By Claus D. Volko, MD, MSc


Symbiont Conversion Theory is a new scientific theory, summarizing and generalizing efforts that  have been made by various researchers in the past years; it could even be perceived as a new  scientific paradigm. This theory states that microorganisms and cells which are commonly  considered to display parasitic behaviour can be “educated” and transformed into symbionts. This is not just a hypothesis but a theory since there is already evidence that proves that this is possible.  The primary motivation for developing this theory is the failure of classical approaches to therapy  of cancer and infectious diseases that follow the paradigm “destroy and kill”. It is common  knowledge about medical doctors that chemotherapy and radiation therapy have detrimental side  effects on healthy, functional tissue, and also that antibiotics can harm benevolent cells. These  negative side effects can possibly be avoided by the new approach of treating parasitic diseases by  converting the culprits into symbionts of which the human organism profits. Another motivation for developing this theory is that some researchers have suggested bacteria and other microbes have  certain innate rights themselves [Cockell]. 

Motivation and Goals 

Symbiont Conversion Theory is the statement that parasites can be converted into symbionts, and it  explains by a couple of examples how this can be done. There is both a practical and an ethical  motivation for the development of this theory. Some may dismiss the ethical dimension as being  unimportant; after all, who empathizes with microorganisms, except perhaps some crazy people?  However, even if you dismiss the ethical component, Symbiont Conversion Theory has a practical  value: it is just too well-known a matter of fact that chemotherapy, radiation therapy and antibiotics  can have harmful side-effects which are better to be avoided. 

The long-term goal is to create organisms, most of all humanoid organisms, that have an improved  immune system. Instead of destroying and killing intruders, the immune system of this post-human  species should educate the parasites and convert them into symbionts. This, of course, is only a  long-term goal. It requires synthetic biology to reach a level that allows to create artificial immune  systems. It also requires artificial life and computational systems biology to be far more developed  than now, so that synthetic organisms can be simulated on a computer before the modifications are  actually implemented, to avoid mistakes. This may sound more like fiction than science, but it  actually is science. Moreover, this is only the long-term goal. The short-term goal is to make new  treatments of cancer and infectious diseases possible by means of signalling cascades triggered by  hormones and by modification of microorganisms using synthetically engineered bacteriophages  that do not kill bacteria but rather alter their behaviour. 

Microorganisms acting as pathogens 

In the 19th century Robert Koch made the discovery that certain diseases are caused by infection  with microorganisms. Since then, it has become common knowledge that infectious diseases may  be caused by bacteria or other types of microorganisms, such as protozoa or fungi. While symbionts are microorganisms that live in us and from which we profit, parasites harm us  while taking advantage of our organisms. Bacteria are known to be both parasites and symbionts,  for instance in the intestinal flora there are bacteria that act as symbionts, while pathogens that  cause diseases are to be considered parasites. 

The harmful thing about bacteria is primarily their toxins, which are chemical compounds  synthesized and secreted by them that interfere with the metabolism of the host organism and thus  affect it in a negative way. However, one must not forget either that the actual symptoms of  bacterial infections are most of all caused by the way the immune system reacts to them, i. e. by  inflammation. We notice pain, see the doctor, and the doctor makes the diagnosis pharyngitis,  laryngitis, pneumonia etc. Then the doctor concludes that the cause of the inflammation is the  bacteria and he or she is most likely to prescribe antibiotics to destroy and kill these invaders. From  


a strictly scientific point of view, it is of course not true to say that the direct cause of the  inflammation is bacterial infection; it is just an indirect cause. The actual “culprit”, so to speak, is  the human immune system. 

We must, however, not make the mistake to believe that the immune system were a bad thing and  that the patient would profit from disabling the immune system entirely. It is easy to observe in  immune-deficiency syndroms such as AIDS what negative effects on health a heavily suppressed  immune system may have. The actual problem is not the immune system per se but inflammation.  Many doctors prescribe cortisone to suppress inflammation and treat some infectious diseases this  way, partly in addition to antibiotics. However, cortisone is a bad thing since it not only suppresses  inflammation but also the immune system as such. What would be more desirable would be  suppression of inflammation while sustaining the other mechanisms of immunity such as  phagocytosis and antigen-antibody reactions. According to my late mentor Uwe Rohr, this can be  achieved by means of the so-called adiols (androstenediol and androstanediol). The adiols are  steroidal hormones just like cortisone. Uwe Rohr proposed that giving the patient high doses of soy  isoflavones would lead to a conversion of other steroidal hormones into adiols and thus  inflammation would be suppressed while at the same time the other functions of the immune system would not be hampered but, on the contrary, would be boosted [Rohr]. 

