عنوان البحث(Papers / Research Title)
Antibiotic Susceptibility Pattern of Some Clinical Gram Positive Isolates
الناشر \ المحرر \ الكاتب (Author / Editor / Publisher)
ايمان محمد جار الله مسير
Citation Information
ايمان,محمد,جار,الله,مسير ,Antibiotic Susceptibility Pattern of Some Clinical Gram Positive Isolates , Time 21/01/2019 19:45:05 : كلية العلوم
وصف الابستركت (Abstract)
sientific research
الوصف الكامل (Full Abstract)
ISSN: 0975-8542 Journal of Global Pharma Technology Available Online at www.jgpt.co.in Research Paper ©2009-2017, JGPT. All Rights Reserved 262 Antibiotic Susceptibility Pattern of Some Clinical Gram Positive Isolates Ehsan F. Hussein1*, Eman M. Jarallah2 1 University of Sumer, Iraq. 2 University of Babylon, Iraq. *Corresponding Author: Ehsan F. Hussein (E mail: ehsan.algrani@yahoo.com) Abstract One hundred fifty samples have been collected through the period from July/2016 to December/2016. Were for isolation and identification of pathogenic gram positive bacteria. The samples were involved fifty samples from each skin, mouth and soil for isolate Staphylococcus aureus, Streptococcus pyogenes and Bacillus spp., respectively. Isolates were identified according to microscopic features and biochemical tests .Antibiotics susceptibility pattern were examined by disc diffusion method. The antibiotics explained different action modes and some of the have significant differences when comparisons together. The Trimethoprim antibiotic has high activity against Staph. aureus, and Strep. pyogenes while the Carbnicillin, Rifaxim in and Trimethoprim antibiotics have high activity against Bacillus spp. These antibiotics were Amoxicillin, Ampicillin, Trimethoprim, Aztreonam, Phamethoxazole, Carbnicillin, Novobiocin, Erythromycin, Rifaximin, Penicillin-G, Oxolinic Acid, Bacitracin and Clindamycin. Trimethoprim antibiotic has high activity when comparison the activity of these antibiotics together. Keywords: Pathogenic bacteria, Trimethoprim, Antibiotics, Resistant. Introduction The resistant in bacteria is occurring worldwide endangering the efficacy of antibiotics which have transformed medicines and save lives of millions [1]. Many reports showed that the after use of antibiotics in treated the first patient, the infections of bacteria become a threat again [2]. The causes of antibiotics resistance have been attributed to the misuse of these medications and overuse as well as a loss of development of new drug by the pharmaceutical industry caused by reduced challenging regulatory requirements and economic incentives [3]. Emergency of bacterial resistant threat the extraordinary health benefit that has been achieved with antibiotics treatment [4]. Staphylococcus is heterogeneous bacterial group and consists of thirty species but the Staphylococcus aurous is the most clinically important species [5]. This in the family of Staphylococcaceae, an important opportunistic pathogen and can causes infections for both human and animals [6]. Staph. aureus is gram positive with diameter 0.8-1 ?m, non-motile, non-speculated and non-capsulated [7]. Staphylococcus aurous was considered has over the past studies as one of the most important pathogens for human and leading to causes of community acquired infections and hospital [8]. Infections of staphylococcal associated with wide spectrum of diseases in humans [9]. This bacterium can colonize of the skin and mucous membrane and from which it have ability to invade other organs in body [10], and considered as an important causative agent for skin and soft tissue infections [10].In despite of, Staphylococcus infections can easily treated with antibiotics, but in recent years, this bacterium developed resist against most commonly used and effective antibiotics [11- 12]. Now, the methicillin resistant Staph. aurous (MRSA) has become prevalence problem in hospitals and wide range of acquired infections [13]. Furthermore, the multi drug Ehsan F. Hussein et. al.: Journal of Global Pharma Technology. 