TY - JOUR
T1 - Genomics accurately predicts antimicrobial resistance in Staphylococcus pseudintermedius collected as part of Vet-LIRN resistance monitoring
AU - Tyson, Gregory H.
AU - Ceric, Olgica
AU - Guag, Jake
AU - Nemser, Sarah
AU - Borenstein, Stacey
AU - Slavic, Durda
AU - Lippert, Sarah
AU - McDowell, Rebecca
AU - Krishnamurthy, Aparna
AU - Korosec, Shannon
AU - Friday, Cheryl
AU - Pople, Neil
AU - Saab, Matthew E.
AU - Fairbrother, Julie Hélène
AU - Janelle, Isabelle
AU - McMillan, Deanna
AU - Bommineni, Yugendar R.
AU - Simon, David
AU - Mohan, Shipra
AU - Sanchez, Susan
AU - Phillips, Ashley
AU - Bartlett, Paula
AU - Naikare, Hemant
AU - Watson, Cynthia
AU - Sahin, Orhan
AU - Stinman, Chloe
AU - Wang, Leyi
AU - Maddox, Carol
AU - DeShambo, Vanessa
AU - Hendrix, Kenitra
AU - Lubelski, Debra
AU - Burklund, Amy
AU - Lubbers, Brian
AU - Reed, Debbie
AU - Jenkins, Tracie
AU - Erol, Erdal
AU - Patel, Mukeshbhai
AU - Locke, Stephan
AU - Fortner, Jordan
AU - Peak, Laura
AU - Balasuriya, Udeni
AU - Mani, Rinosh
AU - Kettler, Niesa
AU - Olsen, Karen
AU - Zhang, Shuping
AU - Shen, Zhenyu
AU - Landinez, Martha Pulido
AU - Thornton, Jay Kay
AU - Thachil, Anil
AU - Byrd, Melissa
AU - Jacob, Megan
AU - Krogh, Darlene
AU - Webb, Brett
AU - Schaan, Lynn
AU - Patil, Amar
AU - Dasgupta, Sarmila
AU - Mann, Shannon
AU - Goodman, Laura B.
AU - Franklin-Guild, Rebecca June
AU - Anderson, Renee R.
AU - Mitchell, Patrick K.
AU - Cronk, Brittany D.
AU - Aprea, Missy
AU - Cui, Jing
AU - Jurkovic, Dominika
AU - Prarat, Melanie
AU - Zhang, Yan
AU - Shiplett, Katherine
AU - Campos, Dubra Diaz
AU - Rubio, Joany Van Balen
AU - Ramanchandran, Akhilesh
AU - Talent, Scott
AU - Tewari, Deepanker
AU - Thirumalapura, Nagaraja
AU - Kelly, Donna
AU - Barnhart, Denise
AU - Hall, Lacey
AU - Rankin, Shelley
AU - Dietrich, Jaclyn
AU - Cole, Stephen
AU - Scaria, Joy
AU - Antony, Linto
AU - Lawhon, Sara D.
AU - Wu, Jing
AU - McCoy, Christine
AU - Dietz, Kelly
AU - Wolking, Rebecca
AU - Alexander, Trevor
AU - Burbick, Claire
AU - Reimschuessel, Renate
N1 - Funding Information:
We would like to acknowledge Jill Johnson, Brooke Adams, Teresa Register, Danielle Kenne, the Bacteria K State Group, Hannah Rawza, Tamara Gull, Jesse Bowman, Jana Morgan, Megan Fauls, Jasmin Huang, Leah Scarborough, Gianna Goldman, Megan Cleary, Noah Allen, Christian Holcomb, Donna Krouse, the members of the Clinical Microbiology Laboratory of the Texas A&M Veterinary Medical Teaching Hospital, Daniel Bradway, Tim Baszler, Rachel Olson, and Marla Francis. This work was supported by FDA Vet-LIRN grants 1U18FD006453 , 5U18FD006180 , 1U18FD006460-01 , 5U18FD006670-02 , 1U18FD006562 , 1U18FD006862 , 5U18FD006172 , 5U18FD006157 , 5U18FD006173 , 5U18FD006667-02 , AWD00007382 , 5U18FD006245 , U18FD006175A , 1U18FD006593-01 , U18-FD-006713 , 1U18FD004849-01 , 1U18FD006164 , 1U18FD006671 , 1U18FD006673-01 , 5U18FD006156 , 5U18FD006160-02 , 5U18FD006170-04 , 5U18FD006179 , 5U18FD006377 , 5U18FD006378 , 5U18FD006379 , 1U18FD006567 , U18FD006171 , U18FD005164 , U18FD006151 , U18FD006181 , U18FD006558 , 1U18FD006165-01 , 1U18FD0051544 , 1U18FD0051544 , 3U18FD005144 , 1U18FD006716 , 5U18FD006379 , 3U18FD005144 , 1U18FD006716 , 1U18FD006448 , 1U18FD006567 , 5U18FD006379 , 5U18FD006155-04 , and 5U18FD006712 .
