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Drug-resistant infections are a crucial issue in the modern medical field. These infections,
developed by the irresponsible prescription and use of antibiotics have the potential to become a
worldwide, life-threatening epidemic if researchers are unable to find efficient and potent
treatments. Current efforts to develop these treatments are poorly coordinated and have little
concentration as there are almost too many potential methods of treatment being researched. This
lack of coordination and cooperation in research efforts has lead to repetition in projects and a
lack of directed effort. By coordinating research activities and compiling findings, the path to
collaboration in drug resistant infection research. The purpose of this paper is to explain why
historical and present collaborations are leading to discoveries in related fields. The audience for
this paper is intended to be those in charge of coordinating and organizing research in academia
or industry, including CTOs, senior scientists and lab coordinators. Those in the intended
audience would see this paper published in a scientific journal, such as PLOS One, or other
Abstract
decreased over the past 3 decades. Collaboration in this research is rarely seen in this field of
study and this lack of coordination has lead to inefficiencies and prolonged advancement. This
paper asserts that increased collaboration in drug-resistant infection research will allow for the
sharing of resources, increased oversight of research and accelerated advancement. The benefits
of collaboration can be seen in both historical collaborations, the Human Genome Project and the
discovery of bacterial gene control, as well as in recent research collaborations, the Accelerating
Medicine Partnership and CFAR HIC Continuum of Care Working Group. Funding from both
public and private organizations have an increased focus on collaboration in research and will be
Starting in 1911, the development of novel antibiotics was plentiful. However, since the
mid to late 1990s, antimicrobial agent discovery has stalled heavily with the discovery of only 17
new treatments in the past 25 years [3]. This is out of the 150 already readily used today [3].
With approximately four treatments per year being developed from 1978 to 1993 and
plummeting to less than one per year from 1993 to the present, this marks a significant decrease
in drug-resistant treatment progress [3]. This substantial decrease in advancement is not due to a
lack of interest in this research, but due to the emergence of new drug resistant infections making
discovery and development has called into question the methods that are being used to develop
these treatments. The general research community has tried to combat this decrease is progress
by diversifying the types of treatments that they are working to develop, however this has shown
to have little effect as the rate of developing new treatments has not been significantly increased.
On the contrary, by diversifying research efforts, collaboration and coordination has been
negatively impacted. This independent mentality to research has led to many groups being
With that being said, the purpose of this essay will be to explain how collaboration in
drug-resistant treatment research is beneficial to the greater good and researchers alike as well as
demonstrate how historical and present collaborations have succeeded in streamlining research
efforts. Popular topics of contention, including sacrifices of intellectually property and concerns
with potential economic loss, will also be addressed to prove how all costs associated with
collaboration are greatly outweighed by their benefits to mankind. By doing this, it is hoped that
the drug-resistant infection treatment research community will be convinced of the importance of
Collaboration through the sharing of data and research plans will allow for more research
to be done in a shorter period of time as individuals working in separate labs researching similar
treatment options will be able to coordinate what research they are conducting. This will
decrease the likelihood of overlap in research pipelines. This decrease in redundant research will
streamlining of information for the development of cures, there is a multitude of other benefits
associated with this approach. Large collaborations between groups of scientists have been seen
to improve the quality and robustness of data and experimental results [10]. This is due to the
increased oversight of having multiple entities invested in the research being conducted and
those entities being knowledgeable of the work being done. Currently, many research efforts are
financially backed by the government and private investors that have minimal technical
knowledge of the research being conducted and because of this have little ability to know the
quality of research being produced [10]. By having other research organizations investing in
research, not financially but with manpower and intellect, there is greater emphasis and
expectation for data to be reproducible between entities and for a strong commitment to good
scientific practices. This increased oversight also positively impacts the credibility and validity
of the research being conducted, thus through collaboration the quality of research is improved.
Collaboration and coordination also offer the opportunity for discussion and
disagreement [10]. While conducting research, there is often the tendency for data that is is not
While many times this may be the case, there is the potential that this overlooked data could
contain vital information to the development of the treatment being investigated. Collaboration
increases the likelihood that this obscure data will be reviewed and considered seriously as the
progression of the research will greatly effect more individual career goals and financial security.
