Scholl Peter F, Kongkasuriyachai Darin, Demirev Plamen A, Feldman Andrew B, Lin Jeffrey S, Sullivan David J, Kumar Nirbhay
M. S. Eisenhower Research and Technology Development Center, Johns Hopkins University Applied Physics Laboratory, 11100 Johns Hopkins Road, Laurel, MD 20723-6099, USA.
Am J Trop Med Hyg. 2004 Nov;71(5):546-51.
Rapid diagnosis leading to effective treatment is essential to control escalating infectious diseases such as malaria. Malaria pigment (hemozoin) detection by laser desorption mass spectometry (LDMS) was recently shown to be a sensitive (<10 parasites/muL) technique for detecting Plasmodium falciparum parasites cultured in human blood. To examine the use of LDMS in a rapid new malaria screening assay, we followed the time course of P. yoelii infections in mice in parallel with light microscopy and a colorimetric hemozoin assay. Hemozoin was detected by LDMS in 0.3 muL of blood within two days of infection independently of the inoculating dose of 10(6), 10(4), or 10(2) parasite-infected erythrocytes. Microscopy and colorimetric hemozoin determinations lagged the LDMS detection of infections by 2-4 and 3-5 days, respectively, except at the highest inoculation dose. The LDMS detection of hemozoin is a potentially more rapid screen than light microscopy for detecting malaria infection in this mouse model at parasitemias <0.1%.
快速诊断并进行有效治疗对于控制疟疾等不断升级的传染病至关重要。最近有研究表明,通过激光解吸质谱法(LDMS)检测疟色素(疟原虫血红素)是一种灵敏的技术(检测限<10个寄生虫/微升),可用于检测在人血中培养的恶性疟原虫。为了研究LDMS在一种快速新型疟疾筛查试验中的应用,我们通过光学显微镜和比色法疟色素检测试验,并行跟踪了约氏疟原虫感染小鼠的时间进程。感染后两天内,无论接种剂量是10⁶、10⁴还是10²个感染寄生虫的红细胞,均可通过LDMS在0.3微升血液中检测到疟色素。除最高接种剂量外,显微镜检查和比色法疟色素测定分别比LDMS检测感染滞后2 - 4天和3 - 5天。在该小鼠模型中,当疟原虫血症<0.1%时,与光学显微镜相比,LDMS检测疟色素可能是一种更快速的疟疾感染筛查方法。