Oral application of Escherichia coli bacteriophage: safety tests in healthy and diarrheal children from Bangladesh
Shafiqul Alam Sarker
International Centre for Diarrheal Diseases Research, Bangladesh (icddr,b), Clinical Sciences Division, 68 Shaheed Tajuddin Ahmed Sharani, Mohakhali, Dhaka, 1212 Bangladesh
Search for more papers by this authorBernard Berger
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorYing Deng
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorSilas Kieser
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorFrancis Foata
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorDeborah Moine
Nestlé Institute of Health Sciences, EPFL Innovation Park, Functional Genomics Group, CH-1015 Lausanne, Switzerland
Search for more papers by this authorPatrick Descombes
Nestlé Institute of Health Sciences, EPFL Innovation Park, Functional Genomics Group, CH-1015 Lausanne, Switzerland
Search for more papers by this authorShamima Sultana
International Centre for Diarrheal Diseases Research, Bangladesh (icddr,b), Clinical Sciences Division, 68 Shaheed Tajuddin Ahmed Sharani, Mohakhali, Dhaka, 1212 Bangladesh
Search for more papers by this authorSayeeda Huq
International Centre for Diarrheal Diseases Research, Bangladesh (icddr,b), Clinical Sciences Division, 68 Shaheed Tajuddin Ahmed Sharani, Mohakhali, Dhaka, 1212 Bangladesh
Search for more papers by this authorPradip Kumar Bardhan
International Centre for Diarrheal Diseases Research, Bangladesh (icddr,b), Clinical Sciences Division, 68 Shaheed Tajuddin Ahmed Sharani, Mohakhali, Dhaka, 1212 Bangladesh
Search for more papers by this authorValérie Vuillet
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorFabienne Praplan
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorCorresponding Author
Harald Brüssow
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
For correspondence. E-mail: [email protected]; Tel. +41 21 785 8676; Fax +41 21 785 8544.Search for more papers by this authorShafiqul Alam Sarker
International Centre for Diarrheal Diseases Research, Bangladesh (icddr,b), Clinical Sciences Division, 68 Shaheed Tajuddin Ahmed Sharani, Mohakhali, Dhaka, 1212 Bangladesh
Search for more papers by this authorBernard Berger
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorYing Deng
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorSilas Kieser
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorFrancis Foata
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorDeborah Moine
Nestlé Institute of Health Sciences, EPFL Innovation Park, Functional Genomics Group, CH-1015 Lausanne, Switzerland
Search for more papers by this authorPatrick Descombes
Nestlé Institute of Health Sciences, EPFL Innovation Park, Functional Genomics Group, CH-1015 Lausanne, Switzerland
Search for more papers by this authorShamima Sultana
International Centre for Diarrheal Diseases Research, Bangladesh (icddr,b), Clinical Sciences Division, 68 Shaheed Tajuddin Ahmed Sharani, Mohakhali, Dhaka, 1212 Bangladesh
Search for more papers by this authorSayeeda Huq
International Centre for Diarrheal Diseases Research, Bangladesh (icddr,b), Clinical Sciences Division, 68 Shaheed Tajuddin Ahmed Sharani, Mohakhali, Dhaka, 1212 Bangladesh
Search for more papers by this authorPradip Kumar Bardhan
International Centre for Diarrheal Diseases Research, Bangladesh (icddr,b), Clinical Sciences Division, 68 Shaheed Tajuddin Ahmed Sharani, Mohakhali, Dhaka, 1212 Bangladesh
Search for more papers by this authorValérie Vuillet
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorFabienne Praplan
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
Search for more papers by this authorCorresponding Author
Harald Brüssow
Nutrition Health Research, Nestlé Research Centre, Nestec Ltd, Vers-chez-les-Blanc, Lausanne, 26 CH-1000 Switzerland
For correspondence. E-mail: [email protected]; Tel. +41 21 785 8676; Fax +41 21 785 8544.Search for more papers by this authorSummary
A T4-like coliphage cocktail was given with different oral doses to healthy Bangladeshi children in a placebo-controlled randomized phase I safety trial. Fecal phage detection was oral dose dependent suggesting passive gut transit of coliphages through the gut. No adverse effects of phage application were seen clinically and by clinical chemistry. Similar results were obtained for a commercial phage preparation (Coliproteus from Microgen/Russia). By 16S rRNA gene sequencing, only a low degree of fecal microbiota conservation was seen in healthy children from Bangladesh who were sampled over a time interval of 7 days suggesting a substantial temporal fluctuation of the fecal microbiota composition. Microbiota variability was not associated with the age of the children or the presence of phage in the stool. Stool microbiota composition of Bangladeshi children resembled that found in children of other regions of the world. Marked variability in fecal microbiota composition was also seen in 71 pediatric diarrhea patients receiving only oral rehydration therapy and in 38 patients receiving coliphage preparations or placebo when sampled 1.2 or 4 days apart respectively. Temporal stability of the gut microbiota should be assessed in case-control studies involving children before associating fecal microbiota composition with health or disease phenotypes.
