Borreliacidal activity of Borrelia metal transporter A (BmtA) binding small molecules by manganese transport inhibition

作者：Wagh Dhananjay; Pothineni Venkata Raveendra; Inayathullah Mohammed; Liu Song; Kim Kwang Min; Rajadas Jayakumar^*

来源：Drug Design, Development and Therapy, 2015, 9: 805-815.

DOI：10.2147/DDDT.S77063

• Lyme disease
• BmtA
• Borrelia burgdorferi
• desloratadine
• Bac Titer-Glo assay

Borrelia burgdorferi, the causative agent of Lyme disease, utilizes manganese (Mn) for its various metabolic needs. We hypothesized that blocking Mn transporter could be a possible approach to inhibit metabolic activity of this pathogen and eliminate the infection. We used a combination of in silico protein structure prediction together with molecular docking to target the Borrelia metal transporter A (BmtA), a single known Mn transporter in Borrelia and screened libraries of FDA approved compounds that could potentially bind to the predicted BmtA structure with high affinity. Tricyclic antihistamines such as loratadine, desloratadine, and 3-hydroxydesloratadine as well as yohimbine and tadalafil demonstrated a tight binding to the in silico folded BmtA transporter. We, then, tested borreliacidal activity and dose response of the shortlisted compounds from this screen using a series of in vitro assays. Amongst the probed compounds, desloratadine exhibited potent borreliacidal activity in vitro at and above 78 mu g/mL (250 mu M). Borrelia treated with lethal doses of desloratadine exhibited a significant loss of intracellular Mn specifically and a severe structural damage to the bacterial cell wall. Our results support the possibility of developing a novel, targeted therapy to treat Lyme disease by targeting specific metabolic needs of Borrelia.

• 出版日期2015