We need to talk about chloramphenicol — how does this antibiotic cause damage to eukaryotes?

A group of scientists from Japan–led by Prof Takashi Kamakura of Tokyo University of Science–has demonstrated, for the first time, the molecular and cellular basis of the “adverse” effects of the antibiotic chloramphenicol on eukaryotic cells. Concluding their study published in Scientific Reports, they state, “Identification of the molecular target of chloramphenicol may lead to better elucidation and resolution of its side effects in humans.”

Antibiotics are often the treatment of choice for bacterial or fungal infections. Chloramphenicol is an example of a broad-spectrum antibiotic that’s active against most bacteria and widely used in human and veterinary medicine. However, it has varied side effects–such as human aplastic anemia, bone marrow suppression, and gray baby syndrome–which limit its prescription. A drug’s side effects are usually thought to be due to its interaction with entities other than the “target” molecules. The causes of the side effects of chloramphenicol have remained unknown to date, but this team of scientists from Japan has demonstrated one of the possible mechanisms of the effect of chloramphenicol on eukaryotic cells. The researchers state, “High doses of chloramphenicol have been known to cause mitochondrial damage in eukaryotes,” but also go on to say, “Our study shows that drugs have novel secondary targets in eukaryotes.”

As the model eukaryotic organism for the study, they used the rice blast fungus Pyricularia (Magnaporthe) oryzae. When asked about the significance of this model organism, Prof Kamakura says, “The rice blast fungus is an economically important pathogen that causes destructive disease in rice, which is the staple food of Japan. Thus, from the perspective of food security, it is important to understand the infection strategy of this pathogen and implement ways to control the damage to crops.” He also cites another interesting fact, “the genome of this fungus has considerably less ‘junk’ DNA–the ‘noncoding’ part of the genome that does not code for any functional proteins. This, along with the low number of targetable functional proteins, makes the rice blast fungus an ideal model for the screening of novel molecular targets of drugs.”

The rice blast fungus uses a peculiar structure called the “appressorium,” which functions in surface recognition, binding, and subsequent infection. The fungus infects the plant using a 3-cell structure called “conidium,” which has a “germ tube” with the appressorium at the end. The appressorium initiates contact with the host (plant) cell and is crucial in the infection cycle. This entire process is known to be dependent on the mitotic division of the single-cell germ tube and cell differentiation. Given the fact that cell differentiation depends on several different molecular components, these molecules can also be “targets” of several drugs. It is this principle, validated by previous studies in the field, that was exploited by the research team led by Prof Kamakura.

The researchers first exposed a suspension of the fungal “conidia” to different concentrations of chloramphenicol. After 6 hours, they found via microscopic observation that the germination of the conidia or the length of the germ tube remained unaffected, but the percentage of appressorium formation significantly dwindled. Prof Kamakura’s team thus concluded that chloramphenicol specifically targets appressorium formation in the rice blast fungus, which is a novel finding.

Next, they “screened” for chloramphenicol targets in the entire genome of the rice blast fungus. Of the 86 peptides that were targeted, 14 were known rice blast fungus peptides, and only 2 were functionally active proteins (proteins from the “coding region” of a gene). One of these was extremely similar to a highly conserved eukaryotic protein called Dullard, and the researchers termed this “MoDullard.” The Dullard protein is known to play a role in cell differentiation in eukaryotes. The researchers found that MoDullard was expressed the most at the appressorium formation stage. They also performed functional analysis by “knocking out” the MoDullard gene, and found that mutants with no MoDullard were not able to produce the appressorium, but were also resistant to chloramphenicol. This confirmed that chloramphenicol targets this protein.

Finally, to determine the target in humans, they identified 5 candidate peptides from the human genome that bore resemblance to MoDullard. They isolated the gene for each of these peptides and transferred it into the MoDullard-knockout mutant. They found that one of the peptides, called CTDSP1, complemented the “lost” function of MoDullard in the mutant cells–meaning that the cells with CTDSP1 introduced were able to produce appressorium. Chloramphenicol was again found to block the formation of this appressorium, which led the researchers to confirm that CTDSP1 is indeed a target of chloramphenicol in humans.

To put these results into perspective, Prof Kamakura states, “A more detailed analysis of the mechanism of inhibition of appressorium formation revealed for the first time here may lead to the development of new control methods for the rice blast fungus. Also, drug screening using the rice blast fungus may lead to the elucidation of yet-unknown side effects or drug repositioning to discover novel effects of existing drugs whose safety profiles have been confirmed.”

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Tokyo University of Science (TUS) is a well-known and respected university, and the largest science-specialized private research university in Japan, with four campuses in central Tokyo and its suburbs and in Hokkaido. Established in 1881, the university has continually contributed to Japan’s development in science through inculcating the love for science in researchers, technicians, and educators.

With a mission of “Creating science and technology for the harmonious development of nature, human beings, and society”, TUS has undertaken a wide range of research from basic to applied science. TUS has embraced a multidisciplinary approach to research and undertaken intensive study in some of today’s most vital fields. TUS is a meritocracy where the best in science is recognized and nurtured. It is the only private university in Japan that has produced a Nobel Prize winner and the only private university in Asia to produce Nobel Prize winners within the natural sciences field.

Website: https://www.tus.ac.jp/en/mediarelations/

Dr. Takashi Kamakura is a Professor in the Department of Applied Biological Science, Faculty of Science and Technology at the Tokyo University of Science. He is a distinguished researcher with over 55 publications, and is also the corresponding author of this paper. He has been associated with the Japan Society for Bioscience, Biotechnology, and Agrochemistry and the Pesticide Science Society of Japan in the past. His areas of research include molecular biology, microbial toxicology, applied genetics, molecular pathology, applied microbiology, and agricultural science.

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