Again, this increased oversight by collaboration participants will decrease the potential of
Finally, collaboration allows for the sharing of resources between institutions. More often
than not, those in private industry or in private research institutions have more resources
available to them than those in academia or publicly funded research groups [8]. This is mostly
due to the affluence of private industry over public funding. By opening collaboration between
the two separate worlds of research there is the potential for the private institutions to share
contribute in manpower and ingenuity. This trade off in resources will meet the needs of both
Although not the standard in the field of medical research historically, there are many
examples of past successful collaborations; one of which is the Human Genome Project. This
notable example of human collaboration and directed effort allowed for major strides in the field
of genetics and molecular biology, specifically the case of mapping of the human genome in only
four years [9]. This would not have been possible without the transparent data sharing that was
conducted throughout the project. By conducting data sharing, results were no longer thought of
as being owned by any given individual, but by all that were participating in the research. This
created a remarkable shift in how intellectual property was treated not as something personally
owned, but as property of the scientific community. By increasing the amount of data in
circulation and dividing the amount of work over a larger group of researchers, discovery was
streamlined. The culmination of research efforts allowed for the maximization of advancements
with the minimizing of redundancies. This giant example of global collaboration is viewed as
one of the greatest research achievements in the field of genetics and biology in the past 100
years.
Successful collaborations have also historically been successful on a smaller scale. The
collaboration between Francois Jacob and Jacques Monod in the 1960s led to the discovery of
bacterial gene control and has also led to the development of numerous DNA sequencing
techniques and indicators using the lac operon [5]. This partnership between a biologist and
accomplished in their individual fields prior to the collaboration and by working in conjunction,
lead to even greater scientific advancement. This is an excellent example of how each party in a
Successful collaborations in research are not only limited to the distant past, but can also
be observed recently in the field of medical research. One example of this is the Accelerating
Medicines Partnership (AMP), created by the NIH in 2014 [1]. In hopes to dissuade the
independent research tendencies of biopharmaceutical companies, the NIH has created a
accelerate research progression in the development of new diagnostics and treatments for
Alzheimer’s, type 2 diabetes and lupus [1]. This structure of shared expertise and resources
allows for the best-informed contribution of all parties involved. An important intricacy of this
partnership is that all partners have agreed to make all AMP data generated public to the greater
those within and outside of this partnership as well as allowing others to benefit from their data
whether it be the discovery of new mechanisms or the identifying of failed experiments. This
partnership has lead to the decrease in the number of failures in Phase II and Phase III clinical
trials, increasing the number of treatments that will likely make it to commercialization per
investment. Phase II trials for lupus treatment developed through this collaboration are set to
begin in early 2018, months to years earlier than expected prior to the formation of this
partnership [1].
The CFAR HIC Continuum of Care Working Group, formed in 2011, is another excellent
example of recent and continually current medical collaborations [2]. The goal of this
implementation science with local Departments of Health [2]. This collaboration has positively
impacted the relationship between private research institutions and the local, publically funded
Departments of Health to further understand the continuum of health of those inflicted with HIV,
work to manage infections and move toward a non detectable prognosis. This collaboration has
been financially beneficial and has also publically shown committed support from the national
government to control the current infection rate of HIV as well as work to manage those
inflected with the disease. This formal partnership has made major strides in treatment research,
treatment-as-prevention campaigns and the institutionalization of PrEP into the medical field [2].
By combining the public outreach of local Departments of Health and the financial resources of
private research institutions, this successfully illustrates how those involved in collaborations
and the fear that one entity of the collaboration will be financially burdened by the partnership.
This concern has been addressed by both public and private organizations that have created
funding opportunities through grants specifically reserved for collaborative efforts. In 2008, the
National Health and Medical Research Counsel of Australia announced that they would be
investing more than $132 million dollars into program grants and fellowships specifically
reserved for collaborative research in efforts to inspire partnerships and other working
relationships with EU scientists [7]. These grants will be focused on medical research
specifically related to mental health, diabetes and cardiovascular issues, however could also be
open to a broad range of research areas [7]. This investment in collaborative research is meant to
property and potential economic benefit while also inspiring not only collaborative research
within Australia but throughout the global scientific community. Financial incentives to
party foundations have also begun to support and subsidize similar research. The JPB
diseases of high interest [6]. Through this program, they require scientists to meet multiple times
over the course of the grant period to discuss how their research can be better streamlined, both
for individual and joint research efforts [6]. They believe that the variety of perspective that the
multiple scientists from all over the world can offer and the trust established through this
formally-funded collaboration will leave to expedited advancement that could not occur without
data sharing and research coordination. This framework can serve as a template for initiatives
that inspire and coordinate medical research collaboration, specifically within the field of drug
The University of Melbourne in Australia in 2016 announced that they will be establishing a
relationship with Monash University and other associated medical research institutes and
hospitals [4]. This partnership is seen as an opportunity to bring two leading universities together
to “enable new significant new discovered to be translated more rapidly into new medicines.” [4]
By bringing people together around key goals, they hope to expand partnerships with hospitals,
It can be seen that government agencies, third party foundation and academic institutions
are all willing and eager to participate and encourage collaborative research. The field of drug-
resistant infection research should capitalize on these opportunities. These options to fund
collaborative research should dissuade any financial fears of institutions considering research
collaborations.
