Richard P. Novick

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Richard P. Novick is an American microbiologist best known for his work in the fields of plasmid biology, staphylococcal pathobiology and antimicrobial resistance. [1] He is the Recanati Family Professor of Science, Emeritus, at NYU Grossman School of Medicine and is a member of the American National Academy of Sciences. [2] [3] Novick has published over 250 peer-reviewed articles, and several book reviews for the Times Literary Supplement, and is a member of the Editorial Board of the Proceedings of the National Academy of Sciences. [4] [5]

Contents

Early life

Novick was born in New York City on August 10, 1932. He as spent most of his life in that city, with the exception of college and medical internship at Yale, residency at Vanderbilt, and a post-doctoral fellowship in London.

Education and career

Novick received a B.A, magna cum laude from Yale and an MD with honors in Microbiology from NYU School of Medicine, performing his honors thesis research in the laboratory of Werner Maas on the biochemistry of leaky mutants in arginine biosynthesis in Escherichia coli, coining the term bradytroph as a descriptor. [6] [7] [8] [9] He interned at Yale-New Haven Hospital under Paul Beeson and performed post-doctoral research along with Mark Richmond in the Laboratory of Martin Pollock, at the National Institute for Medical Research in London, where he developed the micro-iodometric assay for beta-lactamase, [10] and identified the first plasmid in S. aureus. [11] [12] [13] [14] [15] Following a year as a resident in Medicine at Vanderbilt, under David Rogers, he returned to New York for a second post-doctoral, with Rollin Hotchkiss at the Rockefeller Institute, where he published a seminal paper on staphylococcal plasmids [16] [17] and then moved to the Public Health Research Institute of the City of New York (PHRI), . While at PHRI, he discovered heavy metal resistance in bacteria, [18] showing that was carried by plasmids [19] [20] developed a set of molecular tools for the study of staphylococcal molecular genetics [21] [22] and schemes for the nomenclature of bacterial plasmids [23] [24] and transposons. [25] [26] At the 1975 Asilomar Conference on Recombinant DNA, he served as Chairman of the ”plasmid group” ( with members Roy Clowes, Stan Cohen, Roy Curtiss, and Stanley Falkow), and wrote a major portion of the NIH Guidelines for Research with Recombinant DNA. [27] In 1981 he succeeded George Hirst as Director of the Institute and, in 1993, moved to NYU School of Medicine, becoming the Recanati Family Professor of Science in 2010. [28] There, he developed a cassette-based set of cloning vectors [29] now in worldwide use, and over the years developed the world’s largest collection of staphylococcal research strains (>12,000). [30] [31]

Novick has mentored 25 PhD students and 49 Post-doctorals, notably Saleem Khan and Emmanuelle Charpentier. [32]

Research

Novick’s research has mainly been in the field of staphylococcal pathobiology. His mathematical analysis of plasmid incompatibility, in collaboration with Frank Hoppensteadt, was a major advance in plasmid biology [33] as was his demonstration that plasmid replication initiator proteins are, de rigueur, used only once and then inactivated. [34] At NYU, he discovered and characterized a key global regulator of staphylococcal virulence, the agr system [35] of which the effector is RNAIII, and discovered a pathogenicity island family in the staphylococcal chromosome, now known as SaPIs, many of which encode toxic shock toxin. [36] SaPIs turned out to be highly mobile and very widespread in staphylococci and to have a major role in horizontal gene transfer; his lab, led by Drs. Geeta Ram and Hope Ross, converted these mobile islands from agents of disease into antibacterial therapeutic agents (Antibacterial Drones (ABDs)), [37] [38] that could have a major role in the therapy of staphylococcal and other bacterial infections in this era of rampant antibiotic resistance. A patent on this technology has recently been issued, with Drs. Ram, Ross and Novick as joint inventors, and the Novick lab is currently working on commercialization. [39]

Personal life

Novick is married to Barbara Zabin Novick, a retired neuropsychologist. They have two children, Lynn Novick, a documentary film maker and Dorothy Novick, a pediatrician and journalist, and 5 grandchildren.

