<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJPathology</journal-id><journal-title-group><journal-title>Open Journal of Pathology</journal-title></journal-title-group><issn pub-type="epub">2164-6775</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojpathology.2019.92003</article-id><article-id pub-id-type="publisher-id">OJPathology-91590</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Prevalence of Different Types of Micro-Organisms and Levels of Complement C5a in Patients with Acute-Phase Wound Infections
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mohemid</surname><given-names>M. Al-Jebouri</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Balsam</surname><given-names>Yahya R. Al-Mahmood</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Microbiology, College of Veterinary Medicine, University of Mosul, Mosul, Iraq</addr-line></aff><aff id="aff1"><addr-line>Department of Microbiology, College of Medicine, University of Tikrit, Tikrit, Iraq</addr-line></aff><pub-date pub-type="epub"><day>03</day><month>04</month><year>2019</year></pub-date><volume>09</volume><issue>02</issue><fpage>19</fpage><lpage>28</lpage><history><date date-type="received"><day>28,</day>	<month>January</month>	<year>2019</year></date><date date-type="rev-recd"><day>31,</day>	<month>March</month>	<year>2019</year>	</date><date date-type="accepted"><day>3,</day>	<month>April</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Background: An acute wound infection might be caused by external damage to the skin including abrasions, lacerations, bites, burns, accidents, war injuries and surgical incisions. When a wound fails to heal within a week, it should be considered a chronic type. Complement system potent inflammatory cascade in wound infection, is important and altered wound healing. Complement activation leads to the generation of many potent effectors including anaphylatoxin C5a. C5a has induced synthesis of TNF-
  <em>α</em> and IL-1
  <em>β</em> in macrophage and monocyte which are all together the goal of the present paper. 
  Methodology: This study was conducted in Al-Kindy and Al-Wasity hospitals in Baghdad on 200 patients suffering from wounds. One hundred patients were with acute wounds infection and the other 100 patients considered as control wounds
  <em> i.e.</em> without infection. The procedure method was followed according to manufacturer’s instructions (Elabscience, USA) utilizing C5a ELISA kit for conducting the test. Blood samples were taken at 24, 48, 72, 96 and 120 hours of hospitalization of the patients. 
  Results: It was found that the highest concentration of C5a was found at 120 hours after patients hospitalization who were with wound infection, and the mean value of C5a was 4898 pg/ml. 4661 pg/ml of C5a was recorded among patients with acute-phase infection compared to 4387 pg/ml concentration of the same complement among control group without wound infection at 96 hours post residence in hospital. 
  Conclusions: Gram-positive bacteria were more prevalent causing wound infections. 
  <em>Dermacoccus nishinomiyaensis</em>, 
  <em>Kocuria rosea</em> and 
  <em>Kocuria kristinae</em> were isolated for the first time in this locality. A complement 5a (C5a) revealed a very high concentration in acute-phase of wound infections. It was found that C5a was serially elevated with time of hospitalization of wounded and infected patients. C5a was highly elevated with wound infection by Gram-negative bacteria compared to infections by Gram-negatives.
 
</p></abstract><kwd-group><kwd>Acute-Phase Wounds</kwd><kwd> Complement 5a</kwd><kwd> Patients</kwd><kwd> Iraq</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Wound infection is invasive with pathogen to a level that invokes local and systemic response host. Presence of pathogen causes delayed wound healing. Bacteria are one of the most important pathogens contaminated wound and cause infection [<xref ref-type="bibr" rid="scirp.91590-ref1">1</xref>] . The wounds are commonly colonized by Staphylococcus aureus within the first week and later by Pseudomonas aeruginosa and other Enterobacteriaceae like Escherichia coli, Klebsiella sp, and Proteus mirabilis. All these events usually lead to stimulation of innate immune system and play a role in acute inflammation [<xref ref-type="bibr" rid="scirp.91590-ref2">2</xref>] . Complement system potent inflammatory cascade in wound infection, is important and altered wound healing [<xref ref-type="bibr" rid="scirp.91590-ref3">3</xref>] . Complement activation leads to the generation of many potent effectors including anaphylatoxin C5a [<xref ref-type="bibr" rid="scirp.91590-ref4">4</xref>] , which is important for leukocyte recruitment and activation [<xref ref-type="bibr" rid="scirp.91590-ref5">5</xref>] . The activity of the anaphylatoxins is regulated by carboxypeptidase N which is present in tissues [<xref ref-type="bibr" rid="scirp.91590-ref6">6</xref>] . C5a has induced synthesis of TNF-α and IL-1β in macrophage and monocyte [<xref ref-type="bibr" rid="scirp.91590-ref7">7</xref>] . Thrombin and plasmin resulted in release of C5a and C3a possessed significant chemotactic activity for neutrophils in inflammatory pathway [<xref ref-type="bibr" rid="scirp.91590-ref8">8</xref>] . C5a is playing a role as Chemoattractant of macrophage and neutrophil to the site of inflammation, also induces increase oxidative burst, phagocytosis and release of granule enzyme. Allergy inducing C5a and production of huge amounts of histamine will lead to dilatation of blood vessels to facilitate passage of large size and number of leucocytes toward site of infection.