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\title{Effects of African Panaxia Extracts on Staphylococcus Aureus and Klebsiella Pneumoniae from Bacteria Wound Infection in Tiko}
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             \author[1]{Augustine Eyong  Bate}

             \author[2]{Junior Dinkah  Libah}

             \author[3]{Walter Ojong  Ebot}

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\date{\small \em Received: 1 January 1970 Accepted: 1 January 1970 Published: 1 January 1970}

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\begin{abstract}
        


Background: Wound is the disruption of cellular and anatomic continuity of living tissue produced by physical, chemical, electrical or microbial insults to the tissue. Wound healing is the dynamic process of regeneration or repair of broken tissue, due to increasing health care costs, an ageing population, and a sharp rise in the incidence of diseases such as diabetes and obesity worldwide, the present study was aimed to achieve the following objectives.Objectives: This study aimed to determine the effect of African panaxia on bacteria wound infection.Methods: It was a Laboratory based experimental study made up of bacterial isolates from wounds, cultured on blood, EMB agar, followed by confirmatory biochemical tests and MI and MBC was done turbidity absorbance measured using spectrophotometry at 660nm. Data was analyzed using Microsoft excel 2010.

\end{abstract}


\keywords{minimum inhibitory concentration; minimum bactericidal concentration.}

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\section[{Introduction}]{Introduction}\par
ound is the disruption of cellular and anatomic continuity of living tissue produced by physical, chemical, electrical or microbial insults to the tissue. Wound healing is the dynamic process of regeneration or repair of broken tissue \hyperref[b0]{[1]}. Chronic wounds are rapidly growing problem worldwide, due to increasing health care costs, an ageing population, and a sharp rise in the incidence of diseases such as diabetes and obesity \hyperref[b1]{[2]}. The skin is under constant stress from the sun, smog, friction, tension, temperature, and other external factors. Therefore, under sufficient stress that causes injury, it results in wounds. Wounds may be classified as; open and closed, acute and chronic, avulsion and degloving, clean and contaminated, infected and colonized, laceration, incision and abrasion, puncture, penetration, and gunshot wounds. Nonetheless, they exist in various forms comprising crush injuries, ulcers, skin tears, bruises, and post-operative, which directly or indirectly affect human health conditions. If it is not treated correctly, it may ultimately lead to death. Wounds can be caused by various microorganisms such as bacteria, fungi, parasites, and viruses. Some of the commonly associated bacteria organisms include Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, Klebsiellaspp., Acinetobacterspp \hyperref[b2]{[3]}. Studies conducted in 2014 and 2021 reported a wound infection prevalence of 10\% and 5.95\% respectively  {\ref [4,}\hyperref[b3]{5]}.Medicinal plants and synthetic drugs have been the most valuable sources of molecules with therapeutic potential throughout the history of mankind. Folk medicine of each civilization is based on natural products and, nowadays, medicinal plants still represent an important pool for the identification of novel drug leads \hyperref[b4]{[6]}. African panaxia being a synthesized herbal medicine is made from various herbal plants such as ginseng root, Optimum gratisimum, Panaxquiquifolium, Aloe-vera and water with active ingredients ginsenosides, methyl eugenol, saponins and salicylic acid respectively \hyperref[b5]{[7]}. 
\section[{a) Rationale}]{a) Rationale}\par
The advent of the resistance that pathogenic microorganisms have developed against antibiotics has necessitated much attention to be paid on plant extracts and biologically active compounds isolated from natural plants used in herbal medicine \hyperref[b6]{[8]}. Despite the use of various synthesized herbal plants in the treatment of bacteria wound infection, there is limited information regarding the use of African panaxia in the treatment of wound infections. Furthermore, no study has been carried out in this study area. Hence there is need to investigate on the in-vitro activity of African panaxia on bacteria wound infections. 
\section[{b) Goal of study}]{b) Goal of study}\par
