Cytochrome bc1 Complex: Potential Breach to Improve the Activity of Phenazines on Xanthomonas.

The effects of the natural pesticides, phenazines, were reported to be limited by some tolerant metabolism processes within Xanthomonas. Our previous studies suggested that the functional cytochrome bc1 complex, the indispensable component of the respiration chain, might participate in tolerating phenazines in Xanthomonas. In this study, the cytochrome bc1 mutants of Xanthomonas campestris pv. campestris (Xcc) and Xanthomonas oryzae pv. oryzae (Xoo), which exhibit different tolerance abilities to phenazines, were constructed, and the cytochrome bc1 complex was proven to partake a critical and conserved role in tolerating phenazines in Xanthomonas. In addition, results of the cytochrome c mutants suggested the different functions of the various cytochrome c proteins in Xanthomonas and that the electron channeled by the cytochrome bc1 complex to cytochrome C4 is the key to reveal the tolerance mechanism. In conclusion, the study of the cytochrome bc1 complex provides a potential strategy to improve the activity of phenazines against Xanthomonas.

First report of Ustilago planetellacausing Smut on Eragrostis japonica (Thunb.) Trin in central region of China.

Eragrostis japonica (Thunb.) Trin, a kind of grass weeds in paddy rice fields, has recently been developing rapidly as the most harmful weed for rice production in addition to Echinochloa crusgalli and Leptochloa chinensis in partial areas of Anhui, Jiangsu, and Zhejiang provinces (Zhou et al.). In September 2019, inflated sori in the ovaries of E. japonica were identified in fields in Chuzhou County, Anhui Province. The disease incidence was approximately 50% at the survey site. Smut sori were in some spikelets of infected inflorescence destroying the inner most floral organs. Sori were ovoid and initially covered with a thin peridium (Figure 1). The sori busted after maturation, and the black powdery spores spread to the plant and soil. The sori were crushed using the sterilized tweezers. The black powdery spores were suspended with sterilized water and spread onto potato dextrose agar (PDA) medium. Spores were covered with spines, and the shape of spores varied from globose to ovoid. Scanning electron microscope was used to observe the morphology of spores. The spores were 7.5-12.3 µm × 5.8-11.8 µm (n=50). The surface of spores was covered with spines, and dense verruca were identified between the spines (Figure 2). For molecular identification, the primers ITS1/ITS4 and GAPDH-F/R were employed to amplify the rDNA region. The resulting sequences from the studied material were submitted to Genbank (MW819938 and MZ508441). BLASTn analysis revealed that ITS sequence shared 99% similarity with EF040584 (719/728) the ITS sequence from type specimen of Ustilago planetella. Based on the above results, the pathogen was identified as Ustilago planetella (Vánky, 2007). To verify the Koch's postulates, a pathogenicity test was performed by infiltrating the inflorescence with microspore suspensions of the strain SMZF-2 (1×106 spores/mL) when the E. japonica flowers for 30 minutes. The plants were inoculated in a moist chamber (with a relative humidity >80%) with a 12-h light cycle at 28℃. Inflated sori were observed after inoculated for 2 weeks, and U. planetella was isolated and identified with the methods described above. No sori were observed in the water-inoculated control plants. U. planetella had been reported to infect Eragrostis japonica in Thailand (Vánky, 2007). To our knowledge, this is the first report of U. planetella causing Smut on E. japonica (Thunb.) Trin in central region of China. The current study may help solve the negative effect of E. japonica in paddy rice production via using U. planetella in the future.