Advances in Animal and Veterinary Sciences

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AAVS_MH20170531190538_Abbas

 

 

Research Article

 

Potential of House Mice in Harboring Multipel Bacteria and Threats to Public Health

 

Maysoon S. Abbas

Zoonosis Unit, College of Veterinary Medicine, University of Baghdad, Iraq.

 

Abstract | The aim of study was to explore the potential of house mice in carrying bacterial populations. For this purpose, a total of 100 stool samples were collected directly from intestine of individual (n=100) mice. To isolate and characterize bacteria, these samples were cultured on different types of growth media and isolates were identified based on rate of growth, characteristics of colonies, gram staining, acid fast staining, biochemical characteristics and chromogen production. Cumulative outcome of these properties guided the identification of Mycobacterium kansasii in 10% samples, Mycobacterium chelonae in 8%, Mycobacterium scrofulaceum in 7%, Salmonella typhimurium in 15%, Escherichia coli in 10%, Shigella dysenteriae in 30%, Proteus vulgaris in 5%, Pseudomonas aeruginosa 2% and Klebisella pneumoniae in 3%, Nocardia asteroides in 15%, where as Vibrio cholerae in 5% of tested samples. Many of these bacteria are important zoonotic pathogens. Therefore, house mice may act as important source of disease to humans. These results highlight the circulation of multiple bacterial populations in Iraqi house mice for the first time.

 

Keywords | Mice, Bacteria, Human

 

Editor | Kuldeep Dhama, Indian Veterinary Research Institute, Uttar Pradesh, India.

Received | June 02, 2017; Accepted | August 13, 2017; Published | August 22, 2017

*Correspondence | Maysoon S Abbas, Zoonosis Unit, College of Veterinary Medicine, University of Baghdad, Iraq; Email: maysoon.S.Abbas@gmail.com

Citation | Abbas MS (2017). Potential of house mice in harboring multipel bacteria and threats to public health. Adv. Anim. Vet. Sci. 5(8): 346-349.

DOI | http://dx.doi.org/10.17582/journal.aavs/2017/5.8.346.349

ISSN (Online) | 2307-8316; ISSN (Print) | 2309-3331

Copyright © 2017 Abbas et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

 

INTRODUCTION

 

The house mouse (Mus musculus) is a small mammal and mainly lives in close vicinity with humans and animals. House mice can notoriously contaminate food and water with their feces and may transmit diseases. The infectious agents in house mice may not result in clinical disease but may persistently shed pathogens in feces. In fact, these mammals are associated with subclinical disease and their dropping cause illness in human and other animals in vicinity (Treuting et al., 2012, Nathaniel et al., 2017). Changes in ecological dynamics and food webs enable house mice to establish pathogen populations that expand with human societies (Bonhomme et al., 2011, Frankova et al., 2016). However, any change in behavior and ecology may cause acute impact on the host through increasing in resident bacteria in the small intestine. (Nathaniel et al., 2017). Infection of mice with bacteria such as Staphylococcus aureus and Escherichiacoli release virulent factors that effect the infertility of mice (Sharma et al., 2017). It has been proposed that mice can transmit Lymphocytic choriomening it is virus (LCMV) an infection that may cause lethal impact in pregnant women (Bonthius, 2012). Additionally, mice can transmit endemicty phusrickettsial, chickenpox (Eremeeva et al., 2008), Leptospirosis through urine (Brown and Prescott, 2008) and mycobacteria through feces. Recent genetic studies in mice indicate that tuberculosis in mice is under multigenic control (Collette et al., 2017). Mice can be infected with mycobacteria through ingested food, contaminated with the feces of infected animals or humans. These pathogenic and opportunistic mycobacteria resistant to acid and can pass through the stomach of mice without being digested and mycobacteria can survive in tissues and organs in mice and can spread over long distances with the migration of mice (Biet et al., 2005). Salmonella typhi, causative agent of Typhoid fever, a systemic disease, can also be transmitted by mice as a consequence of systemic bacterial infection (Doutsch et al., 2016). Another study identified that mice carry Salmonella spp and can transmit to humans via the fecal-oral route. Shigella produce intestinal damage and bloody mucoid dysentery represents a major threat public health in humans and animal (Benoit and Marteyn, 2016). Nocardiosis is caused by the environmentally actinomycete Nocardia. It caused an emerging pyogranulomatous disease causing severe illness in humans and animals worldwide (Munoz et al., 2007). Escherichia coli is a major cause of diarrhoea and mortality in low-income countries. Vibrio is a facultative anaerobes mainly causing gastroenteritis and septicemia (Thompson et al., 2005) where as Proteus is opportunistic pathogen causing septic infection (Jessica et al., 2015). Klebsiella cause pneumonia, urinary tract infections, septicemia meningitis and diarrhea (Rashid and Ebringer, 2007).