</p><p>Among activation of C5 to generation of the C5a thereby assembly of membrane attack complex given prominent the role of C5a in septic patients [<xref ref-type="bibr" rid="scirp.91590-ref9">9</xref>] .</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Patients</title><p>The study was conducted at AL-Wasity and AL-Kindy hospitals of Baghdad city from December 2017 to August 2018. The number of patients was 100 Patients who were with infected wound due to sign of inflammation (acute wounds infection) like: surgical wounds, burn wounds, laceration, abrasions, cut and bites, and 100 patients included as control groups who had wounds without infection. All patients with acute was surveyed for clinical sign like erythema, malodour, pain, heat and exudate. Ethical clearance for the study was obtained from the Committee of Higher Studies in College of Medicine, University of Tikrit.</p></sec><sec id="s2_2"><title>2.2. Isolation and Identification of Bacteria</title><p>Before taking a wound swab, the wound was gently cleaned with sterile gauze, rotate the swab over a one cm area of the wound, applying sufficient pressure to express fluid from the wound bed [<xref ref-type="bibr" rid="scirp.91590-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.91590-ref11">11</xref>] . After sampling, each swab was applied on to blood and MacConkey agars and incubated for 24 h at 37˚C under aerobic condition. Colonies were identified by Gram’s staining [<xref ref-type="bibr" rid="scirp.91590-ref12">12</xref>] differentiated, and identification by API 20E, and VITEK-2 compact system (bioMerieux Deutschland, Nurtingen, Germany).</p></sec><sec id="s2_3"><title>2.3. Complement C5a Estimation</title><p>Five milliliters of blood was collected by vein puncture using disposable syringe. Blood samples were placed into plan tube for 15 - 30 at room temperature to clott, then were centrifuge for 5 minutes at 3000 rpm for serum separation. Sera were stored at −70˚C for further studies [<xref ref-type="bibr" rid="scirp.91590-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.91590-ref14">14</xref>] . ELISA kits were used utilizing sandwich ELISA principle. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm according to manufacturer instructions.</p></sec><sec id="s2_4"><title>2.4. Statistical Analysis</title><p>F-test utilizing ANOVA computer program was used for data analysis and the significance was considered at P value of less than 0.05.</p></sec></sec><sec id="s3"><title>3. Results</title><p>The present study on acute-phase wound infection revealed that 17 bacterial types were isolated and identified (<xref ref-type="table" rid="table1">Table 1</xref>). A highest frequency of isolation was recorded with Staphylococcus aureus which was 30/105 (28.6%) whereas the lowest frequency was seen with Morganella morganii spp morganii (1%).</p><p>Gram positive bacteria were the most common isolates (53.30%). Gram-negatives were also isolated from different infected wounds and the most prevalent pathogen was Acinetobacter baumannii (<xref ref-type="table" rid="table1">Table 1</xref>). The present study revealed a mixed culture with frequency of 8.60% (<xref ref-type="table" rid="table1">Table 1</xref>, <xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>The present study showed that C5a concentration was increased with time of residence of patient with wound infections e.g., the C5a concentration was 4113 pg/ml at the end of the second day of residence, and this value was elevated to be 4898 pg/ml at 120 hours of hospitalization (<xref ref-type="fig" rid="fig2">Figure 2</xref>). The C5a concentration estimation among control patients was decreased with the time of residence in hospital, e.g. the C5a concentration was 4699 pg/ml after 48 hours of residence and this value started to decrease at 96 hours of hospitalization to be 4387 pg/ml (<xref ref-type="fig" rid="fig3">Figure 3</xref>). A statistical analysis using F-test showed significant differences of the values estimated (P &lt; 0.05).