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梨火疫病菌对四霉素敏感基线的建立及抗药性评价

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[目的]建立新疆库尔勒地区和阿克苏地区梨火疫病菌(Erwinia amylovora)对四霉素的敏感基线,监测梨火疫病菌对四霉素的抗药性水平,为四霉素防治梨火疫病田间用药、抗药性监测与抗药性治理提供理论依据.[方法]采用抑菌圈法测定100株梨火疫病菌株对四霉素的敏感性;采用平板划线法和含药培养基法药剂驯化抗药突变体,进行抗药性评价.[结果]共监测到敏感菌株74个,低抗菌株26个.100株菌株对四霉素的敏感性频率接近正态分布,因此可将该曲线(平均EC50=1.59±1.029 μg·mL-1)作为新疆库尔勒地区和阿克苏地区梨火疫病菌对四霉素的敏感基线;共获得4株抗药突变体,均不具有稳定遗传性;四霉素与84%噻霉酮、中生菌素均会产生交互抗药性.[结论]建立了新疆梨火疫病菌分离菌株对四霉素药剂的敏感基线,仅监测到少数低抗菌株,梨火疫病菌对四霉素的抗性风险低.
Establishment of sensitivity baseline and evaluation of resistance to tetra-mycin of Erwinia amylovora
[Objective]Pear fire blight caused by Erwinia amylovora is an international quarantine bac-terial disease.It is one of the top ten plant pathogenic bacteria in the world with fast transmission speed,multiple transmission routes and wide host range.Biopesticide tetramycin is a pure green biopesticide developed by Liaoning Academy of Microbial Sciences in the 1970s and was productized in the early 1990s.Tetramycin can inhibit both bacterial and fungal plant diseases.At present,there are no reports on the establishment of sensitivity baseline and the evaluation of resistance to tetramycin of E.amylovo-ra in China.The study aimed to establish a sensitivity baseline for E.amylovora to tetramycin in Korla and Aksu regions of Xinjiang,and monitor the resistance level of pear fire blight to tetramycin in the re-gion and provide a scientific basis for the field administration of tetramycin against pear fire blight,anti-biotic resistance monitoring and antibiotic resistance management.[Methods]The samples were col-lected,in ten areas in Xinjing,including Bayinguoleng and Aksu in 2021 and 2023.The bacterial strains were isolated from the infected plant materials of Korla fragrant pear.The sensitivity of 100 strains of E.amylovora isolated to tetramycin was determined by the inhibition zone method.The drug-resistant mutants were acclimated by streak plate method and drug containing medium method,followed by drug resistance evaluation.The preserved strains were separated in the NA medium,incubated at 28 ℃ for 48 h,and single colonies were obtained by secondary activation.The single colony was transferred to the NB culture medium at 28 ℃,180 r·min-1 for 12 h,and the test bacterial suspension was obtained when OD600 was determined to be 1.0.After the bacterial suspension was diluted to 1 × 104 cfu·mL-1,100 μL was coated in the NA medium until dry.Three pieces of sterilized filter paper with a diameter of 6 mm were placed on the NA medium in the petri dish.6 μL of different concentrations of drug drops were absorbed on the filter paper sheet,with 5 treatment concentrations for each drug solution and 2 dishes for each concentration,for a total of 6 repetitions,with sterile water as the control.After being in-cubated at 28 ℃ for 36 h,the diameter of the antibacterial zone was measured by the cross method,and the antibacterial rate was calculated according to the formula.The correlation coefficient and EC50 val-ue were calculated according to the bacteriostasis rate.Based on the average EC50 values of the all test-ed strains,the sensitivity baseline of tetramycin in Xinjiang was established.[Results]The results showed that from the all tested strains,74 sensitive strains were detected,accounting for 74%,and 26 re-sistant strains were detected,accounting for 26%.The distribution of EC50 values of 100 strains of E.am-ylovora ranged from 0.199 to 4.84 μg mL-1,with the maximum ECs0 was 24.32 times as high as the mini-mum EC50,the average EC50 was(1.59±1.029)μg·mL-1,and the 95%confidence interval was 1.389 2-1.797 4 μg mL-1 The distribution of tetramycin to E.amylovora strains showed a unimodal curve,which was similar to the normal distribution,and no E.amylovora strains with significantly decreased sensi-tivity were found.Therefore,the mean ECs0 value of(1.59±1.029)μg·mL-1 could be used as the base-line for the sensitivity of E.amylovora strains to tetramycin in southern Xinjiang.There were some dif-ferences in the sensitivity of the 100 strains of E.amylovora between 4 regions,the strains from Aksu were more sensitive,with mean EC50 value of 0.780±0.436 μg·mL-1,which was significantly different from the strains from Awati Township,Halayugong Township and Tiemengguan.After the four resistance mutants of E.amylovora were transferred to the NA medium for 10 successive generations,the resis-tance levels of the 11th generation resistance mutants were 0.275 μg·mL-1,0.43 μg·mL-1,0.145 μg·mL-1 and 0.564 μg·mL-1,respectively,which all decreased from the resistance level of low antibacterial strains to the resistance level of sensitive strains.The results indicated that the 4 resistant mutants was not genetically stabile.The EC50 values of the E.amylovora resistance mutant against tetramycin were highly correlated with the ECs0 values of 84%benziothiazolinone and zhongshengmycin,and the corre-lation coefficients were 0.765 8 and 0.900 8,respectively,and the absolute values of all correlation co-efficients were higher than 0.75.It can be seen that there is a cross-resistance problem between tetra-mycin and 84%benziothiazolinone and zhongshengmycin,which are commonly used in field to con-trol E.amylovora,so the three fungicides should be avoided as alternate standby pesticides in the field to avoid cross-resistance problems.Thus,it was confirmed that tetramycin had cross-resistance with the 84%benziothiazolinone and zhongshengmycin.[Conclusion]The basic resistance of the strains of E.amylovora from different regions to fungicides was determined by both the agent and the pathogen it-self.The sensitivity baseline value of the E.amylovora isolated strains in Xinjiang to benziothiazoli-none could be established according to this study.Only a few low resistant subgroup strains were detect-ed,and the risk of resistance to tetramycin was at low level.

Erwinia amylovoraTetramycinLaboratory toxicity testSensitive baselineResistance stability

吕振豪、杨雨薇、刘琦、于蕊、陈晓晓、周伊航、陈晶

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新疆农业大学农学院·农业农村部西北荒漠绿洲农林外来入侵生物防控重点实验室(部省共建)·新疆维吾尔自治区农林有害生物监测与安全防控重点实验室,乌鲁木齐 830052

梨火疫病菌 四霉素 室内毒力测定 敏感基线 抗性稳定性

国家重点研发计划

2021YFD1400200

2024

果树学报
中国农业科学院郑州果树研究所

果树学报

CSTPCD北大核心
影响因子:1.486
ISSN:1009-9980
年,卷(期):2024.41(7)
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