Antibiogram, prevalence of methicillin-resistant and multi-drug resistant Staphylococcus spp. in different clinical samples

Methicillin-resistant Staphylococcus spp. (MRSS) are causing numerous forms of illness in humans ranging from mild to fatal infections. We need to investigate the resistant pattern for different clinical isolates to control the resistance phenomena. This study was designed to provide the resistance pattern of isolated Staphylococcus spp. from various clinical samples in Khartoum State and to elucidate the frequencies of Multidrug-resistant (MDR), Extensively drug-resistant (XDR) and pan-drug resistant (PDR). Two hundred and ten bacterial isolates were from different sources (catheter tip, sputum, vaginal swab, urine, tracheal aspirate, blood, pus, nasal swab, stool, throat swab, pleural fluid, and ear swab). Isolates were identified based on their morphological characters and biochemical reaction. Antibiotics susceptibility screening was performed using twenty-three antibiotics from eighteen classes against all isolated Staphylococcus spp. following the Clinical and Laboratory Standards Institute (CLSI) guideline. The result revealed that out of 63 Gram-positive isolated bacteria, 52 (82.5%) were Staphylococcus spp. with a high incidence of S. aureus 37(71.2%). Out of all Staphylococcus spp., 38 (73.1%) were Methicillin-resistant (MR). The prevalence of MDR was higher in S. aureus (89.2%) than in S. epidermidis (75%). All Staphylococcus spp. displayed resistance to ampicillin and penicillin, while all S. aureus were sensitive to daptomycin and fosfomycin. One isolate was XDR possible PDR, while no PDR was reported in all isolated bacteria. This study provided evidence for the antimicrobial-resistant (AMR) burden in Sudan and highlighted the need for a practical and functional stewardship program to reduce the unreasonable costs of antibiotics.


Introduction
Staphylococcus spp. is a bacterial pathogen that quickly obtains antibiotic resistance (Kot et al., 2020, Boucher et al., 2009. Antibiotics are one of our most powerful tools for preventing life-threatening infections, and bacteria become antibiotic-resistant by the capability to defeat the drugs used to kill them, which is a critical global public health challenge of our time. Now, people live in an era when people die because of untreatable infections due to the emergence and spread of antibiotic resistance (CDC, 2019). Moreover, microbial infections with antimicrobial-resistant strains make the disease worse by increasing the possibility of mortality and rising treatment expenses compared to disease by susceptible strains (Mulvey and Simor, 2009).
Furthermore, methicillin-resistant S. aureus (MRSA) is one of the significant problems globally which can cause both community and healthcare-acquired infections; it is reported that infections by MRSA affect more than 150,000 patients yearly in the healthcare setting alone in the European Union (Baldan et al., 2009, Köck et al., 2010, the emergence of resistant bacterial pathogens mainly due to extensive and prolonged use of antibiotics. It affects increasing morbidity and mortality rates (Tsige et al., 2020). The MRSA infection is multifold (Ben Zakour et al., 2008 et al., 2005) and is connected with worse outcomes, extended hospital stay, more treatment expenditure, and high mortality (Zahar et al., 2005, Shorr et al., 2006. According to the WHO, nearly 80 % of S. aureus infections in Africa are resistant to methicillin, making the traditional antibiotics worthless for infection treatment. (WHO, 2014). Other studies in Ethiopia revealed that MRSA is a significant problem in public health (Kahsay et al., 2014;Godebo et al., 2013;Dilnessa and Bitew, 2016). In addition, in Sudan, one of the African countries with a border with Ethiopia, the prevention and governor policies are not well recognised to reduce MRSA. Antibiotics are routinely and incorrectly utilised, increasing the prevalence of drug resistance strain bacteria like MRSA. Therefore, exploring increased drug-resistant MRSA is essential for controlling and treating staphylococcal infections.
Accordingly, global epidemiological surveillance is critical to complete antimicrobial-resistant (AMR) response. Knowledge of local and provincial AMR is essential for medical selection formation. Nonetheless, there is a lack of investigation capabilities for AMR requests across Sudan, and current AMR records are sparse. According to our knowledge, no previous studies in the study area. Therefore, we aim to study the current prevalence of clinical isolates of Staphylococcus spp. and their resistance profile, including the determination of the MDR, XDR and PDR. In general, the findings of this study can be used as a source to develop a guide to reduce the burden of MRSA, and it provides modernised information that is useful for health care professionals responsible for patient supervision and monitoring the emergence of AMR.

Study population and sample size
This study was cross-sectional and conducted at three hospitals in Khartoum, Sudan (Omdurman, Soba and Bahri Teaching Hospitals). The study lasted six months, from October 2019 to March 2020. A total of 210 clinical bacterial isolates were recovered from the catheter tip, sputum, vaginal swab, urine, tracheal aspirate, blood, pus, nasal swab, stool, throat swab, pleural fluid, and ear swab samples. All specimens received in the hospital's microbiology laboratory were included during the study.

Culturing of bacterial isolate
According to the sample sources, the specimens were cultured in XLD, MacConkey Agar and Blood agar and incubated at 37°C for 24 h. The sample showed dense pure colonies were examined for Gram stain (Cheesbourgh, 2006).

Identification of Staphylococcus spp.
All Gram-positive bacteria (GPB) were tested for catalase production, and positive bacteria were identified by culture characteristics on Mannitol Salt Agar (MSA) and blood agar. Biochemical reactions, such as DNase and coagulase production tests, are also used to recognise the species.

