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microbiota is involved in their vector competence and may help in developing novel disease control tools. Pseudomonas aeruginosa is reported to be ubiquitous in the natural environment, humans, and animals. It has been used for biocontrol in plants.

Methods: Twenty-five live tsetse flies, collected from Yankari Game Reserve, Nigeria, were dissected under sterile conditions. The midgut was incubated successively in standard culture media. Suspected isolates were then subjected to biochemical tests. The 16S rRNA gene sequence was used to confirm the genotype. The positive isolate was also tested for susceptibility to 17 antimicrobials.

Results: Eight (32%) of the 25 flies tested were positive for P. aeruginosa. They were positive for oxidase, catalase, citrate, and motility tests and negative for urease, indole, Methyl Red tests. Analysis of 16S rRNA gene confirmed the identity of the isolate, and the phylogenetic relationship with other strains was established. The isolate was sensitive to fluoroquinolones and intermediate to chloramphenicol. Drug resistance was observed against aminoglycosides, penicillin, erythromycin, clindamycin and imipenem

Conclusion: The presence of P. aeruginosa in tsetse gut contributes to the repertoire of cultivable tsetse gut bacteria. It is crucial to investigate whether it could play a role in modulating the fly vector’s competence.

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References

  1. WHO. Trypanosomiasis, human African (sleeping sickness) 2021. https://www.who.int/news-room/fact-sheets/detail/trypanosomiasis-human-african-(sleeping-sickness) (accessed August 9, 2021).
     Google Scholar
  2. Kasozi KI, MacLeod ET, Ntulume I, Welburn SC. An update on african trypanocide pharmaceutics and resistance. Front Vet Sci. 2022;9.
    DOI  |   Google Scholar
  3. Doudoumis V, Alam U, Aksoy E, Abd-Alla AMM, Tsiamis G, Brelsfoard C, et al. Tsetse-Wolbachia symbiosis: Comes of age and has great potential for pest and disease control. J Invertebr Pathol. 2013;112:S94–103. https://doi.org/10.1016/j.jip.2012.05.010.
    DOI  |   Google Scholar
  4. Doudoumis V, Blow F, Saridaki A, Augustinos A, Dyer NA, Goodhead I, et al. Challenging the Wigglesworthia, Sodalis, Wolbachia symbiosis dogma in tsetse flies: Spiroplasma is present in both laboratory and natural populations. Sci Rep. 2017;7:4699. https://doi.org/10.1038/s41598-017-04740-3.
    DOI  |   Google Scholar
  5. Geiger A, Fardeau M-L, Njiokou F, Ollivier B. Glossina spp. gut bacterial flora and their putative role in fly-hosted trypanosome development. Front Cell Infect Microbiol. 2013;3. https://doi.org/10.3389/fcimb.2013.00034.
    DOI  |   Google Scholar
  6. Doudoumis V, Augustinos A, Saridaki A, Parker A, Abd-Alla AMM, Bourtzis K, et al. Different laboratory populations similar bacterial profile? The case of Glossina palpalis gambiensis. BMC Microbiol. 2018;18:148. https://doi.org/10.1186/s12866-018-1290-9.
    DOI  |   Google Scholar
  7. Geiger A, Fardeau M-L, Njiokou F, Joseph M, Asonganyi T, Ollivier B, et al. Bacterial Diversity Associated with Populations of Glossina spp. from Cameroon and Distribution within the Campo Sleeping Sickness Focus. Microb Ecol. 2011;62:632–43. https://doi.org/10.1007/s00248-011-9830-y.
    DOI  |   Google Scholar
  8. Griffith BC, Weiss BL, Aksoy E, Mireji PO, Auma JE, Wamwiri FN, et al. Analysis of the gut-specific microbiome from field-captured tsetse flies, and its potential relevance to host trypanosome vector competence. BMC Microbiol. 2018;18:146. https://doi.org/10.1186/s12866-018-1284-7.
    DOI  |   Google Scholar
  9. Lindh JM, Lehane MJ. The tsetse fly Glossina fuscipes fuscipes (Diptera: Glossina) harbours a surprising diversity of bacteria other than symbionts. Antonie Van Leeuwenhoek. 2011;99:711–20. https://doi.org/10.1007/s10482-010-9546-x.
    DOI  |   Google Scholar
  10. Bekele T, Tesfaye A, Sewunet T, Waktola HD. Pseudomonas aeruginosa isolates and their antimicrobial susceptibility pattern among catheterized patients at Jimma University Teaching Hospital, Jimma, Ethiopia. BMC Res Notes. 2015;8:488. https://doi.org/10.1186/s13104-015-1497-x.
