The outer membrane of Gram-negative bacteria has a highly complex asymmetrical architecture, containing a mixture of phospholipids in the inner leaflet and almost exclusively lipopolysaccharide (LPS) molecules in the outer leaflet. Coli, the outer membrane contains a wide range of proteins with a β barrel architecture, that vary in size from the smallest having eight strands to larger.
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Kecuali Mac OS X Server 1.0 dan rilis beta, versi OS X diberi nama kucing besar hingga OS X 10.9 Maveriks, ketika Apple beralih menggunakan lokasi di California. Ultimate cardio training session with god mac os. Sebelum dirilis, Mac OS X 10.0 memiliki kode 'Cheetah' dan Mac OS X 10.1 memilliki kode 'Puma' secara internal. Earlier versions of macOS have been around since the mid-1980s. There have been many versions since then, but the most recent ones include macOS Mojave (2018), High Sierra (2017), Sierra (2016).El Capitan (2015), and Yosemite (2014). In some older versions, macOS was called OS X (pronounced O-S ten).However, many people use the terms OS X and macOS interchangeably because the basic.
Summary of TCB Hardware Resources
NVidia DGX-2
Machine | OS | RAM | Cores | GPU | Count | ||||
Intel(R) Xeon(R) Platinum 8168 CPU @ 2.70GHz | Ubuntu | 48 | |||||||
Machine | OS | RAM | Cores | GPU | Count | ||||
Intel(R) Xeon(R) Gold 6154 CPU @ 3.00GHz | CentOS | 36 | Intel(R) Xeon(R) Gold 6154 CPU @ 3.00GHz | CentOS | 36 | Dual Intel(R) Xeon(R) Gold 6134 CPU @ 3.20GHz | CentOS | 16 | |
Machine | OS | RAM | Cores | GPU | Count | ||||
Intel(R) Xeon(R) CPU E5-2680 v3 @ 2.50GHz | CentOS | 24 | |||||||
Machine | OS | RAM | Cores | Count | |||||
AMD Opteron(TM) Processor 6272 | CentOS | 64 | 11 | ||||||
AMD Opteron(tm) Processor 6174 | CentOS | 48 | 2 |
Linux Clusters
Machine | OS | RAM | Cores | Nodes |
AMD Opteron(tm) Processor 6174 with InifiniBand connection | CentOS | 48 | 5 | |
AMD Opteron(tm) Processor 6376 with InifiniBand connection | CentOS | 64 | 14 |
Remote visualization and analysis servers
Machine | OS | RAM | Cores | GPU | Count | |||||||||||||
Intel(R) Xeon(R) CPU E5-2660 v3 @ 2.60GHz | CentOS | 20 | Intel(R) Xeon(R) CPU E5-2687W v3 @ 3.10GHz | CentOS | 20 | Intel(R) Xeon(R) CPU E5-2650 v2 @ 2.60GHz | CentOS | 16 | Intel(R) Xeon(R) CPU X5650 @ 2.67GHz | CentOS | 12 | Intel(R) Xeon(R) CPU X5550 @ 2.67GHz | CentOS | 8 | Intel(R) Xeon(R) CPU W3520 @ 2.67GHz | CentOS | 4 | |
Machine | OS | RAM | Cores | GPU | Count | |||||||||||||
Intel(R) Xeon(R) CPU E5-2643 v4 @ 3.40GHz with 49' 4K stereoscopic 3D displays | CentOS | 24 | Intel(R) Xeon(R) CPU E5-2643 v4 @ 3.40GHz with 49' 4K stereoscopic 3D displays | CentOS | 24 | Intel(R) Xeon(R) CPU E5-2643 v4 @ 3.40GHz with 49' 4K stereoscopic 3D displays | CentOS | 24 | Intel(R) Xeon(R) CPU X5550 @ 2.67GHz | Dual Quadro 7000 Graphics | 1 | |||||||
Intel(R) Xeon(R) CPU E5-2687W 0 @ 3.10GHz w/Quadro K6000 Graphics | Quadro K6000 Graphics | 1 | ||||||||||||||||
2.8GHz Apple Mac Pro | NVIDIA GTX 285 | 1 | ||||||||||||||||
2.4GHz Apple Mac Pro | NVIDIA Quadro FX 4800 | 1 |
Data Storage
Machine | OS | RAM | Cores | File System | Storage Space | Raid | Storage connected | Count |
Intel(R) Xeon(R) CPU E5-2637 v3 @ 3.50GHz | 128 GB | ZFS | RAID 6 | Internal Storage | 2 | |||
Dual Intel(R) Xeon(R) CPU E5-2623 v4 @ 2.60GHz | 128 GB | ZFS | RAID 6 | Internal Storage | 4 | |||
Dual Intel(R) Xeon(R) CPU E5-2623 v4 @ 2.60GHz | 128 GB | ZFS | RAID 6 | Internal Storage | 9 |
Desktop Workstations
Machine | OS | RAM | Procs | Count |
Apple iMac | 16 GB | 4 | 3 | |
Dell Workstation | 16 GB | 4 | 4 | |
Custom Linux Workstation most of them with high-end NVIDIA GPU(s) and 42' 4K displays | 24 GB to 512 GB | |||
Machine | OS | RAM | Procs | Count |
Apple MacBook Pro 15' most of them with SSD and retina display | varies | 40 |
Infrastructure Servers
Machine | OS | RAM | Procs | Count |
UltraSPARC-IIIi Sparcv9 processor | 2 GB | 2 | 1 | |
UltraSPARC-IIe Sparcv9 processor | 640 MB | 1 | 2 | |
UltraSPARC-IIe Sparcv9 processor | 512 MB | 1 | 1 | |
Intel(R) Core(TM)2 Quad CPU Q6600 @ 2.40GHz | 8 GB | 4 | 2 | |
AMD Opteron(tm) Processor 148 | 2 GB | 1 | 1 |
Public Servers
Machine | OS | RAM | Procs | Count | |
Intel(R) Xeon(R) CPU E3-1230 v3 @ 3.30GHz - Multi-Processor Server (with 8 processor) | 32 GB * 8 | Intel(r) Xeon(r) CPU E5540 @ 2.53GHz | 24 GB | 2 | 1 |
UltraSPARC-IIIi Sparcv9 processor | 2 GB | 2 | 2 | ||
UltraSPARC-IIe Sparcv9 processor | 256 MB | 1 | 1 | ||
AMD Opteron(tm) Processor 250 | 4 GB | 2 | 1 |
Development/Other
Machine | OS | RAM | Procs | Count |
Intel(R) Xeon Phi(TM) CPU 7210 @ 1.30GHz | 104 GB | 256 | 1 |
Información en españolTitle
