Khayeka-Wandabwa Christopher, Kutima Helen, Nyambati Venny C S, Ingonga Johnstone, Oyoo-Okoth Elijah, Karani Lucy, Jumba Bernard, Githuku Kiige, Anjili Christopher O
Parasit Vectors. 2013 Aug 22;6:244. doi: 10.1186/1756-3305-6-244.
Most natural host populations are exposed to a diversity of parasite communities and co-infection of hosts by multiple parasites is commonplace across a diverse range of systems. Co-infection with Leishmania major and Schistosoma mansoni may have important consequences for disease development, severity and transmission dynamics. Pentavalent antimonials and Praziquantel (PZQ) have been relied upon as a first line of treatment for Leishmania and Schistosoma infections respectively. However, it is not clear how combined therapy with the standard drugs will affect the host and parasite burden in concomitance. The aim of the current study was to determine the efficacy of combined chemotherapy using Pentostam and PZQ in BALB/c mice co-infected with L. major and S. mansoni.
The study used BALB/c mice infected with L. major and S. mansoni. A 3 × 4 factorial design with three parasite infection groups (Lm, Sm, Lm + Sm designated as groups infected with L. major, S. mansoni and L. major + S. mansoni, respectively) and four treatment regimens [P, PZQ, P + PZQ and PBS designating Pentostam®(GlaxoSmithKline UK), Praziquantel (Biltricide®, Bayer Ag. Leverkusen, Germany), Pentostam + Praziquantel and Phosphate buffered saline] as factors was applied. In each treatment group, there were 10 mice. Lesion development was monitored for 10 weeks. The parasite load, body weight, weight of the spleen and liver were determined between week 8 and week 10.
Chemotherapy using the first line of treatment for L. major and S. mansoni reduced the lesion size and parasite loads but did not affect the growth response, spleen and liver. In the co-infected BALB/c mice, the use of Pentostam or PZQ did not result in any appreciable disease management. However, treatment with P + PZQ resulted in significantly (p < 0.05) larger reduction of lesions, net increase in the body weight, no changes in the spleen and liver weight and reduced Leishman-Donovan Units (LDU) and worm counts than BALB/c mice treated with Pentostam or PZQ alone.
The present study demonstrated that the combined first line of treatment is a more effective strategy in managing co-infection of L. major and S. mansoni in BALB/c mice.
大多数自然宿主群体都会接触到多种寄生虫群落,宿主被多种寄生虫共同感染在各种各样的系统中都很常见。利什曼原虫(Leishmania major)和曼氏血吸虫(Schistosoma mansoni)共同感染可能对疾病发展、严重程度及传播动态产生重要影响。五价锑化合物和吡喹酮(PZQ)分别一直被用作治疗利什曼原虫和血吸虫感染的一线药物。然而,尚不清楚标准药物联合治疗会如何同时影响宿主和寄生虫负荷。本研究的目的是确定在同时感染利什曼原虫和曼氏血吸虫的BALB/c小鼠中,使用葡酸锑钠(Pentostam)和吡喹酮联合化疗的疗效。
本研究使用感染了利什曼原虫和曼氏血吸虫的BALB/c小鼠。采用3×4析因设计,有三个寄生虫感染组(分别将感染利什曼原虫、曼氏血吸虫和利什曼原虫 + 曼氏血吸虫的组指定为Lm、Sm、Lm + Sm组)和四种治疗方案[分别将葡酸锑钠(英国葛兰素史克公司的Pentostam®)、吡喹酮(德国拜耳公司的Biltricide®)、葡酸锑钠 + 吡喹酮和磷酸盐缓冲盐水指定为P、PZQ、P + PZQ和PBS]作为因素。每个治疗组有10只小鼠。对病变发展情况监测10周。在第8周和第10周期间测定寄生虫负荷、体重、脾脏和肝脏重量。
使用治疗利什曼原虫和曼氏血吸虫的一线药物进行化疗可减小病变大小和降低寄生虫负荷,但不影响生长反应、脾脏和肝脏。在同时感染的BALB/c小鼠中,使用葡酸锑钠或吡喹酮并未带来任何明显的疾病控制效果。然而,与单独使用葡酸锑钠或吡喹酮治疗的BALB/c小鼠相比,P + PZQ治疗导致病变显著减小(p < 0.05)、体重净增加、脾脏和肝脏重量无变化、利什曼 - 多诺万单位(LDU)减少且虫数减少。
本研究表明,联合一线治疗是管理BALB/c小鼠中利什曼原虫和曼氏血吸虫共同感染的更有效策略。