Novick is a wood turner, a collector of Pre-Columbian figurines, a home brewer of apple cider and apple jack, a wild mushroom expert and a political activist, focusing primarily on the misuse of antibiotics in animal feed, a position for which he was profiled in The New Yorker. [40] He and colleagues Roy Curtiss, Julian Davies and others resigned in protest from the CAST Task Force on Antibiotics in Feed, in 1979, [41] and his prophetic paper, Antibiotics, Wonder Drugs or Chicken Feed, was published in The Sciences. [42]

Related Research Articles

<i>Staphylococcus aureus</i> Species of Gram-positive bacterium

Staphylococcus aureus is a gram-positive spherically shaped bacterium, a member of the Bacillota, and is a usual member of the microbiota of the body, frequently found in the upper respiratory tract and on the skin. It is often positive for catalase and nitrate reduction and is a facultative anaerobe that can grow without the need for oxygen. Although S. aureus usually acts as a commensal of the human microbiota, it can also become an opportunistic pathogen, being a common cause of skin infections including abscesses, respiratory infections such as sinusitis, and food poisoning. Pathogenic strains often promote infections by producing virulence factors such as potent protein toxins, and the expression of a cell-surface protein that binds and inactivates antibodies. S. aureus is one of the leading pathogens for deaths associated with antimicrobial resistance and the emergence of antibiotic-resistant strains, such as methicillin-resistant S. aureus (MRSA), is a worldwide problem in clinical medicine. Despite much research and development, no vaccine for S. aureus has been approved.

Vancomycin-resistant <i>Staphylococcus aureus</i> Antibiotica resistant bacteria

Vancomycin-resistant Staphylococcus aureus (VRSA) are strains of Staphylococcus aureus that have acquired resistance to the glycopeptide antibiotic vancomycin. Bacteria can acquire resistant genes either by random mutation or through the transfer of DNA from one bacterium to another. Resistance genes interfere with the normal antibiotic function and allow bacteria to grow in the presence of the antibiotic. Resistance in VRSA is conferred by the plasmid-mediated vanA gene and operon. Although VRSA infections are uncommon, VRSA is often resistant to other types of antibiotics and a potential threat to public health because treatment options are limited. VRSA is resistant to many of the standard drugs used to treat S. aureus infections. Furthermore, resistance can be transferred from one bacterium to another.

<span class="mw-page-title-main">Stanley Falkow</span> American microbiologist

Stanley "Stan" Falkow was an American microbiologist and a professor of microbiology at Georgetown University, University of Washington, and Stanford University School of Medicine. Falkow is known as the father of the field of molecular microbial pathogenesis. He formulated molecular Koch's postulates, which have guided the study of the microbial determinants of infectious diseases since the late 1980s. Falkow spent over 50 years uncovering molecular mechanisms of how bacteria cause disease and how to disarm them. Falkow also was one of the first scientists to investigate antimicrobial resistance, and presented his research extensively to scientific, government, and lay audiences explaining the spread of resistance from one organism to another, now known as horizontal gene transfer, and the implications of this phenomenon on our ability to combat infections in the future.

<i>Staphylococcus haemolyticus</i> Species of bacterium

Staphylococcus haemolyticus is a member of the coagulase-negative staphylococci (CoNS). It is part of the skin flora of humans, and its largest populations are usually found at the axillae, perineum, and inguinal areas. S. haemolyticus also colonizes primates and domestic animals. It is a well-known opportunistic pathogen, and is the second-most frequently isolated CoNS. Infections can be localized or systemic, and are often associated with the insertion of medical devices. The highly antibiotic-resistant phenotype and ability to form biofilms make S. haemolyticus a difficult pathogen to treat. Its most closely related species is Staphylococcus borealis.

<i>Staphylococcus epidermidis</i> Species of bacterium

Staphylococcus epidermidis is a Gram-positive bacterium, and one of over 40 species belonging to the genus Staphylococcus. It is part of the normal human microbiota, typically the skin microbiota, and less commonly the mucosal microbiota and also found in marine sponges. It is a facultative anaerobic bacteria. Although S. epidermidis is not usually pathogenic, patients with compromised immune systems are at risk of developing infection. These infections are generally hospital-acquired. S. epidermidis is a particular concern for people with catheters or other surgical implants because it is known to form biofilms that grow on these devices. Being part of the normal skin microbiota, S. epidermidis is a frequent contaminant of specimens sent to the diagnostic laboratory.