The goal of this study was to provide base line data on the effect of African panaxia on bacteria wound infection. 
\section[{c) Hypothesis}]{c) Hypothesis}\par
There is no significant effect of African panaxia on bacterial wound infections. 
\section[{d) Objectives of study i. General objective}]{d) Objectives of study i. General objective}\par
The general objective of this study was to determine the effect of African panaxia on bacteria wound infection. 
\section[{ii. Specific objectives}]{ii. Specific objectives}\par
To determine the efficacy of distilled water extract of African panaxia on Staphylococcus aureus and Klebsiella species bacteria from wound infection.\par
To determine the efficacy of Luke warm water extract of African panaxia on Staphylococcus aureusand Klebsiella species bacteria from wound infection.\par
To determine the efficacy of ethanoic extract of African panaxia on Staphylococcus aureus and Klebsiella species bacteria from wound infection. 
\section[{II.}]{II.} 
\section[{Materials and Methods}]{Materials and Methods} 
\section[{a) Study area and setting}]{a) Study area and setting}\par
This study was carried out in Tiko, in Maflekumen Medical Teaching and Research Laboratory situated in Tiko is a subdivision of Fako Division in the South West Region of Cameroon with a \hyperref[b79]{[81]}. The life style and occupation of inhabitants of Tiko including the dusty, windy and hot nature, farming, bike riding and much more favours the acquisition of wounds b humans thus making the area suitable for this study. 
\section[{b) Study design and duration}]{b) Study design and duration}\par
This was a Laboratory based experimental study designed that was conducted from November 2022, to June 2023. 
\section[{c) Specimens and sampling}]{c) Specimens and sampling}\par
This study made use of bacteria isolates from people with bacteria wound infection in Tiko community. 
\section[{d) Ethical consideration}]{d) Ethical consideration}\par
An introductory letter was obtained from MAFLEKUMEN Higher Institute of Health Sciences TIKO (APPENDIX A) and was taken to regional delegation in Buea for the approval of the project. An administrative authorization was obtained from the regional delegation (APPENDIX B) and was presented to the administration of MAFLEKUMEN. An authorisation was gotten from the MAFLEKUMEN administration to carry out the research. 
\section[{e) Data collection and techniques i. Sample collection}]{e) Data collection and techniques i. Sample collection}\par
Bacterial isolates were obtained from Maflekumen diagnostic laboratory. Preparation of MacConkey agar, blood agar and EMB was done byweighing the powder using an electronic balance and dissolved in distilled water following the manufacturer's instructions and was cooked to obtain the gel using a Bunsen burner and allowed to cool to 40?C. The agar was poured into petri dishes and allowed to solidify. The samples were inoculated in the plate and read after 24hrs. Presumptive identification of bacteria was done based on colony characteristics, gram reactions were recorded. Confirmatory biochemical tests were done to confirm the bacteria. For staphylococcus aureus, and Klebsiella species respectively. 
\section[{ii. Catalase test}]{ii. Catalase test}\par
A drop of Hydrogen peroxide was placed on a slide and a colony of isolated bacteria picked and emulsified on the slide containing the hydrogen peroxide. The appearance of air bubbles indicate catalase positive. 
\section[{iii. Coagulase test}]{iii. Coagulase test}\par
A drop of normal saline was placed at both ends of the same slide, one labeled test and the other control. A colony of the isolated bacteria was emulsified on each drop of the normal saline. Serum was placed on the test path and emulsified and nothing was added on the control. The presence of coagulation indicates coagulase. 
\section[{iv. Indole test}]{iv. Indole test}\par
Test organism was inoculated in a bijou bottle containing 3 ml of sterile tryptone water. Incubate at 35-37 o C for up to 48 h. 0.5 ml of Kovac's reagent was added and shake gently, examination for a red color in the surface layer within 10 minutes macroscopically. 
\section[{v. Extraction of African panaxia (Alcohol, distilled water and luke warm water)}]{v. Extraction of African panaxia (Alcohol, distilled water and luke warm water)}\par
