African Journal of
Microbiology Research

  • Abbreviation: Afr. J. Microbiol. Res.
  • Language: English
  • ISSN: 1996-0808
  • DOI: 10.5897/AJMR
  • Start Year: 2007
  • Published Articles: 5233

Full Length Research Paper

Microbiology spectrum and antibiotic susceptibility of bacterial pathogen from ready-to-eat sliced pineapple and water melon

Ajao O.
  • Ajao O.
  • Department of Biology, The Polytechnic, Ibadan, Oyo State, Nigeria.
  • Google Scholar
Nwose A. M.
  • Nwose A. M.
  • Department of Microbiology, University of Ibadan, Oyo State, Nigeria.
  • Google Scholar
Olateru C. T.
  • Olateru C. T.
  • Department of Biology, The Polytechnic, Ibadan, Oyo State, Nigeria.
  • Google Scholar
Onifade D. A.
  • Onifade D. A.
  • Department of Science Laboratory Technology, The Polytechnic, Ibadan, Oyo State, Nigeria.
  • Google Scholar
Abdulfatai A. I.
  • Abdulfatai A. I.
  • Department of Science Laboratory Technology, The Polytechnic, Ibadan, Oyo State, Nigeria.
  • Google Scholar
Bolarinwa O. O.
  • Bolarinwa O. O.
  • Department of Biology, The Polytechnic, Ibadan, Oyo State, Nigeria.
  • Google Scholar
Morakinyo Y. M.
  • Morakinyo Y. M.
  • Department of Biology, The Polytechnic, Ibadan, Oyo State, Nigeria.
  • Google Scholar


  •  Received: 10 January 2021
  •  Accepted: 14 September 2022
  •  Published: 31 October 2022

 ABSTRACT

This study was conducted to examine microbiological quality and antibiotic susceptibility of bacterial pathogen of ready to eat sliced pineapple and water melon. Pineapples and water melon were purchased from three different vendors in Sango, University of Ibadan and Apete markets. Isolation and identification of pathogens were carried out using culture dependent method, morphological and biochemical characterization, respectively. Bacterial isolates were tested for antibiotic susceptibility. Results showed that all samples were contaminated. Lactobacillus species had the highest percentage frequency of occurrence (35%), while Proteus, Pseudomonas, Shigella and Salmonella species had the least (5%). Multiple drug resistances were observed among the isolates when subjected to Ampicillin, Ceftazidine, Cefuroxine, and Augumentin. Despite the dominance of Lactobacillus spp. in this study, the presence of Escherichia coli, Shigella spp., and Salmonella spp., Staphylococcus aureus, Klebsiella pneumonia and Enterobacter species together with their multiple drug resistance call for public health attention. Quality of vended fruits will be better assured if there are improved hygienic practices and awareness among fruit vendors as well as the consumers. There is need to monitor the spread of multiple drug resistant antimicrobial pathogens in vended fruits to avoid outbreaks.

 

Key words: Microbiological quality, antibiotic susceptibility, multiple drug resistance ready to eat, pineapple, water melon.


 INTRODUCTION

Balanced diets enriched by fruits and vegetables are of utmost importance due to their nutritional values and ability to reduce risk of illnesses (Mahmoud et al., 2019). Fruits could be eaten wholly or sliced (Erhirhie et al., 2020). Ready-to-eat sliced fruits are fruits that have been cut open, sliced into bits, but remain in the fresh state and sold from retail outlets. They are usually eaten immediately, easily accessible, convenient and most especially cheaper than the whole fruit (Nwachukwu et al., 2008).

 

In Nigeria where street fruit vending is very common probably due to modern lifestyle, industrialization, economic downturn, materialism and lack of time to prepare proper meal (Fowoyo, 2012), there is little information on the incidence of food borne diseases as related to the street vending fruits. However, microbial studies on each fruits in American, Asian, European and some African countries have revealed increased bacteria pathogen in ready to eat fruits (Mahale et al., 2008). Several bacteria such as Salmonella species, Shigella species, Listeria monocytogens, Campylobacter species, Aeromonas species, Escherichia coli, Staphylococcus aureus, and Pseudomonas species have been associated with contaminated sliced fruits (Eni et al., 2010; Fowoyo, 2012; Asmaru and Sahile, 2013; Nwachukwu and Osuocha, 2014; Shenge et al., 2015).

 

Additionally, increase in the incidence of antimicrobial resistance bacteria in humans, animals and the environment is a major concern in both human and veterinary medicine and Infectious Diseases Report noted that drug resistant organisms are prevalent worldwide (WHO, 2000). Fruits can be infected with antibiotic resistance contaminants though several sources. Manure use in enhancing soil fertility harbours bacteria that can be carrying the Antibiotic Resistant Genes (ARG), which can be horizontally transferred to soil bacteria. This in turn, can contaminate fruits and vegetables. This is also applicable when there is faecal contamination of soil or spray of soil with antimicrobial agents. Also, during plant tissue culture, inclusion of antimicrobial agents in the culture medium can prevent or often treat microbial contamination but increase the chance of build-up of antibiotic resistance (Rashmi et al., 2017).