Supporting Information
Additional Supporting Information may be found in the online version of this article at the publisher's web-site:
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emi13574-sup-0001-suppinfo1.pptx79.9 KB |
Fig. 1. High conservation of stool microbiota composition repeat DNA extractions from the same stool sample in six healthy Swiss children < 2 year of age (A to H). The DNA extraction was directly done from the frozen sample (three different aliquots from the stool, samples 1–3), after thawing and homogenization (samples 4) and one (samples 5) and two (samples 6) further rounds of freezing-thawing. The microbiota composition was highly reproducible for each child. |
emi13574-sup-0002-suppinfo2.tif133.1 KB |
Fig. 2. 3D Principal Coordinate Biplot of Unweighted UniFrac distances for duplicates of fecal microbiota of the same stool sample from children of Bangladesh. Lines connect the duplicate evaluations for the same stool. PC1 is 63%. The right cluster (blue ball symbols) represent diarrhea patients, the left cluster healthy control children. |
emi13574-sup-0003-suppinfo3.tif189 KB |
Fig. 3. Microbiota analysis in paired stool samples from Bangladeshi children with acute diarrhea treated with standard therapy. Same data as in Fig. 7 except that here the stool microbiota composition was analysed at genus level (colour code at bottom). |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
References
- Barletta, F., Ochoa, T.J., Mercado, E., Ruiz, J., Ecker, L., Lopez, G., et al. (2011) Quantitative real-time polymerase chain reaction for enteropathogenic Escherichia coli: a tool for investigation of asymptomatic versus symptomatic infections. Clin Infect Dis 53: 1223–1229.
- Bourdin, G., Schmitt, B., Marvin Guy, L., Germond, J.E., Zuber, S., Michot, L., et al. (2014a) Amplification and purification of T4-like Escherichia coli phages for phage therapy: from laboratory to pilot scale. Appl Environ Microbiol 80: 1469–1476.
- Bourdin, G., Navarro, A., Sarker, S.A., Pittet, A.C., Qadri, F., Sultana, S., et al. (2014b) Coverage of diarrhoea-associated Escherichia coli isolates from different origins with two types of phage cocktails. Microb Biotechnol 7: 165–176.
- Brüssow, H. (2005) Phage therapy: the Escherichia coli experience. Microbiology 151: 2133–2140.
- Brüssow, H. (2016) How stable is the human gut microbiota? And why this question matters. Environ Microbiol 18: 2779–2783.
- Brüssow, H., Sidoti, J., Link, H., Hoang, Y.K., Barclay, D., Dirren, H., and Freire, W.B. (1990) Age-specific prevalence of antibody to enterotoxigenic Escherichia coli in Ecuadorian and German children. J Infect Dis 162: 974–977.
- Bruttin, A., and Brüssow, H. (2005) Human volunteers receiving Escherichia coli phage T4 orally: a safety test of phage therapy. Antimicrob Agents Chemother 49: 2874–2878.
- Chibani-Chennoufi, S., Sidoti, J., Bruttin, A., Dillmann, M.L., Kutter, E., Qadri, F., et al. (2004) Isolation of Escherichia coli bacteriophages from the stool of pediatric diarrhea patients in Bangladesh. J Bacteriol 186: 8287–8294.
- David, L.A., Weil, A., Ryan, E.T., Calderwood, S.B., Harris, J.B., Chowdhury, F., et al. (2015) Gut microbial succession follows acute secretory diarrhea in humans. MBio 6: e00381–e00315.
- Dethlefsen, L., and Relman, D.A. (2011) Incomplete recovery and individualized responses of the human distal gut microbiota to repeated antibiotic perturbation. Proc Natl Acad Sci USA 108(Suppl.1): 4554–4561.
- Flores, G.E., Caporaso, J.G., Henley, J.B., Rideout, J.R., Domogala, D., Chase, J., et al. (2014) Temporal variability is a personalized feature of the human microbiome. Genome Biol 15: 531–544.
- Galtier, M., De Sordi, L., Maura, D., Arachchi, H., Volant, S., Dillies, M.A., and Debarbieux, L. (2016) Bacteriophages to reduce gut carriage of antibiotic resistant uropathogens with low impact on microbiota composition. Environ Microbiol 18: 2237–2245.
- Hurley, J.C. (1992) Antibiotic-induced release of endotoxin: A reappraisal. Clin Infect Dis 15: 840–854.
- Jiang, Z.D., Lowe, B., Verenkar, M.P., Ashley, D., Steffen, R., Tornieporth, N., et al. (2002) Prevalence of enteric pathogens among international travelers with diarrhea acquired in Kenya (Mombasa), India (Goa), or Jamaica (Montego Bay). J Infect Dis 185: 497–502.
