were 0.9075 mg/mL and 4.8213 mg/mL, respectively. The antifungal metabolites can disrupt the internal structure of the pathogenic fungal mycelium, thereby impeding its growth. This study is expected to contribute to the existing knowledge of Czk1-produced metabolites and their future antifungal applications. This study is also expected to provide a new biopreservative perspective on unexplored antifungal metabolites produced by Czk1 as a biocontrol agent.