Diversity and Distribution of Spa types among Methicillin Resistant Staphylococcus Aureus Isolated from Humans and Livestock in Kabale District - South Western Uganda

Background: S. aureus is a skin and mucosal bacterial commensal of both humans and animals which has evolved as an important pathogen implicated to cause various infections. High levels of antibiotic use have resulted into multi-drug resistance MRSA, especially among HA-MRSA, CA-and LA - MRSA. Awareness on coexistence and diversity of MRSA clones among humans and household Livestock particularly cattle and swine in our region is limited. We used spa typing method to determine spa diversity, distribution and coexistence in outpatients, household contacts and respective livestock (cattle and swine) in Kabale region, south western Uganda. Methods: This was a cross sectional study by design consisting of outpatients, household contacts and livestock. Outpatients (n =100) colonized with MRSA were traced back to their respective homesteads where household members, domestic cattle, and, swine were tested for S. aureus and subsequently MRSA colonization. High-resolution DNA melting analysis was used to determine spa types among MRSA isolates. Overlap of MRSA isolates among humans and livestock was based on the presence of similar spa types.Results: A total of 3371 S.aureus isolates were collected from outpatients (n =376), household contacts (n = 1531), Cattle (n = 1159) and Swine (n = 305), among which 482 had mecA gene where 27% (100/376) and 8% (123/1531) were outpatients and household contacts respectively while 11% (132/1159) and 42% (127/305) were cattle and swine respectively. Twenty different spa types were identified; t034, t4677, t108, t1451, t9377, t1081, t040, t701, t041, t002, t044, t037,t121, t127, t922, t032, t019, t018, t012 and t030, among which t034 (109/482), t4677 (53/482), t9377 (63/482) and t1081 (53/482) were most prevalent and distributed among human and livestock. All the MRSA isolates were multidrug resistant to antibiotics tested. Conclusion: In Kabale region, there is high diversity of spa types among MRSA. Presence of similar spa types was found circulating among humans and their respective livestock which demonstrates a possible bidirectional transmission. Presence of MDR - MRSA highlights the need for effective prevention and control of MRSA among livestock and in the community using One Health approach.

[1]  S. Karki,et al.  Prevalence of methicillin-resistant Staphylococcus aureus and pattern of antimicrobial resistance in mastitis milk of cattle in Chitwan, Nepal , 2021, BMC Veterinary Research.

[2]  C. Jenne,et al.  The Prevalence, Risk, and Management of Methicillin-Resistant Staphylococcus aureus Infection in Diverse Populations across Canada: A Systematic Review , 2021, Pathogens.

[3]  A. Bitrus,et al.  Nasal Colonization of Pigs and Farm attendants by Staphylococcus aureus and Methicillin-Resistant Staphylococcus aureus (MRSA) in Kebbi, Northwestern Nigeria , 2021, The Thai Journal of Veterinary Medicine.

[4]  O. Perovic,et al.  Diversity of SCCmec elements and spa types in South African Staphylococcus aureus mecA-positive blood culture isolates , 2020, BMC Infectious Diseases.

[5]  N. Bandarra,et al.  Genetic Relatedness and Diversity of Staphylococcus aureus from Different Reservoirs: Humans and Animals of Livestock, Poultry, Zoo, and Aquaculture , 2020, Microorganisms.

[6]  A. Laglaoui,et al.  Nasal carriage of Staphylococcus aureus in farm animals and breeders in north of Morocco , 2020, BMC Infectious Diseases.

[7]  A. Bazargani,et al.  Determining spa-type of methicillin-resistant Staphylococcus aureus (MRSA) via high-resolution melting (HRM) analysis, Shiraz, Iran , 2019, BMC Research Notes.

[8]  M. Masika,et al.  Methicillin-resistant Staphylococcus aureus (MRSA) in East Africa: red alert or red herring? , 2019, BMC Infectious Diseases.

[9]  B. Kot,et al.  Antimicrobial Resistance Patterns in Methicillin-Resistant Staphylococcus aureus from Patients Hospitalized during 2015–2017 in Hospitals in Poland , 2019, Medical Principles and Practice.

[10]  E. Rutebemberwa,et al.  CA-MRSA and HA-MRSA coexist in community and hospital settings in Uganda , 2019, Antimicrobial Resistance & Infection Control.

[11]  Wei Gao,et al.  Comparison of community- and healthcare-associated methicillin-resistant Staphylococcus aureus isolates at a Chinese tertiary hospital, 2012–2017 , 2018, Scientific Reports.

[12]  M. E. El Zowalaty,et al.  Methicillin-resistant Staphylococcus aureus: livestock-associated, antimicrobial, and heavy metal resistance , 2018, Infection and drug resistance.

