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Disease-mediated ecosystem services: Pathogens, plants, and people 期刊论文
TRENDS IN ECOLOGY & EVOLUTION, 2020, 35 (8) : 731-743
作者:  Paseka, Rachel E.;  White, Lauren A.;  Van de Waal, Dedmer B.;  Strauss, Alex T.;  Gonzalez, Angelica L.;  Everett, Rebecca A.;  Peace, Angela;  Seabloom, Eric W.;  Frenken, Thijs;  Borer, Elizabeth T.
收藏  |  浏览/下载:10/0  |  提交时间:2020/06/22
The arms race between bacteria and their phage foes 期刊论文
NATURE, 2020, 577 (7790) : 327-336
作者:  Hirschey, Matthew
收藏  |  浏览/下载:20/0  |  提交时间:2020/07/03

Bacteria are under immense evolutionary pressure from their viral invaders-bacteriophages. Bacteria have evolved numerous immune mechanisms, both innate and adaptive, to cope with this pressure. The discovery and exploitation of CRISPR-Cas systems have stimulated a resurgence in the identification and characterization of anti-phage mechanisms. Bacteriophages use an extensive battery of counter-defence strategies to co-exist in the presence of these diverse phage defence mechanisms. Understanding the dynamics of the interactions between these microorganisms has implications for phage-based therapies, microbial ecology and evolution, and the development of new biotechnological tools. Here we review the spectrum of anti-phage systems and highlight their evasion by bacteriophages.


  
Social immunity modulates competition between coinfecting pathogens 期刊论文
ECOLOGY LETTERS, 2020, 23 (3) : 565-574
作者:  Milutinovic, Barbara;  Stock, Miriam;  Grasse, Anna V.;  Naderlinger, Elisabeth;  Hilbe, Christian;  Cremer, Sylvia
收藏  |  浏览/下载:7/0  |  提交时间:2020/07/02
Argentine ants  grooming  host-pathogen interactions  immune-mediated competition  infectious disease  Metarhizium fungus  multiple infections  pathogen competition  pathogen diversity  social insects  
Robust and persistent reactivation of SIV and HIV by N-803 and depletion of CD8(+) cells 期刊论文
NATURE, 2020, 578 (7793) : 154-+
作者:  Diaz-Cuadros, Margarete;  Wagner, Daniel E.;  Budjan, Christoph;  Hubaud, Alexis;  Tarazona, Oscar A.;  Donelly, Sophia;  Michaut, Arthur;  Al Tanoury, Ziad;  Yoshioka-Kobayashi, Kumiko;  Niino, Yusuke;  Kageyama, Ryoichiro;  Miyawaki, Atsushi;  Touboul, Jonathan;  Pourquie, Olivier
收藏  |  浏览/下载:33/0  |  提交时间:2020/07/03

Human immunodeficiency virus (HIV) persists indefinitely in individuals with HIV who receive antiretroviral therapy (ART) owing to a reservoir of latently infected cells that contain replication-competent virus(1-4). Here, to better understand the mechanisms responsible for latency persistence and reversal, we used the interleukin-15 superagonist N-803 in conjunction with the depletion of CD8(+) lymphocytes in ART-treated macaques infected with simian immunodeficiency virus (SIV). Although N-803 alone did not reactivate virus production, its administration after the depletion of CD8(+) lymphocytes in conjunction with ART treatment induced robust and persistent reactivation of the virus in vivo. We found viraemia of more than 60 copies per ml in all macaques (n = 14  100%) and in 41 out of a total of 56 samples (73.2%) that were collected each week after N-803 administration. Notably, concordant results were obtained in ART-treated HIV-infected humanized mice. In addition, we observed that co-culture with CD8(+) T cells blocked the in vitro latency-reversing effect of N-803 on primary human CD4(+) T cells that were latently infected with HIV. These results advance our understanding of the mechanisms responsible for latency reversal and lentivirus reactivation during ART-suppressed infection.


The interleukin-15 superagonist N-803, combined with the depletion of CD8(+) lymphocytes, induced a robust and persistent reactivation of the virus in vivo in both antiretroviral-therapy-treated SIV-infected macaques and HIV-infected humanized mice.


  
Targeting of temperate phages drives loss of type I CRISPR-Cas systems 期刊论文
NATURE, 2020, 578 (7793) : 149-+
作者:  Xiang, Lifeng;  Yin, Yu;  Zheng, Yun;  Ma, Yanping;  Li, Yonggang;  Zhao, Zhigang;  Guo, Junqiang;  Ai, Zongyong;  Niu, Yuyu;  Duan, Kui;  He, Jingjing;  Ren, Shuchao;  Wu, Dan;  Bai, Yun;  Shang, Zhouchun;  Dai, Xi;  Ji, Weizhi;  Li, Tianqing
收藏  |  浏览/下载:33/0  |  提交时间:2020/07/03