Basu Bacteria Mac Os Catalina
and Mycobacteriumintracellulare.[1][2] MAC bacteria do not make most people sick. However, people with immune systems that do not work well (from HIV/AIDS or certain cancers for example) or people with lung disease (such as chronic obstructive pulmonary disease (COPD) or cystic fibrosis) are at the greatest risk for getting sick from MAC Infections. Elderly women are also at higher risk to get sick from MAC infections.[2][3]There are 3 types of MAC infections.
- Pulmonary MAC infections - Affect the lungs and are the most common type. These mainly affect elderly women and people who already have lung disease.[2][3]
- Disseminated MAC infections - Have spread throughout the body. This type is usually seen in people with advanced AIDS.[1]
- MAC-associated lymphadenitis - Causes swelling of the lymph nodes (especially in the neck) and is the most common in young children who have normal immune systems.[3][4]
The symptoms of pulmonary MAC infection start slowly, get worse over time and may last for weeks to months. People with pulmonary MAC infections may experience cough, weight loss, fever, fatigue, and night sweats.[2]
Symptoms of disseminated MAC infection include: [1][4]
- Fever
- Sweating
- Weight loss
- Fatigue
- Diarrhea
- Shortness of breath
- Abdominal pain
- Anemia
There have been a few reports of families with more than one family member with a MAC infection. In these families, it is thought that there is a variation in a gene or genes involved with the body's immune response. A genetic variant in an immune system gene may make some people more likely to get sick from an infection than others. There are many genes involved in the human immune response, and there is no single gene known to be responsible for MAC infections.[3][4]
Diagnosis of disseminated MAC infection is suspected based on symptoms and is confirmed in cultures of blood and often lymph node cells. Cultures of cells from urine, stool, liver or bone marrow may also be helpful. CT scans may be used to try to determine the different sites of infection in the body. If pulmonary or disseminated MAC infection is suspected, an HIV test may be done, as well as other tests, to rule out other associated medical conditions.[1][2][3]
A diagnosis of MAC lymphadenitis is confirmed by finding the bacteria in the culture of lymph node cells. These cells are collected by a biopsy of a swollen lymph node.[2][3]
- Pulmonary MAC infection, which affects the lungs
- Disseminated MAC infection, which affects many different parts of the body
- MAC lymphadenitis, which causes swollen lymph nodes
Treatment options for MAC infections vary by type of infection and by the presence of other medical conditions such as AIDS, cystic fibrosis, COPD, or cancer.[3]
Pulmonary MAC infections and disseminated MAC infections are usually treated with a combination of antibiotic medications. There are many types of antibiotics approved for treating MAC infections A combination of medicines is used because some of the disease-causing bacteria can be resistant to certain types of antibiotics. Using more than one antibiotic reduces the chance for the MAC bacteria to come back after treatment is over.[1][3]For people who have both HIV/AIDS and a MAC infection, treatment usually involves a combination of different antibiotics for the MAC infection and antiretroviral therapy to treat the HIV infection.[1][4]
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In special circumstances, there is some evidence to suggest that surgery to remove a single spot of infection in one lung can be helpful in people who have had a poor response to drug therapy. Surgery is usually only done when the infection is found in only one lung and the surgery won't cause any long-term harm.[3][4]Treatment of MAC lymphadenitis usually involves surgical removal of affected lymph nodes. Antibiotics may also be prescribed depending on the severity of infection and the response to surgery.[3]
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[4]FDA-Approved Treatments
The medication(s) listed below have been approved by the Food and Drug Administration (FDA) as orphan products for treatment of this condition. Learn more orphan products.- Liposomal amikacin(Brand name: Arikayce) - Manufactured by Insmed Incorporated
FDA-approved indication: September 2018, liposomal amikacin (Arikayce) was approved for the treatment of Mycobacterium avium complex (MAC) lung disease as part of a combination antibacterial drug regimen in patients who do not achieve negative sputum cultures after a minimum of 6 consecutive months of a multidrug background regimen therapy.