Funding Information:
We would like to acknowledge Jill Johnson, Brooke Adams, Teresa Register, Danielle Kenne, the Bacteria K State Group, Hannah Rawza, Tamara Gull, Jesse Bowman, Jana Morgan, Megan Fauls, Jasmin Huang, Leah Scarborough, Gianna Goldman, Megan Cleary, Noah Allen, Christian Holcomb, Donna Krouse, the members of the Clinical Microbiology Laboratory of the Texas A&M Veterinary Medical Teaching Hospital, Daniel Bradway, Tim Baszler, Rachel Olson, and Marla Francis. This work was supported by FDA Vet-LIRN grants 1U18FD006453, 5U18FD006180, 1U18FD006460-01, 5U18FD006670-02, 1U18FD006562, 1U18FD006862, 5U18FD006172, 5U18FD006157, 5U18FD006173, 5U18FD006667-02, AWD00007382, 5U18FD006245, U18FD006175A, 1U18FD006593-01, U18-FD-006713, 1U18FD004849-01, 1U18FD006164, 1U18FD006671, 1U18FD006673-01, 5U18FD006156, 5U18FD006160-02, 5U18FD006170-04, 5U18FD006179, 5U18FD006377, 5U18FD006378, 5U18FD006379, 1U18FD006567, U18FD006171, U18FD005164, U18FD006151, U18FD006181, U18FD006558, 1U18FD006165-01, 1U18FD0051544, 1U18FD0051544, 3U18FD005144, 1U18FD006716, 5U18FD006379, 3U18FD005144, 1U18FD006716, 1U18FD006448, 1U18FD006567, 5U18FD006379, 5U18FD006155-04, and 5U18FD006712.
Publisher Copyright:
© 2021
PY - 2021/3
Y1 - 2021/3
N2 - Whole-genome sequencing (WGS) has changed our understanding of bacterial pathogens, aiding outbreak investigations and advancing our knowledge of their genetic features. However, there has been limited use of genomics to understand antimicrobial resistance of veterinary pathogens, which would help identify emerging resistance mechanisms and track their spread. The objectives of this study were to evaluate the correlation between resistance genotypes and phenotypes for Staphylococcus pseudintermedius, a major pathogen of companion animals, by comparing broth microdilution antimicrobial susceptibility testing and WGS. From 2017–2019, we conducted antimicrobial susceptibility testing and WGS on S. pseudintermedius isolates collected from dogs in the United States as a part of the Veterinary Laboratory Investigation and Response Network (Vet-LIRN) antimicrobial resistance monitoring program. Across thirteen antimicrobials in nine classes, resistance genotypes correlated with clinical resistance phenotypes 98.4 % of the time among a collection of 592 isolates. Our findings represent isolates from diverse lineages based on phylogenetic analyses, and these strong correlations are comparable to those from studies of several human pathogens such as Staphylococcus aureus and Salmonella enterica. We uncovered some important findings, including that 32.3 % of isolates had the mecA gene, which correlated with oxacillin resistance 97.0 % of the time. We also identified a novel rpoB mutation likely encoding rifampin resistance. These results show the value in using WGS to assess antimicrobial resistance in veterinary pathogens and to reveal putative new mechanisms of resistance.
AB - Whole-genome sequencing (WGS) has changed our understanding of bacterial pathogens, aiding outbreak investigations and advancing our knowledge of their genetic features. However, there has been limited use of genomics to understand antimicrobial resistance of veterinary pathogens, which would help identify emerging resistance mechanisms and track their spread. The objectives of this study were to evaluate the correlation between resistance genotypes and phenotypes for Staphylococcus pseudintermedius, a major pathogen of companion animals, by comparing broth microdilution antimicrobial susceptibility testing and WGS. From 2017–2019, we conducted antimicrobial susceptibility testing and WGS on S. pseudintermedius isolates collected from dogs in the United States as a part of the Veterinary Laboratory Investigation and Response Network (Vet-LIRN) antimicrobial resistance monitoring program. Across thirteen antimicrobials in nine classes, resistance genotypes correlated with clinical resistance phenotypes 98.4 % of the time among a collection of 592 isolates. Our findings represent isolates from diverse lineages based on phylogenetic analyses, and these strong correlations are comparable to those from studies of several human pathogens such as Staphylococcus aureus and Salmonella enterica. We uncovered some important findings, including that 32.3 % of isolates had the mecA gene, which correlated with oxacillin resistance 97.0 % of the time. We also identified a novel rpoB mutation likely encoding rifampin resistance. These results show the value in using WGS to assess antimicrobial resistance in veterinary pathogens and to reveal putative new mechanisms of resistance.
KW - Antimicrobial resistance
KW - Genomics
KW - Staphylococcus pseudintermedius
UR - http://www.scopus.com/inward/record.url?scp=85100655419&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85100655419&partnerID=8YFLogxK
U2 - 10.1016/j.vetmic.2021.109006
DO - 10.1016/j.vetmic.2021.109006
M3 - Article
C2 - 33581494
AN - SCOPUS:85100655419
SN - 0378-1135
VL - 254
JO - Veterinary Microbiology
JF - Veterinary Microbiology
M1 - 109006
ER -