 

This work therefore aimed to determine microbial spectrum of ready-to-eat sliced pineapple and water melon fruits together with the assessment of bacteria susceptibility to antibiotics.


 MATERIALS AND METHODS

Sample collection

 

On the 2nd of January, 2020, samples of sliced pineapple (Ananas comosus) and watermelon (Citrullus lanatus) were purchase randomly at three different sellers in three markets (Apete, Sango and University of Ibadan), Oyo State, Nigeria. All samples were collected in sterile plastic bags and transported to laboratory for analysis.

 

Enumeration and identification of microorganisms

 

Isolation of bacteria from the fruit samples

 

From each fruit sample, 2 g was cut and mashed in a mortal using a pestle and 1 g of sample was weighed into 9 ml of sterile distilled water in McCartney bottle. A 10-fold serial dilution of the solution was done in sterile distilled water and 0.1 ml of dilutions 10-3, 10-5 and 10-6 were plated using pour plate technique on eosin methylene blue agar (EMB), Salmonella-Shigella agar (SSA) for bacterial isolation and identification. All samples were duplicated and incubated at 37°C for 24 h for bacteria and 72 h at 30°C (Cheesbrough, 2011). After incubation, the cultured plates were observed for growth and distinct colonies were selected and streaked on their respective medium, the pure cultures were inoculated on slant and stored in the refrigerator for further studies. Phenotypic identification of the bacteria isolates were carried out according to Boone et al. (2005).

 

Antibiotic sensitivity test

 

The susceptibility of each isolate to commonly available antibiotics was carried out using disc diffusion method. Mueller Hilton agar was prepared according to manufacturer’s specification and sterilized in an autoclave at 121°C for 15 min. The isolated organisms were inoculated on the agar using a swab stick. Each antibiotic disc (10 µg) was aseptically placed on the surface of the plate with sterile forceps, to ensure complete contact with the agar surface. The plates were incubated for 24 h at 37°C, clear zone of incubation around the antibiotic disc on the plate indicated susceptibility of the isolates. Inhibition clear zones were measured in millimetre and grouped into antibiotics sensitive and resistant isolates (Cheesbrough, 2011).


 RESULTS AND DISCUSSION

All the pineapple samples were contaminated. Pineapple bought from Apete pineapple (APP) had average viable count of 2.3 × 10-4 - 4.5 × 10-5 cfu/ml bacteria cells, Sango pineapple (SPP) had a viable count of 1.8 × 10-3 - 4.5 × 10-5 cfu/ml and University of Ibadan pineapple had a viable count of 4.7 × 10-3- 4.0 ×10-5 cfu/ml. Water melon bought from Apete had total viable count of 3.7 × 10-4 - 1.1 × 10-7, Sango 1.2 × 10-4 - 1.7 × 10-4 and University of Ibadan 2.5 × 10-4 - 2.5 × 10-7 (Table 1).

 

 
Apete pineapple (APP) had three major groups of bacteria isolated and identified as E. coli, Lactobacillus species and S. aureus. Sango pineapple samples (SPP) had a wider spread of organisms such as S. aureus, E. coli, Lactobacillus spp., Salmonella spp, Proteus and Bacillus subtilis while Shigella spp., Pseudomonas aeruginosa, S. aureus and B. subtilis were isolated from University of Ibadan pineapple samples (UPP) sample. The water melon samples had seven similar bacteria isolates, identified as S. aureus, Enterobacter species, P. aeruginosa, Lactobacillus spp., E. coli, Klebsiella pneumonia and Shigella spp.
 

 

Among all the bacterial isolates from sliced pineapples (Figure 1a), Lactobacillus spp. had the higher percentage occurrence of 35%, followed by S. aureus at 18%, E. coli and B. subtilis at 12% while Proteus, Pseudomonas spp., Shigella spp. and Salmomella spp. had the occurrence rate of 5%. With the exception of Pseudomonas and Klebsiella spp. which are the least (8%), all other bacteria isolates had same occurrence level (16.8%) in water melon (Figure 1b).

 

 

According to Wadamori et al. (2016), various pathogenic microbes can contaminate fresh fruits and vegetables at any point in the chain. The presence of these bacteria contaminants indicated that, microbial contaminants of fruits and vegetables occur mainly because of resident microflora in the soil, application of non-resident microflora via animal manures, sewage or irrigation water, transportation and handling (Ray and Bhunia, 2007; Ofor et al., 2009). Similar report had been previously shown though not in Oyo State (Adebolu and Ifesan, 2001; Tambekar and Mundhada, 2006; Uzeh et al., 2009; Eni et al., 2010). Although it is worthy to note that Lactobacillus spp. are normal flora of the fruit. Their presence could also be due to the fact that they are obiquitious occurring naturally in a variety of niches, including the gastrointestinal tract and plants (Mohania et al., 2008). Their dominance could be traced to their ability to inhibit the growth of pathogenic bacteria by producing antimicrobial substances (such as lactic acid) (Olateru et al., 2020).

 

The presence of Staphylococcus indicates unhygienic handling of fruits. The samples obtained from Sango pineapples had variety of organisms; this might be attributed to poor handling and storage condition (Bello et al., 2016)

 

The prevalence of pathogenic organism in all samples can be as a result of improper washing and decontamination of these produce. In support, Eni et al. (2010) isolated S. aureus with percentage occurrence rate of 29.2%, followed by Klebsiella spp. (12.5%), Salmonella spp. (12.5%), E. coli (4.2%) and Actinomycetes (4.2%) from ready to eat fruits and vegetable in Sango-Ota, Ogun State Nigeria. As noted by Buck et al. (2003), enteric pathogens such as E. coli and Salmonella spp. are among the greatest concerns during food-related outbreaks. Several cases of typhoid fever outbreak have been associated with eating contaminated vegetables grown in or fertilized with contaminated soil or sewage (Beuchat, 2002). Besides, contamination observed in this study may be attributed to storage conditions or cross contamination between fruits as a result re-washing with used water or water recycled by the vendor or processor (Topalcengiz et al., 2017).

 

Tables 2 and 3 present the distribution of isolates susceptibility and resistance to specific antibiotic agents. The result showed that susceptibility of the isolates to different antibiotic varied. Ofloxacin, Gentamycin, and Ciprofloxacin, have the highest inhibitory properties against all isolates while Nitrofurantoin has the lowest inhibitory properties. All isolates showed high resistance to Ampicillin, Ceftazidine, Cefuroxine, and Augumentin. E. coli, B. subtilis, P. aeruginosa and Salmonella spp., were partially susceptible to Gentamycin, Ciprofloxacin, Nitrofurantoin and Ofloxacin. S. aureus was sensitive to Gentamycin, Ciprofloxacin, Nitrofurantoin and Ofloxacin. Shigella spp. was sensitive to Gentamycin and partially sensitive to Ciprofloxacin, Nitrofurantoin and Ofloxacin. Proteus species was resistant to Gentamycin and Nitrofurantoin and partially sensitive to Ciprofloxacin and Ofloxacin. However, Pseudomonas spp. isolated from ready to eat water melon was resistant to Gentamycin and Klebisella to Ampicillin. The presence of resistant bacteria pathogen may be attributed to continuous indiscrete use of antibiotics as therapy and as an additive. In support, Meher et al. (2011) reported that emergence of drug resistance is one of the most serious health problems in developing countries. Abuse of antibiotics have resulted in increase in prevalence of antibiotic resistant bacteria strains, vice-verse increase bacterial infections (Nuermberger and Bishai, 2004; Kummerer, 2004; Rashmi et al., 2017).

 


 CONCLUSION

It is very important to note that the outward appearance of fruits gave a wrong assessment of the microbial quality. Hence, awareness is to be created both for the consumers and the vendors. There is also need to increase surveillance of antibiotic resistant pathogen in ready to eat foods.


 CONFLICT OF INTERESTS

The authors have not declared any conflict of interests.



 REFERENCES

Adebolu TT, Ifesan BO (2001). Bacteriological quality of vegetable salads. Nigerian. Journal of Microbiology 15(1): 81-85.

 

Asmaru G, Samuel S (2013). Microbial Spectrum of Fruit in Gondar town main markets, North Western Ethiopia. Journal of Microbiology Research 3(1):1-10.

 

Mahmoud AM, Hernández Bautista RJ, Mansur AS, Omnia EH (2019). Beneficial Effects of Citrus Flavonoids on Cardiovascular and Metabolic Health, Review Article. Hindawi pp. 1-19.
Crossref

 

Bello OB, Olawuyi OJ, Azeez AH, Adebisi OS, Owoade TA (2016). Microorganisms causing post-harvest tomato (solanum lycopersicum l.) fruit decay in Nigeria. Scientia Agriculturae 13(2):93-96.
Crossref

 

Beuchat LR (2002). Ecological factors influencing survival and growth of human pathogens on raw fruits and vegetables. Microbes infection 4:413-423.
Crossref

 

Boone DR, Castenholz RW, Garrity GM, Brenner DJ, Krieg NR, Staley JR (2005). Bergey's Manual of Systematic Bacteriology. Second Edition. New York: SpringerVerlag.

 

Buck JW, Walcott RR, Beuchat LR (2003). Recent trends in microbiology safety of fruits and vegetables. Plant Health Progress 10:1094.
Crossref

 

Cheesbrough M (2011). District Laboratory Practice in tropical countries part 2. Cambridge University Press pp. 163-169.

 

Eni AO, Ibukunoluwa AO, Orannusi US (2010). Microbial quality of fruits and vegetables sold in Sango Ota, Nigeria. African Journal of Food Science 4(5):291-296.

 

Erhirhie EO, Omoirri MA, Chikodiri SC, Ujam TN, Kesiena EE, Oseyomon JO (2020). Evaluation of microbial quality of vegetables and fruits in Nigeria: a review. International Journal of Nutrition Sciences 5(3):99-108.

 

Fowoyo PT (2012). Microbiological Assessment of Air contamination of vended fruits sold in the main markets in Lokoja, Kogi state Nigeria. Research Journal of Biological Sciences 7(9-12):355-360.

 

Kummerer K (2004). Resistance in the environment. Journal of Antimicrobial. Chemotherapy 54(2):311-320.
Crossref

 

Meher NN, Reaz MM, Mahmudul H, Fakruddin SI, Bhuiyan HR, Asif I (2011). Prevalence of Multi Drug Resistant Bacteria on Raw Salad Vegetables Sold in Major Markets of Chittagong City, Bangladesh, Middle-East Journal of Scientific Research 10(1):70-77.

 

Mohania D, Ravinder N, Manoj K, Aarti B, Mukesh Y, Shalini J, Francesco M, Vinod S, Om P, Hariom Y (2008). Molecular approaches for identification and characterization of lactic acid bacteria. Journal of Digestive Diseases 9(4):190-198.
Crossref

 

Nuermberger EL, Bishai WR (2004). Antibiotic resistance in Streptococcus pneumoniae: what does the future hold? Clinical Infectious Diseases 38(4):363-371.
Crossref

 

Nwachukwu E, Ezeama CF, Ezeanya BN (2008). Microbiology of polyethylene packaged sliced watermelon (Citrullus lanatus) sold by street vendors in Nigeria. African Journal of Microbiology Research 2:192-195.

 

Nwachukwu E, Osuocha HU (2014). Microbiological Assessment of Ready-to-Eat Sliced Pawpaw (Carica papaya) and Watermelon (Citrullus lanatus) Vended in Umuahia, Nigeria. International Journal of Current Microbiology and Applied Sciences 3(6):910-91691.

 

Ofor MO, Okorie VC, Ibeawuchi II, Ihejirika GO, Obilo OP, Dialoke SA (2009). Microbial contaminants in fresh Tomato Wash Water and Food Safety Considerations in south- Eastern Nigeria. Life Science Journal 1:80-82.

 

Olateru CT, Popoola BM, Alagbe GO, Ajao O (2020). Lactic acid bacteria fermentation of coconut milk and its effect on the Nutritional, Phytochemical, Antibacterial and Sensory Properties of Virgin Coconut oil produced. African Journal of Biotechnology 19(6):362-367.
Crossref

 

Rashmi HB, Bharti SK, Gogai M, Devi S, Anita, Ganguly S (2017). Antibiotic Resistance: Role of Fruits and Vegetables in the Food Basket. International Journal of Pure Applied Bioscience 5(4):169-173.
Crossref

 

Ray B, Bhunia AK (2007). Fundamental Food Microbiology. 4th Edition, CRC Press, USA P 492.

 

Shenge KC, Whong CM, Yakubu LL, Omolehin RA, Erbaugh JM, Miller SA, LeJeune, JT (2015). Contamination of tomatoes with coliforms and Escherichia coli on farms and in markets of northwest Nigeria. Journal of Food Protection 78(1):57-64.
Crossref

 

Tambekar DH, Mundhada RH (2006). Bacteriological quality of salad vegetables sold in Amravati City (India). Journal of Biological Sciences 6(1):28-30.
Crossref

 

Topalcengiz Z, Strawn LK, Danyluk MD (2017). Microbial quality of agricultural water in Central Florida. PLoSONE 12(4):e0174889.
Crossref

 

Uzeh RE, Alade FA, Bankole M (2009). The microbial quality of prepacked mixed vegetable salad in some retail outlets in Lagos, Nigeria. African Journal of Food Science 3(9):270-272.

 

Wadamori Y, John F, Malik AH (2016). Microbiological risk assessment and antibiotic resistance profiling of fresh produce from different soil enrichment system: A preliminary study. Cogent Food and Agriculture 2:1.
Crossref

 

World Health Organization (WHO) (2000). Overcoming Antimicrobial Resistance World Health Report on Infectious Diseases.

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