1. Introduction
Diabetes mellitus (DM) is the name applied to the concurrence of certain processes which can be characterized with the occurrence of hyperglycemia, resulting from physio-pathological alterations, mainly induced by SIRT1 gene mutation [1] . DM is a potential problem for human health and knowledge over said etiological diversity arises as means to identify each one of the consequences involved from the disease. One of the major sources of distress regarding complications related with diabetes mellitus (DM) is the diabetic foot syndrome; the World Health Organization (WHO) defines diabetic foot as infection and destruction of deep tissues, related with neurological disorders and different degrees of peripheral vascular illness in lower limbs occurring in diabetes patients [2] [3] [4] [5] [6] . The depicted situation carries a high morbidity degree and a high risk of amputation. The aim of the present research was to characterize those microorganisms with a higher level of incidence in diabetic foot clinic pictures through microbiological analysis, this to enhance further prevention programmes [7] . One of the most important factor prompting to foot infection in diabetic patients are skin barrier integrity losses, as a result of decreasing in chemotactic, phagocytic, and cytotoxic capacity; as a consequence of diabetic neuropathy, losses in protective sensations may occur, which enhances the presence of lesions on the skin (mainly from traumatic origin), sensation losses, foot deformities, and joints mobility constraints, featured frequently in diabetes patients; the aforementioned usually produce changes in feet biomechanics; callus is formed and disrupts the skin barrier [2] . Microorganisms then can penetrate through those cracks formed in the skin concomitantly. Alongside with the depicted neuropathy, an ischemic factor contributing to hamper wounds and infection curative processes can be presented as an outcome [8] [9] . Symptoms may range from absence of clinic sings, evidenced by feet losing their sensitivity with ulceration risk, to unbearable neuropathic pain presence [10] . DM1 autoimmune reaction comes alongside autoantibodies production humoral counteraction. Currently, anti-glutamate decarboxylase antibodies (GAD), the most-commonly used antibodies at clinic level, are the ones used against insulin (anti-insulin IAA), decarboxylase glutamic acid (GAD) and anti-tyrosine phosphatase 2 (Langerhans’ antibodies anti-isletsIA2). From a predictive point of view, the three previously-mentioned types presence in the same individual assures practically the disease development. Nonetheless, if just one of them is detected, its predictive value does not exceed 60%. IA2 antibodies, when and if detected, are often associated with diabetes quick evolution [11] [12] . Patients with a diabetes mellitus diagnosis show vascular disease clinical signs, infection or neuropathy, in at least one of the lower limbs. Diabetic foot Wagner classification is the more commonly used parameter to quantify trophic lesions; in the case of diabetic foot, this classification corresponds to: Type I, evidenced with superficial ulcers without deep tissue involvement; Type II, where wounds reach tendons, joint capsule, and bones; Type III, where abscess is occurred (pus fluids accumulation), osteomyelitis (bone infection), osteoarthritis (joint wearing and tearing), and tendonitis (tendon inflammation); Type IV, evidenced with gangrene or localized gangrene incidence, usually in one part of the foot; Type V, [13] where gangrene is spread throughout the foot. Among those diabetes mellitus chronic complications, resulting from micro and macrovascular damages, diabetic foot is considered as one of the most-feared complications when patients are asked [14] . Diabetic foot aetiology includes gram-positive or gram- negative pathogens with both, aerobic or anaerobic metabolism; Staphylococcus aureus has been found to be the most important pathogen in diabetic foot infections, either as a single agent or alongside mixed infection [15] [16] .
Three microorganisms can predominate in diabetic foot: Staphylococcus aureus, Escherichia coli, Klebbsiella; since diabetic foot infection is polymicrobial, leading to a rapid and progressive synergistic so-called wet gangrene; if not treated properly, the latter may be fatal. A fulminant infection pathognomonic sign can be described with subcutaneous emphysema development; although this might also occur in diabetes patients with infections caused by less-pathogen microorganisms such as Escherichia coli and other coliforms [17] [18] [19] . The tables (Table 1 & Table 2) below show a compilation of toxins secreted by Gram- positive and Gram-negative bacteria:
2. Methodology
A descriptive-retrospective study was conducted to determine the more-commonly occurred microorganisms in diabetic foot ulcers infection. The study population consisted in 70 clinical records depicting type 2 diabetes mellitus diagnosis, diabetic foot ulcer at any stage, culture application, and antibiogram. Prior au-
Table 1. Gram-positive bacteria toxins [20] [21] [22] [23] .