RNAIII is a stable 514 nt regulatory RNA transcribed by the P3 promoter of the Staphylococcus aureus quorum-sensing agr system ). It is the major effector of the agr regulon, which controls the expression of many S. aureus genes encoding exoproteins and cell wall associated proteins plus others encoding regulatory proteins The RNAIII transcript also encodes the 26 amino acid δ-haemolysin peptide (Hld). RNAIII contains many stem loops, most of which match the Shine-Dalgarno sequence involved in translation initiation of the regulated genes. Some of these interactions are inhibitory, others stimulatory; among the former is the regulatory protein Rot. In vitro, RNAIII is expressed post exponentially, inhibiting translation of the surface proteins, notably protein A, while stimulating that of the exoproteins, many of which are tissue-degrading enzymes or cytolysins. Among the latter is the important virulence factor, α-hemolysin (Hla), whose translation RNAIII activates by preventing the formation of an inhibitory foldback loop in the hla mRNA leader.

Plant transformation vectors are plasmids that have been specifically designed to facilitate the generation of transgenic plants. The most commonly used plant transformation vectors are T-DNA binary vectors and are often replicated in both E. coli, a common lab bacterium, and Agrobacterium tumefaciens, a plant-virulent bacterium used to insert the recombinant DNA into plants.

Lysostaphin is a Staphylococcus simulans metalloendopeptidase. It can function as a bacteriocin (antimicrobial) against Staphylococcus aureus.

<span class="mw-page-title-main">Toxic shock syndrome toxin-1</span>

Toxic shock syndrome toxin-1 (TSST-1) is a superantigen with a size of 22 kDa produced by 5 to 25% of Staphylococcus aureus isolates. It causes toxic shock syndrome (TSS) by stimulating the release of large amounts of interleukin-1, interleukin-2 and tumour necrosis factor. In general, the toxin is not produced by bacteria growing in the blood; rather, it is produced at the local site of an infection, and then enters the blood stream.

<span class="mw-page-title-main">Staphylococcal infection</span> Medical condition

A staphylococcal infection or staph infection is an infection caused by members of the Staphylococcus genus of bacteria.

mecA is a gene found in bacterial cells which allows them to be resistant to antibiotics such as methicillin, penicillin and other penicillin-like antibiotics.

<i>Staphylococcus capitis</i> Species of bacterium

Staphylococcus capitis is a coagulase-negative species (CoNS) of Staphylococcus. It is part of the normal flora of the skin of the human scalp, face, neck, scrotum, and ears and has been associated with prosthetic valve endocarditis, but is rarely associated with native valve infection.

<i>Staphylococcus</i> Genus of Gram-positive bacteria

Staphylococcus is a genus of Gram-positive bacteria in the family Staphylococcaceae from the order Bacillales. Under the microscope, they appear spherical (cocci), and form in grape-like clusters. Staphylococcus species are facultative anaerobic organisms.

Roberto Kolter is Professor of Microbiology, Emeritus at Harvard Medical School, an author, and past president of the American Society for Microbiology. Kolter has been a professor at Harvard Medical School since 1983 and was Co-director of Harvard's Microbial Sciences Initiative from 2003-2018. During the 35-year term of the Kolter laboratory from 1983 to 2018, more than 130 graduate student and postdoctoral trainees explored an eclectic mix of topics gravitating around the study of microbes. Kolter is a fellow of the American Association for the Advancement of Science and of the American Academy of Microbiology.

SaPIs are a family of ~15 kb mobile genetic elements resident in the genomes of the vast majority of S. aureus strains. Much like bacteriophages, SaPIs can be transferred to uninfected cells and integrate into the host chromosome. Unlike the bacterial viruses, however, integrated SaPIs are mobilized by host infection with "helper" bacteriophages. SaPIs are used by the host bacteria to co-opt the phage reproduction cycle for their own genetic transduction and also inhibit phage reproduction in the process.

SCCmec, or staphylococcal cassette chromosome mec, is a mobile genetic element of Staphylococcus bacterial species. This genetic sequence includes the mecA gene coding for resistance to the antibiotic methicillin and is the only known way for Staphylococcus strains to spread the gene in the wild by horizontal gene transfer. SCCmec is a 21 to 60 kb long genetic element that confers broad-spectrum β-lactam resistance to MRSA. Moreover, additional genetic elements like Tn554, pT181, and pUB110 can be found in SCCmec, which have the capability to render resistance to various non-β-lactam drugs.

The CidA/LrgA Holin Family is a group of proteins named after CidA and LrgA of Staphylococcus aureus. CidA and LrgA are homologous holin and anti-holin proteins, each with 4 putative transmembrane segments (TMSs). Members of the CidA/LrgA holin family also include putative murine hydrolase exporters from a wide range of Gram-positive and Gram-negative bacteria as well as archaea. Most CidA/LrgA holin family proteins vary in size between 100 and 160 amino acyl residues (aas) in length although a few are larger.