2017; 10(9):262-274 ©2009-2017, JGPT. All Rights Reserved 263 methicillin resistant Staph. aureus with very limited treatment choice also increased [14]. Streptococcus pyogenes the major causes pathogen and associated with acute respiratory tract infections [15]. This bacterium can cause several types of infections such as pharyngitis and pyoderma [16]. This microorganism have been distinguished as one of infectious agents that leading to puerperal fever in human and also contributing in the skin, ear, vagina and throat infections[17]. Invasive infections like streptococcal toxic shock syndrome and sepsis began to receive attention from epidemiologists and recently reported as higher incidence rates and even epidemics these bacteria [18]. The number of such infections associated with Streptococcus pyogenes especially in developed countries caused May by loses of diagnostic methods and therapeutic problem [19]. Increasing the resistance of antibiotics among Streptococcus pyogenes have been observed during the last decade in worldwide [20]. The increase in the rate of antibiotic resistant among clinical isolates of Streptococcus pyogenes, this contributes in the needs for continuous studies for known the patterns of antimicrobial resistance [21]. Species of Bacillus bacteria are spore forming, gram-positive and chemo heterotrophic bacilli which are usually aerobic or facultative anaerobic [22]. The members of these bacteria are generally found in soils and have abilities for grow in every environment as well as have capability to formation resistant spores and metabolite products [23]. Bacillus spp. is a gram positive rods bacteria usually found in soil [24]. These bacteria responsible for No socomial infections [25]. Also, the spores produced by Bacillus are frequently causes foods contamination which resulting in diseases like diarrhea and vomiting[26]. Bacillus spp. have ability to resistant several types of antibiotic [27]. However, there are limited information about antibiotics resistance by these bacteria [28]. Materials and Methods Isolation of Pathogenic Positive Bacteria One hundred fifty samples have been collected were for isolation of pathogenic gram positive bacteria. The samples were involve fifty skin samples for is oblate Staphylococcus aureus, fifty mouth samples for isolate Streptococcus pyogenes and fifty soil samples for Bacillus spp. Figure1: Number and percent of pathogenic gram positive isolated bacteria Figure (1) the number and percent of Staph. aurous isolated from Skin, Strep. Pyogenes isolated from Mouth and Bacillus spp. isolated from Soil were (20; 33%), (16; 27%) and (24; 40%) respectively. Identification of bacterial Isolates The isolates of Staph aureus were characterized and identified according to [29]. This done by use of microscope and biochemical tests such as gram staining, coagulates test and catalase test [9]. The isolates of Strep Pyogenes were identified and determined according to [30]. This carries out by use of microscope and biochemical tests such as gram staining, catalase test and blood agar hemolytic [31]. The isolates of Bacillus spp were isolated by use of serial diluted of soil samples in sterile distilled water and plated on nutrients agar media [32]. As well as descriptive and identified according to [33]. This worked by use of microscope and biochemical tests such as gram staining, catalase test, oxidase test and indol test [34]. Ehsan F. Hussein et. al.: Journal of Global Pharma Technology. 