    DOI  |   Google Scholar
  11. Ezeador CO, Ejikeugwu PC, Ushie SN, Agbakoba NR. Isolation, Identification And Prevalence Of Pseudomonas Aeruginosa Isolates From Clinical And Environmental Sources In Onitsha Metropolis, Anambra State. Eur J Med Health Sci. 2020;2. https://doi.org/10.24018/ejmed.2020.2.2.188.
    DOI  |   Google Scholar
  12. Gad GF, El-Domany RA, Zaki S, Ashour HM. Characterization of Pseudomonas aeruginosa isolated from clinical and environmental samples in Minia, Egypt: prevalence, antibiogram and resistance mechanisms. J Antimicrob Chemother. 2007;60:1010–7. https://doi.org/10.1093/jac/dkm348.
    DOI  |   Google Scholar
  13. Chin-A-Woeng TFC, Bloemberg GV, Mulders IHM, Dekkers LC, Lugtenberg BJJ. Root colonization by Phenazine-1-Carboxamide-Producing bacterium Pseudomonas chlororaphis PCL1391 is essential for Biocontrol of tomato foot and root rot. Mol Plant-Microbe Interactions®. 2000;13:1340–5. https://doi.org/10.1094/MPMI.2000.13.12.1340.
    DOI  |   Google Scholar
  14. Haas D, Défago G. Biological control of soil-borne pathogens by fluorescent pseudomonads. Nat Rev Microbiol. 2005;3:307–19. https://doi.org/10.1038/nrmicro1129.
    DOI  |   Google Scholar
  15. Lanotte P, Watt S, Mereghetti L, Dartiguelongue N, Rastegar-Lari A, Goudeau A, et al. Genetic features of Pseudomonas aeruginosa isolates from cystic fibrosis patients compared with those of isolates from other origins. J Med Microbiol. 2004;53:73–81. https://doi.org/10.1099/jmm.0.05324-0.
    DOI  |   Google Scholar
  16. Anayo OF, Scholastica EC, Peter OC, Nneji UG, Obinna A, Mistura LO. The Beneficial Roles of Pseudomonas in Medicine, Industries, and Environment: A Review. IntechOpen. 2019. https://doi.org/10.5772/intechopen.85996.
    DOI  |   Google Scholar
  17. Vaishnav P, Demain AL. Unexpected applications of secondary metabolites. Biotechnol Adv. 2011;29:223–9. https://doi.org/10.1016/j.biotechadv.2010.11.006.
    DOI  |   Google Scholar
  18. Challier A, Laveissière C. Un nouveau piège pour la capture des glossines (Glossina : Diptera, Muscidae) : description et essais sur le terrain [A new trap for catching tsetse flies (Glossina: Diptera, Muscidae): description and field trials]. Cah ORSTOMSérie Entomol Médicale Parasitol. 1973;11:251–62. French.
     Google Scholar
  19. Pollock JN. Training manual for Tsetse control personnel. Tsetse biology, systematics and distribution, techniques. Vol. 1. Rome, Italy: FAO; 1982.
     Google Scholar
  20. Bauer AW, Kirby WMM, Sherris JC, Turck M. Antibiotic Susceptibility testing by a standardized single disk method. Am J Clin Pathol. 1966;45:493–6. https://doi.org/10.1093/ajcp/45.4_ts.493.
    DOI  |   Google Scholar
  21. Grönemeyer JL, Burbano CS, Hurek T, Reinhold-Hurek B. Isolation and characterization of root-associated bacteria from agricultural crops in the Kavango region of Namibia. Plant Soil. 2012;356:67–82. https://doi.org/10.1007/s11104-011-0798-7.
    DOI  |   Google Scholar
  22. Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: Molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol. 2018;35:1547–9. https://doi.org/10.1093/molbev/msy096.
    DOI  |   Google Scholar
  23. Felsenstein J. Confidence limits on phylogenies: an approach using the bootstrap. Evol Int J Org Evol. 1985;39:783–91. https://doi.org/10.1111/j.1558-5646.1985.tb00420.x.
    DOI  |   Google Scholar
  24. Stover CK, Pham XQ, Erwin AL, Mizoguchi SD, Warrener P, Hickey MJ, et al. Complete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogen. Nature. 2000;406:959–64. https://doi.org/10.1038/35023079.
    DOI  |   Google Scholar
  25. Gaithuma A, Yamagishi J, Hayashida K, Kawai N, Namangala B, Sugimoto C. Blood meal sources and bacterial microbiome diversity in wild-caught tsetse flies. Sci Rep. 2020;10:5005. https://doi.org/10.1038/s41598-020-61817-2.
    DOI  |   Google Scholar
  26. Adejobi A, Ojo O, Alaka O, Odetoyin B, Onipede A. Antibiotic resistance pattern of Pseudomonas spp. from patients in a tertiary hospital in South-West Nigeria. Germs. 2021;11:238. https://doi.org/10.18683/germs.2021.1260.
    DOI  |   Google Scholar