[13]  A. Nienhaus,et al.  Prevalence and risk factors of MRSA colonisations: a cross-sectional study among personnel in outpatient care settings in Hamburg, Germany , 2018, BMJ Open.

[14]  E. Ghaznavi-Rad,et al.  Molecular Characterization of Methicillin-Resistant Staphylococcus aureus Isolates, Isolated from a Burn Hospital in Southwest Iran in 2006 and 2014 , 2018, International journal of microbiology.

[15]  B. Joel,et al.  High Rates of Methicillin-Resistant Staphylococcus aureus Colonization of Domesticated Swine of Kabale District – Southwestern Uganda , 2018 .

[16]  A. van Belkum,et al.  Distribution of the Most Prevalent Spa Types among Clinical Isolates of Methicillin-Resistant and -Susceptible Staphylococcus aureus around the World: A Review , 2018, Front. Microbiol..

[17]  M. Mohammadi,et al.  The spa typing of methicillin-resistant Staphylococcus aureus isolates by High Resolution Melting (HRM) analysis. , 2017, Journal of medical microbiology.

[18]  N. Mbembati,et al.  Prevalence of methicillin-resistant Staphylococcus aureus carriage on admission among patients attending regional hospitals in Dar es Salaam, Tanzania , 2017, BMC Research Notes.

[19]  E. Choo Community-Associated Methicillin-Resistant Staphylococcus aureus in Nosocomial Infections , 2017, Infection & chemotherapy.

[20]  M. García-nuñez,et al.  Prevalence of colonization by methicillin-resistant Staphylococcus aureus ST398 in pigs and pig farm workers in an area of Catalonia, Spain , 2016, BMC Infectious Diseases.

[21]  K. Bierowiec,et al.  Is the Colonisation of Staphylococcus aureus in Pets Associated with Their Close Contact with Owners? , 2016, PloS one.

[22]  J. Morschhäuser The development of fluconazole resistance in Candida albicans – an example of microevolution of a fungal pathogen , 2016, Journal of Microbiology.

[23]  M. Castanheira,et al.  Nosocomial Candidiasis: Antifungal Stewardship and the Importance of Rapid Diagnosis. , 2015, Medical mycology.

[24]  A. Grgurevic,et al.  Carriage and Genetic Diversity of Methicillin-Resistant Staphylococcus aureus among Patients and Healthcare Workers in a Serbian University Hospital , 2015, PloS one.

[25]  D. Coleman,et al.  Staphylococcal cassette chromosome mec: recent advances and new insights. , 2013, International journal of medical microbiology : IJMM.

[26]  A. Mellmann,et al.  Livestock-Associated Methicillin-Resistant Staphylococcus aureus (MRSA) as Causes of Human Infection and Colonization in Germany , 2013, PloS one.

[27]  B. Grenfell,et al.  Hospital-Community Interactions Foster Coexistence between Methicillin-Resistant Strains of Staphylococcus aureus , 2013, PLoS pathogens.

[28]  P. Andersen,et al.  Rapid detection, differentiation and typing of methicillin-resistant Staphylococcus aureus harbouring either mecA or the new mecA homologue mecA(LGA251). , 2012, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

[29]  H. Heesterbeek,et al.  Persistence of Livestock Associated MRSA CC398 in Humans Is Dependent on Intensity of Animal Contact , 2011, PloS one.

[30]  M. D. de Jong,et al.  MRSA CC398 in the pig production chain. , 2011, Preventive veterinary medicine.

[31]  R. Daum,et al.  Community-Associated Methicillin-Resistant Staphylococcus aureus: Epidemiology and Clinical Consequences of an Emerging Epidemic , 2010, Clinical Microbiology Reviews.

[32]  A. Widmer,et al.  Distribution of spa types among meticillin-resistant Staphylococcus aureus isolates during a 6 year period at a low-prevalence University Hospital. , 2008, Journal of medical microbiology.

[33]  F. Allerberger,et al.  Classifying spa Types in Complexes Improves Interpretation of Typing Results for Methicillin-Resistant Staphylococcus aureus , 2006, Journal of Clinical Microbiology.

[34]  A. Friedrich,et al.  Assignment of Staphylococcus Isolates to Groups by spa Typing, SmaI Macrorestriction Analysis, and Multilocus Sequence Typing , 2006, Journal of Clinical Microbiology.

[35]  R. Rohde Molecular Characterization of Methicillin Resistant Staphylococcus aureus (MRSA) Isolates , 2006 .

[36]  Nagler Test UK Standards for Microbiology Investigations , 2014 .