Cultivated chrysanthemum (Chrysanthemum morifolium) is a popular flower species from China, where it is widely planted for use as tea and in medicines, as well as for ornamental purposes. In July 2016, a serious stem necrotic disease was observed on chrysanthemum in a commercial greenhouse in Beijing, China. Most chrysanthemum varieties were infected, with a total disease incidence above 50%, rising to over 90% in some sensitive cultivars. Infected chrysanthemum plants exhibited two main symptoms: (i) irregular chlorotic spots on the upper leaves with shortened internodes (cultivar Silvia), or (ii) discontiguous black streaks on stems near the base of the upper petioles, followed by eventual dieback (cultivars Dante, Radost, Stellini, and Olive). These symptoms are very similar to those of chrysanthemum infected with the tospoviruses Tomato spotted wilt virus (TSWV) or Chrysanthemum stem necrotic virus (CSNV). To identify the pathogen, infected chrysanthemum leaves were analyzed using reverse-transcription polymerase chain reaction (RT-PCR) with tospovirus universal primers (Hassani-Mehraban et al. 2016). After extracting the total RNA with a Plant RNA kit (Tiangen, Beijing, China), RT-PCR was performed using an RT-PCR kit (Vazyme, Nanjing, China), with infected chrysanthemum showing black streaks on stems as positive controls and virus-free plantlets as negative controls. RT-PCR products were bidirectionally sequenced by Sangon Biotech (Shanghai, China) and aligned in DNAstar. Three clones of 10 infected leaf samples (two of each cultivar) were collected from different sections of the greenhouse and sequenced, revealing high sequence similarity with fewer than 2-bp difference between them. The most conserved sequence, isolated from sample BLZ01, was deposited in GenBank under accession number MF196915. This sequence was 99% identical to TSWV S RNA segments in GenBank and distinctly different from CSNV RNAs, indicating that the devastating disease was caused by TSWV, not CSNV. This diagnosis was further confirmed using commercial ELISA kits (Luyuan Bode Biological, Beijing, China), which revealed TSWV but not CSNV in all symptomatic tissue. Additional RT-PCRs were performed using TSWV-specific (Chung et al. 2006; Qiu et al. 1998) and CSNV-specific (Takeshita et al. 2011) primers complementing the RNA-dependence RNA polymerase gene (L RNA), Gn/Gc gene (M RNA), and nucleocapsid protein gene (NP, S RNA), respectively, and the results confirmed those of the ELISA. Finally, the virus isolated from BLZ01 was mechanically transmitted from infected cultivar Olive collected from the original greenhouse to 1-month-old virus-free chrysanthemum seedlings using chilled 0.01 M phosphate buffer (pH 7.2) containing 0.1% sodium sulfite. After 2 weeks, most inoculated plants (13 of 18) exhibited localized necrotic spots and black streaks on their stems. RT-PCR and sequencing revealed that the partial sequence of the TSWV NP gene from the inoculated chrysanthemum was identical to the virus from the greenhouse materials. TSWV has spread and is causing epidemics on chrysanthemum in many countries. To our knowledge, this is the first report of TSWV detected on chrysanthemum in China, and this article will act as a warning to prevent the spread of TSWV in Beijing.