Genetic description of VanD phenotype vanA genotype in vancomycin-resistant Enterococcus faecium isolates from a Bone Marrow Transplantation Unit

被引:1
|
作者
Marchi, Ana Paula [1 ,2 ]
Perdigao Neto, Lauro Vieira [1 ,2 ,3 ]
Cortes, Marina Farrel [1 ,2 ]
Camarinha de Castro Lima, Victor Augusto [1 ,2 ]
Ruedas Martins, Roberta Cristina [2 ]
Moyses Franco, Lucas Augusto [1 ,4 ]
Rossi, Flavia [5 ]
Rocha, Vanderson [6 ]
Levin, Anna S. [1 ,2 ,3 ]
Costa, Silvia Figueiredo [1 ,2 ,3 ]
机构
[1] Univ Sao Paulo, Dept Molestias Infecciosas & Parasitarias, Fac Med, Av Dr Arnaldo 455, BR-01246903 Sao Paulo, Brazil
[2] Inst Med Trop FMUSP, Lab Invest Med LIM 49, Bacteriol & Resistencia Antimicrobiana, Av Dr Eneas Carvalho de Aguiar 470, BR-05403000 Sao Paulo, Brazil
[3] Hosp Clin Univ Sao Paulo, Dept Controle Infeccao, Rua Dr Ovidio Pires de Campos 225, BR-05403010 Sao Paulo, Brazil
[4] Inst Med Trop FMUSP, Lab Invest Med LIM46, Parasitol, Av Dr Eneas Carvalho de Aguiar 470, BR-05403000 Sao Paulo, Brazil
[5] Univ Sao Paulo, Div Lab Lab Cent, Hosp Clin, Sessao Microbiol,Fac Med, Av Dr Eneas de Carvalho Aguiar 155, BR-05403010 Sao Paulo, Brazil
[6] Univ Sao Paulo, Dept Hematol Hemoterapia & Terapia Celular, Fac Med, Hosp Clin, Av Dr Eneas de Carvalho Aguiar 155, BR-05403010 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Enterococcus faecium; Whole-genome sequence; Resistance; Molecular characterization; SURVEILLANCE; OUTBREAK; STRAIN;
D O I
10.1007/s42770-021-00634-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background Vancomycin-resistant Enterococcus faecium (VREfm) is an important agent of hospital-acquired infection. VanA phenotype is characterized by resistance to high levels of vancomycin and teicoplanin and is encoded by the vanA gene, whereas VanD phenotype is characterized by resistance to vancomycin and susceptibility or intermediate resistance to teicoplanin; however, some isolates carry a VanD phenotype with a vanA genotype, but there are many gaps in the knowledge about the genetic mechanisms behind this pattern. Objective To characterize the genetic structure, clonality, and mobile genetic elements of VRE isolates that display a VanD-vanA phenotype. Results All vanA VRE-fm isolates displayed minimum inhibitory concentration (MIC) for vancomycin > 32 mu g/mL and intermediate or susceptible MIC range for teicoplanin (8-16 mu g/mL). The isolates were not clonal, and whole-genome sequencing analysis showed that they belonged to five different STs (ST478, ST412, ST792, ST896, and ST1393). The absence of some van complex genes were observed in three isolates: Ef5 lacked vanY and vanZ, Ef2 lacked vanY, and Ef9 lacked orf1 and orf2; moreover, another three isolates had inverted positions of orf1, orf2, vanR, and vanS genes. IS1542 was observed in all isolates, whereas IS1216 in only five. Moreover, presence of other hypothetical protein-encoding genes located downstream the vanZ gene were observed in six isolates. Conclusion VRE isolates can display some phenotypes associated to vanA genotype, including VanA and VanB, as well as VanD; however, further studies are needed to understand the exact role of genetic variability, rearrangement of the transposon Tn1546, and presence of insertion elements in isolates with this profile.
引用
收藏
页码:245 / 250
页数:6
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