</p><p>The present study revealed that among 100 patients 40 were with acute-phase wound infection by Gram-negative bacteria and the mean value of the C5a in their sera was 4686.2 pg/ml. Whereas 56/100 patients were infected with Gram-positive bacteria and the mean value of the same complement was lower</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of gram positive and gram negative isolates</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="2"  >Bacteria</th><th align="center" valign="middle" >number</th><th align="center" valign="middle" >%</th></tr></thead><tr><td align="center" valign="middle"  rowspan="9"  >Gram positive cocci</td><td align="center" valign="middle" >Staphylococcus aureus</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >28.6</td></tr><tr><td align="center" valign="middle" >Staphylococcus epidermidis</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >5.7</td></tr><tr><td align="center" valign="middle" >Staphylococcus haemolyticus</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >Kocuria rosea</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >Enterococcus faecalis</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >Aerococcus viridans</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Staphylococcus hominis spp hominis</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Kocuria kristinae</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Dermacoccus nishinomiyaensis</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle"  rowspan="8"  >Gram negative bacilli</td><td align="center" valign="middle" >Acinetobacter baumannii</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >12.4</td></tr><tr><td align="center" valign="middle" >Pseudomonas aeruginosa</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >9.5</td></tr><tr><td align="center" valign="middle" >Escherichia coli</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >5.7</td></tr><tr><td align="center" valign="middle" >Proteus mirabilis</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >Pseudomonas oryzihabitans</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Klebsiella pneumoniae</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Enterobacter cloacae</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Morganella morganii spp morganii</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle"  rowspan="3"  >Mixed</td><td align="center" valign="middle" >Pseudomonas aeruginosa &amp; Klebsiella pneumoniae</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >Staphylococcus haemolyticus &amp; Kocuria kristinae &amp; Acinetobacter baumannii</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >2.9</td></tr><tr><td align="center" valign="middle" >Pseudomonas aeruginosa &amp; Serratia liquefaciens</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Grand total</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >105</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><p>compared to those infected with Gram-negative bacteria i.e. the mean value was 4546.8 pg/ml i.e. Gram-negatives induced higher amount of C5a compared to Gram-positive pathogens (<xref ref-type="fig" rid="fig4">Figure 4</xref>). Statistical analysis revealed a significant difference between these values (P &lt; 0.05).</p></sec><sec id="s4"><title>4. Discussion</title><p>The present study revealed that Staphylococcus aureus was more prevalent</p><p>causing acute-phase wound infection and the frequency of isolation was 28.6% This result was almost similar to that obtained by Nagoba and others who found that the incidence of this bacteria was 28.12% [<xref ref-type="bibr" rid="scirp.91590-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.91590-ref15">15</xref>] and Yin (2013) who showed Staphylococcus aureus was responsible for the majority of skin and soft tissue infection. S. aureus causes invasive and life threatening infection such as abscesses, and sepsis [<xref ref-type="bibr" rid="scirp.91590-ref16">16</xref>] . Others workers concluded different frequencies of isolation e.g. Rajan showed that 44.6% of the wounds studied were infected by S. aureus [<xref ref-type="bibr" rid="scirp.91590-ref17">17</xref>] . Almost 25% of the infections recorded in the present study were collectively caused by other Gram-positive bacteria which was almost similar to that obtained by Alwan and his co-workers [<xref ref-type="bibr" rid="scirp.91590-ref18">18</xref>] . Dermacoccus nishinomiyaensis, Kocuria rosea and Kocuria kristinae were isolated for the first time among patients of Baghdad district. However, the pathogens were also recorded elsewhere [<xref ref-type="bibr" rid="scirp.91590-ref19">19</xref>] - [<xref ref-type="bibr" rid="scirp.91590-ref24">24</xref>] . Therefore, these new isolated bacteria should be considered as a true pathogen contributed to clinical sepsis and proper treatment should be provided to all susceptible patients [<xref ref-type="bibr" rid="scirp.91590-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.91590-ref20">20</xref>] . Moreover, isolation of Kocuria kristinae with others bacteria was similar to that obtained by some authors who recorded K. kristinae as commensal of humans, animal and environment to be contaminants of wounds [<xref ref-type="bibr" rid="scirp.91590-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.91590-ref22">22</xref>] . In the present study, among the Gram negatives, Acinetobacter baumannii was isolated with the highest frequency (12.4%) followed by Pseudomonas aeruginosa (9.5%) from the total isolates of wound and the two types were isolated by Al-Ali who found that the isolation frequencies by both were 19.5% and 39.5% respectively [<xref ref-type="bibr" rid="scirp.91590-ref25">25</xref>] . E. coli was isolated with percentage of 5.7% which was different from that obtained by Rashid et al. who showed almost 2% of their isolates from wounds was E. coli [<xref ref-type="bibr" rid="scirp.91590-ref26">26</xref>] . In contrast, Idomir et al. estimated an incidence of by E. coli to be 11.5% [<xref ref-type="bibr" rid="scirp.91590-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.91590-ref28">28</xref>] . The isolation patterns of the other pathogens showed different frequencies compared to other workers [<xref ref-type="bibr" rid="scirp.91590-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.91590-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.91590-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.91590-ref29">29</xref>] .