The SPP1 Holin Family consists of proteins of between 90 and 160 amino acyl residues (aas) in length that exhibit two transmembrane segments (TMSs). SPP1 is a double-stranded DNA phage that infects the Gram-positive bacteria. Although annotated as holins, members of the SPP1 family are not yet functionally characterized. A representative list of proteins belonging to the SPP1 Holin family can be found in Transporter Classification Database.

Accessory gene regulator (agr) is a complex 5 gene locus that is a global regulator of virulence in Staphylococcus aureus. It encodes a two-component transcriptional quorum-sensing (QS) system activated by an autoinducing, thiolactone-containing cyclic peptide (AIP).

Staphylococcus cornubiensis is a species of Gram-positive cocci in the Staphylococcus intermedius Group (SIG): a group of genetically and phenotypically similar bacterial species that were previously identified as S. intermedius. The bacterium was first isolated from a human skin infection in Cornwall, United Kingdom. However, its presence in other species and/or pathologies has yet to be discussed in the literature. Another SIG bacterium, S. pseudintermedius, has also been implicated in cutaneous infections in humans–as a result of zoonotic transmission from domestic animals. The other SIG species have been isolated from various wild and domestic animals; such as dogs, cats, horses, camels, and dolphins, among others.

References

  1. Novick, R. P. (December 1987). "journals.asm.org". Microbiological Reviews. 51 (4): 381–395. doi:10.1128/mr.51.4.381-395.1987. PMC   373122 . PMID   3325793.
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  4. Marino, Melissa (2007-09-04). "Profile of Richard P. Novick". Proceedings of the National Academy of Sciences. 104 (36): 14179–14181. Bibcode:2007PNAS..10414179M. doi: 10.1073/pnas.0707438104 . ISSN   0027-8424. PMC   1964851 . PMID   17728399.
  5. Ram, Geeta; Chen, John; Ross, Hope F; Novick, Richard P (2015-04-03). "An insight into staphylococcal pathogenicity island-mediated interference with phage late gene transcription". Bacteriophage. 5 (2): e1028608. doi:10.1080/21597081.2015.1028608. ISSN   2159-7081. PMC   4588161 . PMID   26459624.
  6. Novick, Richard P.; Maas, Werner K. (February 1961). "CONTROL BY ENDOGENOUSLY SYNTHESIZED ARGININE OF THE FORMATION OF ORNITHINE TRANSCARBAMYLASE IN ESCHERICHIA COLI". Journal of Bacteriology. 81 (2): 236–240. doi:10.1128/jb.81.2.236-240.1961. ISSN   0021-9193. PMC   278992 . PMID   13729753.
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  10. Novick, Rp (1962-05-01). "Micro-iodometric assay for penicillinase". Biochemical Journal. 83 (2): 236–240. doi:10.1042/bj0830236. ISSN   0006-2936. PMC   1243538 . PMID   14480578.
  11. Novick, R. P.; Richmond, M. H. (August 1965). "Nature and Interactions of the Genetic Elements Governing Penicillinase Synthesis in Staphylococcus aureus". Journal of Bacteriology. 90 (2): 467–480. doi:10.1128/jb.90.2.467-480.1965. ISSN   0021-9193. PMC   315668 . PMID   14329463.
  12. Marino, Melissa (2007-09-04). "Profile of Richard P. Novick". Proceedings of the National Academy of Sciences. 104 (36): 14179–14181. Bibcode:2007PNAS..10414179M. doi: 10.1073/pnas.0707438104 . ISSN   0027-8424. PMC   1964851 . PMID   17728399.
  13. Fournier, Bénédicte; Klier, André (November 2003). "Response to the criticisms of Richard P. Novick in his review 'Autoinduction and signal transduction in the regulation of staphylococcal virulence' (Novick, 2003, Mol Microbiol 48: 1429–1449)". Molecular Microbiology. 50 (3): 1085–1086. doi: 10.1046/j.1365-2958.2003.03792.x . ISSN   0950-382X. PMID   14617163. S2CID   27453467.