2017; 10(9):262-274 ©2009-2017, JGPT. All Rights Reserved 264 Antibiotic Susceptibility Test Antibiotic susceptibility tests for pathogenic gram positive bacteria were carried out by technique of disc diffusion method on Muller Hinton agar plates [35]. Statistical Analysis The results were analyzed by the Statistical Package Social Sciences (SPSS) version 20 for determine of Mean, Medium, Standard deviation and Standard error of mean, in addition the significance between antibiotics calculated according to One Way ANOVA by descriptive excluded cases analysis by analysis with LSD at (95%) confidence and significant level at (P=0.05). Figure 2: Inhibition zones formed by antibiotic types Results One hundred fifty samples have been collected were for isolation of pathogenic gram positive bacteria. This carries out through the period from July/2016 to December/2016. The samples were involve fifty skin samples of isolate Staphylococcus aureus, fifty mouth samples of isolate Streptococcus pyogenes and fifty soil samples of Bacillus spp. these isolated were characterized and identified by use of several type of biochemical tests as well as the antibiotics sensitivity and resistant were doing by use 13 types of antibiotics. These antibiotics have different modes of action as well as showed the Trimethoprim antibiotic has high activity against both Staphs. aureus and Strep. pyogenes while the Carbnicillin antibiotic has high activity against Bacillus spp. Also explained the Trimethoprim antibiotic has high activity when comparison the activity of these antibiotics together. Also the antibiotics have significant differences and their activity against the bacteria. Figure (2) the inhibition zones that formed by different types of antibiotics on Muller Hinton Agar after (24 h) against experimental pathogenic gram positive bacteria when cultured with antibiotics together on this medium. Table1: Replicates of inhibition zones formed by antibiotic types against Staph. aurous Inhibition zones replicates measured by (mm) CC 5 ?g B 10 ?g OA 2 ?g P 10 ?g R 40 ?g E 15 ?g NV 30 ?g PY 100 ?g SMZ 25 ?g ATM 30 ?g TMP 10 ?g AM 10 ?g AX 15 ?g Replicates/* 1 6 7 16 9 6 6 0 7 4 8 6 5 5 2 7 8 6 12 0 2 7 0 9 2 6 3 8 3 8 10 10 9 0 3 11 0 0 1 0 12 4 4 20 10 25 6 25 4 4 0 4 8 11 3 11 5 25 11 25 4 6 2 6 0 5 0 6 4 3 6 16 13 20 13 11 7 9 5 7 6 9 6 2 7 6 5 8 14 22 0 20 0 5 12 18 0 11 8 32 26 32 20 0 14 0 10 6 0 0 6 6 9 0 18 11 24 18 4 10 7 6 8 10 9 0 10 10 8 29 4 4 10 8 3 9 6 8 2 8 11 18 15 22 13 13 9 5 8 18 2 11 8 9 12 12 8 19 16 20 18 6 0 7 16 0 7 7 13 30 29 30 6 6 0 20 16 16 0 22 4 13 14 15 10 14 12 16 9 10 6 12 4 18 2 15 15 18 13 25 2 10 9 14 12 8 10 6 14 5 Mean 14.866 12.734 19.467 10.933 10.466 6.467 8.666 4.933 7.7334 5.533 8.734 5.666 7.133 Median 15.000 10.000 20.000 12.000 10.000 6.000 8.000 5.000 7.000 6.000 8.000 5.000 7.000 9.226 6.861 8.339 6.158 8.279 5.139 5.961 5.119 4.667 4.853 6.649 3.848 4.189 Std. Deviation 2.382 1.771 2.153 1.591 2.137 1.326 1.538 1.321 1.205 1.253 1.716 0.993 1.081 Std. Error of Mean Ehsan F. Hussein et. al.: Journal of Global Pharma Technology. 2017; 10(9):262-274 ©2009-2017, JGPT. All Rights Reserved 265 Table (1) the Mean, Median, Standard deviation and Standard error for replicates of inhibition zones were measured by (mm) of each antibiotics against Staph. aurous bacteria and found the Trimethoprim antibiotic has high activity (19.467 mm) while the (Erythromycin) antibiotic has low activity (4.933mm) against this bacterium by measured of mean. ? *AX 15=Amoxicillin15 *E 15= Erythromycin15 ? *AM 10= Ampicillin10 *R 40=Rifaximin40 ? *TMP 10= Trimethoprim10 *P 10=Penicillin-G10 ? *ATM 30= Aztreonam30 *OA 2= Oxolinic Acid2 ? *SMZ 25= Phamethoxazole25 *B 10=Bacitracin10 ? *PY 100= Carbnicillin100 *CC 5= Clindamycin5 ? *NV 30=Novobiocin3 Table2: LSD system for study of significant differences between of antibiotic types against Staph. aurous Significantly results according to LSD system at P-Value= 0.05 Y side / X side (antibiotics) AX15 ?g AM10 ?g TMP10 ?g ATM30 ?g SMZ25 ?g PY100 ?g NV30 ?g E 15 ?g R 40 ?g P 10 ?g OA 2 ?g B 10 ?g CC 5 ?g AX15 ?g Sig. 0.356 0.048* 0.090 0.058 0.001* 0.008* 0.001* 0.002* 0.001* 0.009* 0.001* 0.001* M.D. ** -2.133 4.601 -3.933 -4.401 -8.401 -6.201 -9.933 -7.133 -9.333 -6.133 -9.201 -7.733 AM10 ?g Sig. 0.356 0.004* 0.436 0.327 0.007* 0.079 0.001* 0.031* 0.002* 0.048* 0.003* 0.016* M.D. ** 2.133 6.733 -1.801 -2.266 -6.266 -4.066 -7.801 -5.001 -7.201 -4.001 -7.066 -5.601 TMP10 ?g Sig. 0.048* 0.004* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* M.D. ** -4.601 -6.733 -8.533 -9.001 -13.001 -10.801 -14.533 -11.733 -13.933 -10.733 -13.801 -12.333 ATM30 ?g Sig. 0.090 0.436 0.001* 0.840 0.054 0.327 0.001* 0.167 0.001* 0.341 0.001* 0.101 M.D. ** 3.933 1.801 8.533 -0.466 -4.466 -2.266 -6.001 -3.201 -5.401 -2.201 -5.266 -3.801 SMZ25 ?g Sig. 0.058 0.327 0.001* 0.840 0.084 0.436 0.001* 0.237 0.034* 0.453 0.039* 0.150 M.D. ** 4.401 2.266 9.001 0.466 -4.001 -1.801 -5.533 -2.733 -4.933 -1.733 -4.801 -3.333 PY100 ?g Sig. 0.001* 0.007* 0.001* 0.054 0.084 0.341 0.507 0.583 0.686 0.327 0.729 0.773 M.D. ** 8.401 6.266 13.001 4.466 4.001 2.201 -1.533 1.266 0.933 2.266 -0.801 0.666 NV30 ?g Sig. 0.008* 0.079 0.001* 0.327 0.436 0.341 0.107 0.686 0.176 0.977 0.195 0.507 M.D. ** 6.201 4.066 10.801 2.266 1.801 -2.201 -3.733 -0.933 -3.133 0.066 -3.001 -1.533 E15 ?g Sig. 0.001* 0.001* 0.001* 0.001* 0.001* 0.507 0.107 0.226 0.795 0.101 0.751 0.341 M.D. ** 9.933 7.801 14.533 6.001 5.533 1.533 3.733 2.801 0.601 3.801 0.733 2.201 R40 ?g Sig. 0.002* 0.031* 0.001* 0.167 0.237 0.583 0.686 0.226 0.341 0.665 0.371 0.795 M.D. ** 7.133 5.001 11.733 3.201 2.733 -1.266 0.933 -2.801 -2.201 1.001 -2.066 -0.601 P10 ?g Sig. 0.001* 0.002* 0.001* 0.001* 0.034* 0.686 0.176 0.795 0.341 0.167 0.954 0.489 M.D. ** 9.333 7.201 13.933 5.401 4.933 0.933 3.133 -0.601 2.201 3.201 0.133 1.601 OA2 ?g Sig. 0.009* 0.048* 0.001* 0.341 0.453 0.327 0.977 0.101 0.665 0.167 0.185 0.489 M.D. ** 6.133 4.001 10.733 2.201 1.733 -2.266 -0.066 -3.801 -1.001 -3.201 -3.066 -1.601 B10 ?g Sig. 0.001* 0.003* 0.001* 0.001* 0.039* 0.729 0.195 0.751 0.371 0.954 0.185 0.525 M.D. ** 9.201 7.066 13.801 5.266 4.801 0.801 3.001 -0.733 2.066 -0.133 3.066 1.466 CC5 ?g Sig. 0.001* 0.016* 0.001* 0.101 0.150 0.773 0.507 0.341 0.795 0.489 0.489 0.525 M.D. ** 7.733 5.601 12.333 3.801 3.333 -0.666 1.533 -2.201 0.601 -1.601 1.601 -1.466 *Significant differences of mean at the p-valve equal to 0.05 level **Differences of Mean Table (2) the significant differences between types of different antibiotics when study the activities of these antibiotics against Staph. aurous by statistical analysis by used of LSD system.Also explained the significant differences that found between used antibiotics and this showed through the star that present at p-valve equal to 0.05 levels.Not all antibiotics that studied have significant differences through comparison together, some of these antibiotics have significant differences and this showed through the star that found at p-valve equal to 0.05 levels. Comparisons involved two types. First, involve the (X) side antibiotics with the (Y) side antibiotics and second involved comparison the (Y) side antibiotics with the (X) side antibiotics. Figure 3: Action modes of antibiotic types against Staph. aurous Ehsan F. Hussein et. al.: Journal of Global Pharma Technology. 2017; 10(9):262-274 ©2009-2017, JGPT. All Rights Reserved 266 Figure (3) the types of antibiotics give different action modes, this mean each antibiotic explained inhibition zones with different size against same bacteria at fifteen replicates, as well as (AX 15 & TMP 10) antibiotics have high inhibition zones were (32 mm). Figure4: Percent of antibiotic types against Staph. aureus Figure (4) action percentages of different types of antibiotic; also showed (TMP 10) antibiotics has high percent equal to 16% as well as the (E 15) antibiotic has low percent equal to 4% from all activities of antibiotics against Staph. aureus. Table3: Replicates of inhibition zones formed by antibiotic types against Strep. pyogenes Inhibition zones replicates measured by (mm) CC 5 ?g B 10 ?g OA 2 ?g P 10 ?g R 40 ?g E 15 ?g NV 30 ?g PY 100 ?g SMZ 25 ?g ATM 30 ?g TMP 10 ?g AM 10 ?g AX 15 ?g Replicates/* 1 0 7 16 10 10 3 16 4 6 0 0 0 3 2 6 4 18 12 8 4 15 0 7 5 3 10 0 3 12 0 10 7 12 5 18 10 10 6 0 0 5 4 5 8 25 10 13 7 13 3 6 5 3 2 8 5 0 9 25 12 7 2 14 0 9 8 0 0 9 6 5 3 24 22 16 9 17 3 6 4 3 3 6 7 4 9 23 16 11 4 19 2 11 9 2 8 4 8 10 2 20 12 10 5 12 10 5 7 7 2 5 9 3 10 19 9 8 0 15 6 4 4 2 5 4 10 