Wang Xue, Zhao Jianan, Ji Fang, Wang Meng, Wu Bin, Qin Jianhua, Dong Guoying, Zhao Ruili, Wang Chengmin
Guangdong Key Laboratory of Animal Conservation and Resource Utilization, Institute of Zoology, Guangdong Academy of Science, Guangzhou, China.
College of Veterinary Medicine, Agricultural University of Hebei, Baoding, China.
Microbiol Spectr. 2023 Feb 22;11(2):e0269122. doi: 10.1128/spectrum.02691-22.
This study aimed to explore the relationship between wild birds and the transmission of multidrug-resistant strains. Klebsiella pneumoniae was isolated from fresh feces of captured wild birds and assessed by the broth microdilution method and comparative genomics. Four Klebsiella pneumoniae isolates showed different resistance phenotypes; S90-2 and S141 were both resistant to ampicillin, cefuroxime, and cefazolin, while M911-1 and S130-1 were sensitive to most of the 14 antibiotics tested. S90-2 belongs to sequence type 629 (ST629), and its genome includes 30 resistance genes, including and , while its plasmid pS90-2.3 (IncR) carries , , and . S141 belongs to ST1662, and its genome includes a total of 27 resistance genes, including . M911-1 is a new ST, carrying and , and its plasmid pM911-1.1 (novel) carries , , and (A). S130-1 belongs to ST3753, carrying and , and its plasmid pS130-1 [IncFIB(K)] carries only one resistance gene, (A). pM911-1.1 and pS90-2.3 do not have conjugative transfer ability, but their resistance gene fragments are derived from multiple homologous strain chromosomes or plasmids, and the formation of resistance gene fragments (multidrug resistance region) involves interactions between multiple mobile element genes, resulting in a complex and diverse resistance plasmid structure. The homologous plasmids related to pM911-1.1 and pS90-2.3 were mainly from isolated human-infecting bacteria in China, namely, K. pneumoniae and Escherichia coli. The multidrug-resistant K. pneumoniae isolates carried by wild birds in this study had drug resistance phenotypes conferred primarily by multidrug resistance plasmids that were closely related to human-infecting bacteria. Little is known about the pathogenic microorganisms carried by wild animals. This study found that the multidrug resistance phenotype of Klebsiella pneumoniae isolates carried by wild birds was mainly attributed to multidrug resistance plasmids, and these multidrug resistance plasmids from wild birds were closely related to human-infecting bacteria. Wild bird habitats overlap to a great extent with human and livestock habitats, which further increases the potential for horizontal transfer of multidrug-resistant bacteria among humans, animals, and the environment. Therefore, wild birds, as potential transmission hosts of multidrug-resistant bacteria, should be given attention and monitored.
本研究旨在探讨野生鸟类与多重耐药菌株传播之间的关系。从捕获的野生鸟类新鲜粪便中分离出肺炎克雷伯菌,并通过肉汤微量稀释法和比较基因组学进行评估。四株肺炎克雷伯菌分离株表现出不同的耐药表型;S90 - 2和S141对氨苄西林、头孢呋辛和头孢唑林均耐药,而M911 - 1和S130 - 1对所测试的14种抗生素中的大多数敏感。S90 - 2属于序列型629(ST629),其基因组包含30个耐药基因,包括 和 ,而其质粒pS90 - 2.3(IncR)携带 、 和 。S141属于ST1662,其基因组共有27个耐药基因,包括 。M911 - 1是一种新的序列型,携带 和 ,其质粒pM911 - 1.1(新型)携带 、 和(A)。S130 - 1属于ST3753,携带 和 ,其质粒pS130 - 1 [IncFIB(K)]仅携带一个耐药基因,(A)。pM911 - 1.1和pS90 - 2.3没有接合转移能力,但其耐药基因片段源自多个同源 菌株染色体或质粒,耐药基因片段(多重耐药区域)的形成涉及多个移动元件基因之间的相互作用,导致耐药质粒结构复杂多样。与pM911 - 1.1和pS90 - 2.3相关的同源质粒主要来自中国分离的人感染细菌,即肺炎克雷伯菌和大肠杆菌。本研究中野生鸟类携带的多重耐药肺炎克雷伯菌分离株的耐药表型主要由与人类感染细菌密切相关的多重耐药质粒赋予。关于野生动物携带的致病微生物知之甚少。本研究发现野生鸟类携带的肺炎克雷伯菌分离株的多重耐药表型主要归因于多重耐药质粒,并且这些来自野生鸟类的多重耐药质粒与人类感染细菌密切相关。野生鸟类栖息地与人类和牲畜栖息地在很大程度上重叠,这进一步增加了多重耐药细菌在人、动物和环境之间水平转移的可能性。因此,野生鸟类作为多重耐药细菌的潜在传播宿主,应受到关注并进行监测。