Bacterial proximity effects on the transfer of antibiotic resistance genes within the alimentary tract of yellow mealworm larvae

被引:0
作者
Crippen, Tawni L. [1 ]
Sullivan, John P. [1 ]
Anderson, Robin C. [1 ]
机构
[1] USDA, ARS, Southern Plains Agr Res Ctr, Food & Feed Safety Res Unit, 2881 F&B Rd, College Stn, TX 77845 USA
关键词
insects as feed; darkling beetle; bacterial conjugation; horizontal gene transfer; LESSER MEALWORM; ALPHITOBIUS-DIAPERINUS; ESCHERICHIA-COLI; HORIZONTAL TRANSFER; TENEBRIO-MOLITOR; PLASMID TRANSFER; GASTROINTESTINAL-TRACT; CONJUGATIVE TRANSFER; ERWINIA-HERBICOLA; SALMONELLA;
D O I
10.1093/jee/toae019
中图分类号
Q96 [昆虫学];
学科分类号
摘要
The arthropod intestinal tract and other anatomical parts naturally carry microorganisms. Some of which are pathogens, secrete toxins, or carry transferable antibiotic-resistance genes. The risks associated with the production and consumption of edible arthropods are dependent on indigenous microbes, as well as microbes introduced during the processes of rearing. This mass arthropod production puts individual arthropods in close proximity, which increases the possibility of their exposure to antibiotic-resistant bacteria carried by bacteria from fellow insects, industry workers, or rearing hardware and substrates. The purpose of this study was to determine if the alimentary tract of the yellow mealworm provided an environment permitting horizontal gene transfer between bacteria. The effect of the concentration of bacterial exposure was also assessed. Antibiotic resistance gene transfer between marker Salmonella Lignieres (Enterobacterales: Enterobacteriaceae) and Escherichia coli (Migula) (Enterobacterales: Enterobacteriaceae) introduced into the larval gut demonstrated that the nutrient-rich environment of the yellow mealworm gut provided favorable conditions for the transfer of antibiotic resistance genes. Conjugation frequencies were similar across inoculum concentrations; however, transconjugant production correlated positively to increased exposure concentration. The lowest concentration of bacterial exposure required enrichment to detect and thus may have been approaching a threshold level for the 2 bacteria to colocate within the expanse of the larval gut. While many factors can affect this transfer, the simple factor of the proximity of donor and recipient bacteria, as defined by the concentration of bacteria within the volume of the insect gut, likely primarily contributed to the efficiency of antibiotic gene transfer.
引用
收藏
页码:417 / 426
页数:10
相关论文
共 52 条
  • [1] Horizontal Transfer of the Tetracycline Resistance Gene tetM Mediated by pCF10 Among Enterococcus faecalis in the House Fly (Musca domestica L.) Alimentary Canal
    Akhtar, Mastura
    Hirt, Helmut
    Zurek, Ludek
    [J]. MICROBIAL ECOLOGY, 2009, 58 (03) : 509 - 518
  • [2] [Anonymous], 2023, Food Waste FAQs
  • [3] [Anonymous], 2018, Nitrogen inputs to agricultural soils from livestock manure. New statistics
  • [4] TRANSCONJUGATION BETWEEN BACTERIA IN THE DIGESTIVE-TRACT OF THE CUTWORM PERIDROMA-SAUCIA
    ARMSTRONG, JL
    WOOD, ND
    PORTEOUS, LA
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (05) : 1492 - 1493
  • [5] Gene transfer and plasmid instability within pilot-scale sewage filter beds and the invertebrates that live in them
    Ashelford, KE
    Learner, MA
    Fry, JC
    [J]. FEMS MICROBIOLOGY ECOLOGY, 2001, 35 (02) : 197 - 205
  • [6] Becker GeoffreyS., 2008, Livestock Feed Costs: Concerns and Options
  • [7] Characterization of antimicrobial resistant Salmonella Kinshasa from dairy calves in Texas
    Bischoff, KM
    Edrington, TS
    Callaway, TR
    Genovese, KJ
    Nisbet, DJ
    [J]. LETTERS IN APPLIED MICROBIOLOGY, 2004, 38 (02) : 140 - 145
  • [8] Identification of plasmids by PCR-based replicon typing
    Carattoli, A
    Bertini, A
    Villa, L
    Falbo, V
    Hopkins, KL
    Threlfall, EJ
    [J]. JOURNAL OF MICROBIOLOGICAL METHODS, 2005, 63 (03) : 219 - 228
  • [9] Clinical and Laboratory Standards Institute (CLSI), 2023, M100-performance standards for antimicrobial susceptibility testing, V28th
  • [10] CLSI, 2018, M07ED11 CLSI, DOI DOI 10.1016/J.DIAGMICROBIO.2013.01.001