African panaxia was bought from the Moghamo express in Mutengene and transported to the laboratory for sensitivity testing on the bacteria isolates. One gram of African panaxia was weighted on an electric scale balance and put in a 250 ml flask, followed by adding 100 ml of solvent (95\% ethanol). The flask was then left at room temperature for two days preceding filtration funnel and Wattman No. 1 filter paper. The filtrate was concentrated under decreased pressure with an evaporator at 40°C. This crude extract was saved at 4°C until use, this extract of African panaxia was considered as the 100\% concentration for ethanol extract, different stock solution for distilled water were made equally and also for look warm water respectively. Then the concentrations (100\%, 75\%, 50\%, and 25\%) were made by diluting the concentrated extract of African panaxia with appropriate volumes of sterile distilled respectively for luke warm water. Serial dilutions were made to determine the minimum inhibitory, and bactericidal concentration respectively.\par
i. Different stock solutions of African panaxia were made (Absolute alcohol, luke warm water and distilled water, in which different volumes were used 100, 75, 50 and 25 in which the isolated species of bacteria were used to test for the minimum inhibitory concentration and minimum bactericidal concentration using dilution technique and absorbance was measured using a spectrophotometry machine at a wavelength of 660nm.\par
ii. A solution of the isolated bacteria was prepared and standardized by matching to the 0.5 McFarland turbidity standards using sterile saline to produce approximately 1.5×10 8 colony forming units per ml. iii. Serial dilutions were made on the different stock solutions of African panaxia using four sterile dry tubes per isolate and per stock solution respectively. iv. Two (2ml) of nutrient broth was placed in each sterile test tube, followed by adding 2ml of each stock solution in the first tube, mix well and transfer 2ml to the next tube continuously and to the fourth to remove 2ml and discard respectively 1drop of the bacterial suspension was place in each test tube respectively.\par
v. They labeled test tubes were sealed and incubated at 37 o C for 18 to 24hours in which the and minimum inhibitory concentration and minimum bactericidal concentration recorded by checking the turbidity of each tube and absorbance was measured using a spectrophotometer at 660nm following the control of the absorbance of 0.5 McFarland standard and Azithromycin.\par
f) Data analysis Data was analyzed using Microsoft excel and the results was presented in tables and figures III. 
\section[{Results and Discussion}]{Results and Discussion} 
\section[{a) Results}]{a) Results}\par
This chapter presents the results obtained from the effect of African panaxia on Staphylococcus and Klebsiella isolated from wounds. Based on extract with distilled water the concentration with 75\% and 50\% stocks were effective in inhibiting the growth of Staphylococcus and Klebsiella respectively. Also using a stock of 50\% and 25\%, it exhibited bactericidal properties on Staphylococcus and Klebsiella respectively as presented on figure 1 below.     \hyperref[b81]{[83]}. Also,  {\ref Mohammed et al., in 2019}, also revealed that the most common bacteria isolated from wounds were Staphylococcus aureus, and Klebsiella pneumonia \hyperref[b82]{[84]}. Also, these findings agree with other findings by \hyperref[b83]{Obi et al., in 2015} who reported that common bacteria isolates from the different types of wounds were Pseudomonas aeruginosa, Klebsiella pneumonia, Staphylococcus aureus, Enterococcus faecalis and Acinetobacter baumannii \hyperref[b83]{[85]}. 
\section[{To determine the minimum inhibitory concentration of African panaxiaon Staphylococcus aureus and Klebsiella pneumoniae from wound infections}]{To determine the minimum inhibitory concentration of African panaxiaon Staphylococcus aureus and Klebsiella pneumoniae from wound infections}\par
The minimum inhibitory concentrations were determined using extract from different concentrations such as distilled water, luke warm water and ethanoic extracts of the African panaxia. From the findings it was revealed that African panxia extracts of distilled water and luke warm water were more inhibitory at 75\%, 50\% stock respectively than Bactericidal. These findings are similar to results of Korukluoglu et al. in 2010 who reported that extraction of aqueous solvent resulted in a product with greater overall antimicrobial activity than extraction with water, as aqueous extracts of all the olive oil displayed little or no antimicrobial activity against any of the bacteria tested  {\ref [86]}. Similarly Weerakkody et al., (2010) \hyperref[b3]{[5]} observed that water extracts of oregano and rosemary had little or no antimicrobial activity compared to ethanol or hexane extracts. Again, Sofia et al., (2007) \hyperref[b4]{[6]} reported that water extracts of mustard, cinnamon, garlic and clove had good inhibitory activities against E. coli and S. aureus, 