While being a loyal disciple of Uwe Rohr, I would like to go even beyond that. It is not desirable  from an ethical point of view that the immune system destroys and kills bacteria and other cells that  have a detrimental effect on the host organism. After all, these pathogens are living things as well,  so they should also have a right to life. That is why I propose a mechanism to “educate” and convert pathogens to cells that are beneficial for the host organism. 


What applies to microorganisms goes for cancer as well, at least to some extent. Cancer is a  potentially deadly disease caused by cells of the host organism that have undergone mutation and  behave in a manner that harms the host organism. Why should it not be possible to convert these  cancer cells back into normal, functional tissue? 

Uwe Rohr has in particular dealt with cancer. He shared Rudolf Virchow’s view that cancer cells are basically cells that “have lost the ability to convert themselves into functional epithelial tissue”. He  proposed a method to resolve this, for which he adopted the term “Modify and Repair”, which had  originally been coined by researchers from Harvard Medical School and MIT in context of repair of 

blood capillaries in a malignant tumor [Jain]. In Uwe Rohr’s opinion, this process could be  undergone by application of steroid hormones that have previously been blocked. Isoflavones such  as daidzein, which share biochemical similarities with a particular group of steroidal hormones  known as adiols, modulate stem cells in plants where they have been derived from, such as soy and  red clover, and this effect can apparently be obtained in the human organism as well [Schilling]. In  pregnancy, adiol and 2-methoxy-estradiol stabilize membranes and convert stem cells into  differentiated functional cells [Tagawa, Rohr, Kobayashi]. This, according to Uwe Rohr, could be  used to treat cancer în humans effectively without aiming to destroy or kill the malignant cells. 

Reprogramming of B cell leukemia cells 

A paper that takes the same line as Uwe Rohr has recently been published by James Scott  McClellan and his team [McClellan]. It states that BCR-ABL1+ precursor B-cell acute  lymphoblastic leukemia is “characterized by a block in differentiation due in part to the somatic loss of transcription factors required for B-cell development” and that the authors “hypothesized that  overcoming this differentiation block by forcing cells to reprogram to the myeloid lineage would  reduce the leukemogenicity of these cells”. This could be achieved “by exposure to myeloid  differentiation-promoting cytokines in vitro or by transient expression of the myeloid transcription  factor C/EBP alpha or PU.1”. According to the authors, “[t]he resultant cells were clonally related to 


the primary leukemic blasts but resembled normal macrophages in appearance, immunophenotype,  gene expression, and function”. 

The paper also refers to a publication by Nowak which gives an overview of several other  hypotheses regarding the possibility to treat leukemia by stimulating the differentiation of the  malignant cells [Nowak], but it also states that “[t]o date, […] differentiation therapy has only been  used routinely in a subtype of acute myeloid leukemia, namely, acute promyelocytic leukemia  (APL)”. 

Furthermore, the authors refer to work by Graf and coworkers, which “has demonstrated that  immature B cells can be reprogrammed to apparently normal macrophages although enforced  expression of C/EBP alpha” and has “also demonstrated that a human B-ALL cell line can be  

induced to reprogram into macrophages” [Xie, Rapino]. In contrast to these older publications,  McClellan and his co-authors “report here the first example to our knowledge of myeloid  reprogramming of primary human BCR-ABL1+ B-ALL cells occurring in samples from multiple  different patients” and “demonstrate that myeloid reprogramming can be accomplished through the  action of soluble cytokines without genetic manipulation of leukemic cells”. However, there is still an unsolved problem: “Even after a second round of sorting and culturing B ALL blasts in reprogramming conditions, a population of residual blasts remains.” The authors  “speculate that our culture methods are not yet optimized for maximal reprogramming”. Another recent publication on the reprogramming of cancer cells has been authored by Akihiro  Fujikawa [Fujikawa]. This paper states that targeting a receptor-type protein tyrosine phosphatase  called PTPRZ “inhibits stem cell-like properties and tumorigenicity in glioblastoma cells”.  Moreover, an Israeli group around Anna Shteinfer-Kuzmine has published a paper that deals with  selective induction of apoptosis in cancer cells [Shteinfer-Kuzmine]. Although apoptosis is  generally considered to be a form of cell death, according to Uwe Rohr the same processes that  initiate apoptosis may also lead to differentiation of stem cells into functional tissue. 

Reprogramming Bacteria 

In a recent study by Liao et al., it was found that adding an acetyl tag to the histone HU modified  both “the thermal stability and DNA binding kinetics of HU” [Liao]. “Accordingly, this  modification likely destabilizes the chromosome structure and regulates bacterial gene transcription. This work indicates that acetyllysine plays an important role in bacterial epigenetics.” In their  conclusions, the authors point out that “[i]ntroducing two mutations into E. coli HU alpha converts  a commensal strain into an invasive form, so it is likely that post-translational modification of HU  may exert similar effect” [Koli]. Moreover, “[s]uch molecules may modulate the transcription activation profile of pathogen and eliminate the virulence without killing the bacteria, thereby  preventing the emergence of drug resistance” [Dickey]. 