National Library of Medicine Drug Information Portal
Medline Plus Health Information
Mac Os Mojave
People who are HIV-positive with MAC infections may have a shortened lifespan depending on their immune systems and their response to HIV medications. For people who have had successful treatment, there is still a chance that the infection will come back, so people who have been sick from a MAC infection need to be monitored over time.[2][3]
In HIV-negative people with lung disease from a MAC infection, the treatment success rates range from 20-90% in different studies.[2] People with certain types of lung disease, people who are underweight, and people with anemia are more likely to have a poor outcome than other HIV-negative people affected by a MAC infection.
MAC lymphadenitis in children generally does not impact their health. In some cases, the condition may go away even without treatment.[3]
Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn about medical research and ways to get involved.
Clinical Research Resources
- ClinicalTrials.gov lists trials that are related to Mycobacterium Avium Complex infections. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.
Please note: Studies listed on the ClinicalTrials.gov website are listed for informational purposes only; being listed does not reflect an endorsement by GARD or the NIH. We strongly recommend that you talk with a trusted healthcare provider before choosing to participate in any clinical study.
Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group's website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
Organizations Supporting this Disease
- NTM Info & Research (supports pulmonary NTM infections)
550 Madruga Avenue, Suite 230
Coral Gables, FL 33146
Telephone: 305-667-6461, ext 26 and 32
E-mail: ntmmail@ntminfo.org
Website: http://www.ntminfo.org/
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
Where to Start
- The National Organization for Rare Disorders (NORD) has a report for patients and families about this condition. NORD is a patient advocacy organization for individuals with rare diseases and the organizations that serve them.
In-Depth Information
- Medscape Reference provides information on this topic. You may need to register to view the medical textbook, but registration is free.
- The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch's tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Mycobacterium Avium Complex infections. Click on the link to view a sample search on this topic.
- The AIDS Education and Training Center (AETC) offers information on Mycobacterium Avium Complex infections. Click on the link to view this information page.
Questions sent to GARD may be posted here if the information could be helpful to others. We remove all identifying information when posting a question to protect your privacy. If you do not want your question posted, please let us know.
- Currier JS. Mycobacterium avium complex (MAC) infections in HIV-infected patients. UpToDate. 2017; https://www.uptodate.com/contents/mycobacterium-avium-complex-mac-infections-in-hiv-infected-patients.
- Griffith DE. Overview of nontuberculous mycobacterial infections in HIV-negative patients. UpToDate. 2017; https://www.uptodate.com/contents/overview-of-nontuberculous-mycobacterial-infections-in-hiv-negative-patients.
- Daley CL. Mycobacterium avium Complex Disease. Microbiol Spectr. April, 2017; 5(2):https://www.ncbi.nlm.nih.gov/pubmed/28429679.
- Koirala J. Mycobacterium Avium-Intracellulare. Medscape Reference. 2018; http://emedicine.medscape.com/article/222664-overview.
- Disseminated mycobacterium avium complex disease. US Department of Health and Human Services. 2017; https://aidsinfo.nih.gov/guidelines/html/4/adult-and-adolescent-opportunistic-infection/326/mac.
- Diel R, Lipman M, Hoefsloot W. High mortality in patients with Mycobacterium avium complex lung disease: a systematic review. BMC Infect Dis. 2018; 18(206):1-10. https://bmcinfectdis.biomedcentral.com/track/pdf/10.1186/s12879-018-3113-x.