Hybrid mandevilla (Mandevilla × amabilis) is an ornamental plant widely grown in southern China, appreciated for its large bright-color flowers and heat tolerance (Oder et al. 2016). In June to August 2019, an anthracnose disease was observed on hybrid mandevilla plants in a nursery in Nanning, Guangxi, China (108˚14’30’’E, 22˚51’02’’N). Symptoms began as red-brown spots, which gradually enlarged (0.2 to 1.1 cm in width and 0.3 to 1.5 cm in length), overlapped, and extended until the leaves wilted. Of the 70 plants surveyed, more than 80% of leaves showed these symptoms. To determine the causal agent, samples were gathered from symptomatic leaves, cut into 3 × 3 mm pieces, surface-sterilized with 75% ethanol for 10 s and 2% NaClO for two min, and rinsed three times in sterile water. The pieces were placed onto potato dextrose agar (PDA) and incubated at 25°C in the darkness. After six days, hyphal margins were transferred onto fresh PDA and incubated at 25°C. Cultures grown on PDA started as grey-white, turned dark grey after nine days of growth, and conidia were produced after 13 days. Conidia were hyaline, guttulate, unicellular, cylindrical, and averaged 15.74 × 5.84 μm. Three single-spore isolates, PXT1-1, PXT1-5, and PXT2-1, were selected for molecular identification. The rDNA internal transcribed spacer region (ITS), a partial sequence of the actin gene (ACT), the chitin synthase 1 gene (CHS), glyceraldehyde-3-phosphate dehydrogenase gene (GAPDH), beta-tubulin (TUB2), and the intergenic region of apn2 and MAT1-2-1 genes (ApMat) of isolates PXT1-1, PXT1-5, and PXT2-1 were amplified with the primer pairs ITS1/ITS4, ACT-512F/ACT-783R, CHS-79F/CHS-354R, GDF1/GDR1, T1/Bt-2b (Weir et al. 2012), and AM-F/AM-R (Silva et al. 2012), respectively. The sequences were compared with the GenBank nucleotide sequence database and had more than 99% similarity to ITS (JX010165), ACT (FJ907426), CHS (JX009866), GAPDH (JX010033), TUB2 (JX010405), and ApMat (JQ807838) of isolate ICMP18581 of Colletotrichum fructicola Prihastuti, L. Cai & K. D. Hyde. The sequences were deposited into GenBank (Accessions MT193419 to MT193421 for ITS, MT193101 to MT193103 for ACT, MT193098 to MT193100 for CHS, MT193095 to MT193097 for GAPDH, MT193092 to MT193094 for TUB2, and MT193089 to MT193091 for ApMat of the three isolates, respectively). Based on the genetic and morphological results, the isolates were identified as C. fructicola. Pathogenicity was tested on 72 healthy leaves from nine 2-year-old hybrid mandevilla plants (eight leaves per plant) in November 2019 in a greenhouse using isolates PXT1-1, PXT1-5, and PXT2-1. Two wounds were made slightly on both sides of the middle vein on each leave using a sterilized toothpick, and each wounded site was inoculated with 10 μl of a 1 × 106 conidia/ml suspension. Leaves of three plants were treated with sterile water for the control. Plants were covered with plastic bags to maintain high humidity and placed in a greenhouse kept at 28°C with a 12-h photoperiod. At five days post-inoculation, all the inoculated leaves developed dark brown lesions (0.1 to 1.4 cm in width and 0.2 to 1.6 cm in length), while controls remained disease free. The fungus was re-isolated from symptomatic inoculated leaves and identification confirmed by morphology and sequencing, fulfilling Koch’s postulates. Colletotrichum fructicola can cause leaf diseases in a variety of crops and ornamental plants, including apple, tea plants, sage, and orchid (Guarnaccia et al. 2019; Kim et al. 2018). To our knowledge, this is the first report of C. fructicola causing anthracnose on hybrid mandevilla in China. These findings provide a foundation for future studies on the epidemiology and control of anthracnose caused by C. fructicola on hybrid mandevilla.