Summary and Conclusions 

This paper marks only the beginning of the new scientific paradigm of Symbiont Conversion  Theory. In this paper, several publications have been cited which demonstrate that it is possible to  “transform”, “convert” or “reprogram” malignant cells as well as intruders (i. e., bacteria) into  differentiated, functional cells that actually have a beneficial effect for the host organism. Thus, it  has been shown that parasites can be “educated” to become symbionts. This makes Symbiont  Conversion Theory not just a hypothesis, but a theory. My own contribution is that I have  generalized several novel attempts at treating various forms of disease and pointed out what they  have in common, i. e. that their mechanism is to convert parasites into symbionts. This theory also has certain implications for politics. Just like Charles Darwin’s principle of natural  selection can be transferred to political reality, which results in the concept of Social Darwinism  (that itself is sometimes considered inhumane), Symbiont Conversion Theory lays the foundation of a political concept that prefers integration of foreigners, no matter whether they are initially  


benevolent or hostile, instead of segregating and removing them from the country. Thus, Symbiont  Conversion Theory when applied to politics is a modern form of Social Darwinism, but a far more  positive and humane one. 

A final note: Originally I wanted to call Symbiont Conversion Theory simply Symbiosis Theory.  But then I realized that there is another theory, namely Serial Endosymbiotic Theory, coined by  Lynn Margulis, which would also deserve to be called Symbiosis Theory. I therefore propose that  the term Symbiosis Theory should be used as an umbrella term for the two of these theories. 


[Cockell] C.S. Cockell, “Microbial rights?”, EMBO Rep. 2011 Mar 3; 12(3): 181 

[Dickey] S.W. Dickey, “Different drugs for bad bugs: antivirulence strategies in the age of antibiotic resistance”, Nat Rev Drug Discov. 2017 Jul;16(7):457-471 

[Fujikawa] A. Fujikawa et al., “Targeting PTPRZ inhibits stem cell-like properties and  tumorigenicity in glioblastoma cells”, Scientific Reports volume 7, Article number: 5609 (2017), doi:10.1038/s41598-017-05931-8 

[Jain] R.K. Jain, “Taming vessels to treat cancer”, Sci Am. 2008 Jan;298(1):56-63 

[Kobayashi] S. Kobayashi et al., “Reproductive history and breast cancer risk”, Breast Cancer. 2012 Oct; 19(4): 302–308 

[Koli] P. Koli et al., “Conversion of commensal Escherichia coli K-12 to an invasive form via  expression of a mutant histone-like protein”, MBio. 2011 Sep 6;2(5). pii: e00182-11 

[Liao] J.H. Liao et al., “Acetylome of Acinetobacter baumannii SR17 Reveals a Highly-Conserved  Modification of Histone-Like Protein HU”, Front Mol Biosci. 2017 Nov 27;4:77 

[McClellan] S. McClellan et al., “Reprogramming of primary human Philadelphia chromosome positive B cell acute lymphoblastic leukemia cells into nonleukemic macrophages”, Proc Natl Acad  Sci U S A. 2015 Mar 31;112(13):4074-9 

[Nowak] D. Nowak et al., “Differentiation therapy of leukemia: 3 decades of development”, Blood.  2009 Apr 16;113(16):3655-65 

[Rapino] F. Rapino et al., “C/EBP alpha induces highly efficient macrophage transdifferentiation of B lymphoma and leukemia cell lines and impairs their tumorigenicity”, Cell Rep. 2013 Apr  25;3(4):1153-63 

[Rohr] U.D. Rohr et al., “Cancer protection of soy resembles cancer protection during pregnancy”,  Horm Mol Biol Clin Invest 2010; 3(2):391-409 

[Schilling] T. Schilling et al., “Effects of phytoestrogens and other plant-derived compounds on  mesenchymal stem cells, bone maintenance and regeneration”, J Steroid Biochem Mol Biol 2014;  139:252-261 

[Shteinfer-Kuzmine] A. Shteinfer-Kuzmine et al., “Selective Induction of Cancer Cell Death by  VDAC1-Based Peptides” (BGN), Molecular Oncology, April 2018 


[Tagawa] N. Tagawa et al., “Serum concentrations of androstenediol and androstanediol sulfate, and their relation to cytokine production during and after normal pregnancy”, Steroids 2004;  69(10):675-680 

[Xie] H. Xie et al., “Stepwise reprogramming of B cells into macrophages”, Cell. 2004 May  28;117(5):663-76 

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