Department of Food Science and Technology, Yeungnam University, 280 Daehak-ro, Gyeongsan-si, Gyeongsangbuk-do 712-749, Republic of Korea.
Food Standard Research Center, Korea Food Research Institute, Anyangpangyo-ro 62, 1201 Beon-gil, Seongnam-si, Gyeonggi-do 13539, Republic of Korea.
Biosens Bioelectron. 2016 Mar 15;77:986-94. doi: 10.1016/j.bios.2015.10.077. Epub 2015 Oct 28.
This study aimed to develop an immunoliposome-based immunomagnetic concentration and separation assay for the rapid detection of Cronobacter sakazakii (C. sakazakii), an acute opportunistic foodborne pathogenic bacterium, in both pure culture and infant formula. To develop the assay, magnetic nanoparticles (diameter 30 nm) were coated with immunoglobulin G (IgG), specifically anti-C. sakazakii IgG, and applied for the sensitive and efficient detection of C. sakazakii using immunoliposomes. The binding efficiency of anti-C. sakazakii IgG to the magnetic nanoparticles was 86.23 ± 0.59%. The assay developed in this study detected as few as 3.3 × 10(3) CFUmL(-1) of C. sakazakii in pure culture within 2h 30 min; in comparison, an indirect non-competitive enzyme-linked immunosorbent assay was able to detect 6.2 × 10(5) CFUmL(-1) of C. sakazakii in pure culture after 17 h. The developed assay did not show any cross-reactivity with other Cronobacter spp. or pathogens belonging to other genera. In addition, the method was able to detect 10(3) CFUmL(-1) of C. sakazakii in infant formula without any pre-incubation. These results confirm that the immunoliposome-based immunomagnetic concentration and separation assay may facilitate highly sensitive, efficient, and rapid detection of C. sakazakii.
本研究旨在开发一种基于免疫脂质体的免疫磁浓缩分离检测法,用于快速检测阪崎克罗诺杆菌(Cronobacter sakazakii,C. sakazakii),这是一种急性机会性食源致病菌,可应用于纯培养物和婴儿配方奶粉中。为了开发该检测方法,我们将直径为 30nm 的磁性纳米颗粒(magnetic nanoparticles)包被免疫球蛋白 G(immunoglobulin G,IgG),即抗 C. sakazakii IgG,并应用免疫脂质体进行 C. sakazakii 的灵敏高效检测。抗 C. sakazakii IgG 与磁性纳米颗粒的结合效率为 86.23±0.59%。本研究中开发的检测方法在 2 小时 30 分钟内即可检测到纯培养物中低至 3.3×10(3) CFUmL(-1)的 C. sakazakii;相比之下,间接非竞争酶联免疫吸附测定法(indirect non-competitive enzyme-linked immunosorbent assay)在 17 小时后才能检测到纯培养物中 6.2×10(5) CFUmL(-1)的 C. sakazakii。该检测方法与其他阪崎克罗诺杆菌或其他属的病原体均无交叉反应。此外,该方法无需预孵育即可检测到婴儿配方奶粉中 10(3) CFUmL(-1)的 C. sakazakii。这些结果证实,基于免疫脂质体的免疫磁浓缩分离检测法可实现 C. sakazakii 的高度敏感、高效和快速检测。