Preparation of wild-plant extract: The leaves of Juniperusprocera were collected and were classified from the Ranyah, KSA, at the flowering time. They were prepared to produce the boiling water extract according to the Saudi Arabian customs. Five grams of the leaves were simmered into two hundred and fifty mL of purified water. The boil water was filtered, the gradual dilution was made using distilled water to (1/4 crude, 1/2 crude, 3/4 crude, and 1 crude) 14

 Preparation of infectious-pathogens: They were obtained from the laboratory after diagnosis, isolation and identification. They were included wound causes (Staphylococcus sp., and Streptococcus sp.). Tonsillitis cause was Streptococcus pyogenes. Gastroenteritis causes were (Salmonella sp., and Shigella sp.). Urinary tract infection cause was Escherichia coli. Oral and vagina candidiasis causes were Candida albicans. Activation of them were by culturing on "Mueller Hinton Broth"; (Lab. M. Ltd., UK)for 18-24 hour at 35-37 oC. Theywere attuned to 106 Living cell / mL for exposure to wild-plant extract graduated dilutions 15.

Interaction to wild-plant extract: The microtitration plates were used for mixing the fixed infectious-pathogens suspensions and the wild-plant extract graduated dilutions. The microtitration plates were incubated at room temperature for the following times (overnight (12-18 hour), and one day) 16

Direct total cell count by "Bread Test": The degraded slide was used, a loop full was placed from each microtitration plate well. The film was fixed and was simple stained then was washed. The cells were counted in ten microscopic fields. The following laws were applied to calculate the number and percent of dead cells.

Number of dead cells / mL = *106 - (Mean cells in ten fields X *100 X *5000).

*106: Basic living cells / mL.

*100: Volume of one loop full.

*5000: Constant Standard Numbers.

Percent of dead cells = (Number of dead cells / *106) X 100. 17

Data analysis: The results were designed via "IBM Simple Statistics"; (IBM, Armonk, NY, United States) 18.

Number of dead cells / mL and percent of dead cells after interaction to wild-plant extract: Table (1 & 2) observed Juniperusprocera one crude concentration killed all infectious-pathogens during one day. Lower Juniperusprocera crude extract concentrations eliminated infectious-pathogens within more than one day. Only three Staphylococcus sp., Streptococcus sp, and Streptococcus pyogenes were eliminated by concentration of Juniperusprocera extract three quarters crude during one day 1234567.

The effects were different on the infectious-pathogens, the most affected were Staphylococcus sp., Streptococcus sp, and Streptococcus pyogenes. The mean number of dead sells / mL were (84.9 / mL, 87.0 / mL, and 77.8 / mL) respectively. The mean percentage of dead cells were (80.0%, 82.0%, and 73.4%) respectively. They were most affected by the Juniperusprocera extract at all concentrations were completely eliminated by concentration of three quarters of crude before other infectious-pathogens 891011.

The less affected were Salmonella sp., Shigella sp, also Escherichia coli. The mean number of dead sells / mL were (72.6 / mL, 76.1 / mL, and 79.0 / mL) respectively. The mean percent of dead cells were (68.5%, 71.8%, and 74.5%) respectively. They were less pretentious by the Juniperusprocera extract at all concentrations were completely eliminated by concentration of one crude 891011.

The more less affected was Candida albicans, the mean number of dead sells / mL was 69.3 / mL. The mean percent of dead cells was 65.4%. They were more less affected by the extract at all concentrations was completely eliminated by Juniperusprocera extract concentration of one crude 111213.

Through the results, were originated the concentrated extract was more powerful to eliminate all infectious-pathogens within one day. The lowest concentrated extract took more than one day to completely eliminate infectious-pathogens 891011. (Table 1) (Table 2).

Juniperusprocera is usual in the southwest of the KSA. The "Saudi Arabian Customs" use extract is still in line with "Ancient Arab Customs" to treat infectious-pathogens. That is for reducing use of medicines and decreasing the treatment costs 1234567.

However, it is necessary to healthy treated evaluate the extracts through the "Pharmacy Branch" for safe herbal therapeutic use. That is in order to rapidity recovery from infectious-pathogens and do not affect the patient’s health 1234567.