Prevalence of pleuromutilin antibiotic resistance genes in different laying hen breeding stages in China

被引:0
作者
Feng, Jing-Yi [1 ]
Su, Wen [1 ]
Feng, Yu-Xuan [1 ]
Lin, Cong [1 ]
Xie, Xian-Jun [1 ]
Wu, Jie [1 ]
Lai, Shan-Ming [1 ]
Zhang, An-Yun [1 ]
机构
[1] Sichuan Univ, Coll Life Sci, Anim Dis Prevent & Food Safety Key Lab Sichuan Pro, Key Lab Bioresource & Ecoenvironm,Minist Educ, Chengdu 610065, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
antibiotic resistance genes; laying hens; pleuromutilin resistance; qPCR; STAPHYLOCOCCUS-AUREUS ST398; ABC TRANSPORTER GENE; ANTIMICROBIAL RESISTANCE; ERYSIPELOTHRIX-RHUSIOPATHIAE; LSA(E); STREPTOGRAMIN; ENVIRONMENT; PIG; LINCOSAMIDES; PLEUROMUTILINLINCOSAMIDESTREPTOGRAMIN;
D O I
10.1093/femsle/fnad038
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
This is the first comprehensive comparative survey of pleuromutilin resistance genes among laying hen production chain in China. Antimicrobial resistance is a rapidly evolving and extremely complex issue, particularly due to the use of various types of antimicrobials within human, animal, and environmental sectors. Pleuromutilin antibiotics are used to prevent and control respiratory diseases in the rearing stage of hen chicks, but the current status of pleuromutilin resistance in the laying hen breeding process is unclear. ATP-binding cassette transporters encoded by lsa(A), lsa(E), lsa(C), and vga(D) can be transferred by plasmids and transposons, thereby posing a potential dissemination risk. To investigate pleuromutilin resistance genes in the laying hen production chain in China, 95 samples from five environmental types were collected in four breeding stages to determine the abundances of the main resistance genes by qPCR, i.e. lsa(A), lsa(E), lsa(C), and vga(D). The abundance (5.16 log(10)GC/g) and detection rate (100%) of lsa(E) was highest in all of the samples, thereby suggesting high contamination with the lsa(E) gene across the large-scale laying hen breeding environment and feces. The lsa(A) (6.02 log(10)GC/g) and lsa(E) (6.18 log(10)GC/g) genes were most abundant in flies, and the abundance of vga(D) (4.50 log(10)GC/g) was highest in dust (P < .05). In addition to feces, flies and dust were important sources of contamination with pleuromutilin resistance along the laying hen production chain. In summary, we determined the abundances of four pleuromutilin resistance genes in the laying hen production chain and provided direct evidence of pleuromutilin resistance transmission and environmental contamination. In particular, the chicken breeding stage needs further attention.
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页数:8
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共 40 条
  • [1] Characterization of a new staphylococcal gene, vgaB, encoding a putative ABC transporter conferring resistance to streptogramin A and related compounds
    Allignet, J
    El Solh, N
    [J]. GENE, 1997, 202 (1-2) : 133 - 138
  • [2] Spread of airborne antibiotic resistance from animal farms to the environment: Dispersal pattern and exposure risk
    Bai, Hong
    He, Liang-Ying
    Wu, Dai-Ling
    Gao, Fang-Zhou
    Zhang, Min
    Zou, Hai-Yan
    Yao, Mao-Sheng
    Ying, Guang-Guo
    [J]. ENVIRONMENT INTERNATIONAL, 2022, 158
  • [3] A novel genomic island harbouring lsa(E) and lnu(B) genes and a defective prophage in a Streptococcus pyogenes isolate resistant to lincosamide, streptogramin A and pleuromutilin antibiotics
    Berbel, Damaris
    Camara, Jordi
    Garcia, Ernesto
    Tubau, Fe
    Guerin, Francois
    Giard, Jean-Christophe
    Angeles Dominguez, M.
    Cattoir, Vincent
    Ardanuy, Carmen
    [J]. INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2019, 54 (05) : 647 - 651
  • [4] Changing epidemiology of group B streptococcal infections among adults in Iceland: 1975-2014
    Bjoernsdottir, E. S.
    Martins, E. R.
    Erlendsdottir, H.
    Haraldsson, G.
    Melo-Cristino, J.
    Kristinsson, K. G.
    Ramirez, M.
    [J]. CLINICAL MICROBIOLOGY AND INFECTION, 2016, 22 (04) : 379.e9 - 379.e16
  • [5] Streptococcus suis in invasive human infections in Poland: clonality and determinants of virulence and antimicrobial resistance
    Bojarska, A.
    Molska, E.
    Janas, K.
    Skoczynska, A.
    Stefaniuk, E.
    Hryniewicz, W.
    Sadowy, E.
    [J]. EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2016, 35 (06) : 917 - 925
  • [6] Occurrence and removal of antibiotic resistance genes in municipal wastewater and rural domestic sewage treatment systems in eastern China
    Chen, Hong
    Zhang, Mingmei
    [J]. ENVIRONMENT INTERNATIONAL, 2013, 55 : 9 - 14
  • [7] Detection and Genetic Environment of Pleuromutilin-Lincosamide-Streptogramin A Resistance Genes in Staphylococci Isolated from Pets
    Deng, Fengru
    Wang, Huiwen
    Liao, Yifei
    Li, Jun
    Fessler, Andrea T.
    Michael, Geovana B.
    Schwarz, Stefan
    Wang, Yang
    [J]. FRONTIERS IN MICROBIOLOGY, 2017, 8
  • [8] Nonsense mutations in the lsa-like gene in Enterococcus faecalis isolates susceptible to lincosamides and streptogramins A
    Dina, J
    Malbruny, B
    Leclercq, R
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (07) : 2307 - 2309
  • [9] Host specificity in the diversity and transfer of lsa resistance genes in group B Streptococcus
    Douarre, Pierre-Emmanuel
    Sauvage, Elisabeth
    Poyart, Claire
    Glaser, Philippe
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2015, 70 (12) : 3205 - 3213
  • [10] Dissemination of antibiotic resistance genes and human pathogenic bacteria from a pig feedlot to the surrounding stream and agricultural soils
    Fang, Hua
    Han, Lingxi
    Zhang, Houpu
    Long, Zhengnan
    Cai, Lin
    Yu, Yunlong
    [J]. JOURNAL OF HAZARDOUS MATERIALS, 2018, 357 : 53 - 62