Detection of methicillin-resistant Staphylococcus spp. (MRS) by cefoxitin disc screen test
The susceptibility profile of Staphylococcus spp. to cefoxitin (30 lg) was carried out on Mueller-Hinton agar plates using the disc diffusion technique. The tested bacterial isolate was suspended on physiological saline, and then the turbidity was compared with a 0.5 McFarland standard. After incubation at 35°C for 24 h, interpretation of inhibition zone performed using CLSI guidelines 2017 as fallows; S. aureus, resistant 21 mm and sensitive 22 mm whereas MRS were cefoxitin resistant. For quality control, S. aureus ATCC BAA 2313 was used for MRSA, and S. aureus ATCC BAA 1026 was used in each experiment. (CLSI, 2017).

Detection of MDR and XDR
MDR was defined as acquired resistance to at least one antimicrobial agent from 3 or more antimicrobial classes. XDR is characterised by resistance to at least one drug in all antibiotic types except two or fewer; bacterial isolates are only sensitive to one or two categories. The PDR is resistant to all groups of antimicrobial agents (Basak et al., 2016).

Statistical analysis
Statistical package for social sciences (SPSS) software programme version 20 (SPSS Inc., Chicago, IL) was used for analysing all data. Descriptive data is displayed as a percentage. A P-value of 0.05 was considered for significant association between sources of samples and isolated bacteria.

Detection of methicillin-resistant Staphylococcus spp. (MRSS) by cefoxitin disc screen test
Of 52 isolated Staphylococcus spp., 38 (73.1 %) were positive for the Cefoxitin disc screen. The results are demonstrated in Table 2.

Detection of MDR, XDR and PDR
MDR was predominant. Of all isolated species, only S. cohnii are resistant to all tested antibiotics except for mupirocin which was not tested, so it is considered XDR and possible PDR. The results are displayed in Table 2.

Antimicrobial susceptibility profile of isolated Staphylococcus spp.
Twenty-three different antibiotics belong to eighteen different classes used in this study, and the result was interpreted according to CLSI guidelines. All S. aureus were sensitive to daptomycin and fosfomycin, and only two isolates were resistant to teicoplanin and rifampin. While all Staphylococcus spp. were resistant to penicillin and ampicillin, the result is shown in Table 3..
In this study, all Staphylococcus spp. including S. aureus was resistant to penicillin and ampicillin. This finding is unlike the results obtained from Tanzania (97 %) (Mshana et al., 1970), Nigeria (95.8 %) (Uwaezuoke and Aririatu, 2004), and ultimately agreed with a study done in Ethiopia (East border country) which found that all MRSA were 100 % resistant to penicillin and ampicillin (Kejela and Bacha, 2013).
Interestingly, All S. aureus were sensitive to daptomycin and fosfomycin, and numerous proportions of S. aureus isolates, includ- Table 1 Prevalence and association between Gram-positive bacteria and sources of samples.   ing MRSA, were susceptible to vancomycin, synercid, and trimethoprim-sulfamethoxazole were (91.9 %), fusic acid, teicoplanin and rifampin were (94.6 %). These results agree with a study that reported that the susceptibility of S. aureus to vancomycin was 91.7 % (DeLeo et al., 2010). In a review of similar work, these findings disagreed with the study done in Southwest Ethiopia reported that 97 % of all S. aureus isolates were susceptible to vancomycin, 94.7 % to trimethoprim-sulfamethoxazole (Kejela and Bacha, 2013), other study said 96.9 % of S. aureus isolates were susceptible to vancomycin (Rijal et al., 2008). MRSA percentage among all S. aureus isolates was 67.6 %, higher than the previous study done in Sudan, which was 44.6 % (Elboshra et al., 2020). While in Italy reached 35.8 % (Campanile et al., 2015), above 40 % in Philippines (Juayang et al., 2014), and in Saudi Arabia 64.6 % (Moglad, 2021). This result is alarming because MRSA has limited drug choices to treat infections caused by them.
In our study, the first study to screen Twenty-three antibiotics belonging to eighteen different classes of antibiotics, and a significant percentage (88.5 %) of Staphylococcus spp. isolates were MDR. The resistance pattern ranged from five antibiotics to fifteen antibiotics, and for S. aureus MDR was 89.2 % which is higher than that reported in Italy 35.8 % (Campanile et al., 2015) and Ethiopia (82.3 %) (Kahsay et al., 2014). Many of our MDR isolates were MRSA, which shows that the opportunities to treat disease caused by MDR MRSA with conventional antibiotics are very narrow.
Unfortunately, our results showed that S. cohnii was resistant to all tested antibiotics, with an exception for mupirocin was not tested, which made it XDR and possible PDR. Alarmingly resistant bacteria could share their resistance genes even with bacteria not exposed to antibiotics (CDC, 2019). As previously reported in the literature, S. aureus develops resistance to several antibiotics by gaining elements by horizontal transferring of mobile genetic material, modifying the drug-binding sites on molecular targets by mutations, and expressing endogenous efflux pumps (Foster, 2017). MRSA is an important human pathogen with growing resistance to presently used antimicrobial remedies (Pokharel et al., 2019).

Conclusion
This study focused on the current scenario of antimicrobialresistant Staphylococcus spp. and highlighted the frequencies of MDR, XDR, and PDR among clinical isolates of Staphylococcus spp. in Khartoum state Sudan and the incidence of MDR Staphylococcus spp. was high.
Also, this study showed the current resistant patterns, which are essential for the active treatment of diseases caused by MDR and MRSA. This study might evidence the serious need for monitoring and dealing with the development of MDR strain. Finally, this study recommended that antibiotic use be improved, reduce unnecessary uses, and ensure improved access to antibiotics in Sudan.

Declaration of Competing Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper