Previous Page  21 / 30 Next Page
Information
Show Menu
Previous Page 21 / 30 Next Page
Page Background

Page 79

Journal of Infectious Diseases and Therapy ISSN: 2332-0877 | Volume: 6

Infectious Diseases

4

th

Annual Congress on

Neglected Tropical & Infectious Diseases

5

th

International Conference on

August 29-30, 2018 | Boston, USA

&

Trypanosoma congolense

versus geranylacetone:

In vivo

activity with

in vitro

and in silico antisialidase

studies

Saad Bello Saad, Mohammed Auwal Ibrahim

and

Isah Danladi Jatau

Ahmadu Bello University, Nigeria

T

he menace of animal trypanosomiasis, especially caused by

Trypanosoma congolense

, still wreaks havoc in the livestock industry

of the African continent which demands concerted efforts aimed at reducing the disease burden. An important strategy targeted

against the disease is the use of chemotherapeutic agents but the presently available approved drugs are no longer effective which

necessitates the search for novel agents. In the present study, geranylacetone was investigated for

in vivo

activity against

T. congolense

infected rats as well as the effects on trypanosome-induced pathological changes and

in vitro

and in silico anti-

T. congolense

sialidase

activity. At a dose of 100 mg/kg bw, geranylacetone significantly (P<0.05) decreased the number of

T. congolense

in infected animals

whilst an insignificant (P>0.05) reduction was observed with 50mg/kg bw of the compound. Furthermore, the compound was able to

reverse the

T. congolense

-induced anemia and organ damages as evidenced by the significantly (P<0.05) lower values of packed cell

volumes as well as hepatic and renal functions parameters in the treated group compared with infected untreated animals. Considering

the crucial role of anemia in the pathogenesis of the

T. congolense

infection, the effects of geranylacetone on the T. congolense sialidase

was further probed using

in vivo

,

in vitro

and in silico approaches. The

in vitro

studies suggested that the compound inhibited

purified bloodstream

T. congolense

sialidase using an uncompetitive inhibition pattern. The mode of binding and critical interactions

alongside the relevant amino acids were predicted using the molecular docking. We concluded that geranylacetone is also another

molecule with therapeutic potency against

T. congolense

and could be added into the library of compounds with validated

in vivo

activity against trypanosomes for further studies as possible next generation trypanocides.

mauwalibrahim@gmail.com

J Infect Dis Ther 2018, Volume 6

DOI: 10.4172/2332-0877-C3-045