9 2 20 14 12 7 13 2 3 2 1 3 2 11 5 7 24 15 16 10 20 8 13 10 5 7 3 12 11 4 28 12 18 5 18 4 0 2 4 5 6 13 8 8 24 11 20 7 23 2 8 5 3 3 0 14 4 0 20 18 14 3 15 3 9 3 6 4 4 15 7 4 21 20 12 2 19 4 3 6 2 0 12 Mean 5.934 5.133 21.134 13.333 12.467 4.866 16.467 4.066 6.667 5.066 2.734 3.466 4.733 Median 5.000 4.000 21.000 12.000 12.000 5.000 16.000 3.000 6.000 5.000 3.000 3.000 4.000 Std. Deviation 3.614 3.356 4.421 4.186 3.777 2.748 3.044 3.151 3.436 2.737 2.121 3.217 3.217 Std. Error of 0.334 0.866 1.141 1.081 0.975 0.709 0.785 0.813 0.887 0.706 0.546 0.798 0.831 Mean Table (3) the Mean, Median, Standard deviation and Standard error for replicates of inhibition zones were measured by (mm) for each antibiotics against Strep. pyogenes bacteria. And found the Trimethoprim antibiotic has high activity (21.134 mm) while 0.00% 5.00% 10.00% 15.00% 20.00% CC 5?g B 10?g OA 2?g P 10 ?g R 40?g E 15?g NV 30?g PY 100?g SMZ 25?g ATM 30?g TMP 10?g AM 10?g Staph. aureus AX 15?g Ehsan F. Hussein et. al.: Journal of Global Pharma Technology. 2017; 10(9):262-274 ©2009-2017, JGPT. All Rights Reserved 267 the (Oxolinic Acid) antibiotic has low activity (2.734mm) against this bacterium by measured of mean. ? *AX 15=Amoxicillin15 *E 15= Erythromycin15 ? *AM 10= Ampicillin10 *R 40=Rifaximin40 ? *TMP 10= Trimethoprim10 *P 10=Penicillin-G10 ? *ATM 30= Aztreonam30 *OA 2= Oxolinic Acid2 ? *SMZ 25= Phamethoxazole25 *B 10=Bacitracin10 ? *PY 100= Carbnicillin100 *CC 5= Clindamycin5 ? *NV 30=Novobiocin3 Table 4: LSD system for study of significant differences between of antibiotic types against Strep pyogenes Significantly results according to LSD system at P-Value= 0.05 Y side / X side (antibiotics) AX15 ?g AM10 ?g TMP10 ?g ATM30 ?g SMZ25 ?g PY100 ?g NV30 ?g E 15 ?g R 40 ?g P 10 ?g OA 2 ?g B 10 ?g CC 5 ?g AX15 ?g Sig. 0.514 0.001* 0.001* 0.001* 0.385 0.001* 0.129 0.550 0.480 0.011* 0.045* 0.328 M.D. ** -0.801 15.201 7.4001 6.533 -1.066 10.533 -1.866 0.733 -0.866 -3.201 -2.466 -1.201 AM10 ?g Sig. 0.514 0.001* 0.001* 0.001* 0.828 0.001* 0.385 0.212 0.957 0.051 0.175 0.744 M.D. ** 0.801 16.001 8.201 7.333 -0.266 11.333 -1.066 1.533 -0.066 -2.401 -1.666 -0.401 TMP10 ?g Sig. 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* M.D. ** -15.201 -16.001 -7.801 -8.666 -16.266 -4.666 -17.066 -14.466 -16.066 -18.401 -17.666 -16.401 ATM30 ?g Sig. 0.001* 0.001* 0.001* 0.480 0.001* 0.011* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* M.D. ** -7.401 -8.201 7.801 -0.866 -8.466 3.133 -9.266 -6.666 -8.266 -10.601 -9.866 -8.601 SMZ25 ?g Sig. 0.001* 0.001* 0.001* 0.480 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* M.D. ** -6.533 -7.333 8.666 0.866 -7.601 4.001 -8.401 -5.801 -7.401 -9.733 -9.001 -7.733 PY100 ?g Sig. 0.385 0.828 0.001* 0.001* 0.001* 0.001* 0.514 0.143 0.870 0.083 0.254 0.913 M.D. ** 1.066 0.266 16.266 8.466 7.601 11.601 -0.801 1.801 0.201 -2.133 -1.401 -0.133 NV30 ?g Sig. 0.001* 0.001* 0.001* 0.011* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* 0.001* M.D. ** -10.533 -11.333 4.666 -3.133 -4.001 -11.601 -12.401 -9.801 -11.401 -13.733 -13.001 -11.733 E15 ?g Sig. 0.129 0.385 0.001* 0.001* 0.001* 0.514 0.001* 0.035* 0.415 0.278 0.625 0.587 M.D. ** 1.866 1.066 17.066 9.266 8.401 0.801 12.401 2.601 1.001 -1.333 -0.600 0.666 R40 ?g Sig. 0.550 0.212 0.001* 0.001* 0.001* 0.143 0.001* 0.035* 0.193 0.002* 0.011* 0.116 M.D. ** -0.733 -1.533 14.466 6.666 5.801 -1.801 9.801 -2.601 -1.601 -3.933 -3.201 -1.933 P10 ?g Sig. 0.480 0.957 0.001* 0.001* 0.001* 0.870 0.001* 0.415 0.193 0.058 0.193 0.786 M.D. ** 0.866 0.066 16.066 8.266 7.401 -0.201 11.401 -1.001 1.601 -2.333 -1.601 -0.333 OA2 ?g Sig. 0.011* 0.051 0.001* 0.001* 0.001* 0.083 0.001* 0.278 0.002* 0.058 0.550 0.104 M.D. ** 3.201 2.401 18.401 10.601 9.733 2.133 13.733 1.333 3.933 2.333 -0.733 -0.551 B10 ?g Sig. 0.045* 0.175 0.001* 0.001* 0.001* 0.254 0.001* 0.625 0.011* 0.193 0.550 0.302 M.D. ** 2.466 1.666 17.666 9.866 9.001 1.401 13.001 0.600 3.201 1.601 -0.733 1.266 CC5 ?g Sig. 0.328 0.744 0.001* 0.001* 0.001* 0.913 0.001* 0.587 0.116 0.786 0.104 0.302 M.D. ** 1.201 0.401 16.401 8.601 7.733 0.133 11.733 -0.666 1.933 0.333 0.551 -1.266 *Significant differences of mean at the p-valve equal to 0.05 level **Differences of Mean Table (4) the significant differences between types of different antibiotics when study the activities of these antibiotics against Strep. pyogenes by statistical analysis by used of LSD system. Also explained the significant differences that found between used antibiotics and this showed through the star that present at pvalve equal to 0.05 levels. Not all antibiotics that studied have significant differences through comparison together, some of these antibiotics have significant differences and this showed through the star that found at pvalve equal to 0.05 levels. Comparisons involved two types. First, involve the (X) side antibiotics with the (Y) side antibiotics and second involved comparison the (Y) side antibiotics with the (X) side antibiotics. Figure 5: Action modes of antibiotic types against Strep. Pyogenes Ehsan F. Hussein et. al.: Journal of Global Pharma Technology. 2017; 10(9):262-274 ©2009-2017, JGPT. All Rights Reserved 268 Figure (5) the types of antibiotics give differentiation modes, this mean each antibiotic explained inhibition zones with different size against same bacteria at fifteen replicates, as well as (TMP 10) antibiotics has high inhibition zone was (28 mm). Figure 6: Percent of antibiotic types against Strep. Pyogenes Figure (6) action percentages of different types of antibiotic; also showed (TMP 10) antibiotics has high percent equal to 20% as well as the (OA 2) antibiotic has low percent equal to 3% from all activities of antibiotics against Strep. pyogenes. Table 5: Replicates of inhibition zones formed by antibiotic types against Bacillus spp Inhibition zones replicates measured by (mm) CC 5 ?g B 10 ?g OA 2 ?g P 10 ?g R 40 ?g E 15 ?g NV 30 ?g PY 100 ?g SMZ 25 ?g ATM 30 ?g TMP 10 ?g AM 10 ?g AX 15 ?g Replicates/* 1 4 7 7 3 8 12 5 5 10 8 4 3 0 2 12 3 17 0 3 13 4 9 8 8 13 5 3 3 6 7 8 6 9 7 3 8 6 13 6 4 0 4 13 6 2 0 4 10 3 5 12 5 9 5 2 5 5 5 5 11 3 8 8 15 9 13 10 0 4 6 8 0 13 5 6 12 0 7 10 8 8 6 5 7 16 6 16 4 4 14 4 6 12 6 16 4 3 8 10 7 15 7 6 19 11 10 16 6 10 8 7 9 6 6 8 6 8 9 5 6 14 15 6 9 2 10 6 8 7 9 5 18 4 7 9 6 7 3 8 11 3 9 11 5 5 13 6 9 13 7 10 8 6 12 8 6 8 4 12 6 6 5 11 11 8 5 5 13 12 10 15 7 5 20 6 0 15 6 15 6 5 14 9 13 11 0 2 10 8 8 7 9 9 0 8 15 0 5 9 6 9 16 4 7 18 4 8 8 9 Mean 7.866 6.533 10.134 4.866 5.933 12.467 5.133 7.134 11.333 8.334 9.266 4.933 4.466 Median 8.000 6.000 9.000 5.000 5.000 12.000 5.000 7.000 11.000 8.000 9.000 5.000 5.000 Std. Deviation 4.241 2.972 4.356 3.204 2.763 4.323 2.587 3.226 3.415 3.265 3.305 3.326 2.825 1.064 0.767 1.124 0.827 0.713 1.116 0.668 0.883 0.881 0.843 0.858 0.853 0.792 Std. Error of Mean Table (5) the Mean, Median, Standard deviation and Standard error for replicates of inhibition zones were measured by (mm) for each antibiotics against Bacillus spp. bacteria. And found the Carbnicillin has high activity was (12.467mm) while the Clindamycin antibiotics have low activity 0.00% 5.00% 10.00% 15.00% 20.00% 25.00% CC 5?g B 10?g OA 2?g P 10 ?g R 40?g E 15?g NV 30?g PY 100?g SMZ 25?g ATM 30?g TMP 10?g AM 10?g Strep. pyogenes AX 15?g Ehsan F. Hussein et. al.: Journal of Global Pharma Technology. 2017; 10(9):262-274 ©2009-2017, JGPT. All Rights Reserved 269 (4.466mm) against this bacterium by measured of mean. ? *AX 15=Amoxicillin15 *E 15= Erythromycin15 ? *AM 10= Ampicillin10 *R 40=Rifaximin40 ? *TMP 10= Trimethoprim10 *P 10=Penicillin-G10 ? *ATM 30= Aztreonam30 *OA 2= Oxolinic Acid2 ? *SMZ 25= Phamethoxazole25 *B 10=Bacitracin10 ? *PY 100= Carbnicillin100 *CC 5= Clindamycin5 ? *NV 30=Novobiocin3 Table 6: LSD system for study of significant differences between of antibiotic types against Bacillus spp Significantly results according to LSDsystem at P-Value= 0.05 Y side / X side (antibiotics) AX15 ?g AM10 ?g TMP10 ?g ATM30 ?g SMZ25 ?g PY100 ?g NV30 ?g E 15 ?g R 40 ?g P 10 ?g