  14. Maiques, Elisa; Úbeda, Carles; Campoy, Susana; Salvador, Noelia; Lasa, Íñigo; Novick, Richard P.; Barbé, Jordi; Penadés, José R. (April 2006). "β-Lactam Antibiotics Induce the SOS Response and Horizontal Transfer of Virulence Factors in Staphylococcus aureus". Journal of Bacteriology. 188 (7): 2726–2729. doi:10.1128/JB.188.7.2726-2729.2006. ISSN   0021-9193. PMC   1428414 . PMID   16547063.
  15. Novick, Richard P.; Maas, Werner K. (February 1961). "CONTROL BY ENDOGENOUSLY SYNTHESIZED ARGININE OF THE FORMATION OF ORNITHINE TRANSCARBAMYLASE IN ESCHERICHIA COLI". Journal of Bacteriology. 81 (2): 236–240. doi:10.1128/jb.81.2.236-240.1961. ISSN   0021-9193. PMC   278992 . PMID   13729753.
  16. Maguin, E; Duwat, P; Hege, T; Ehrlich, D; Gruss, A (September 1992). "New thermosensitive plasmid for gram-positive bacteria". Journal of Bacteriology. 174 (17): 5633–5638. doi:10.1128/jb.174.17.5633-5638.1992. ISSN   0021-9193. PMC   206509 . PMID   1324906.
  17. Marino, Melissa (2007-09-04). "Profile of Richard P. Novick". Proceedings of the National Academy of Sciences. 104 (36): 14179–14181. Bibcode:2007PNAS..10414179M. doi: 10.1073/pnas.0707438104 . ISSN   0027-8424. PMC   1964851 . PMID   17728399.
  18. Dhasmana, Neha; Ram, Geeta; McAllister, Kathleen N.; Chupalova, Yulia; Lopez, Peter; Ross, Hope F.; Novick, Richard P. (2021-12-21). Vidaver, Anne K. (ed.). "Dynamics of Antibacterial Drone Establishment in Staphylococcus aureus: Unexpected Effects of Antibiotic Resistance Genes". mBio. 12 (6): e0208321. doi:10.1128/mBio.02083-21. ISSN   2150-7511. PMC   8593670 . PMID   34781740.
  19. Novick, Richard P.; Roth, Christine (April 1968). "Plasmid-linked Resistance to Inorganic Salts in Staphylococcus aureus". Journal of Bacteriology. 95 (4): 1335–1342. doi:10.1128/jb.95.4.1335-1342.1968. ISSN   0021-9193. PMC   315091 . PMID   5646621.
  20. Dhasmana, Neha; Ram, Geeta; McAllister, Kathleen N.; Chupalova, Yulia; Lopez, Peter; Ross, Hope F.; Novick, Richard P. (2021-12-21). Vidaver, Anne K. (ed.). "Dynamics of Antibacterial Drone Establishment in Staphylococcus aureus: Unexpected Effects of Antibiotic Resistance Genes". mBio. 12 (6): e0208321. doi:10.1128/mBio.02083-21. ISSN   2150-7511. PMC   8593670 . PMID   34781740.
  21. Novick, Richard P. (1991), "Genetic systems in Staphylococci", Bacterial Genetic Systems, Methods in Enzymology, vol. 204, Elsevier, pp. 587–636, doi:10.1016/0076-6879(91)04029-n, ISBN   978-0-12-182105-0, PMID   1658572 , retrieved 2023-07-20
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  23. Novick, R. P.; Clowes, R. C.; Cohen, S. N.; Curtiss, R.; Datta, N.; Falkow, S. (March 1976). "Uniform nomenclature for bacterial plasmids: a proposal". Bacteriological Reviews. 40 (1): 168–189. doi:10.1128/br.40.1.168-189.1976. ISSN   0005-3678. PMC   413948 . PMID   1267736.
  24. Novick, Richard (1967-09-01). "Properties of a cryptic high-frequency transducing phage in Staphylococcus aureus". Virology. 33 (1): 155–166. doi:10.1016/0042-6822(67)90105-5. ISSN   0042-6822. PMID   4227577.
  25. Campbell, A.; Berg, D.; Botstein, D.; Lederberg, E. M.; Novick, R. P.; Starlinger, P.; Szybalski, W. (1979-03-01). "Nomenclature of transposable elements in prokaryotes". Gene. 5 (3): 197–206. doi:10.1016/0378-1119(79)90078-7. ISSN   0378-1119. PMID   467979.
  26. Projan, Steven J.; Novick, Richard (1988-05-01). "Comparative analysis of five related staphylococcal plasmids". Plasmid. 19 (3): 203–221. doi:10.1016/0147-619X(88)90039-X. ISSN   0147-619X. PMID   2852816.