Table 2. Gram-negative bacteria toxins [24] - [29] .
thorization from the private clinic staff, the complete set-up of the clinical records was analysed. The following variables were studied: age (measured in years), gender, origin, lesion Wagner’s classification, cultures, isolated microorganism, and antibiogram report. Analysis and data processing were performed through descriptive statistics with Origin, Statgrahics Plus Version 5.0. statistics package. The hypothesis stablished was: there is a high diabetic foot incidence with presence of both, Gram-positive bacteria Staphylococcus aureus and gram-negative bacteria Escherichia coli.
3. Results
Socio-demographic characteristics:
Clinic characteristics
70 patients were attended; the highest precedence index (where these patients came from) was Machala (30%). The Pareto analysis carried out showed that the masculine gender reached a number of 42 patients (60%), thus the highest number of cases, whereas the feminine gender reached the number of 28 (40%) Figures 1-3 features that the age group with the highest presence was the one representing ages between 51 - 55 years, with a total number of 34 and representing the 48.57% of cases.
Table 3 shows that the highest occurrence frequency, according to Wagner classification, was diabetic foot type III (36 cases―51.43%). A correlation between Wagner classification and microorganism type was carried out. Gram- negative bacteria showed the highest incidence of occurrence with 20 patients in type III as featured in Table 4 and Figure 4.
4. Discussion
Diabetic foot is one of the most prevalent complications found among those
Source: Authors.
Figure 1. Percentage of diabetic foot incidence in the population studied distributed according to gender.
Source: Authors.
Figure 2. Percentage of patients subjected to study distributed regarding place of origin within El Oro province.
Source: Authors.
Figure 3. Distribution (in percentage) of diabetic foot incidence in the studied group accordingly to age group used.
Table 3. Pareto analysis in Wagner classification.
Source: Authors.
provoked by diabetes clinical pictures; this is a pathology which does not make any distinction regarding gender, ethnicity, and age. In the context taken in the present investigation, data were obtained through a survey applied to a known number of patients with this anomaly; data showed that the illness was occurred
Table 4. Diabetic foot patients’ distribution accordingly to microorganism type and Wagner classification.
Source: Authors.
Source: Authors.
Figure 4. Wagner classification distribution (in percentage values) of patients subjected as part of the research.
predominantly in male gender (42 patients―60%), while the figure for the female gender was 28 patients (40%). In addition to this information, data were also obtained concerning to the age factor; the disease was found predominantly between 51 - 55 years, occurred in 34 patients (48.75%). Figure 1 and Figure 2 show origin of patients; most patients came from the urban region of Machala, representing approximately 30%.
Currently, the number of diabetic patients is increasing significantly, consequently the number of cases of diabetic foot increases concomitantly, hence, to expand the knowledge over prevention of complications due to diagnosis based on analysis of bacteria present in foot tissue injuries is necessary [30] [31] [32] . In addition, as marked out in the Pareto analysis in Table 5, it shall be noted that microorganisms found in cultures carried out for the sake of the present work pertain to Gram-negative bacteria (39 cases―55.77%) and Gram-positive (31 cases―42%) as illustrated in Figure 5 and in Pareto analysis in Table 6. Staphylococcus Aureus (Gram-positive bacteria found in diabetic foot clinical pictures) is sensitive to antibiotics: Aztreonan, Amikacin, Imipenen, Gentamicin, Tetracycline, Chloramphenicol and is, in the other hand, resistant to antibiotics such as Ampicillin, Clindamycin, Penicillin, and Ciprofloxacin. Escherichia coli (Gram-negative bacteria found in diabetic foot clinical pictures), featured in Figure 6, proved to be sensitive to antibiotics Ceftazidime Imipenem, and Phospomicia Meropenen; it was also proved to be resistant to Amikacin.
Table 5. Pareto analysis of gram-negative bacteria incidence.
Source: Authors.
Table 6. Pareto analysis of gram-positive bacteria incidence.
Source: Authors.
Source: Authors.
Figure 5. Gram-positive bacteria occurred in diabetic foot cases registered and distributing accordingly to its incidence (in percentage values).
Source: Authors.
Figure 6. Gram-negative bacteria occurred in diabetic foot cases registered and distributing accordingly to its incidence (in percentage values).
5. Conclusion
Ulcer infection in diabetic foot clinic cases was characterized to be Type III, according to Wagner scale. Most frequent microorganisms found pertained to the Gram-negative Escherichia coli 27 (69.28%) and gram-positive bacteria Staphylococcus aerus 25 (80%) species, according to Pareto analysis results.
Acknowledgements
Lam, A. and Espinoza, F.M. are associate lecturers at UTMACH. Lam, A. carried out literature review previous to the present work research and carried out data compilation and experimental work; Espinoza, F.M., contributed with experimental work and interpretation. Cuenca, F. is a lecturer at UTMACH. He contributed with statistical and data interpretation review; he also contributed with text translation from its original language and subsequent redaction of the present written article. The three authors contributed equally to the present work development and review.