OA 2 ?g B 10 ?g CC 5 ?g AX15 ?g Sig. 0.287 0.071 0.017* 0.123 0.001* 0.031* 0.557 0.006* 0.709 0.263 0.021* 0.007* M.D. ** -1.333 2.266 -3.001 -1.933 4.601 -2.733 -0.733 3.466 0.466 1.400 -2.933 -3.401 AM10 ?g Sig. 0.287 0.004* 0.183 0.631 0.001* 0.263 0.631 0.001* 0.151 0.030* 0.201 0.099 M.D. ** 1.333 3.601 -1.666 0.601 5.933 -1.401 0.601 4.801 1.801 2.733 -1.601 -2.066 TMP10 ?g Sig. 0.071 0.004* 0.001* 0.001* 0.063 0.001* 0.017* 0.337 0.151 0.488 0.001* 0.001* M.D. ** -2.266 -3.601 -5.266 -4.201 2.333 -5.001 -3.001 1.201 -1.801 -0.866 -5.201 -5.666 ATM30 ?g Sig. 0.017* 0.183 0.001* 0.394 0.001* 0.831 0.071 0.001* 0.006* 0.001* 0.957 0.749 M.D. ** 3.001 1.666 5.266 1.066 7.601 0.266 2.266 6.466 3.466 4.401 0.066 -0.401 SMZ25 ?g Sig. 0.123 0.631 0.001* 0.394 0.001* 0.522 0.337 0.001* 0.056 0.008* 0.424 0.241 M.D. ** 1.933 0.601 4.201 -1.066 6.533 -0.801 1.201 5.401 2.401 3.333 -1.001 -1.466 PY100 ?g Sig. 0.001* 0.001* 0.063 0.001* 0.001* 0.001* 0.001* 0.365* 0.001* 0.001* 0.001* 0.001* M.D. ** -4.601 -5.933 -2.333 -7.601 -6.533 7.333 5.333 -1.133 -4.133 -3.201 -7.533 -8.001 NV30 ?g Sig. 0.031* 0.263 0.001* 0.831 0.522 0.001* 0.111 0.001* 0.011* 0.001* 0.873 0.594 M.D. ** 2.733 1.401 5.001 -0.266 0.801 7.333 2.001 6.201 3.201 4.133 -0.201 -0.666 E15 ?g Sig. 0.557 0.631 0.017* 0.071 0.337 0.001* 0.111 0.001* 0.337 0.089 0.080 0.034* M.D. ** 0.733 -0.601 3.001 -2.266 1.201 -5.333 -2.001 4.201 1.201 2.133 -2.201 -2.666 R40 ?g Sig. 0.006* 0.001* 0.337 0.001* 0.001* 0.365* 0.001* 0.001* 0.017* 0.099 0.001* 0.001* M.D. ** -3.466 -4.801 -1.201 -6.466 -5.401 1.133 -6.201 -4.201 -3.001 -2.066 -6.401 -6.866 P10 ?g Sig. 0.709 0.151 0.151 0.006* 0.056 0.001* 0.011* 0.337 0.017* 0.455 0.007* 0.002* M.D. ** -0.466 -1.801 1.801 -3.466 -2.401 4.133 -3.201 -1.201 3.001 0.933 -3.401 -3.866 OA2 ?g Sig. 0.263 0.030* 0.488 0.001* 0.008* 0.001* 0.001* 0.089 0.099 0.455 0.001* 0.001* M.D. ** -1.400 -2.733 0.866 -4.401 -3.333 3.201 -4.133 -2.133 2.066 -0.933 -4.333 -4.801 B10 ?g Sig. 0.021* 0.201 0.001* 0.957 0.424 0.001* 0.873 0.080 0.001* 0.007* 0.001* 0.709 M.D. ** 2.933 1.601 5.201 -0.066 1.001 7.533 0.201 2.201 6.401 3.401 4.333 -0.466 CC5 ?g Sig. 0.007* 0.099 0.001* 0.749 0.241 0.001* 0.594 0.034* 0.001* 0.002* 0.001* 0.709 M.D. ** 3.401 2.066 5.666 0.401 1.466 8.001 0.666 2.666 6.866 3.866 4.801 0.466 *Significant differences of mean at the p-valve equal to 0.05 level **Differences of Mean Table (6) the significant differences between types of different antibiotics when study the activities of these antibiotics against Bacillus spp. By statistical analysis by used of LSD system. Also explained the significant differences that found between used antibiotics and this showed through the star that present at pvalve equal to 0.05 levels. Not all antibiotics that studied have significant differences through comparison together, some of these antibiotics have significant differences and this showed through the star that found at p-valve equal to 0.05 levels. Comparisons involved two types. First, involve the (X) side antibiotics with the (Y) side antibiotics and second involved comparison the (Y) side antibiotics with the (X) side antibiotics. Figure7: Action modes of antibiotic types against Bacillus spp Ehsan F. Hussein et. al.: Journal of Global Pharma Technology. 2017; 10(9):262-274 ©2009-2017, JGPT. All Rights Reserved 270 Figure (7) the types of antibiotics give differentiation modes, this mean each antibiotic explained inhibition zones with different size against same bacteria at fifteen replicates, as well as (PY 100) antibiotics has high inhibition zone was (20 mm). Figure 8: Percent of antibiotic types against Bacillus spp Figure (8) action percentages of different types of antibiotic; also showed (PY 100) antibiotics has high percent equal to 13% as well as the (CC 5) antibiotic has low percent equal to 5% from all activities of antibiotics against Bacillus spp. Figure 9: Comparisons between all antibiotics means against pathogenic positive bacteria Figure (9) the Trimethoprim antibiotic has high activity when comparison the activity of the all antibiotic types against pathogenic gram positive bacteria. Discussion In this study the trimethoprim antibiotic has high activity against Staphylococcus aurous (Table: 1 and Figure: 4). These were agreed with the Kaka et al who found this antibiotic has bactericidal activity against these bacteria [36]. While dis agreed with Tiwar et al who presented some isolate of this bacteria were resistant to trimethoprim [37]. The current study explained the erythromycin antibiotic has low activity against Staph. aureus (Table: 1 and Figure: 4). These were agreed with Brown who found the isolate of this bacteria were resistant to this antibiotic [38]. Staphylococcus aureus is the major causes of acquired infections in hospital and demonstrated this pathogen in community acquired infection [39]. These bacteria now have capacity to resistant most antibiotic types [40]. In the present study the trimethoprim antibiotic has high activity against Streptococcus Pyogenes (Table:3 and Figure:6). These results were agreed with Bowen et al who found these bacteria were Susceptible to this antibiotic [41]. But dis agreed with study of Bergmann who found these bacteria were resistant to this antibiotic [42]. And with Dangwetngam et al who found this antibiotic has no activity but against Streptococcus agalactiae [43]. The 0.00% 5.00% 10.00% 15.00% CC 5?g B 10?g OA 2?g P 10 ?g R 40?g E 15?g NV 30?g PY 100?g SMZ 25?g ATM 30?g TMP 10?g AM 10?g Bacillus spp. AX 15?g Ehsan F. Hussein et. al.: Journal of Global Pharma Technology. 2017; 10(9):262-274 ©2009-2017, JGPT. All Rights Reserved 271 current study showed the Oxolinic acid antibiotic has low activity against Strep. pyogenes. These were agreed with Matsuoka and Wada who found this antibiotic has low activity but against Streptococcus iniae [44]. Also agreed with Dangwetngamet al but against the Streptococcus agalactiae [43]. Streptococcus pyogenes can causes infection and has ability for large number of diseases [16]. Also this bacteria can resistant wide range of antibiotic types [15]. In the current study the Carbnicillin antibiotic has high activity against Bacillus spp. (Table:5 andFigure:8). These results were agreed with Naik et al who found the isolates of B. cereus were sensitive to this antibiotic, but dis agreed with Naik et al who found the isolate of B. subtilis were resistant to this antibiotic[45]. In the current study showed the Clindamycin antibiotic has low activity against Bacillus spp. This was agreed with Kervick et al who explained the isolates of Bacillus spp. were resistant to Clindamycin [46]. However, Bacillus spp. are the widely distributed in soil and have ability to resistant of essential antibiotics [47]. In addition, these bacteria can causes and associated with several types of infections [48]. Figures (2, 3, 5, and 7) showed the antibiotic types in current study have different action modes. These differences may cause by types of antibiotics that used and types of bacteria under study as well as type of antibiotics targets, however, some type of antibiotics act by destroyed the nucleic acids DNA and/or RNA, inactive protein synthesis, cell wall breaking, cell wall destroyed and stopped of essential path ways [49]. Antibiotics can be classified to whether they induce death of cell called bactericidal antibiotics or inhibit growth of cell called bacteriostatic antibiotics [50]. Also, this depended on mechanisms of antimicrobial resistance such as, multi antibiotic efflux pumps, antibiotic modified or breakdown enzymes and change or invisible of antibiotic targeting [51]. Figure (9) explained the trimethoprim antibiotic has high activity when comparison the activity of all antibiotic types together. Trimethoprim has activity against wide range of gram positive aerobic bacteria and comparable in efficacy with ampicillin, oxolinic acid and cephalexin [52]. 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