- Junick, J., and Blaut, M. (2012) Quantification of human fecal bifidobacterium species by use of quantitative real-time PCR analysis targeting the groEL gene. Appl Environ Microbiol 78: 2613–2622.
- Koenig, J.E., Spor, A., Scalfone, N., Fricker, A.D., Stombaugh, J., Knight, R., et al. (2011) Succession of microbial consortia in the developing infant gut microbiome. Proc Natl Acad Sci USA 108(Suppl.1): 4578–4585.
- Kotloff, K.L., Nataro, J.P., Blackwelder, W.C., Nasrin, D., Farag, T.H., Panchalingam, S., et al. (2013) Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the Global Enteric Multicenter Study, GEMS): a prospective, case-control study. Lancet 382: 209–222.
- Lin, A., Bik, E.M., Costello, E.K., Dethlefsen, L., Haque, R., Relman, D.A., and Singh, U. (2013) Distinct distal gut microbiome diversity and composition in healthy children from Bangladesh and the United States. PLoS One 8: e53838.
- Liu, J., Kabir, F., Manneh, J., Lertsethtakarn, P., Begum, S., Gratz, J., et al. (2014) Development and assessment of molecular diagnostic tests for 15 enteropathogens causing childhood diarrhoea: a multicentre study. Lancet Infect Dis 14: 716–724.
- Martinez, L. (2012) The evolving threat of antimicrobial resistance. Options for Action. Geneva: WHO.
- McCallin, S., Sarker, S.A., Barretto, C., Sultana, S., Berger, B., Huq, S., et al. (2013) Safety analysis of a Russian phage cocktail: from metagenomic analysis to oral application in healthy human subjects. Virology 443: 187–196.
- Qadri, F., Svennerholm, A.M., Faruque, A.S., and Sack, R.B. (2005) Enterotoxigenic Escherichia coli in developing countries: epidemiology, microbiology, clinical features, treatment, and prevention. Clin Microbiol Rev 18: 465–483.
- Sarker, S.A., McCallin, S., Barretto, C., Berger, B., Pittet, A.C., Sultana, S., et al. (2012) Oral T4-like phage cocktail application to healthy adult volunteers from Bangladesh. Virology 434: 222–232.
- Sarker, S.A., Sultana, S., Reuteler, G., Moine, D., Descombes, P., Charton, F., et al. (2016) Oral phage therapy of acute bacterial diarrhea with two coliphage preparations: a randomized trial in children from Bangladesh. EBioMedicine 4: 124–137.
- Simeoni, U., Berger, B., Junick, J., Blaut, M., Pecquet, S., Rezzonico, E., et al. (2015) Gut microbiota analysis reveals a marked shift to bifidobacteria by a starter infant formula containing a synbiotic of bovine milk-derived oligosaccharides and Bifidobacterium animalis subsp. lactis CNCM I-3446. Environ Microbiol 18: 2185–2195.
- Smith, M.I., Yatsunenko, T., Manary, M.J., Trehan, I., Mkakosya, R., Cheng, J., et al. (2013) Gut microbiomes of Malawian twin pairs discordant for kwashiorkor. Science 339: 548–554.
- Subramanian, S., Huq, S., Yatsunenko, T., Haque, R., Mahfuz, M., Alam, M.A., et al. (2014) Persistent gut microbiota immaturity in malnourished Bangladeshi children. Nature 510: 417–421.
- Taniuchi, M., Sobuz, S.U., Begum, S., Platts-Mills, J.A., Liu, J., Yang, Z., et al. (2013) Etiology of diarrhea in Bangladeshi infants in the first year of life analyzed using molecular methods. J Infect Dis 208: 1794–1802.
- Thaiss, C.A., Zeevi, D., Levy, M., Zilberman-Schapira, G., Suez, J., Tengeler, A.C., et al. (2014) Transkingdom control of microbiota diurnal oscillations promotes metabolic homeostasis. Cell 159: 514–529.
- Vandenheuvel, D., Lavigne, R., and Brüssow, H. (2015) Bacteriophage therapy: Advances in formulation strategies and human clinical trials. Annu Rev Virol 2: 599–618.
- Weiss, M., Denou, E., Bruttin, A., Serra-Moreno, R., Dillmann, M.L., and Brüssow, H. (2009) In vivo replication of T4 and T7 bacteriophages in germ-free mice colonized with Escherichia coli. Virology 393: 16–23.
- Yang, C.J., Lee, N.Y., Lin, Y.H., Lee, H.C., Ko, W.C., Liao, C.H., et al. (2010) Jarisch-Herxheimer reaction after penicillin therapy among patients with syphilis in the era of the HIV infection epidemic: incidence and risk factors. Clin Infect Dis 51: 976–979.