Konecka Edyta, Mokracka Joanna, Krzymińska Sylwia, Kaznowski Adam
Department of Microbiology, Faculty of Biology, Adam Mickiewicz University in Poznań , Poland.
Pol J Microbiol. 2019;68(2):185-191. doi: 10.21307/pjm-2019-018.
We observed the death of insect caterpillars of in the laboratory culture line and identified as the bacterial causative agent of the insect death. We confirmed that had insecticidal activity against and caused high mortality of larvae. The LC values of CFU per 1 cm of insect diet surface were similar for all isolates. Our research reports novel strains with high pesticidal activity as candidates for future research on a new bioinsecticide. As bioinsecticides cannot be harmful to non-target organisms, we determined the pathogenic properties of to humans. We proved the ability of to damage mammalian epithelial cells. All strains had cytopathic effects to Vero cells with a cytotoxic index ranging from 51.2% ± 3.8% to 79.2% ± 4.1%. We found that all of the strains excreted catecholate siderophore - enterobactin. All isolates were resistant to sulfamethoxazole, tobramycin, gentamicin, cefepime, and aztreonam. We did not observe the ESBL phenotype and the integrons' integrase genes. Resistance to sulfamethoxazole was due to the presence of the or gene. The use of resistant strains that are pathogenic to humans in plant protection may cause infections difficult to cure and lead to the spread of resistance genes. The results of our study emphasize the necessity of determination of the safety to vertebrates of the bacteria that are proposed to serve as biocontrol agents. The novelty of our study lies in the demonstration of the indispensability of the bacteria verification towards the lack of hazardous properties to humans. We observed the death of insect caterpillars of in the laboratory culture line and identified as the bacterial causative agent of the insect death. We confirmed that had insecticidal activity against and caused high mortality of larvae. The LC values of CFU per 1 cm of insect diet surface were similar for all isolates. Our research reports novel strains with high pesticidal activity as candidates for future research on a new bioinsecticide. As bioinsecticides cannot be harmful to non-target organisms, we determined the pathogenic properties of to humans. We proved the ability of to damage mammalian epithelial cells. All strains had cytopathic effects to Vero cells with a cytotoxic index ranging from 51.2% ± 3.8% to 79.2% ± 4.1%. We found that all of the strains excreted catecholate siderophore – enterobactin. All isolates were resistant to sulfamethoxazole, tobramycin, gentamicin, cefepime, and aztreonam. We did not observe the ESBL phenotype and the integrons’ integrase genes. Resistance to sulfamethoxazole was due to the presence of the or gene. The use of resistant strains that are pathogenic to humans in plant protection may cause infections difficult to cure and lead to the spread of resistance genes. The results of our study emphasize the necessity of determination of the safety to vertebrates of the bacteria that are proposed to serve as biocontrol agents. The novelty of our study lies in the demonstration of the indispensability of the bacteria verification towards the lack of hazardous properties to humans.
我们在实验室培养品系中观察到昆虫毛虫死亡,并鉴定出[细菌名称]为昆虫死亡的细菌病原体。我们证实[细菌名称]对[昆虫名称]具有杀虫活性,并导致幼虫高死亡率。每1平方厘米昆虫饲料表面[细菌名称]菌落形成单位(CFU)的半数致死浓度(LC)值在所有分离株中相似。我们的研究报告了具有高杀虫活性的新型菌株,作为未来新型生物杀虫剂研究的候选菌株。由于生物杀虫剂不能对非目标生物有害,我们测定了[细菌名称]对人类的致病特性。我们证明了[细菌名称]破坏哺乳动物上皮细胞的能力。所有菌株对Vero细胞都有细胞病变效应,细胞毒性指数范围为51.2%±3.8%至79.2%±4.1%。我们发现所有菌株都分泌儿茶酚型铁载体——肠杆菌素。所有分离株对磺胺甲恶唑、妥布霉素、庆大霉素、头孢吡肟和氨曲南均有抗性。我们未观察到超广谱β-内酰胺酶(ESBL)表型和整合子的整合酶基因。对磺胺甲恶唑的抗性归因于[基因名称]或[基因名称]的存在。在植物保护中使用对人类致病的抗性[细菌名称]菌株可能会导致难以治愈的感染,并导致抗性基因的传播。我们的研究结果强调了确定拟用作生物防治剂的细菌对脊椎动物安全性的必要性。我们研究的新颖之处在于证明了对细菌进行无危害人类特性验证的必要性。我们在实验室培养品系中观察到昆虫毛虫死亡,并鉴定出[细菌名称]为昆虫死亡的细菌病原体。我们证实[细菌名称]对[昆虫名称]具有杀虫活性,并导致幼虫高死亡率。每1平方厘米昆虫饲料表面[细菌名称]菌落形成单位(CFU)的半数致死浓度(LC)值在所有分离株中相似。我们的研究报告了具有高杀虫活性的新型菌株,作为未来新型生物杀虫剂研究的候选菌株。由于生物杀虫剂不能对非目标生物有害,我们测定了[细菌名称]对人类的致病特性。我们证明了[细菌名称]破坏哺乳动物上皮细胞的能力。所有菌株对Vero细胞都有细胞病变效应,细胞毒性指数范围为51.2%±3.8%至79.2%±4.1%。我们发现所有菌株都分泌儿茶酚型铁载体——肠杆菌素。所有分离株对磺胺甲恶唑、妥布霉素、庆大霉素、头孢吡肟和氨曲南均有抗性。我们未观察到超广谱β-内酰胺酶(ESBL)表型和整合子的整合酶基因。对磺胺甲恶唑的抗性归因于[基因名称]或[基因名称]的存在。在植物保护中使用对人类致病的抗性[细菌名称]菌株可能会导致难以治愈的感染,并导致抗性基因的传播。我们的研究结果强调了确定拟用作生物防治剂的细菌对脊椎动物安全性的必要性。我们研究的新颖之处在于证明了对细菌进行无危害人类特性验证的必要性。