Conclusion
Collaboration is a necessity to improve research efficiency and efficacy and to end the
stall in advancements that have been observed over the past 3 decades. Through the examples
presented above it can be seen that collaboration in drug-resistant infection research will allow
for streamlined research as well as a reduction in redundant efforts. Past examples of successful
the industry and act as a catalyst for future development and discovery. Recent medical
collaborations have illustrated the viability of these relationships in the current research climate.
Findings for these partnerships are plentiful as both government agency and third party
foundations are looking to facilitate collaborative research and are more than willing to
financially support coordinated efforts between leading researchers and research groups.
Benefiting from the sharing of resources, discussion and oversight will allow for improved
advancements in the field of drug-resistant infection research and will leave a positive impact on
mankind.
Works Cited
[1] “Accelerating Medicines Partnership (AMP).” National Institutes of Health, U.S. Department
partnership-amp.
[2] “CFAR HIV Continuum of Care Working Group.” District of Columbia Center for AIDS
working-group.
[3] “Clinical Infectious Diseases | Oxford Academic.” OUP Academic, Oxford University Press,
University, www.monash.edu/news/articles/10158.
[5] Lodish, Harvey. “Bacterial Gene Control: The Jacob-Monod Model.” Molecular Cell
www.ncbi.nlm.nih.gov/books/NBK21683/.
research/.
[7] National Health and Medical Research Council. “Media Releases.” National Health and
and-medical-research-collaboration.
Research Integrity,
ori.hhs.gov/education/products/niu_collabresearch/collabresearch/need/need.html.
[9] “An Overview of the Human Genome Project.” National Human Genome Research Institute
(NHGRI), www.genome.gov/12011238/an-overview-of-the-human-genome-project/.
[10] Parker, Michael, and Patricia Kingori. “Good and Bad Research Collaborations:
Researchers’ Views on Science and Ethics in Global Health Research.” PLoS ONE,
As I began this writing process, I felt as though I had a good handle of how to approach
this paper due to the time I spent on the Unit 2 topic memo. The Unit 2 paper allowed me to
create a framework for my Unit 3 paper and gave me a place to continue to refer back to it and
when I felt overwhelmed by the scale of this paper. I keeps relatively close to my original plan,
however I did choose to write a scholarly essay instead of a proposal as I planned on referencing
multiple other successful collaboration in my paper and a scholarly essay made more sense as the
As I started writing my Unit 3 paper, I again started writing a very rough draft just to get
my thoughts down and to figure out how to organize my final draft. I decided to break my paper
down into 6 sections, each where I address a different aspect of my argument for collaborative
research. This allowed me to easily sort my sources into categories and determine the best way to
use them to build a strong argument. I then continued to revise my draft multiple times to ensure
that I included all that I intended to in my Unit 2 memo as well as took out any redundancies
between sections.
Once I received my peer reviews, I found that I was explain too much of the science of
the argument or the examples that I was presenting. Because the audience of my paper are
experts in the field, this is not necessary and actually decreased the effectiveness of my
argument. To rectify this, I again read through my paper and marked all sections where the
explanation would be elementary for the audience and then replaced them with additional
examples or discussion of the examples that I had already presented. This allowed me to strength
my argument by including addition examples adding credibility to my paper.
Also from my peer revisions, I choose to be more specific in my context note to include
exactly which paper or publication this paper would be in. This help with the focus of my paper
as well as establishing the audience that this paper would be geared toward. Additionally, my
considering what journal this paper would be published in, I was able to better develop the tone
and persona of my paper by referencing other essays published in the journal I selected, PLOS
One.
My experience with rhetorical analysis from Unit 1 again helped me while writing this
paper. The analysis of other documents for purpose, motive and audience aided me when
considering how the word choice and diction I choose to use in my paper would affect these key
characteristics of my paper. Previous experience with rhetorical analysis also was helpful when
reading the sources that I choose to included in my paper and determining any inherent bias that
they may have as well as how they would best fit into my Unit 3 paper.
Overall, I found this experience to difficult but rewarding. I do not often write papers like
a scholarly essay so there was a bit of a learning curve when I began to write my paper.
However, now that it is complete, I have a price of work that I am proud of and I truly believe