</p><p>The present study revealed that complement C5a was very high in concentration at 120 hours of patient residence in hospital with average value of 4898 pg/ml followed by 4765 pg/ml at 48 hours in acute-phase wound infection The most receptive interpretation that the mechanisms of accelerated healing were associated with lack of C5aR1 signaling, and C5a as well as reduced recruitment of inflammatory cells to wounds along with their reduced activation. The increased angiogenesis and high levels of mast cells contribute to more efficient healing process [<xref ref-type="bibr" rid="scirp.91590-ref30">30</xref>] . The same opinion concluded by Rafail and co-workers who showed that C3 and C5 deficiency revealed a reduction in inflammatory and increased accumulation of mast cells and advanced angiogenesis [<xref ref-type="bibr" rid="scirp.91590-ref31">31</xref>] . The increased C5a after 48 hrs in the wounds mentioned by Jang and co-workers showed that after wounds infection the activation of complement system, split fragment C5a and C3a augment inflammatory responses e.g. increased blood flow and vascular permeability and facilitate migration of neutrophils and monocytes to the inflamed tissue also induce mast cell to release histamine and TNF-α which contribute to the proliferation of the inflammatory response. C5a has the ability to stimulate cells to secrete neuropeptides and neurotrophins as the main roles of pain after wounds as well as C5a sensitized C-fiber afferent response to heat in the incision, as noted C5a concentration 1000 pg/ml at 24 hrs begins to decline at 48hrs with concentration 800 pg/ml in the clean wounds and present any infection may causes long wounds healing due to prolonged inflammatory process [<xref ref-type="bibr" rid="scirp.91590-ref32">32</xref>] . The elevated concentrations of C5a described in sepsis due to bacteria particularly Gram-negative types which showed a higher concentration of C5a as compared to Gram-positive bacteria which revealed less elevation in this complement. C5a is an important mediator of neutrophil dysfunction, acting via the major C5a receptor CD88, and CD88 is not directly phagocytic but is marker of exposure to C5a which inhibits phagocytosis [<xref ref-type="bibr" rid="scirp.91590-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.91590-ref34">34</xref>] . Finally, all workers have indicated that reduction of complement component and activation causes improve wound healing, for this reason may be the concentration in control wounds were less than acute-phase of wounds [<xref ref-type="bibr" rid="scirp.91590-ref34">34</xref>] .</p></sec><sec id="s5"><title>5. Conclusion</title><p>The present study revealed that most of acute-phase wound infections were caused by Gram-positive bacteria. Dermacoccus nishinomiyaensis, Kocuria rosea and Kocuria kristinae were isolated for the first time among patients of Baghdad district. Acute-phase wound infection by Gram-negative bacteria caused a higher elevation in C5a concentration of patients compared to infection by Gram-positive types.</p></sec><sec id="s6"><title>Ethical Approval</title><p>Ethical clearance for the study was obtained from the Committee of Higher Studies in College of Medicine, University of Tikrit. The researcher did not in any way expose participants of the study to physical or psychological harm. Participation in the study was strictly voluntary with the informed consent of participants that guaranteed their right to privacy. All authors hereby declare that all experiments have been examined and approved by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in the 1964 declaration of Helsinki.</p></sec><sec id="s7"><title>Limitations</title><p>Single region data of displacement area is not generalized. For this reason a survey of the whole area can reflect the whole region should be done.</p></sec><sec id="s8"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s9"><title>Cite this paper</title><p>Al-Jebouri, M.M. and Al-Mahmood, B.Y.R. (2019) Prevalence of Different Types of Micro-Organisms and Levels of Complement C5a in Patients with Acute-Phase Wound Infections. Open Journal of Pathology, 9, 19-28. https://doi.org/10.4236/ojpathology.2019.92003</p></sec></body><back><ref-list><title>References</title><ref id="scirp.91590-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">White, R.J. (2009) Wound Infection-Associated Pain. 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