I thought I’d give examples of some of the Blastocystis-related activities in which I was involved in April.
I was lucky to be invited as 
part of the faculty for this year’s ECCMID conference in Amsterdam. I 
had an opportunity to give a talk on
Detection of protozoans using molecular techniques in routine clinical practice
(click link to watch it). I also co-authored a poster with the title
Blastocystis colonization correlates with gut
 bacterial diversity which is one of 
several studies recently performed by our group that suggest that 
Blastocystis is a biomarker – or an indicator if you wish – of a healthy
 gut microbial environment and high gut microbiota diversity. 
This very topic was one of the two major topics of my colleague Lee 
O’Brien Andersen’s PhD work; Lee just defended his thesis this Friday 
and being involved in his work is some of the most interesting, rewarding, and 
challenging professional activities I’ve experienced so far. I will soon provide a link to 
an electronic version of his thesis here on this site. I hope that we will be able to
 fund his post doc aiming to expand his work on comparative Blastocystis
 genomics, since he only just started this
 work. Also, I hope that we will be able to do much more research on 
Blastocystis’ impact on host immunity and gut microbiota using in vitro 
and in vivo models. We need to know much more about to which extent 
Blastocystis can actually induce changes in bacterial
 communities and what these changes are. We also need to know whether 
manipulation of gut bacteria in a Blastocystis carrier can lead to 
eradication of the organism. 
Last week, I was so fortunate to
 oversee the production of an e-learning course in faecal microbiota 
transplantation (FMT) for Unite European Gastroenterology (UEG), which will 
probably appear online already in June. FMT is currently used primarily for treating recurrent Clostridium difficile infections, but the application range may extend far beyond this. The presentations included both theoretical and live sessions,
 and it was a lot of fun to do, not only because of the topic, but also 
because my colleagues at the Agostino Gemelli University Hospital in Rome were extremely 
professional, enthusiastic and well-organised. The reason
 why FMT is interesting in a Blastocystis context includes the fact that
 while there are quite standardized guidelines as to what is not 
allowed in donor stool, there is no consensus on what is actually 
allowed in the stool. Obviously, Blastocystis will often
 be present in donor stool, and when conventional microbiological methods are used to screen donor stool for pathogens, Blastocystis will only rarely be picked up. Hence recipients may receive stool containing Blastocystis. And so of course we would like to know 
whether to recommend using or excluding stool positive for Blastocystis 
(and other common parasites such as Dientamoeba) for FMT.
 
 
 