\section[{To determine the minimum bactericidal concentration of African panaxia on Staphylococcus aureus and Klebsiella pneumoniae from wound infections}]{To determine the minimum bactericidal concentration of African panaxia on Staphylococcus aureus and Klebsiella pneumoniae from wound infections}\par
Comparing results found in this study with those of the literature, we notice in a previous work on antimicrobial activity of some medicinal plants from Tunisia, that methanolic extracts of C. monspeliensis leaves have shown an interesting activity against P. aeruginosa, S. aureus, E. faecalis with inhibition zones diameters of 18.0, 20.0 and 15.0 mm, respectively. \hyperref[b24]{26} Whereas, water-methanol extracts of fruit peels of pomegranate (P. granatum) have demonstrated a moderate activity when they were tested on S. aureus, P. aeruginosa and K. pneumoniae (13.0, 18.0 and 16.0 mm, respectively) \hyperref[b25]{[27]}.This activity of pomegranate peels could be attributed to tannins, for which antimicrobial activity has been demonstrated.  {\ref [4]} On the other hand, the results found in the study concerning the activity of R. tripartitaaerial parts extracts are in agreement with other previous works which found significant antibacterial activity of leaves alcoholic extracts against methicillin-resistant S. aureus, 16 and no activity against E. coli and P. aeruginosa. 29 For W. frutescens, El Bouzidi et al. have reported different antibacterial activities of leaves methanolic extracts against S. aureus(11.5 mm), K. pneumoniae (18.0 mm), P. fluorescens (14.5 mm) and no activity against E. coli.30 IV. 
\section[{Conclusion}]{Conclusion}\par
Based on the results obtained from the study, it could be concluded that the most common bacteria isolates obtained from this study were Staphylococcus aureus, Pseudomonas aeruginosa and Klebsiella pneumonae. African panaxia extract from distilled water was more inhibitory than bactriocidal on Staphylococcus aureus and Klebsiella pneumonia and the lastly the African panaxia extract from ethanol was totally bactericidal on both Staphylococcus aureus and Klebsiella pneumonae.\par
V. 
\section[{Recommendations}]{Recommendations}\par
From the results obtained from this study, the following recommendations can be made Ethanoic extract of African panaxia should be used on wounds infected with Klebsiella pneumonae and Staphylococcus aureus to obtain maximum success. Also other natural herbs should be used to determine their inhibitory and bactericidal properties on Klebsiella pneumonae and Staphylococcus aureus.  \begin{figure}[htbp]
\noindent\textbf{1} \par 
\begin{longtable}{P{0.5084821428571429\textwidth}P{0.30682397959183677\textwidth}P{0.014094387755102042\textwidth}P{0.0021683673469387755\textwidth}P{0.015178571428571427\textwidth}P{0.0032525510204081632\textwidth}}
Based on the inhibitory and bactericidal\tabcellsep \multicolumn{5}{l}{concentration on Klebsiella. Finally with alcoholic extract}\\
property of Africa panaxia on staphylococcus and\tabcellsep \multicolumn{5}{l}{of the African panaxia, the plant extract was bactericidal}\\
Klebsiella, of all the different concentrations made with\tabcellsep \multicolumn{5}{l}{at 95\% stock concentration on Staphylococcus and}\\
distilled water, at 25\% stock concentration, the extract of\tabcellsep \multicolumn{5}{l}{Klebsiella and bactericidal and bacteriostatic at 75\%}\\
African panaxia was both inhibitory and bactericidal on\tabcellsep stock\tabcellsep concentration\tabcellsep on\tabcellsep Staphylococcus\tabcellsep and\\
Staphylococcus and Klebsiella. African panaxia extract\tabcellsep \multicolumn{5}{l}{bacteriostatic on Klebsiella as presented on table 1}\\
with look warm water revealed that the extract was\tabcellsep below.\tabcellsep \tabcellsep \tabcellsep \tabcellsep \\
bactericidal at 50\% stock and 25\% stock concentration\tabcellsep \tabcellsep \tabcellsep \tabcellsep \tabcellsep \\
on Staphylococcus and bacteriostatic at 25\% stock\tabcellsep \tabcellsep \tabcellsep \tabcellsep \tabcellsep \end{longtable} \par
 
\caption{\label{tab_0}Table 1 :}\end{figure}
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\end{document}