On infection of their host, temperate viruses that infect bacteria (bacteriophages  hereafter referred to as phages) enter either a lytic or a lysogenic cycle. The former results in lysis of bacterial cells and phage release (resulting in horizontal transmission), whereas lysogeny is characterized by the integration of the phage into the host genome, and dormancy (resulting in vertical transmission)(1). Previous co-culture experiments using bacteria and mutants of temperate phages that are locked in the lytic cycle have shown that CRISPR-Cas systems can efficiently eliminate the invading phages(2,3). Here we show that, when challenged with wild-type temperate phages (which can become lysogenic), type I CRISPR-Cas immune systems cannot eliminate the phages from the bacterial population. Furthermore, our data suggest that, in this context, CRISPR-Cas immune systems are maladaptive to the host, owing to the severe immunopathological effects that are brought about by imperfect matching of spacers to the integrated phage sequences (prophages). These fitness costs drive the loss of CRISPR-Cas from bacterial populations, unless the phage carries anti-CRISPR (acr) genes that suppress the immune system of the host. Using bioinformatics, we show that this imperfect targeting is likely to occur frequently in nature. These findings help to explain the patchy distribution of CRISPR-Cas immune systems within and between bacterial species, and highlight the strong selective benefits of phage-encoded acr genes for both the phage and the host under these circumstances.


CRISPR-Cas systems cannot eliminate temperate bacteriophages from bacterial populations and-in this context-the systems impose immunopathological costs on the host, creating selective pressures that may explain their patchy distribution in bacteria.


  
Interaction between the nasal microbiota and S.pneumoniae in the context of live-attenuated influenza vaccine 期刊论文
NATURE COMMUNICATIONS, 2019, 10
作者:  Piters, Wouter A. A. de Steenhuijsen;  Jochems, Simon P.;  Mitsi, Elena;  Rylance, Jamie;  Pojar, Sherin;  Nikolaou, Elissavet;  German, Esther L.;  Holloway, Mark;  Carniel, Beatriz F.;  Chu, Mei Ling J. N.;  Arp, Kayleigh;  Sanders, Elisabeth A. M.;  Ferreira, Daniela M.;  Bogaert, Debby
收藏  |  浏览/下载:6/0  |  提交时间:2019/11/27
Endemic infection can shape exposure to novel pathogens: Pathogen co-occurrence networks in the Serengeti lions 期刊论文
ECOLOGY LETTERS, 2019, 22 (6) : 904-913
作者:  Fountain-Jones, Nicholas M.;  Packer, Craig;  Jacquot, Maude;  Blanchet, F. Guillaume;  Terio, Karen;  Craft, Meggan E.
收藏  |  浏览/下载:7/0  |  提交时间:2019/11/26
Babesia  calicivirus  canine distemper virus  co-infection  community assembly  coronavirus  feline immunodeficiency virus  parvovirus  
Coordinated host-pathogen transcriptional dynamics revealed using sorted subpopulations and single macrophages infected with Candida albicans 期刊论文
NATURE COMMUNICATIONS, 2019, 10
作者:  Munoz, Jose F.;  Delorey, Toni;  Ford, Christopher B.;  Li, Bi Yu;  Thompson, Dawn A.;  Rao, Reeta P.;  Cuomo, Christina A.
收藏  |  浏览/下载:7/0  |  提交时间:2019/11/27
Mouse models of Loa loa 期刊论文
NATURE COMMUNICATIONS, 2019, 10
作者:  Pionnier, Nicolas P.;  Sjoberg, Hanna;  Chunda, Valerine C.;  Fombad, Fanny F.;  Chounna, Patrick W.;  Njouendou, Abdel J.;  Metuge, Haelly M.;  Ndzeshang, Bertrand L.;  Gandjui, Narcisse, V;  Akumtoh, Desmond N.;  Tayong, Dizzle B.;  Taylor, Mark J.;  Wanji, Samuel;  Turner, Joseph D.
收藏  |  浏览/下载:9/0  |  提交时间:2019/11/27
A potent series targeting the malarial cGMP-dependent protein kinase clears infection and blocks transmission 期刊论文
NATURE COMMUNICATIONS, 2017, 8
作者:  Baker, David A.;  Stewart, Lindsay B.;  Large, Jonathan M.;  Bowyer, Paul W.;  Ansell, Keith H.;  Jimenez-Diaz, Mar-A B.;  El Bakkouri, Majida;  Birchall, Kristian;  Dechering, Koen J.;  Bouloc, Nathalie S.;  Coombs, Peter J.;  Whalley, David;  Harding, Denise J.;  Smiljanic-Hurley, Ela;  Wheldon, Mary C.;  Walker, Eloise M.;  Dessens, Johannes T.;  Lafuente, Maria Jose;  Sanz, Laura M.;  Gamo, Francisco-Javier;  Ferrer, Santiago B.;  Hui, Raymond;  Bousema, Teun;  Angulo-Barturen, I. Igo;  Merritt, Andy T.;  Croft, Simon L.;  Gutteridge, Winston E.;  Kettleborough, Catherine A.;  Osborne, Simon A.
收藏  |  浏览/下载:9/0  |  提交时间:2019/11/27