 

These studies cumulatively highlight the potential of mice in harboring a plethora of pathogens and thus propose mice as a threat to public health (Guansheng et al., 2017; Claire et al., 2017; Meerburg et al., 2007). It is therefore imperative to investigate the dynamics of pathogens that are circulating in house mice in Iraq where these are widely distributed and are housed in close vicinity to human and animals.

 

MATERIALS AND METHODS

 

Al-huria city of Baghdad was chosen for the study and one hundred house mice were captured to collect feces directly from intestine of mice. These samples were then diluted in PBS and were individually inoculated in enrichment broth media for 24 hr at 37 C° before cultured on different type of media (MacConecky agar, Eosin methylene blue agar, Xylose lysine deoxycholate agar, Salmonella-Shigella agar, Thiosulfate-citrate-bile salts-sucrose agar, Blood agar). These selective and enrichment media were chosen based on the possibility of bacterial population in mice. The suspected pathogens were identified by growth of colony in gram staining, motility and different biochemical reaction. All feces samples were also cultured on Lowenstein-Jenson media after using decontamination (5%), oxalic acid, NaoH (4%) and incubated at 37°C for eight weeks. Diagnosis of mycobacteria was based on the rate of growth, characteristics features of bacterial colonies, acid-fast stain and the ability to production of chromo genes (Quinn et al., 2006).

 

RESULTS

 

Based on chemical characteristics, biochemical tests, growth features, a number of bacterial were identified (Table 1). Several collected samples were positive for more than one bacteria and thus represent a dynamic range of multiple pathogen harbored in these house mice. A differential percentage of positivity was mapped within these samples, which ranged from 2-35%. Cumulative results demonstrated that Mycobacterium kansasii (10%), Mycobacterium chelonae (8%), Mycobacterium scrofulaceum (7%), Salmonella typhimurium (15%), Escherichia coli (10%), Shigella dysenteriae (30%), Proteus vulgaris (5%), Pseudomona saeruginosa (2%), Klebisella pneumoniae (3%), Nocardia asteroides (15%), and Vibrio cholerae (5%) were amongst the most common pathogens prevalent in sampled mice.

 

Table 1: Types of bacteria isolated from faecal samples of mice

 

Type of bacteria

Number of positive isolates

Percentage positivity

Mycobacterium kansasii

10

10%

Mycobacterium chelonae

8

8%

Mycobacterium scrofulaceum

7

7%

Salmonella typhimurium

15

15%

Escherichia coli

10

10%

Shigella dysenteriae

30

30%

Proteus vulgaris

5

5%

Pseudomonas aeruginosa

2

2%

Klebisella pneumoniae

3

3%

Nocardia asteroides

15

15%

Vibrio cholera

5

5%

 

DISCUSSION

 

House mouse are the most dangerous rodent species and cause multiple damages to human resources by feeding on crops and stored commodities and by their faecal and urine contamination (Frankova et al., 2016). The present study revealed prevalence of different bacterial species in the feces of house mice. Generally, results of this study are in agreement with previous finding that mice tuberculosisis excreted through the faeces of infected animals and this maybe a source of infection for vertebrates and lead to spread of tuberculosis (Biet et al., 2005). In another study, it was identified that transmission of mycobacteria may occur through inhaling of aerosolized fecal material. Pathogenic mycobacteria in house mice were found in organs and excreted in their feces. Therefore, it is plausible that the infection occur through inhalation or ingestion of contaminated material, ectoparasites and animal bites (Fischer et al., 2000). In another study, based on 708 small mammals, different type of Mycobacterium species (M.parascrofulaceum, M.chimaera, M. arupense, intracellulare where identified in mice (Lies Durnez et al., 2008).

 

Salmonella infection in mice may come from different sources: contact with faeces of infected wild animals or human (Hulst et al., 2004; Guard-Petter et al., 1997). Previous studied have found the presence of S.enteritidis in spleens and livers of houses mice and thus can acquire infections from in different parts in livestock houses. On the other hands, Salmonella from mice can come from faeces of infected wild animals (Hilton et al., 2002).Three S. typhimurium bacteria were isolated from feces ofmice (Søndberg et al., 2016). S. typhimurium bacteria were isolated from feces, livers and spleens of mice. Another study found that house mice were positive for salmonella enteric serotype enteritids (SE) in house mice with a percentage of 3.7%. The results of other study indicate that Eschericia colican be isolated from intestinal contents (Narayanan et al., 2017).There are evidences that Shigella organisms can be isolated from mice and may produce intestinal damage and bloody mucoid dysentery in humans (Ahmed et al.,1990). It has been found that mice can be infected with the eight strains of bacteria, which are localized to different compartments (Martin and Polz, 2004; Meerburg et al., 2009).

 

Not only human, house mice also threaten other species of animals such as birds.Mice can transmit Klebsiella spp. ,Staphylococcus intermedius, Escherichiacoli and Pseudomonas spp., Enterococcusspp (Dagleish et al., 2017) in birds. House mice are recognized carrier of various infective agents and these agents may have zoonotic potential (Roble et al., 2012). In conclusion, this study determined the prevalence of pathogenic bacteria in house mice. These infected mice contaminate their surrounding environment, and may risk public health. Therefore, there is need to not only explore the full spectrum of pathogen in house mice but also to increase awareness in communities to consider isolation and decontamination of possible contaminated premises and food items.

 

ACKNOWLEDGMENTS

 

Authors would like to thank Zoonotic Diseases Unit in University of Baghdad, Veterinary Medicine for their help in the study.

 

CONFLICT OF INTEREST

 

No conflict of interest in this study.

 

AUTHORS CONTRIBUTION

 

All the works in this research was performed by Maysoon Sabah Abbas.

 

REFERENCES

 

  • Ahmed ZU, Sarker MR, Sack SK (1990). Protection of adult rabbitand monkeys from lethal shigellosis by oral immunization with a thyminerequirin and temperature-sensitive mutant of Shigella flexneri Y. Vaccine. 8:153–158. https://doi.org/10.1016/0264-410X(90)90139-D
  • Benoit S, Marteyn (2016). Shigella Vaccine Development: The Model Matters JSM Tropical Medicine and Research Shigella Vaccine Development: The Model Matters. JSM Trop. Med. Res. 1(1): 10115.
  • Biet F, Boschiroli ML, Thorel MF, Guilloteau LA (2005). Zoonotic aspects of Mycobacterium bovis and Mycobacterium avium-intracellulare complex (MAC). J. Vet. Res. 36: 411-436. https://doi.org/10.1051/vetres:2005001
  • Brown K, Prescott J (2008). Leptospirosis in the family dog: a public health perspective. Cmaj. 178 (4): 399–401. https://doi.org/10.1503/cmaj.071097
  • Bonthius DJ (2012). Lymphocytic choriomeningitis virus: an under recognized cause of neurologic disease in the fetus, child, and adult”. Seminars in Pediatric Neurology. 19 (3): 89–95. https://doi.org/10.1016/j.spen.2012.02.002
  • Bonhomme F, Orth A, Davidian JB (2011). Genetic differentiation of the house mouse around the Mediterranean basin: Matrilineal footprints of early and late colonization. Proc. Biol. Sci. 278(1708):1034–43.
  • Claire L Hews, Seav‐Ly Tran, Udo Wegmann Bernard Brett, Alistair DS, Walsham Devon, Kavanaugh Nicole J, Ward Nathalie Juge, Stephanie Schüller (2017). The StcE metalloprotease of enterohaemorrhagic Escherichiacoli reduces the inner mucus layer and promotes adherence to human colonic epithelium ex vivo. Cell. Microbiol. e12717.1-10.
  • Collette S Guy, Esther Tichauer, Gemma L Kay, Daniel J Phillips, Trisha L Bailey, James Harrison ,Christopher M Furze, Andrew D Millard, Matthew I Gibson, Mark J Pallen, Elizabeth Fullam (2017). Identification of the antimycobacterial functional properties of piperidinol derivatives. British J. Pharmacol. https://doi.org/10.1111/bph.13744
  • Dagleish MP, Ryan PG, Girling S, AL Bond (2017) Clinical Pathology of the Critically Endangered Gough Bunting (Rowettia goughensis) J. Comp. Path. 2017 Vol. -, 1e11 Available online .
  • Diane E, McClure DVM, PhD DACLAM (2012) Mycobacteriosis in the Rabbit and Rodent. Vet. Clin. Exot. Anim. 15:85–9929. https://doi.org/10.1016/j.cvex.2011.11.002
  • Doutsch SY, Arrieta MC, Tupin A, Valdez Y, L Caetano, M Antunes, Yen RB, Finlay B (2016). Nutrient Deprivation Affects Salmonella Invasion and its Interaction with the Gastro intestinal Microbiota. *PLOSON.
  • Eremeeva ME, Warashina WR, Sturgeon MM, Buchholz AE, Olmsted GK, Park SY, Effler PV, Karpathy SE (2008). “Rickettsia typhi and R. felis in rat fleas (Xenopsylla cheopis), Oahu, Hawaii”. Emerging Infect. Dis. 14 (10): 1613-1616. https://doi.org/10.3201/eid1410.080571
  • Fischer O, L Matlova, J Bartl, L Dvorska, I Melicharek, I Pavlik (2000).F indings of mycobacteria in insectivores and small rodents. Folia Microbiol. 45:147–152. https://doi.org/10.1007/BF02817414
  • Frankova M, Stejskal V, Rödl P, Aulický R (2016). Current threats of rodents and Integrated Pest Management (IPM) for stored grain and malting barley. Kvasny. Prum. 62(10): 306–311.
  • Garber Smeltzer M, Fedorka-cray P, Ladely S, Ferris K (2003). Salmonella enteric serotype enteritidis in table egg layer house environments and in mice in u.s layer house and associated risk factors. Avian Dis. 47(1): 134-142. https://doi.org/10.1637/0005-2086(2003)047[0134:SESEIT]2.0.CO;2
  • GIllespie RG, Lipman NS (2012). Infectious disease survey of musculus from pet stores in new York city. AM. ASSOC. LAB. ANIM. 51.(1):37-41
  • Guansheng Z, Junchi C, Zhen C Liang, Liang X Weiyang, ChangBao, Zhan YH, Y Yan Yang (2017). Short Syntheiicβ-Sheet Antimicrobial Peptides for the Treatment of Multidrug Resistant Pseudomonas aeruginosa Burn Wound Infections. Adv. Healthcare Mater. 6, 16011341-91-.20.
  • Guard-Petter J, Henzler DJ, Rahman MM, Carlson RW (1997) On farm monitoring of mouse-invasive Salmonella entericase rovar enteritidis and a model for its association with the production of contaminated eggs. Appl. Environ. Microbiol. 63:1588–1593.
  • Hilton AC, Willis RJ, Hickie SJ (2002). Isolation of Salmonella from urban wild brown rats (Rattus norvegicus) in the West Midlands, UK. Int. J. Environ. Health Res. 12:163–168 https://doi.org/10.1080/09603120220129328
  • Hulst VD, Arkel V, Kwakkel RP (2004) Campylobacter and Salmonella infections on organic broiler farms. NJAS-Wageningen. J. Life Sci. 52:101–108.
  • Carson JJ, Husain M, Lin L, David J, Orlicky C, Torres BAV (2016). Cytochrome bd-Dependent Bioenergetics and Antinitrosative Defenses in Salmonella Pathogenesis. 7(6): e02052-1621-25
  • Jessica N, Schaffer,  Melanie M, Pearson (2015). Proteus mirabilis and Urinary Tract. Infect. Microbiol. Spectr. 3(5): https://doi.org/10.1128/microbiolspec.UTI-0017-2013
  • Jun JW, Shin TJ, Kim JH, Shin SP, Han JEG HHeo, ME, Zoysa GW, Shin JI Young, SeChangPark (2014). A bacteriophage, designated pVp1, showed–resistant multiple-antibiotic–resistant V. parahaemolyticus pandemic strain infection. 210: 72–8.
  • Lies Durnez, Miriam Eddyani, Georgies F Mgode, Abdul Katakweba, Charles R. Katholi, Robert R Machang’u, Rudovik R Kazwala, Franc¸oise Portaels, Herwig Leirs (2008). First Detection of Mycobacteria in African Rodents and Insectivores Using Stratified Pool Screening. Appl. Environmen. Microbiol. 74(3): 768–773. https://doi.org/10.1128/AEM.01193-07
  • Martin F Polz (2004). Spatial Distribution and Stability of the Eight Microbial Species of the Altered Schaedler Flora in the Mouse Gastrointestinal. Tract. Appl. Environ. Microbiol. 70(5): 2791–2800. https://doi.org/10.1128/AEM.70.5.2791-2800.2004
  • Meerburg BG, Singleton GR, Kijlstra A (2009). Rodent-borne diseases and their risks for public health. Crit. Rev. Microbiol. 35(3): 221-70 https://doi.org/10.1080/10408410902989837
  • Meerburg BG, Kijlstra A (2007). Role of rodenti in transmission of salmonella and campylobacter. J. Sci. Food Agric. 87: 2774.2781.
  • Munoz J, Mirelis B, Aragon LM, Gutierrez N, Sanchez F, Espanol M (2007). Clinical and microbiological features of no cardiosis 1997-2003. J. Med. Microbiol. 56: 545-50. https://doi.org/10.1099/jmm.0.46774-0
  • Nathaniel L Ritz, Derek M Lin, Larry L Barton, Henry CLin (2017). Small Intestinal Bacterial Overgrowth Accelerates Completion of Maze Taskin Mice USA Annals of Exp. Biol. 2017. 5(1): 1-6.
  • Narayanan MS, Muyyarikkandys K, Venkitanarayanan MA, RA Malaradjou (2017). Oral supplementation of trans cinnamal dehyde reduces uropathogenic Escherichia coli colonization in a mouse model. 64(3):183–2511415.
  • Quinn PJ, Markey BK, Carter ME, Donnelly WJ, Leonard FC (2006). Vet. Microbiol. Microbial. Dis. Blackwell. 97 – 10552
  • Rajamouli P, Bradley EB, Banurekha K, Maher Y, Abdalla Martin (2016). Air way delivery of interferon cover expressing macrophages confers resistance to Mycobacterium avium infection in SCID mice. Physiol. Rep. 4 (21), e1300822.
  • Rashid, T; Ebringer, A (2007). “Ankylosing spondylitis is linked to Klebsiella--the evidence. Clinical Rheumatology. 26 (3): 858–864. https://doi.org/10.1007/s10067-006-0488-7
  • Roble GS, Gillespi, Lipman NS (2012). J. AM. Assoc. Lab. Anim. Sci. 51(1):37-41 IS infectious disease survey of Mus musculus from pet stores in new York city
  • Sharma T, Chauhan AT, Deepali Rana, KG Sonia, P Vijay (2017). Antifertility effect of sperm impairing factor isolated from bacteria in male mice. J. Microbiol. Exp. 5(2). 00141
  • Sondberg E, Jelsbak L (2016). Salmonella Typhimurium undergoes distinct genetic adaption during chronic infections of mice. BMC Microbiol. 16[30]. https://doi.org/10.1186/s12866-016-0646-2
  • Thompson FL, Gevers D, Thompson CC, Dawyndt P, Naser S, Hoste B, Munn CB, Swings J (2005). Phylogeny and Molecular Identification of Vibrioon the Basis of Multilocus Sequence Analysis”. Appl. Environ. Microbiol.71 (9): 5107–5115. https://doi.org/10.1128/AEM.71.9.5107-5115.2005
  • Treuting PM, Clifford CB, Sellers RS, Brayton CF (2012). Of Mice and Microflora: Considerations for Genetically Engineered Mice. Vet. Pathol. 49(1) 44-63. https://doi.org/10.1177/0300985811431446
  •