  27. National Institutes of Health (U.S.). Office of the Director (1976). Recombinant DNA research : documents relating to "NIH guidelines for research involving recombinant DNA molecules". University of Illinois Urbana-Champaign. [Bethesda, Md.] : U. S. Dept. of Health, Education, and Welfare, Public Health Service, National Institutes of Health ; Washington : for sale by the Supt. of Docs., U. S. Govt. Print. Off.
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  29. Charpentier, Emmanuelle; Anton, Ana I.; Barry, Peter; Alfonso, Berenice; Fang, Yuan; Novick, Richard P. (October 2004). "Novel Cassette-Based Shuttle Vector System for Gram-Positive Bacteria". Applied and Environmental Microbiology. 70 (10): 6076–6085. Bibcode:2004ApEnM..70.6076C. doi:10.1128/AEM.70.10.6076-6085.2004. ISSN   0099-2240. PMC   522135 . PMID   15466553.
  30. Traber, Katrina; Novick, Richard (March 2006). "A slipped-mispairing mutation in AgrA of laboratory strains and clinical isolates results in delayed activation of agr and failure to translate δ- and α-haemolysins: agrA mutation resulting in late agr activation". Molecular Microbiology. 59 (5): 1519–1530. doi: 10.1111/j.1365-2958.2006.04986.x . PMID   16468992. S2CID   82413638.
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  34. Rasooly, A.; Novick, R. P. (1993-11-12). "Replication-specific inactivation of the pT181 plasmid initiator protein". Science. 262 (5136): 1048–1050. Bibcode:1993Sci...262.1048R. doi:10.1126/science.8235621. ISSN   0036-8075. PMID   8235621.
  35. Peng, H. L.; Novick, R. P.; Kreiswirth, B.; Kornblum, J.; Schlievert, P. (September 1988). "Cloning, characterization, and sequencing of an accessory gene regulator (agr) in Staphylococcus aureus". Journal of Bacteriology. 170 (9): 4365–4372. doi:10.1128/jb.170.9.4365-4372.1988. ISSN   0021-9193. PMC   211451 . PMID   2457579.
  36. Lindsay, J. A.; Ruzin, A.; Ross, H. F.; Kurepina, N.; Novick, R. P. (July 1998). "The gene for toxic shock toxin is carried by a family of mobile pathogenicity islands in Staphylococcus aureus". Molecular Microbiology. 29 (2): 527–543. doi: 10.1046/j.1365-2958.1998.00947.x . ISSN   0950-382X. PMID   9720870. S2CID   30680160.
  37. Ram, Geeta; Ross, Hope F.; Novick, Richard P.; Rodriguez-Pagan, Ivelisse; Jiang, Dunrong (November 2018). "Conversion of staphylococcal pathogenicity islands to CRISPR-carrying antibacterial agents that cure infections in mice". Nature Biotechnology. 36 (10): 971–976. doi:10.1038/nbt.4203. ISSN   1546-1696. PMC   6511514 . PMID   30247487.
  38. Ram, Geeta; Ross, Hope F.; Novick, Richard P.; Rodriguez-Pagan, Ivelisse; Jiang, Dunrong (November 2018). "Conversion of staphylococcal pathogenicity islands to CRISPR-carrying antibacterial agents that cure infections in mice". Nature Biotechnology. 36 (10): 971–976. doi:10.1038/nbt.4203. ISSN   1546-1696. PMC   6511514 . PMID   30247487.
  39. US 11149269,Novick, Richard; Ross, Hope Forer& Ram, Geeta,"Compositions and methods for non-antibiotic treating of bacterial infections by blocking or disrupting bacterial genes involved in virulence or viability",published 2021-10-19, assigned to New York University
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  41. "Biomedical Politics" (PDF).
  42. Charpentier, Emmanuelle; Anton, Ana I.; Barry, Peter; Alfonso, Berenice; Fang, Yuan; Novick, Richard P. (October 2004). "Novel Cassette-Based Shuttle Vector System for Gram-Positive Bacteria". Applied and Environmental Microbiology. 70 (10): 6076–6085. Bibcode:2004ApEnM..70.6076C. doi:10.1128/AEM.70.10.6076-6085.2004. ISSN   0099-2240. PMC   522135 . PMID   15466553.